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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
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FORM 10-K
[X] ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(D) OF THE
SECURITIES EXCHANGE ACT OF 1934
FOR THE FISCAL YEAR ENDED JUNE 30, 1998
COMMISSION FILE NUMBER: 0-37159
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IOMED, INC.
(EXACT NAME OF REGISTRANT AS SPECIFIED IN ITS CHARTER)
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UTAH 87-0441272
(STATE OR OTHER JURISDICTION OF (I.R.S. EMPLOYER
INCORPORATION OR ORGANIZATION) IDENTIFICATION NO.)
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3385 WEST 1820 SOUTH, SALT LAKE CITY, UTAH 84104
(ADDRESS OF PRINCIPAL EXECUTIVE OFFICES) (ZIP CODE)
(801) 975-1191
(REGISTRANT'S TELEPHONE NUMBER, INCLUDING AREA CODE)
SECURITIES REGISTERED PURSUANT TO SECTION 12(B) OF THE EXCHANGE ACT:
COMMON STOCK, NO PAR VALUE
Indicate by check mark whether the registrant (1) has filed all reports
required to be filed by Section 13 or 15(d) of the Securities Exchange Act of
1934 during the preceding 12 months (or for such shorter period that the
registrant was required to file such reports), and (2) has been subject to such
filing requirements for the past 90 days [ X ] Yes [ ] No.
Indicated by check mark if delinquent filers pursuant to Item 405 of
Regulation S-K is not contained herein, and will not be contained, to the best
of registrant's knowledge, in definitive proxy or information statements
incorporated by reference in Part III of this Form 10-K or any amendment to this
Form 10-K.[ ]
The aggregate market value of the Registrant's voting stock held by
non-affiliates based upon the closing price of the common stock as quoted on the
American Stock Exchange on September 1, 1998 was approximately $10,853,836.
The number of shares of Registrant's common stock outstanding on September
1, 1998, was 6,499,518.
DOCUMENTS INCORPORATED BY REFERENCE
Certain information is incorporated into Part III of this Report on Form
10-K by reference to the Registrant's Proxy Statement for its 1998 Annual
Meeting of Shareholders.
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TABLE OF CONTENTS
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PART I
Item 1 -- Business.................................................... 1
Item 2 -- Properties.................................................. 18
Item 3 -- Legal Proceedings........................................... 18
Item 4 -- Submission of Matters to a Vote of Security Holders......... 18
PART II
Item 5 -- Market for Registrant's Common Equity and Related
Stockholder Matters......................................... 19
Item 6 -- Selected Consolidated Financial Data........................ 20
Item 7 -- Management's Discussion and Analysis of Financial Condition
and Results of Operations................................... 22
Item 7a -- Quantitative and Qualitative Information about Market
Risk........................................................ 33
Item 8 -- Financial Statements and Supplementary Data................. 33
Item 9 -- Changes and Disagreements with Accountants on Accounting and
Financial Disclosure........................................ 33
PART III
Item 10 -- Directors and Executive Officers of the Company............. 50
Item 11 -- Executive Compensation...................................... 50
Item 12 -- Security Ownership of Certain Beneficial Owners and
Management.................................................. 50
Item 13 -- Certain Relationships and Related Transactions.............. 50
PART IV
Item 14 -- Exhibits, Financial Statement Schedules, and Reports on Form
8-K......................................................... 50
Signatures................................................................... 54
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PART I
ITEM 1. BUSINESS
FORWARD-LOOKING STATEMENTS
Certain statements contained in this report on Form 10-K (the "Report") are
"forward-looking statements" within the meaning of Section 21E of the Securities
and Exchange Act of 1934, as amended. Such forward-looking statements may be
identified by the use of terminology such as "may," "will," "expect,"
"anticipate," "intend," "designed," "estimate," "should," or "continue" or the
negatives thereof or other variations thereon or comparable terminology. Such
forward-looking statements involve known and unknown risks, uncertainties and
other factors which may cause the actual results, performance or achievements of
IOMED, Inc. and its subsidiary Dermion, Inc. (collectively the "Company"), or
industry results, to be materially different from any future results,
performance or achievements expressed or implied by such forward-looking
statements. These risks, uncertainties and other factors include, among other
things, the following: the Company's sporadic history of profitability and the
continuing uncertainty of its profitability; the Company's ability to develop
and introduce new products; the uncertainty of market acceptance of the
Company's new and existing products and their market penetration; the
uncertainties related to the Company's product development programs; the
Company's reliance on collaborative partners and licenses; the Company's limited
sales, marketing and distribution experience and current dependence on
distributors; the risks associated with obtaining governmental approval of the
Company's products; the highly competitive industry in which the Company
operates and the rapid pace of technological change within that industry; the
uncertainty of patented and proprietary technology protection and the Company's
reliance on such patented and proprietary technology (including reliance on
technology licensed from third parties); changes in or failure to comply with
governmental regulation; the uncertainty of third party reimbursement for the
Company's products; the Company's dependence on key employees; general economic
and business conditions and other factors referenced in this Report.
INTRODUCTION
The Company commercializes controllable drug delivery systems using
iontophoretic technology. Iontophoresis is a non-invasive method of enhancing
and controlling the transport of water-soluble ionic drugs into and through the
skin using a low level electrical current. The Company's proprietary
iontophoretic drug delivery systems allow rapid onset and cessation of
therapeutic action, as well as programmable dose control. The flexibility of the
Company's proprietary systems provides therapeutic control not possible with
many alternative drug delivery methods, including oral tablets and capsules,
injections, inhalants and passive transdermal patches. The Company's systems may
also increase bioavailability, safety and patient comfort.
The Company currently markets two products, an iontophoretic system used to
deliver dexamethasone sodium phosphate ("Dexamethasone") and an iontophoretic
system used to deliver Iontocaine. The Company's system for the delivery of
Dexamethasone has been used primarily by physical therapists and athletic
trainers in over 11 million patient applications for the treatment of acute
local inflammatory conditions such as tendonitis, tennis elbow and carpal tunnel
syndrome. The Company's system to deliver Iontocaine provides needle-free,
long-lasting local dermal anesthesia up to six times more rapidly and up to
three times deeper than can be achieved using topical anesthetic creams. The
Company is initially marketing its Iontocaine product under the brand name Numby
Stuff in pediatric hospitals in the United States. The Company is also
developing a number of iontophoretic drug delivery systems for other
indications, including conscious sedation, tocolysis, and post operative and
chronic pain control.
The Company was incorporated in Utah in 1974 as Motion Control, Inc. In
1987, the Company merged with JMW Acquisition Corporation, and the name of the
merged entity was changed to IOMED, Inc. All references to the Company include
the Company's predecessor entities, as well as Dermion, Inc. ("Dermion"), the
Company's wholly-owned subsidiary.
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BACKGROUND ON DRUG DELIVERY SYSTEMS
A wide variety of drug delivery methods are currently available in the
market, although not all drugs can be delivered by all routes of administration.
For certain applications, there are clinical benefits in providing rapid onset
of therapeutic action and the minimum drug dosage necessary to achieve the
desired effect. In all applications, drug delivery should be convenient, cost
effective and as non-invasive as possible.
Conventional Oral Methods. Conventional oral drug dosage forms, such as
pills and capsules, are the most common types of drug delivery. These methods
offer ease of administration and low cost-per-use, but their application is
often limited by inconvenient dosage intervals and less than optimal
bioavailability (due to degradation of the drug in the gastro intestinal tract
("GI tract") and the liver) and efficacy. In addition, conventional oral dosage
forms often produce higher initial drug levels than are required to achieve the
desired therapeutic effects, thereby increasing the risk of side effects and
lower than therapeutically optimal levels of the drug as it is metabolized and
cleared from the body. More frequent administration of lower doses can sometimes
mitigate this problem, but can also increase cost, inconvenience and patient
noncompliance.
Injection Methods. Injectable drug dosage forms generally provide rapid
onset of action and offer many of the same advantages as conventional oral drug
dosage methods. Like conventional oral dosage forms, however, they often produce
higher initial drug levels than are required to achieve the desired therapeutic
effect, thereby increasing risk of side effects. Injectable drug delivery
methods require caregiver administration and have the added disadvantage of
using needles as a delivery path into the body, raising the possibility of
needle stick injuries, as well as risk of infection to the caregiver and the
patient. The use of needles also increases patient anxiety due to the pain of
injection.
Controlled Release Methods. Controlled release drug delivery systems
attempt to overcome many of the limitations inherent in conventional drug
delivery methods by maintaining a more consistent and appropriate drug level in
the bloodstream. Sustained release oral dosage forms are designed to release the
active ingredients of the drug into the body at either a predetermined point in
time or at a predetermined rate over an extended period of time, but they
generally do not provide rapid onset of action and may not achieve optimal
bioavailability. Passive transdermal patches allow absorption of drugs through
the skin and generally provide a convenient method of administering drugs at a
steady rate over an extended period of time, but onset of action may take hours
after application, and absorption of the drug may continue for hours after the
patch is removed, which can increase side effects. Additionally, because human
skin is an effective barrier, most drug formulations will not passively permeate
the skin in therapeutic quantities. Continuous infusion pumps introduce drugs
directly into the body, thereby providing rapid onset of action, and may offer
variable controlled dosing. Infusion therapy requires insertion of a needle,
however, and, therefore, can be painful and threatening to the patient. The use
of infusion pumps also increases the risk of infection and generally requires
medical professionals for safe administration, which may significantly increase
costs.
Pulmonary and Nasal Methods. Both pulmonary (inhalation) delivery and nasal
sprays are designed to provide rapid onset of action or to deliver drugs that
are not orally bioavailable. Pulmonary delivery has the disadvantage of variable
drug amounts reaching the alveoli of the lungs, therefore making it difficult to
control the bioavailability of the dose. Nasal sprays can cause irritation in
some patients and can be difficult to administer in variable intranasal
conditions. In addition, the dose of the product cannot be controlled by the
patient over a period of time, and patients and caregivers may have difficulty
maintaining the desired therapeutic effect.
Other. Many existing and emerging pharmaceutical compounds, such as
biotechnology-derived oligonucleotides, peptides and other macromolecular drugs,
cannot be effectively administered by traditional non-invasive methods and are,
therefore, administered only by injection or infusion. Oral delivery of such
molecules is generally inefficient due to the rapid breakdown of the molecules
during digestion and the natural impermeability of the GI tract to larger
molecules. The skin is even less permeable to macromolecules than the GI tract,
which the Company believes is the primary reason passive transdermal delivery of
those molecules using patch technology has not been successful to date.
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IONTOPHORETIC DRUG DELIVERY AND ITS ADVANTAGES
Iontophoretic drug delivery systems are designed to overcome many of the
limitations associated with many other drug delivery methods. Iontophoresis is
an active method of transdermal drug delivery in which water-soluble, ionized
(electrically charged) drugs are transported through the skin for local or
systemic therapeutic applications by applying a low level, external electrical
current. The amount of drug delivered through the skin is proportional to the
total electrical charge applied (which is a function of time and current).
Therefore, it is possible to program the system's electrical current levels to
control more precisely the desired drug dose, delivery rate and the pattern of
delivery.
Iontophoretic drug delivery systems are generally comprised of a power
supply which is used to control drug dose (the "dose controller") and a pair of
electrodes, one containing the drug and one serving as a grounding electrode to
complete the electrical circuit through the skin. The drug delivery electrode is
applied to the patient's skin at a local treatment site (such as for joint or
tendon soreness or to induce local dermal anesthesia), or at any suitable site
on the body for systemic drug delivery. The grounding electrode is applied to
the skin a short distance away from the drug electrode. When an electric current
with the same positive or negative electric charge as the drug is applied to the
drug electrode, the drug is repelled from the electrode and into the skin in the
same way as like poles of two magnets repel each other. Although the Company's
currently marketed products consist of discrete components, the Company has
begun the development of more advanced systems which integrate all components in
a single miniaturized patch.
The Company believes that, for certain applications, iontophoretic drug
delivery systems may offer several advantages over other drug delivery methods,
including:
Broad Applicability. A substantial number of the drugs on the market and in
development today are, the Company believes, ionic and water-soluble and,
therefore, may be amenable to delivery by iontophoresis. In addition,
iontophoretic drug delivery systems may be applicable to a significantly broader
range of pharmaceutical compounds, including larger drug molecules such as
peptides and oligonucleotides, than passive transdermal drug delivery methods.
Increased Convenience and Compliance. Iontophoretic drug delivery systems
are easy to use and offer simple, needle-free administration that eliminates the
inconvenience of frequent dosing, and may, if successfully developed and
approved by applicable regulatory authorities, permit patient
self-administration.
Programmable Control of Drug Delivery. The rate, timing and pattern of drug
delivery using an iontophoretic drug delivery system can be controlled by
varying the electrical current applied to the system's electrodes. The benefits
of this ability to control the drug's delivery include the following:
- Rapid Onset of Action -- The speed with which a drug delivery system can
provide efficacious blood levels of the target drug determines the onset
of therapeutic action. Iontophoretic drug delivery systems allow many
drugs to pass directly through the skin into underlying tissue and the
bloodstream at a rate that is significantly more rapid than oral or
passive transdermal delivery methods. Research has shown that certain
drugs can be delivered by iontophoresis 10 to 1,000 times faster than
drug delivery by passive transdermal patches.
- Rapid Cessation of Administration -- In certain applications, it is
desirable that drug delivery cease once the desired effect has been
obtained. Iontophoretic drug delivery systems allow rapid cessation of
drug delivery since absorption of water-soluble drugs from the skin into
the bloodstream ceases rapidly after the current is turned off or the
drug electrode is removed from the skin.
- Variable Dose Control -- Iontophoretic drug delivery systems may be
designed to offer precision controlled dosing that can be customized for
desired therapeutic profiles or for individual patient needs, including
baseline and/or bolus dosing.
- Patient Controlled Dosing -- Iontophoretic drug delivery systems may be
designed to offer active patient control or intervention in the dosing
regimen, while at the same time incorporating programmed lock-outs for
added safety and dose monitoring capability.
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- Dose-to-Effect -- Iontophoretic drug delivery systems allow caregivers or
patients to monitor the onset of drug effectiveness and maintain,
progressively reduce or cease drug administration once a desired
therapeutic effect is observed.
THE COMPANY'S IONTOPHORETIC SYSTEMS
While the fundamentals of iontophoresis have been understood for decades,
the method has become commercially practicable as a means for delivering drugs
only recently as a result of advances in electronics, materials science and
electrochemistry. These advances have led to the development of more efficient
and adaptable drug containment electrodes and more reliable, compact and
programmable dose controllers. The Company has developed iontophoretic drug
delivery systems which incorporate dose controllers and electrodes that have
enhanced performance characteristics, which the Company believes are adaptable
to a number of clinical settings and therapeutic applications, and which the
Company believes are cost effective in a number of therapeutic applications. The
Company's current iontophoretic drug delivery systems are not designed to
facilitate patient self-administration, but drug delivery systems currently
being developed by the Company may allow patients significant control over the
administration of certain drugs.
In March 1997, the Company entered into a series of agreements with Elan
Corporation, plc ("Elan") pursuant to which the Company acquired certain
in-process research and development programs, including exclusive world-wide
rights to the commercial exploitation of certain technology developed by Elan in
the field of iontophoretic drug delivery and certain other electro-transport
fields (the "Elan Agreements"). The acquisition of the Elan technology is
intended to speed the development and commercialization of products using a
combination of the Company's and Elan's technology, including the miniaturized
integrated, wearable systems currently under development by the Company. The
Company also believes its competitive position in relation to other companies
engaged in the development of iontophoretic drug delivery systems has been
significantly enhanced by Elan's broad base of United States and foreign
patents, in-depth body of in vitro drug transport data and in vivo animal and
human clinical data, in addition to other proprietary know-how.
Dose Controllers. The Company's dose controllers generate the low-level
electrical current needed for iontophoretic drug delivery. The Company presently
markets a compact, fully portable dose controller, the Phoresor(R), that offers
durable microprocessor control, enhanced user interface, versatile programmable
dosing capability, autocalculating treatment time (based on electrical current
settings and selected dose) and constant current output (by automatically
adjusting voltage to compensate for variations in the electrical resistance of
the skin). The Phoresor incorporates a microprocessor, other electronic
circuitry, on-board software that monitors and controls the rate of current
flow, and an easy-to-use control panel. The Company has also developed and
markets a new dose controller for specific use with its pediatric local dermal
anesthetic product. The Company's next generation of dose controllers, both
stand-alone and wearable miniaturized versions, are being designed to include
many of the same features as the Company's current dose controllers. Depending
on the therapeutic application, the new generation dose controllers may be
designed to allow bolus dosing capability and programming (using a physician's
or pharmacist's key) to adjust dosing to match desired delivery profiles or
patterns.
In a clinical setting for short treatment durations, the battery and dose
controller are housed in a small, discrete, reusable unit connected to a pair of
disposable, single-use electrodes to which drug solution is added immediately
prior to application to the patient. This technology is used in the Company's
current products. For longer term or chronic applications or
patient-administered therapy outside the clinical setting, the Company is
developing iontophoretic drug delivery systems in which the battery, dose
controller and electrodes will be combined in a small patch applied to the skin
as a single, integrated unit. The electronic components may be reusable, with
replaceable or rechargeable batteries and single-use, disposable drug and
grounding electrodes, or the entire unit may be disposable after a single use.
The drug may be added to the electrode drug pad during manufacturing, or may be
stored separately in the system and introduced into the drug containment pad
immediately before use by means of proprietary, integrated hydration devices
developed by the Company.
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Electrodes. Electrode design is critical to successful delivery of a drug
by iontophoresis. The Company's electrodes incorporate patented and proprietary
design innovations which the Company believes offer significant advantages to
both patients and health care providers. The Company's proprietary electrode
technology includes patented polymer hydrogels which absorb drug solutions in
seconds, becoming soft and pliable so as to conform better to the body and to be
comfortable to the patient. The Company's electrode technology also employs
special silver and silver chloride inks to distribute electric current more
evenly from the dose controller to the electrodes and control possible changes
in acidity and alkalinity (pH changes) which can occur during iontophoresis.
BUSINESS STRATEGY
The Company's primary business goal is to establish its proprietary
iontophoretic drug delivery systems as a preferred, cost effective means of
delivering a wide range of drugs. To achieve this goal, the Company uses its
multi-disciplinary expertise in pharmacology and drug formulation, regulatory
and product testing, microelectronics, electrochemistry, polymer chemistry and
adhesives. The Company's strategy for achieving this goal includes the following
principal elements:
Develop Systems for Off-Patent Drugs. The Company intends to continue the
independent development of proprietary iontophoretic drug delivery systems for
off-patent drugs with known safety and efficacy and for which the Company
believes its drug delivery technology may be cost competitive with and offer
advantages over other drug delivery methods. The Company believes that, by
developing proprietary products based on currently approved off-patent drugs,
rather than new chemical entities ("NCEs"), it can reduce regulatory and
development risks and shorten the product development cycle for certain
products.
Enter into Collaborative Relationships. In order to gain access to NCEs and
other proprietary drugs, and to reduce the costs and risks associated with the
development of iontophoretic drug delivery systems for such compounds, the
Company intends to enter into collaborative relationships with pharmaceutical
and other biotechnology companies whose drugs could benefit from the Company's
iontophoretic drug delivery technology.
Increase Market Penetration of Existing Products. In order to leverage the
capabilities of its limited number of sales personnel, the Company intends to
expand its existing dealer distribution network and seek additional
collaborative sales and marketing relationships with other parties that have
specific expertise in markets targeted by the Company. In general, the Company
intends to use collaborative sales and marketing relationships in the sale and
distribution of its products.
In addition, the Company is actively seeking to expand the commercial
potential of its local anesthesia and acute inflammation products by pursuing
new applications. The Company will continue to support (i) marketing studies
aimed at expanding the use of its delivery system for Iontocaine to a broader
range of procedures and (ii) clinical trials to further establish the safety and
efficacy of iontophoresis for the treatment of local inflammation using
Dexamethasone or for use in other specific procedures.
Broaden Technology Platform. The Company intends to enhance its proprietary
iontophoretic technology base principally through internal research and
development. The Company will also pursue additional iontophoretic and other
complementary products and technologies owned or developed by third parties, on
a case-by-case basis, through in-licensing or acquisition.
Control Product Manufacturing Processes. The Company has historically
maintained control over the manufacture of its electrode kits in order to retain
control over the quality of its products and capture a larger portion of the
product revenue stream when third parties are involved in the marketing of the
product.
PRODUCTS AND PRODUCTS UNDER DEVELOPMENT
The Company currently has product development programs at various stages of
development for acute local inflammation, local dermal anesthesia, remission of
pre-term labor, conscious sedation and pain control. The following table lists
the therapeutic applications of the principal products developed or currently
under development by the Company. This table is qualified in its entirety by
reference to the more detailed
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descriptions set forth elsewhere in this Report. There can be no assurance that
any products under development will be developed successfully or approved in a
timely manner, if at all, or even if developed or approved, be successfully
manufactured or marketed. In addition, the status of development indicated below
does not necessarily indicate the order in which the products shown may be
submitted to or approved by the Food and Drug Administration ("FDA").
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APPLICATION THERAPEUTIC AGENT PRODUCT STATUS
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Acute local inflammation Dexamethasone Currently marketed (1)
Local dermal anesthetic Iontocaine Currently marketed
Pain control Hydromorphone Phase II clinicals (2)
Conscious sedation Fentanyl Phase I clinicals (3)
Local mucosal anesthetic Iontocaine Preclinical
Remission of pre-term labor Terbutaline Preclinical
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(1) Currently marketed under a 510(k) clearance for use with "ions of soluble
salts or other drugs." The Company is revising its Phase III protocols and
pending subsequent evaluation may file an NDA.
(2) Initial Phase II clinical studies were conducted by Elan. The Company
acquired the rights to the data from those studies under the Elan
Agreements. The Company will be required to conduct expanded Phase II and
Phase III clinical trials.
(3) The Company has conducted, or participated in the conduct of, two
independent human blood level studies for the iontophoretic delivery of
fentanyl.
ACUTE LOCAL INFLAMMATION
Acute local inflammatory conditions resulting from exercise, sports
injuries, trauma or repetitive motion disorders are among the leading types of
injuries occurring in the workplace and among physically active adults. The most
common of these injuries include tendonitis, bursitis, carpal tunnel syndrome
and epicondylitis (tennis elbow). Generally, patients suffering from these
conditions are initially treated with oral nonsteroidal anti-inflammatory drugs
("NSAIDS") for a period of up to fourteen days. Although steroid injections are
generally more effective than NSAIDS, medical professionals usually avoid
steroid injections in all but severe cases because of the negative side effects
that can accompany bolus needle injections of corticosteroids into an inflamed
joint or tendon, including risk of infection, tissue distortion, tendon
weakening and tendon rupture. If patients do not respond to treatment with
NSAIDS, the physician generally has two options -- refer the patient to a
physical therapist, or proceed with injection of anti-inflammatory steroids such
as Dexamethasone. Based on market data with respect to the number of
corticosteroid injections for acute inflammation, as well as data gathered by
the Company in a survey it conducted of 54 physical therapy clinics around the
United States with respect to the number of patients that visit physical therapy
clinics for acute inflammation, the Company estimates that the total potential
retail market in the United States for the sale of iontophoretic drug delivery
systems to clinicians to treat acute local inflammatory conditions may be in
excess of $400 million. In addition, the Company estimates that current total
retail sales into this market by the Company and its competitors are
approximately $35 million.
The Company believes iontophoretic delivery of Dexamethasone provides
significant advantages over other current treatment regimens for acute local
inflammation. The Company believes iontophoresis eliminates many of the risks
and much of the inconvenience associated with bolus steroid injections, avoids
the systemic side effects of oral steroids and eliminates the significant
incidence of GI tract side effects of orally administered NSAIDS. The Company
believes iontophoresis also increases therapeutic efficacy by bypassing
metabolism by the liver, by reducing the possibility of overdosing, and by
providing localized delivery at the target site without trauma. As a result, the
Company believes that it may be advantageous to introduce the iontophoretic
delivery of Dexamethasone into the initial treatment regimen for acute local
inflammation. The Company believes that earlier treatment with Dexamethasone has
the potential to significantly increase the rate of patient recovery and, in
doing so, reduce the overall cost of patient treatment.
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Commercial Products. The Company pioneered the commercial introduction of
an iontophoretic drug delivery system for the treatment of local acute
inflammation in 1979. The product is used principally by physical therapists
(under a doctor's prescription) and has been administered in over 11 million
patient treatments for the iontophoretic delivery of Dexamethasone. More than 9
million of these treatments occurred since 1990, when advancements in electrode
technology made by the Company led to the introduction of its present family of
gel electrodes for use with its microprocessor controlled dose controllers. The
Company's system for the delivery of Dexamethasone is also used by athletic
trainers and physical therapists serving a number of professional athletes,
including professional golfers and tennis players, men's and women's Olympic ski
teams and professional football, basketball and hockey teams. The Company
believes that iontophoretic drug delivery systems have been accepted in the
rehabilitation marketplace due to their ease of use, non-invasiveness,
recognized efficacy and lack of significant side effects.
The Company currently markets nine different electrode kits in four
different configurations and continues to develop additional electrode kits and
configurations for application in different segments of the acute local
inflammation market. The Company's existing electrode kits, as well as those it
has under development, are designed to be user friendly and to offer clinicians
a broad range of electrode sizes, formats, configurations and price ranges.
Products Under Development. Currently, due to limited labeling of
Dexamethasone, neither the Company nor its competitors has the requisite
regulatory approval to promote the use of iontophoretic drug delivery systems
specifically for the delivery of Dexamethasone. The Company believes that its
inability to do so limits its ability to market its system, particularly to the
physician market. The Company further believes that to market iontophoretic drug
delivery systems for a specific drug and therapeutic indication the FDA requires
that each new drug/device combination be approved through a New Drug Application
("NDA"). Therefore, in order to expand the Company's sales of its delivery
systems into the physician market as a first line treatment for acute local
inflammation, the Company has filed an investigational new drug application
("IND") with the FDA. Pending further evaluation of clinical design and
protocols and clarification of the FDA's requirements for an NDA, followed by a
revised economic benefits analysis, the Company may initiate clinical studies in
support of an NDA seeking FDA approval to label a formulation of Dexamethasone
for use with the Company's iontophoretic drug delivery systems. The Company
believes the approval of an NDA (if obtained) would allow the Company to more
actively promote the iontophoretic delivery of Dexamethasone to family
physicians, orthopedists, neurologists and sports and industrial medicine
clinics.
LOCAL DERMAL ANESTHESIA
Medical care providers have long recognized the importance of the
management of pain, including pain associated with certain minimally invasive
medical procedures such as needle injections; venous access (including
phlebotomies and intravenous catheterizations); lumbar punctures; and local
dermatological, gynecological and urological procedures such as wart and mole
removal, LOOP/LETZ procedures, biopsies (including fine needle, punch,
excisional, shave and cervical biopsies), Mohs procedures and vasectomies. To
address this concern, local dermal anesthetics are widely used in medical
practice.
The primary means of administering local dermal anesthetics is by needle
injection, which has the benefit of being fast, effective and long lasting.
However, the fear and pain associated with the needle stick, especially on the
extremities or on other sensitive areas such as the face, vulva and cervix is
compounded by the sting associated with virtually all injectable local
anesthetics. These factors increase patient discomfort and anxiety. In addition,
the local tissue distortion which typically accompanies injections may cause
procedural difficulty for the physician. New topical analgesic formulations have
recently been introduced into the market and are gaining widespread acceptance,
especially in pediatric hospitals and clinics and in pediatric dermatology.
These topical formulations avoid many of the pitfalls of anesthetic injections,
but they generally require significant advance preparation since they take one
to two hours to obtain anesthesia. Even when topical formulations are given
adequate time to achieve anesthesia, they anesthetize only to a maximum depth of
3 to 5 mm. The time required to achieve therapeutic anesthesia and the depth of
anesthesia make these formulations less suitable or impractical for many
potential applications. The Company believes that the
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growing interest in these products, in spite of their clinical limitations, is a
positive indication of the market's desire for an effective, needle-free local
dermal anesthetic.
Commercial Products. The Company's Iontocaine brand of lidocaine HCl 2% and
epinephrine 1:100,000 is FDA approved under an NDA and is specifically labeled
for use with the Company's Phoresor and its proprietary, single use, disposable
electrode kits. The Iontocaine delivery system was shown to be safe and
effective in double blinded, placebo controlled, randomized studies in over 400
adult and pediatric patients. Based on these studies, the Company filed an NDA
with the FDA and received labeling to use the system for all procedures
requiring local dermal anesthesia.
Using the Company's product, clinicians can administer needle-free, long
lasting (up to two hours) local dermal anesthesia up to a depth of 10 mm in
approximately ten minutes. The Company believes the ability to provide painless
local dermal anesthesia up to three times deeper than topical formulations, and
in 85% less time, could make the Company's products a preferred drug delivery
method for many existing applications where topical anesthetic creams are
currently employed, and that the product will provide a means of painlessly
inducing local dermal anesthesia for a broader range of medical procedures where
the use of such creams is not practical.
A leading concern among patients, parents and health care professionals is
the control of pain in the practice of children's medicine, including the pain
associated with needle insertions. With the growing acceptance of topical
anesthetic creams in the pediatric hospital setting, the Company believes there
is a large potential market for an iontophoretic drug delivery system targeted
toward pediatrics. Accordingly, the Company has focused its initial local dermal
anesthesia product launch into the pediatric market under the brand name Numby
Stuff. Numby Stuff, which the Company launched in January of 1997, currently
consists of the Phoresor, the Company's line of proprietary, single use,
disposable electrode kits and Iontocaine, all in a brightly colored, child
friendly product package. Numby Stuff is currently being used to induce local
dermal anesthesia prior to pediatric intravenous starts, blood draws and other
invasive procedures, and the Company believes it provides a cost effective
alternative to the leading topical product. The Company estimates that pediatric
intravenous starts, blood draws and other invasive procedures are performed more
than 20 million times in the United States each year.
The Company has developed a preprogrammed, fixed-dose, dose controller with
push-button operation for use as part of the Numby Stuff product. This new dose
controller was cleared by the FDA in April 1998. The Company believes that the
new dose controller's lower manufacturing cost, anticipated pricing and
simplified operation will enhance the marketability and use of Numby Stuff.
At the Company's request, Numby Stuff was reviewed by the new product
review committee of the Alliance of Children's Hospitals ("ACH"), a consortium
of 36 free standing children's hospitals in the United States. Following the
review, in December 1996, the Company acquired a right from ACH to use ACH's
Seal of Acceptance in the commercialization of Numby Stuff.
Products Under Development. In order to achieve greater market acceptance
of its Iontocaine product in pediatric markets, the Company supports evaluations
conducted by doctors and other medical personnel for the use of its anesthetic
product prior to a wide variety of painful medical procedures. The Company is
currently conducting or planning two studies evaluating the use of Numby Stuff
prior to lumbar punctures and circumcisions in pediatric patients. Depending on
the results of these studies, the Company may develop new electrode kits which
specifically address these opportunities. The Company also believes, in addition
to the pediatric market, the adult hospital market represents additional
opportunities for growth. The Company believes that it could service the adult
hospital market through a collaborative marketing partner by making minor
modifications in its product image. For example, according to published studies,
there are over 250 million venous catheters inserted each year, of which a large
percentage are inserted in adult patients.
The Company also believes Iontocaine, together with the Phoresor and
adaptations of its existing electrode designs, can be successfully used to
induce effective local dermal or mucosal anesthesia prior to certain
gynecological procedures. The Company believes the effective, rapid, painless,
needle-free anesthesia
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provided by the Company's drug delivery technology would increase patient
comfort. In general, the Company believes the promotion of the Company's systems
for use in connection with gynecological procedures involving mucosal membranes
would require additional FDA approval, most likely in the form of a supplement
to the Company's existing Iontocaine NDA. The Company does not believe
gynecological procedures involving the vulva would require additional FDA
approval. The Company has performed preliminary studies which indicate that its
anesthetic system may significantly reduce or eliminate the pain of vulvar
biopsies. The Company has already tested prototype electrodes which are
specifically designed for this application. There are approximately 50 million
pap smears performed each year in the United States, of which the Company
estimates approximately 2.5 million require follow-up procedures that could
benefit from non-invasive local dermal anesthesia. The majority of these
procedures are performed by a relatively small number of gynecologists who are
mainly located in high density population areas.
REMISSION OF PRE-TERM LABOR
Pre-term birth is a leading cause of neonatal morbidity and mortality. Each
year in the United States alone, 10% of all births are premature, resulting in
more than 400,000 babies being born before completing 37 weeks of gestation. The
cost of neonatal intensive care required for pre-term babies exceeds $5.0
billion a year in the United States. The Company believes prolonging pregnancies
threatened by pre-term delivery by even a few days may result in improved
clinical outcomes, which could represent an important opportunity for
significant medical, economic and social benefits.
The Company estimates that each year a significant number of patients in
the United States who are at risk for or experience pre-term labor and pre-term
birth are placed on one or more forms of tocolytic drug therapy. Tocolysis is
the clinical term for the remission of labor. Although many of these therapies
are not specifically FDA approved, the medical literature indicates that they
have been successful in a large number of patients. The Company believes the
number of patients placed on various tocolytic drug therapies will rise with the
increased use of ambulatory external tocodynamometers and the advance of other
new diagnostic techniques and products used to identify patients at risk. These
advances in diagnostics should aid in identifying asymptomatic pregnant women.
A typical therapeutic program for a pregnant woman who is experiencing
acute episodes of pre-term labor consists of intravenous ("IV") infusions of
magnesium sulfate in the hospital. After a period of 12 to 24 hours of
successful tocolysis, the patient is then switched to oral terbutaline sulfate
tablets and released. Usually, after two to three weeks, the therapeutic effects
of oral terbutaline are lost and the patient must be readmitted to the hospital
to begin the treatment cycle again. If symptoms persist, the patient is often
placed on an injectable form of terbutaline sulfate by means of a subcutaneous
infusion pump. Although not approved by the FDA for this indication,
subcutaneous infusion terbutaline therapy has been found to be effective in
controlling pre-term labor and avoiding the loss of therapeutic efficacy
experienced with oral dosing. Subcutaneous infusion terbutaline therapy can last
for over a month, with a mean treatment period of approximately three weeks, and
costs approximately $1,500 to $2,000 per week. Those costs include pump rental,
drugs, disposable infusion kits and central monitoring and home visits by a
skilled medical professional.
Products Under Development. The Company is evaluating a system for
delivering terbutaline using iontophoresis. Based on in vitro feasibility tests
it has conducted, the Company has determined that terbutaline may be delivered
by iontophoresis in therapeutic quantities. The Company intends to seek NDA
approval for the delivery of terbutaline for remission of pre-term labor using
its iontophoretic drug delivery system. The Company has successfully completed
an initial blood level study in healthy volunteers. The results of this study
showed that blood levels of terbutaline, within the anticipated therapeutic
range, were achievable using iontophoresis and that the dosing capabilities of
the system would very closely match the delivery profile of terbutaline therapy
using subcutaneous infusion. The Company is currently finalizing a protocol and
preparing to initiate a second blood level study to be conducted in pregnant
women at a leading medical institution, specializing in women's health. The
Company believes that an iontophoretic drug delivery system for terbutaline
could offer an alternative treatment regimen to oral terbutaline therapies with
all of the benefits of home infusion therapy. The Company also believes an
iontophoretic system may have substantial advantages over subcutaneous infusion
therapy, including being less expensive to produce and service than
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standard infusion therapy devices, potentially providing greater patient comfort
(since the electrodes could be placed at various sites on the body) and being
non-invasive, thereby eliminating the risk of infection and reducing the need
for frequent intervention by a skilled medical professional.
Since the general pharmacology and toxicology of terbutaline are well
known, and because the Company believes this is an area of significant interest
within both the FDA and the medical community, the Company believes that, if,
upon completion, its Phase I blood level studies are deemed successful, it may
be able to progress more rapidly into Phase III studies in at-risk, pregnant
women than would be possible for an NCE. Due to the nature of the condition
being treated, the Company believes the clinical trials should be of relatively
short duration and will have a clearly defined endpoint.
CONSCIOUS SEDATION
Many patients, especially children, experience extreme anxiety before the
start of invasive or painful medical procedures, during stressful diagnostic
tests such as endoscopies, magnetic resonance imaging, and CT scans, and before
and during certain dental and emergency room procedures. Invasive methods of
premedication and sedation, such as intramuscular ("IM") injections or IV
administration of analgesics or sedatives, can cause anxiety. Clinicians have
long sought alternative, non-invasive methods of premedication. Despite the
absence of approved labeling for safety and efficacy for oral administration,
clinicians widely use injectable drugs and drug combinations mixed with flavored
syrups for off-label oral administration in children. Since 1994, clinicians
have also been able to use fentanyl for conscious sedation using an oral
transmucosal delivery system. Oral administration may require up to five times
the amount of drug recommended for injection because of decreased
bioavailability, but is used because the alternative of IV or IM injections are
counterproductive to the goal of relieving anxiety. Based on market data, the
Company estimates that annual worldwide sales of the top two products used for
conscious sedation are approximately $950 million.
Products Under Development. The safety and efficacy of fentanyl as a drug
to induce conscious sedation are well known. Data from two human blood level
studies with fentanyl conducted by the Company and a former collaborative
partner show that it may be possible for therapeutic quantities of fentanyl to
be delivered by iontophoresis. Therefore, the Company believes it could
represent a viable drug for inducing conscious sedation using the Company's
iontophoretic drug delivery systems. The Company's ability to market a product
in the United States using fentanyl may also be limited by certain litigation
now before the United States Patent and Trademark Office (the "PTO").
PAIN MANAGEMENT
The Company estimates that of the 24 million surgeries performed each year
in the United States, 75%, or 18 million, result in moderate to severe
post-operative pain. In addition, there are currently 9.1 million cancer
patients in the United States. Each year roughly 6.6 million patients with
cancer are treated for pain and of these, 65% to 80% experience moderate to
severe pain. In recent years, there has been a growing awareness that many
patients, especially the terminally ill, do not receive adequate analgesic
therapy for their pain. Sales of prescription narcotics in the United States to
treat pain were approximately $1.0 billion in 1996 and, according to market
reports, the market is estimated to grow at a rate of approximately 10.5% per
year. Factors contributing to this growth rate include more relaxed policies for
narcotic administration and the introduction of drug delivery systems that make
administration safer, more controllable and convenient.
Morphine is the most commonly prescribed drug for the management of severe
pain in critically ill patients in the United States. Morphine and hydromorphone
are the most widely used parenteral pain medications for home use because they
are relatively safe, effective and have relatively short half lives.
Hydromorphone is a more potent, highly soluble analog of morphine, which is the
standard against which other analgesics are generally measured.
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The Company believes that iontophoretic delivery systems for narcotic
analgesics for the treatment of post operative and chronic pain control could
offer significant benefits over existing methods of delivery, including infusion
pumps, transdermal patches and transmucosal products. To provide effective pain
relief, a morphine injection is generally administered every four hours.
Repeated injection or continuous infusion of morphine is expensive because the
methods of administration consume substantial hospital staff time or require
frequent visits by a health care provider to a patient receiving home infusion
therapy. An iontophoretic system has the potential to offer all of the benefits
of an infusion pump, including the ability to closely match the delivery profile
with rapid onset and cessation of action characteristics and to provide control
of baseline delivery with bolus dose capability for acute episodes of pain, but
without the need to use needles. The Company believes an iontophoretic delivery
system for pain management may also be more convenient and less expensive, since
the rental of costly infusion pumps and intervention by a skilled medical
professional may not be required. Passive transdermal patches offer convenience
and reduced costs, but they take four to eight hours before effective analgesia
is achieved and take hours or even days for the drug depot to clear from the
skin after the patch is removed. In addition, passive transdermal patches do not
offer precise baseline dosing from patient to patient and do not address the
need for bolus dosing required to address acute episodes of pain.
Products Under Development. The Company believes an iontophoretic delivery
system for hydromorphone may be a favorable alternative to the administration of
morphine by infusion for acute post operative pain and for chronic pain in the
hospice or home care setting. Hydromorphone is approximately ten times more
potent than morphine and has added therapeutic advantages, including lower
incidence of nausea and vomiting (which frequently accompanies the
administration of morphine), and more effective analgesia with no stupefying and
minimal hypnotic effects. Through the Elan Agreements, the Company obtained
rights to prototype wearable iontophoretic drug delivery systems for the
delivery of hydromorphone and to the preclinical, Phase I and limited Phase II
clinical data generated by Elan in testing the device. The Company believes the
additional clinical trials necessary to market this product may be of relatively
short duration in comparison to an NCE, since hydromorphone's safety and
efficacy profile is well known and the clinical endpoints are both well
established and easy to measure.
In addition to a system for the delivery of hydromorphone, the Company
believes a market exists for an iontophoretic drug delivery system for fentanyl,
a narcotic analgesic more potent than hydromorphone, which has been used
primarily during surgery. The Company conducted a preliminary blood level study
using fentanyl and, using data from that study, designed advanced electrodes
which a former collaborative partner used in a subsequent fentanyl human blood
level test. These studies demonstrated that fentanyl can be delivered by
iontophoresis to achieve the delivery rates and blood levels necessary for pain
control.
Due to its short half-life in the body, injectable fentanyl is not
generally used for the treatment of moderate to severe post-operative or chronic
pain. However, the increased use of home infusion therapy and the development of
a passive transdermal patch have demonstrated that fentanyl can be delivered at
therapeutic levels, making the drug suitable for new indications not previously
possible with injections. The Duragesic transdermal fentanyl patch, which was
developed by Alza Corporation ("Alza") and is marketed by Janssen
Pharmaceuticals, was introduced in 1992 and had annual worldwide sales of $205
million in 1996.
The Company's ability to market a product using fentanyl in the United
States may be limited by certain litigation before the PTO.
OTHER POTENTIAL PRODUCT APPLICATIONS
The Company has an active program of identifying and developing
iontophoretic drug delivery products for various therapeutic indications where
the Company believes there is a potential market need, where a suitable
water-soluble ionic drug is available and where that drug can be delivered
through iontophoresis in therapeutic quantities on a cost-competitive basis. The
Company has identified certain drugs and therapeutic indications as potential
product opportunities, and has undertaken preliminary steps toward verifying the
market need and technical feasibility of iontophoretic delivery of those drugs.
In addition, through the Elan Agreements, the Company acquired certain
in-process research and development, including exclusive
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world-wide rights for the commercial exploitation of certain iontophoretic
patents, know-how and clinical data. The Elan technology includes in vitro
feasibility studies conducted on 64 drugs (including several peptide drugs), in
vivo blood level animal studies on 18 of those drugs and human blood level
studies on nine of those drugs.
As part of its continuing product development program, the Company will
evaluate the feasibility of iontophoretic delivery of biotechnology derived
peptides, small proteins and oligonucleotides for applications where existing
drug delivery systems have significant limitations. The Company also intends to
examine the use of its iontophoretic system to deliver anti-emetics to treat
postsurgical nausea and vomiting induced by or secondary to chemotherapy,
surgery, migraine headache or AIDS.
COLLABORATIVE RELATIONSHIPS AND LICENSES
A principal component of the Company's commercial strategy is to develop
products, where appropriate, in collaboration with established pharmaceutical
companies or other strategic partners. These collaborative partners may provide
proprietary drugs, technology, financial resources, research and pharmaceutical
manufacturing capabilities or marketing infrastructure to aid in the development
and commercialization of the Company's products and potential future products.
Depending on the availability of financial, marketing and scientific resources
and other factors, the Company may also license or cross license its technology
or products to others and retain profit sharing, royalty, manufacturing,
co-marketing, co-promotion or similar rights. Any such arrangements could limit
the Company's flexibility in pursuing alternatives for the development or
commercialization of its products.
The Company has entered into the following collaborative relationships and
license arrangements:
Novartis Agreement. In July 1995, as amended in March 1996, the Company
entered into various research and development agreements (the "R&D Agreements")
with the ethical pharmaceuticals division of Ciba-Geigy Corporation ("Ciba") to
evaluate the feasibility of delivering a number of Ciba compounds for several
therapeutic applications utilizing the Company's iontophoretic drug delivery
technologies, including certain of its existing iontophoretic devices. In 1997,
Ciba was merged with Sandoz Corporation to form Novartis Pharma A.G.
("Novartis").
Although the Company met all of the essential development objectives under
the R&D Agreements, in July 1998, Novartis advised the Company that it would not
renew the R&D Agreements beyond the scheduled December 31, 1998, expiration
date. Novartis will continue to fund research through December 31, 1998, in
accordance with the terms of the R&D Agreements.
In connection with the R&D Agreements, the Company granted Novartis a
perpetual non-exclusive, royalty bearing license to the Company's iontophoretic
technology. Following the expiration of the R&D Agreements, Novartis' rights to
exclusivity in those fields covered by the agreements will terminate, and IOMED
will be free to apply the technologies it developed for Novartis to any
available drug candidates, either independently or on behalf of other parties.
The Company believes the application of that technology may shorten the
Company's future product development cycles.
The Company has also agreed that, during the term of the agreement with
Novartis and for a period of five years thereafter, the Company will negotiate
in good faith to license to Novartis rights to any iontophoretic drug delivery
technologies developed or acquired by the Company but which are not covered
under the existing license agreements (the "Second Generation Technology").
Further, the Company has agreed to negotiate such additional licenses prior to
entering into any agreement to license or otherwise transfer any rights to such
Second Generation Technology to a third party. Under the R&D Agreements, as
amended, the parties agreed that they will jointly own the technology developed
in the collaboration.
Elan Agreements. Effective March 1997, the Company entered into the Elan
Agreements. Under the Elan Agreements, the Company acquired exclusive, worldwide
licenses to certain of Elan's iontophoretic drug delivery technologies,
including know-how and over 250 issued and 47 pending United States and foreign
patents.
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Alza Agreement. In 1993, the Company entered into a cross-license agreement
with Alza. Under the agreement, the companies, among other things, exchanged
non-exclusive, royalty free rights to certain patented technologies which each
party believed to be of significant strategic importance to the potential
technological success of many iontophoretic drug delivery applications. One
patent sublicensed by Alza to the Company under the agreement bears a nominal
royalty rate if used.
University of Utah Agreement. In 1974, the Company entered into a licensing
agreement with the University of Utah Research Foundation (the "University").
Under the agreement, which was amended in 1993, the Company obtained an
exclusive license to certain iontophoretic drug delivery and prosthetic
technologies developed at the University. Under the terms of the amended
license, the Company is obligated to pay the University a royalty on all sales
of its iontophoretic drug delivery products through the year 2007. In December
1996, the Company sold the assets comprising its prosthetic technologies
operations to Fillauer, Inc. and, in connection with that sale, sublicensed its
rights in the prosthetic technologies covered by the license to Fillauer, Inc.
Fillauer Agreements. In December 1996, the Company sold the assets of its
prosthetics products and technologies operations to Fillauer, Inc. and granted
Fillauer an exclusive, worldwide license and sublicense to the patents and other
intellectual property of the Company relating to such products. Under the terms
of the sublicense agreement, the Company will receive license fees and royalties
on future sales of such products.
Laboratoires Fournier Agreement. In July 1993, the Company entered into an
agreement with Laboratoires Fournier, S.C.A. ("Laboratoires Fournier"), a
private French pharmaceutical company, for the joint research and development of
wearable integrated iontophoretic systems, with primary effort devoted to the
development of systems for the treatment of acute post operative pain and
patient controlled analgesia. The companies subsequently concluded that certain
United States patents issued to Alza for the iontophoretic delivery of fentanyl
and its analogs after the Company and Laboratoires Fournier had entered into
their agreement posed a potential barrier to the commercial viability of the
proposed system in the United States. As a result, the Company elected to
suspend development efforts in the area. In February 1996, the parties
terminated their collaborative research and development activities and amended
their initial agreement. Under the amended agreements, both companies have
rights to all jointly developed iontophoretic technologies and know-how, and
Laboratoires Fournier has a limited non-exclusive license to the Company's
previously existing proprietary iontophoretic technologies.
Boston University Agreement. In December 1997, the Company acquired a
non-exclusive, fully-paid, perpetual, non-royalty bearing license to certain
iontophoretic drug delivery technology developed by Boston University. The
agreement also provides the Company with the right to sublicense the technology
upon the payment of a sublicense fee.
MANUFACTURING
The Company's manufacturing activities primarily relate to its manufacture
of electrode kits, which are manufactured and assembled using several
proprietary materials, components, processes and production technologies
developed by the Company in conjunction with its equipment and materials
suppliers. The Company has manufactured internally all of the electrodes it has
sold, and believes its electrode manufacturing capacity can be expanded to meet
its needs for the foreseeable future.
The Company does not manufacture or repackage any drugs or compounds used
in its delivery systems and outsources the manufacture and assembly of its
Phoresor dose controllers. The Company's patented Phoresor iontophoretic dose
controllers employ a variety of sub-assemblies and components that are designed
or specified by the Company. These components and subassemblies are manufactured
by third parties, and then shipped to a contract manufacturer for final
assembly. The Company's manufacturing activities for the Phoresor dose
controllers are limited to design, labeling, inspection and packaging.
The Company's second and third generation dose controllers are in various
stages of design, research, and development and may require additional clearance
or a pre-market approval ("PMA") from the FDA prior to marketing. The Company,
alone or in conjunction with its development partners, will design the products
and,
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in combination with its suppliers, will manufacture and assemble prototypes and
clinical quantities. Upon completion of the design, specifications and testing,
the Company intends to subcontract the manufacture and assembly of all
commercial quantities of its dose controllers to electronics companies that
specialize in such work.
The Company and certain of its suppliers are required to comply with FDA
regulations governing manufacturing practices, including the Quality System
Regulation, which mandate controls for product design, control and quality. The
Company believes it is in compliance with the Quality System Regulation. The
Company is also ISO 9001 and CE Mark certified and has good manufacturing
practices audits conducted on a regular basis.
SALES AND DISTRIBUTION
The Company's marketing strategy is to position its proprietary
iontophoretic drug delivery products in the marketplace as the preferred means
of drug delivery for a wide range of drugs. The strategy employs the use of
multiple sales and distribution channels, including (i) a network of medical
supply dealers; (ii) direct sales representatives; and (iii) collaborative
marketing partners. The Company intends to use these distribution channels, both
singly and, for certain products, in combination, to maximize the Company's
marketing resources.
The Company currently sells its drug delivery system for acute local
inflammatory conditions to the rehabilitative medicine, physical therapy and
related specialty markets. The Company employs a nationwide distribution network
consisting of approximately 50 durable medical equipment and physician supply
dealers to sell and distribute its products in those markets. This distribution
network is supported by eight regional business managers and four internal
customer service representatives who are employees of the Company. In addition
to the Company's sales and distribution efforts for its local inflammation
products in the United States, it maintains marketing and sales activities in
international markets, including Europe, Scandinavia, Australia, South Korea,
Singapore and Hong Kong. These sales are made primarily through independent
distributors operating in those countries.
In 1997, the Company launched an iontophoretic drug delivery system for
Iontocaine and initially targeted its sales efforts for this product in the
pediatric hospital market under the name Numby Stuff. In August 1998, the
Company restructured its field sales staff to bring costs more in line with
total product sales. After the restructuring, along with independent sales
representatives, the Company's eight regional business managers and four
internal customer service representatives will also call on the pediatric
hospital market to facilitate the sales of Numby Stuff. The Company also intends
to expand its marketing efforts for its Iontocaine products for other
applications and to the general physician office and international markets. The
Company intends to use collaborative marketing partners or distributors for some
or all of those Iontocaine markets, and is seeking collaborative marketing
partners or distributors to assist its direct sales efforts in the pediatric and
general hospital market.
PATENTS AND PROPRIETARY RIGHTS
The Company's iontophoretic drug delivery technologies include patents,
trademarks, trade secrets and other proprietary know-how. These technologies are
used in various combinations in the testing, evaluation and formulation of
optimal ionic drug solutions and in the research, development, design and
manufacture of microprocessor controlled power supplies and iontophoretic
electrodes which are specifically designed and constructed for particular
therapeutic applications.
The Company has implemented a policy of actively patenting and maintaining
as trade secrets and proprietary information all inventions and technologies
which it believes are important to its business operations. The Company
generally seeks patent protection for its key proprietary technologies and
technological products in the United States, Canada, Europe and Japan. The
Company also relies on a number of trade secrets, know-how, continuing
technological innovations and licensing opportunities to develop and maintain
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its competitive position. The Company's patent committee meets regularly to
review and make recommendations to the Company's management regarding patent and
invention issues.
As of June 30, 1998, the Company held or had rights to utilize 61 United
States patents and 256 foreign patents relating to its iontophoretic drug
delivery technology, and has (or has the rights to utilize) 14 pending patent
applications in the United States and 35 pending patent applications in foreign
countries for that technology. The Company also owns or has licensed rights to
issued and pending United States patents governing the design and manufacture of
certain myoelectric prosthetic devices which it has sublicensed to a third party
in connection with the sale of the Company's Motion Control division.
GOVERNMENT REGULATION
Both drugs and medical devices, including the Company's iontophoretic drug
delivery systems, are subject to extensive regulation by the FDA in the United
States and by comparable authorities in other foreign countries.
The Company's iontophoretic drug delivery products involve a medical device
component, thereby subjecting such products to compliance with the FDA's
regulations governing medical devices. Where such medical devices are labeled
for use with a specific pharmaceutical product for a specific therapeutic
indication, they are subject to the FDA's regulations governing both medical
devices and pharmaceutical products. The Company believes that most, if not all,
of its future iontophoretic drug delivery systems will involve a pharmaceutical
component or specific labeling for use with a pharmaceutical product.
Products regulated as medical devices may not be commercially distributed
in the United States unless they have been cleared or approved by the FDA, or
unless they are otherwise exempted from the FDA's regulations. Currently, there
are two methods for obtaining FDA clearance or approval of medical devices.
Devices deemed to pose less risk are placed in class I (general controls) or
class II (general and special controls) and qualify for 510(k) notification, a
procedure under sec. 510(k) of the Federal Food, Drug, and Cosmetic Act (the
"FDC Act"). In order for a device to qualify under the sec. 510(k) notification
procedure, the manufacturer must, among other things, establish that the product
to be marketed is substantially equivalent in intended use and safety and
effectiveness to another legally marketed class I or class II device or to a
"preamendment" class III device (as defined below) for which FDA has not called
for PMAs. In such cases, marketing of the product may commence when the FDA
issues a letter finding that there is a substantial equivalence to the legally
marketed device. The FDA may require, in connection with a 510(k) notification,
the manufacturer to provide the FDA with test results from animal studies and/or
human clinical trials. The Company believes that it typically takes between four
and 12 months to obtain a 510(k) clearance, but it can take longer. A 510(k)
clearance is also required when the manufacturer makes changes or modifications
to a cleared device that could significantly affect safety or effectiveness, or
where there is a major change or modification in the intended use of a cleared
device.
A medical device that does not qualify for the 510(k) clearance is placed
in class III, which is reserved for devices deemed by the FDA to pose the
greatest risk (e.g., life-sustaining, life supporting or implantable devices, or
devices that are not substantially equivalent to a legally marketed class I or
II device). The manufacturer of such a device must file a PMA application under
sec. 515 of the Drug Act. A PMA application generally requires a much more
complex submission than a 510(k) notification and typically requires a showing
that the device is safe and effective based on extensive and costly preclinical
and clinical testing, as well as information about the device and its components
regarding, among other things, manufacturing, labeling and promotion. Upon
submission, the FDA determines if the PMA application is sufficiently complete
to permit substantive review and, if so, the application is accepted for filing.
The FDA then commences an in-depth review of the PMA application, which the
Company believes can last from one to three years, or even longer. Even after
approval of a PMA, a new PMA or PMA supplement is required in the event of a
modification to the device, its labeling or its manufacturing process.
A preamendment class III device is one that was on the market before May
28, 1976. A device that is substantially equivalent to a preamendment class III
device can be brought to market through the 510(k) process until the FDA either
calls for the submission of PMA applications or downclassifies the device to
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class I or II. Manufacturers of preamendment class III devices that the FDA
retains in class III must submit PMA applications 90 days after the publication
of a final regulation calling for PMAs. In such event, a PMA must be submitted
even if the device has already received 510(k) premarket clearance. On the other
hand, if the FDA downclassifies a preamendment class III device to class I or
II, a PMA application is not required and such devices may continue to be
marketed through the 510(k) process.
An even more lengthy and complex regulatory framework applies to the
labeling and marketing of specific drugs for use with an iontophoresis device.
The activities required before a pharmaceutical product may be marketed in the
United States primarily begin with preclinical testing. Preclinical tests
include extensive laboratory evaluation of product chemistry and other end
points and animal studies to assess the potential safety and efficacy of the
product as formulated. Almost all preclinical studies pertinent to drug approval
are regulated by the FDA under a series of regulations called the Good
Laboratory Practice (GLP) regulations. Violations of these regulations can, in
some cases, lead to invalidation of the studies, requiring such studies to be
replicated.
If the drug is subject to full NDA requirements, FDA approval process
entails (i) conducting preclinical laboratory and animal testing to enable FDA
authorization of an IND application, (ii) initial IND clinical studies to define
safety and dose parameters, (iii) well controlled IND clinical trials to
demonstrate product safety and efficacy, and (iv) submission to the FDA of an
NDA. Preclinical studies involve laboratory evaluation of product
characteristics and animal studies to assess the efficacy and safety of the
drug. Human clinical trials are typically conducted in three sequential phases.
Phase I trials normally consist of testing the product in a small number of
healthy volunteers for safety and pharmacokinetic parameters using single and
multiple dosing regimens. In Phase II trials, the manufacturer evaluates safety,
initial efficacy, and dose ranging of the product for specific indications in a
somewhat larger patient population. Phase III trials typically involve expanded
testing for safety and clinical efficacy in a broad patient population at
multiple clinical testing centers. The manufacturer must also submit a clinical
plan, or "protocol," accompanied by the approval of the institution
participating in the trials, to the FDA prior to commencing each clinical trial
and must obtain the informed consent of subjects in the clinical trial. The FDA
may order the temporary or permanent discontinuation of clinical trials at any
time. All the results of the preclinical and clinical studies on a product are
then submitted to the FDA in the form of an NDA for review. In responding to an
NDA, the FDA may grant marketing approval, require additional testing and/or
information, or deny the application altogether. The process of obtaining FDA
approval for a new product through the IND/NDA process may take several years
and typically involves the expenditure of substantial resources.
The Company may be subject to certain user fees that the FDA is authorized
to collect under the Food and Drug Modernization Act of 1997, which reauthorized
the user fees established in the Prescription Drug User Fees Act of 1992 for
certain drugs.
The regulatory status of iontophoresis devices is also complex. The FDA has
classified them as class II devices eligible for marketing through 510(k)
premarket clearance when intended for use with a drug whose labeling bears
adequate directions for the device's use with that drug. However, if an
iontophoresis device is intended for use with a drug that is not labeled for use
with the device, the FDA considers the iontophoresis device to be a preamendment
class III device. This status means that the device at present can be marketed
through a 510(k) clearance, but it remains subject to a call for PMAs.
In an April 1994 document setting forth the FDA's strategy for addressing
preamendment class III devices, the FDA indicated that preamendment class III
iontophoresis devices were among fifteen "high priority" devices that presented
an unreasonably high risk to public health because significant issues of safety
and/or effectiveness were not being resolved or, to the agency's knowledge, had
little probability of being resolved. The FDA indicated that these devices were
not considered candidates for downclassification and were very likely to be
required to be subject to PMAs. This process would involve two steps. First, the
FDA would publish a proposed regulation to require PMAs for iontophoresis
devices having preamendment class III status. After a comment period, FDA would
then publish a final regulation imposing the requirement. The FDA's strategy
document stated the agency's intent to publish a proposed regulation requiring
PMAs for
16
<PAGE> 19
preamendment class III iontophoresis devices in 1996. The agency, to date, has
not published such a regulation.
The Company's Phoresor received 510(k) clearance in 1990 as a preamendment
class III device labeled for use with ions of soluble salts or other drugs. In
1995, the FDA approved an NDA for Iontocaine to be used as a local anesthetic
and delivered iontophoretically by the Phoresor, which effectively moved the
Phoresor into class II for this intended use. Unlike Iontocaine, Dexamethasone
does not have an NDA approval allowing it to be labeled for iontophoretic
delivery. Thus, the Company's Phoresor is a preamendment class III device when
used with Dexamethasone (or any drug other than Iontocaine). No assurance can be
given that the Company will ever obtain an approved NDA for the iontophoretic
delivery of Dexamethasone.
The FDA also regulates the Company's quality control and manufacturing
procedures by requiring the Company and its contract manufacturers to comply
with current Good Manufacturing Practices ("GMP"), including compliance with the
Quality System Regulation (for devices) and the current GMP regulations (for
drugs). The FDA's GMPs require, among other things, that (i) the manufacturing
process be regulated and controlled by the use of written procedures, and (ii)
the ability to produce products which meet the manufacturer's specifications be
validated by extensive and detailed testing at various steps of the
manufacturing process. These regulations also require investigation of any
deficiencies in the manufacturing process, the products produced, or record
keeping. The FDA monitors compliance with these requirements by requiring
manufacturers to register their manufacturing facilities with the FDA and by
conducting periodic FDA inspections of those facilities. If an FDA inspector
observes conditions that might be in violation of GMP requirements, the
manufacturer is generally required to correct those conditions or explain them
satisfactorily. If a manufacturer fails to adhere to GMP requirements, the
devices manufactured by the manufacturer could be considered to be manufactured
in violation of the FDC Act and the manufacturer could be subject to FDA
enforcement action that could include fines, plant closure, or a recall of the
company's product.
Agencies similar to the FDA regulate medical devices and pharmaceutical
products in most foreign countries. The Company will be required to meet the
regulations of any foreign country where it markets its products. In addition,
various aspects of the Company's business and operations are also regulated by a
number of other governmental agencies including the Drug Enforcement Agency,
U.S. Department of Agriculture, the Environmental Protection Agency, the
Occupational Safety and Health Administration as well as by other federal, state
and local authorities. In addition, international sales are regulated by
numerous foreign authorities. Unanticipated changes in existing regulatory
requirements, failure of the Company to comply with such requirements or
adoption of new requirements could have a material adverse effect on the
Company.
COMPETITION
The drug delivery, pharmaceutical and biotechnology industries are highly
competitive and rapidly evolving, with significant developments expected to
continue at a rapid pace. The Company's success will depend upon maintaining a
competitive position and developing products and technologies for efficient and
cost effective drug delivery. The Company's products will compete with other
formulations of drugs and with other drug delivery systems, including other
iontophoretic delivery systems. The Company believes its products will compete
on the basis of quality, efficacy, cost, convenience, safety and patient
compliance.
The Company is aware of many other competitors in the general field of drug
delivery, including competitors developing injectable or implantable drug
delivery systems, oral drug delivery technologies, passive transdermal systems,
oral transmucosal systems and intranasal and inhalation systems. The Company is
also aware of other companies that have developed or are currently developing
iontophoretic and other electrotransport drug delivery systems.
Both Alza and Empi, Inc. ("Empi") are engaged in the development and/or
marketing of iontophoretic devices. Alza, a licensee of the Company, is
undertaking the development of iontophoretic drug delivery systems, but does not
currently market any iontophoretic products. Empi is the Company's primary
17
<PAGE> 20
competitor in the treatment of acute local inflammation in the physical therapy
market and, the Company estimates, controls a majority of the retail
iontophoresis market for that indication.
In connection with their collaboration, the Company granted Novartis a
perpetual, non-exclusive, royalty bearing license to certain of the Company's
iontophoretic technology which will survive the termination of the
collaboration. After the termination of the collaboration on December 31, 1998,
Novartis may, pursuant to the royalty-bearing license, independently develop
products using the licensed technology, including products which may compete
directly with those currently marketed or under development by the Company.
Currently, no other company markets an iontophoretic system for the
inducement of local anesthesia. The Company's iontophoretic system for
delivering Iontocaine for the inducement of local dermal anesthesia will
therefore primarily compete with traditional methods of delivering local dermal
anesthetics by needle injection or will be used in circumstances where either no
anesthesia is used, due to the pain associated with the needle injection
(including needle injections themselves), or where topical anesthetic creams are
used. The most effective and widely used topical anesthetic cream, EMLA, is
manufactured and sold by Astra Corporation, a large Swedish pharmaceutical
company. There can be no assurance that the Company can effectively compete with
these products or any other drug delivery systems.
EMPLOYEES
The Company has assembled a team of medical-products managers and
scientists with considerable experience in iontophoresis, encompassing all of
the key disciplines which the Company believes are necessary to further the
development and implementation of the Company's business.
As of June 30, 1998, the Company had 80 full-time employees, 6 of whom hold
doctorate degrees. Six others hold advanced business or technical degrees. Of
the Company's 80 full-time employees on that date, 14 were engaged in research
and development, 34 in manufacturing and quality control, and 32 in marketing
and general administration. The Company's future success depends in significant
part upon the continued service of its key technical and senior management
personnel and its continuing ability to attract and retain highly qualified
technical and managerial personnel. None of the Company's employees is
represented by a labor union. The Company has not experienced any work stoppages
and considers its relations with its employees to be good.
ITEM 2. PROPERTIES
The Company maintains leased administrative, manufacturing and research
office space at two facilities. The Company's principal executive offices and
manufacturing facility, which consists of approximately 18,000 square feet of
useable space, are located at 3385 West 1820 South in Salt Lake City, Utah. Its
research facility, which consists of approximately 8,000 square feet of useable
space, is located at 1290 West 2320 South in Salt Lake City, Utah. These
facilities are leased to the Company until December 31, 1999. The Company
believes its existing facilities are adequate and suitable for its present needs
and that additional space will be available as needed.
ITEM 3. LEGAL PROCEEDINGS
The Company is not involved in, nor is it aware of, any litigation or
impending litigation.
ITEM 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS
No matters were submitted to a vote of security holders during the fourth
quarter of the fiscal year covered by this Report.
18
<PAGE> 21
PART II
ITEM 5. MARKET FOR REGISTRANT'S COMMON EQUITY AND RELATED STOCKHOLDER MATTERS
The Company's common stock has traded on the American Stock Exchange (the
"AMEX") since April 24, 1998, under the symbol "IOX". The following table sets
forth monthly information on the price range of the Company's common stock since
that date. This information indicates the high and low sales prices as reported
by the AMEX. These prices represent quotations between dealers and do not
include retail mark-up, mark-down or commission, and do not necessarily
represent actual transactions.
<TABLE>
<CAPTION>
HIGH LOW
------ ------
<S> <C> <C>
April 1998........................................... $8.250 $7.000
May 1998............................................. $7.875 $6.125
June 1998............................................ $7.500 $5.000
</TABLE>
As of June 30, 1998, there were approximately 139 shareholders of record of
the Company's common stock. Included in the number of shareholders of record are
shares held in "nominee" or "street" names. Because many of such shares are held
by brokers and other institutions on behalf of individual investors, the Company
is unable to estimate the total number of shareholders represented by these
record holders.
The Company has not paid dividends to date and does not anticipate or
contemplate paying cash dividends in the foreseeable future. It is the present
intention of management to utilize all available funds for the development and
growth of the Company's business.
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<PAGE> 22
ITEM 6. SELECTED CONSOLIDATED FINANCIAL DATA
The following selected statements of operations data for the years ended
June 30, 1996, 1997 and 1998, and the balance sheet data as of June 30, 1997 and
1998 are derived from the audited consolidated financial statements included in
this report and should be read in conjunction with those consolidated financial
statements and the notes thereto. The selected statement of operations data for
the years ended June 30, 1994 and 1995, and the balance sheet data as of June
30, 1994, 1995 and 1996 are derived from the audited consolidated financial
statements of the Company, which are not included herein and are qualified by
reference to such financial statements and the notes thereto. Certain
reclassifications have been made to the audited financial statements for the
years ended June 30, 1994 and 1995 to reflect the results of discontinued
operations in a manner consistent with the presentation of the discontinued
operations for the years ended June 30, 1996 and 1997.
<TABLE>
<CAPTION>
FISCAL YEAR ENDED JUNE 30,
-------------------------------------------------------------------
1994 1995 1996 1997 1998
---------- ---------- ---------- ------------ -----------
<S> <C> <C> <C> <C> <C>
STATEMENT OF OPERATIONS DATA:
Revenues:
Product Sales..................................... $6,991,000 $6,964,000 $6,829,000 $ 7,483,000 $ 8,489,000
Contract research revenues, royalties and license
fees............................................ -- -- 2,409,000 1,800,000 1,788,000
---------- ---------- ---------- ------------ -----------
Total revenues.............................. 6,991,000 6,964,000 9,238,000 9,283,000 10,277,000
Operating costs and expenses:
Cost of products sold............................. 3,499,000 3,369,000 3,138,000 3,338,000 3,890,000
Research and development.......................... 1,665,000 1,467,000 1,099,000 1,488,000 1,559,000
Selling, general and administrative............... 3,307,000 3,338,000 3,283,000 3,501,000 5,389,000
Non-recurring charges............................. -- -- 430,000(1) 15,059,000(2) --
Total costs and expenses.................... 8,471,000 8,174,000 7,950,000 23,386,000 10,838,000
---------- ---------- ---------- ------------ -----------
Income (loss) from operations....................... (1,480,000) (1,210,000) 1,288,000 (14,103,000) (561,000)
Interest expense.................................... 39,000 32,000 9,000 242,000 930,000
Interest income and other, net...................... 102,000 120,000 167,000 291,000 402,000
---------- ---------- ---------- ------------ -----------
Income (loss) from continuing operations before
income taxes and minority interest................ (1,417,000) (1,122,000) 1,446,000 (14,054,000) (1,089,000)
Minority interest................................... -- -- (17,000) 23,000 11,000
Income tax expense (benefit)........................ (264,000) (173,000) (79,000) 5,000 --
---------- ---------- ---------- ------------ -----------
Income (loss) from continuing operations............ (1,153,000) (949,000) 1,542,000 (14,082,000) (1,100,000)
Income from discontinued operations (3)............. 444,000 290,000 201,000 44,000 --
Net income (loss)................................... $ (709,000) $ (659,000) $1,743,000 $(14,038,000) $(1,100,000)
========== ========== ========== ============ ===========
DILUTED PER COMMON SHARE AMOUNTS:
Income (loss) from continuing operations............ $ (0.63) $ (0.47) $ 0.42 $ (4.52) $ (0.29)
Income from discontinued operations................. 0.24 0.14 0.05 0.01 --
Net income (loss)................................... $ (0.39) $ (0.33) $ 0.47 $ (4.51) $ (0.29)
========== ========== ========== ============ ===========
Shares used in computing diluted per share amounts
(4)............................................... 1,823,000 2,038,000 3,710,000 3,109,000 3,821,000
BALANCE SHEET DATA:
Cash and cash equivalents........................... $2,541,000 $1,861,000 $4,507,000 $ 6,346,000 $16,709,000
Total assets................................ 5,501,000 4,770,000 7,251,000 8,664,000 20,200,000
Long-term obligations, including current portion.... 3,263,000 3,099,000 44,000 15,240,000(5) 237,000
Redeemable, convertible preferred shares............ 2,308,000 2,235,000 1,270,000 900,000 --
Accumulated deficit................................. (8,584,000) (9,243,000) (7,500,000) (21,538,000) (22,638,000)
Shareholders' equity (deficit)...................... (945,000) (1,592,000) 3,992,000 (9,491,000) 18,651,000
</TABLE>
- ---------------
(1) Costs incurred in connection with the settlement of certain trade dress
litigation.
(2) Reflects the write-off of certain in-process research and development
(including related transaction costs) purchased from Elan.
(3) Discontinued operations include the operating results of the Company's
prosthetics division, which was sold in December 1996.
(4) See Notes to Consolidated Financial Statements for information concerning
the computation of per share amounts.
(5) Reflects $15,240,000 (including accrued interest) in notes issued to Elan at
June 30, 1997.
20
<PAGE> 23
ITEM 7.MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS
OF OPERATIONS
The following discussion of the financial condition and results of
operations of the Company should be read in conjunction with the Consolidated
Financial Statements and the related Notes thereto included elsewhere in this
Report. The following Management's Discussion and Analysis of Financial
Condition and Results of Operations contains forward-looking statements, within
the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the
Securities Exchange Act of 1934, that involve risks and uncertainties. The
Company's actual results of operations could differ significantly from those
anticipated in such forward-looking statements as a result of numerous factors
discussed under Item 1 "Business" and elsewhere in this Report.
OVERVIEW
The Company develops, manufactures and commercializes controllable drug
delivery systems using iontophoretic technology. The majority of the Company's
revenues has been generated through the sale of its iontophoretic drug delivery
products in the physical therapy market for use in the delivery of Dexamethasone
and contract research revenues from the Company's collaboration with Novartis.
The Company recently introduced its local dermal anesthesia products into the
market place and, to date, has not realized significant revenue from the sales
of such products. Since its inception, the Company has generally incurred
operating losses and it expects to incur additional operating losses over the
next several years as a result of anticipated costs associated with a
significant increase in internally funded research, development and clinical
trial activities relating to new applications for its iontophoretic drug
delivery technologies, and the consolidation and equipping of its facilities. As
of June 30, 1998, the Company's accumulated deficit was approximately $22.6
million. The Company's ability to achieve and sustain profitability will depend
on its ability to achieve market acceptance and successfully expand sales of its
existing products; successfully complete the development of, receive regulatory
approvals for, and successfully manufacture and market, its products under
development; as well as successfully negotiate and enter into agreements with
collaborative partners, licensors, licensees and other parties for the
development, clinical testing, manufacture, marketing or commercialization of
certain of its products or products in development, as to which there can be no
assurance.
FISCAL YEARS ENDED JUNE 30, 1997 AND 1998
Revenues. Product sales increased 13% from $7.5 million in fiscal 1997 to
$8.5 million in fiscal 1998. The increase can be attributed to higher sales of
the Company's iontophoretic drug delivery products for the treatment of local
inflammatory conditions resulting from overall market growth in this segment.
Contract research revenues, royalties and license fees were $1.8 million in
both fiscal 1997 and 1998. Contract revenues during fiscal 1997 included a
milestone payment from Novartis and during fiscal 1998, included the Company's
receipt of royalty revenues pursuant to the sale of its Motion Control division.
Contract research revenues received during fiscal 1997 and 1998 pursuant to the
Novartis agreement covered a substantial portion of the Company's research and
development expenses.
In June 1998, Novartis Pharmaceuticals Corporation elected not to renew its
collaborative research and development agreement with the Company beyond its
scheduled expiration date of December 31, 1998. Accordingly, the Company's
contract research revenues may decline during fiscal 1999 and future years. The
effect of the loss of contract research revenue on the Company's future
operating results may be offset, in whole or in part, by a reduction in research
and development expenditures incurred in connection with the collaboration, as
well as by additional contract research revenues, if the Company is successful
in its efforts to enter into new collaborative research and development
arrangements.
Costs of Products Sold. Costs of products sold increased 17% from $3.3
million in fiscal 1997 to $3.9 million in fiscal 1998, reflecting increased
material and labor costs associated with higher unit sales volumes. Costs of
products sold increased as a percentage of product sales primarily as a result
of higher royalty obligations and a less favorable product mix.
22
<PAGE> 24
Research and Development Expense. Research and development expenditures
were approximately $1.5 million in fiscal 1997 and $1.6 million in fiscal 1998.
Fiscal 1998 includes a higher proportion of expenditures on internally financed
product development projects of the Company. This trend is expected to continue
at least through fiscal 1999.
Selling, General and Administrative Expenses. Selling, general and
administrative expenses increased 54%, from $3.5 million in fiscal 1997 to $5.4
million in fiscal 1998. This increase can be attributed primarily to recruiting,
personnel and other sales and marketing costs associated with the Company's
continued investment in the market introduction of Numby Stuff. In addition, the
Company realized increased costs associated with the maintenance and prosecution
of the patent portfolio acquired from Elan.
Although the response to the Company's Numby Stuff product line by medical
professionals and medical organizations, including the ACH, has been very
positive, the process by which such products obtain administrative review and
final approval for use in the hospital environment is extremely complex and time
consuming. Among other things, such new products are subject to extensive
evaluations within each hospital and often each department, require review and
approval by hospital products and therapeutics committees, and must be accepted
for inclusion on the hospital's formulary. As a result, in August 1998, the
Company restructured its sales and marketing organization to reduce overall
costs and bring them in line with current product sales and the slower than
anticipated rate of market penetration of Numby Stuff. In addition, the Company
will seek to expand its sales, marketing and distribution capabilities for all
of its product lines through collaborative partnerships and by broadening its
current dealer distribution network.
Non-Recurring Charges. In fiscal 1997, the Company entered into the Elan
Agreements pursuant to which the Company acquired certain rights to Elan's
in-process research and development relating to iontophoretic drug delivery,
including issued and pending United States and foreign patents, know-how and
clinical data. As a result of this transaction, the Company recorded a
non-recurring charge of approximately $15.1 million.
Other Costs and Expenses. Interest expense increased from $242,000 in
fiscal 1997 to $930,000 in fiscal 1998. This increase can be attributed to the
recognition of interest expense on $15.0 million in notes issued to Elan in
connection with the Elan Agreements. Interest income and other miscellaneous
income was $291,000 in fiscal 1997, compared to $402,000 in fiscal 1998,
reflecting higher interest earnings on higher average invested cash balances,
which included the net proceeds from the Company's initial public offering in
April 1998.
Income (loss) from Continuing Operations. A loss from continuing operations
of $14.1 million in fiscal 1997 compares to a loss from continuing operations of
$1.1 million in fiscal 1998. The loss in fiscal 1997 can be attributed to the
non-recurring charge resulting from the write-off of in-process research and
development acquired from Elan. The loss in fiscal 1998 can be attributed to the
non-cash interest charges on the Elan indebtedness and the Company's investment
in the sales and marketing of Numby Stuff, which, to date, has not generated
significant revenues.
FISCAL YEARS ENDED JUNE 30, 1996 AND 1997
Revenues. Product sales increased 10% from $6.8 million in fiscal 1996 to
$7.5 million in fiscal 1997. This increase can be attributed to increased sales
of the Company's iontophoretic drug delivery products for the treatment of local
inflammatory conditions resulting from the first full year of sales of the
Company's new electrode kits for this market segment.
Contract research revenues, royalties and license fees decreased 25% from
$2.4 million in fiscal 1996 to $1.8 million in fiscal 1997. During fiscal 1996,
the Company entered into a research and development agreement with Novartis to
develop proprietary iontophoretic drug delivery systems for Novartis drugs.
Pursuant to the agreement, the Company received contract research revenues and
other payments of $1.4 million and $1.8 million, respectively, in fiscal 1996
and 1997. In addition, in fiscal 1996, the Company received a one-time license
fee of $1.0 million. Contract research revenues received during fiscal 1996
23
<PAGE> 25
and 1997 pursuant to the Novartis agreement covered a substantial portion of the
Company's research and development expenses.
Costs of Products Sold. Costs of products sold increased 6% from $3.1
million in fiscal 1996 to $3.3 million in fiscal 1997, reflecting increased
costs attributable to higher material and labor costs resulting from higher unit
sales volume. Costs of products sold decreased slightly as a percent of product
sales due to productivity gains which were offset, in part, by increased costs
associated with new product introductions.
Research and Development Expense. Research and development expenditures
increased 36%, from $1.1 million in fiscal 1996 to $1.5 million in fiscal 1997.
The increase reflects increased costs of personnel and other expenditures
associated with the development programs conducted under the Novartis agreement,
as well as research and development expenditures on the Company's internally
financed product development projects.
Selling, General and Administrative Expenses. Selling, general and
administrative expenses increased 6%, from $3.3 million in fiscal 1996 to $3.5
million in fiscal 1997. The increase in fiscal 1997 can be attributed to the
recruiting, personnel and other sales and marketing costs associated with the
Company's market introduction of Numby Stuff. The increase was offset, in part,
by decreases in general and administrative expenses.
Non-Recurring Charges. In March 1997, the Company entered into the Elan
Agreements, pursuant to which the Company acquired certain rights to Elan's
in-process research and development relating to iontophoretic drug delivery,
including issued and pending United States and foreign patents, know-how and
clinical data. As a result of this transaction, the Company recorded a
non-recurring charge of approximately $15.1 million.
During fiscal 1996, the Company recorded a non-recurring charge of $430,000
for costs incurred in connection with the settlement of a trade-dress
infringement suit brought by a competitor of the Company relating to a newly
developed series of the Company's electrode kits for the treatment of acute
local inflammation.
Other Costs and Expenses. Interest expense increased from $9,000 in fiscal
1996 to $242,000 in fiscal 1997. This increase can be attributed to the
recognition of interest expense on $15.0 million in notes issued to Elan in
connection with the Elan Agreements. Interest income and other miscellaneous
income was $167,000 in fiscal 1996, compared to $291,000 in fiscal 1997,
reflecting interest earnings on higher average cash balances during fiscal 1997.
The Company has substantial net operating loss carryforwards. Income taxes
in both periods reflect estimated alternative minimum tax liabilities, offset by
the recognition of future tax benefits resulting from the allocation of income
tax expense, at statutory rates, to the pre-tax income of the Company's
discontinued operations.
Income (loss) from Continuing Operations. Income from continuing operations
of $1.5 million in fiscal 1996 compares to a loss from continuing operations of
$14.1 million in fiscal 1997. Excluding the non-recurring charges in both fiscal
years, income from continuing operations decreased from $2.0 million in fiscal
1996 to $1.0 million in fiscal 1997. The decrease in fiscal 1997 can be
attributed primarily to the one time $1.0 million license fee the Company
received from Novartis in fiscal 1996.
LIQUIDITY AND CAPITAL RESOURCES
Prior to fiscal 1996, the Company funded its operating losses primarily
through private equity financing, convertible debt arrangements, capital lease
financing, and collateralized bank loans. Beginning in fiscal 1996, the
Company's operating and research activities have been internally funded,
primarily as a result of the research and development revenues and license fees
the Company has received from Novartis.
In April 1998, the Company consummated an initial registered public
offering pursuant to which the Company issued 1,850,000 common shares and raised
approximately $11,445,000, net of underwriters' discounts and estimated
expenses. As of June 30, 1998, the Company had cash and cash equivalents
totaling
24
<PAGE> 26
approximately $16.7 million. Cash in excess of immediate requirements is
invested in a manner which is intended to maximize liquidity and return while
minimizing investment risk, and, whenever possible, the Company seeks to
minimize the potential effects of concentration of credit risk.
The Company consumed $251,000 in cash for operating activities during
fiscal 1998 compared to providing $1.0 million in cash during fiscal 1997. This
increased cash consumption can be attributed to the higher cash loss in fiscal
1998 in combination with the Company's continued investment in net non-cash
working capital used to finance its sales growth and expanded product offerings.
The Company generated approximately $1.0 million of cash from operating
activities during fiscal 1997, compared to $2.2 million in fiscal 1996. The
decrease can be attributed primarily to the one-time license fee received from
Novartis in fiscal 1996 and an increased net investment in working capital in
fiscal 1997.
Historically, the Company's operations have not been capital intensive and,
therefore, its investment in property, plant and equipment during the periods
presented has not been significant. The Company anticipates however, that its
investment in facilities and equipment will increase in the future, due to the
Company's desire to consolidate its manufacturing, administrative and research
and development facilities and the need to increase the automation of its
electrode manufacturing processes to meet higher expected sales volumes. The
Company's expenditures for equipment and furniture were $316,000, $231,000 and
$670,000 in each of the fiscal years ended June 30, 1996, 1997 and 1998,
respectively.
During fiscal 1998, the Company purchased a license to certain
iontophoretic drug delivery technology at a cost of $214,000, including
transaction expenses.
In other non-cash transactions related to the initial public offering, (i)
the Company granted warrants to purchase 170,000 common shares to the
underwriters, exercisable after April 23, 1999, at an initial exercise price of
$9.38 per share; (ii) Elan converted the amounts outstanding under the Elan
Notes, including accrued interest thereon, into 1,206,391 common shares and
893,901 shares of newly created Series D preferred shares, at the initial public
offering price of $7.50 per share; (iii) the 28,800 Series C preferred shares of
the Company which were outstanding immediately prior to the offering were
automatically converted, on a share for share basis, into common shares; and
(iv) the Company issued an additional 29,697 common shares to Laboratoires
Fournier, pursuant to the anti-dilution provisions of a prior stock purchase
agreement between the companies.
During fiscal 1997, the Company generated $255,000 in cash from the private
placement of its Common Shares. During fiscal 1996, the Company generated $1.0
million ($892,000, net of related expenses) in cash from the sale of a 20%
equity interest in Dermion to Novartis. (See Note 10 of the Notes to
Consolidated Financial Statements.)
The Company expects to continue to incur substantial costs associated with
the expansion of its research and development activities, including clinical
trials, continued investment in sales and marketing of new product lines,
additional investment in working capital, and the cost of consolidating and
equipping its facilities. The Company anticipates that the net proceeds of the
Company's initial public offering, together with existing cash balances and cash
generated from operations (including funding from Novartis through December
1998) will be sufficient to fund the operations of the Company at least through
fiscal 1999. However, the Company may be required or elect to raise additional
capital before that time. The Company's actual capital requirements will depend
on many factors, some of which are outside the Company's control.
DISCONTINUED OPERATIONS
Prior to January 1997, the Company provided state-of-the-art prosthetics
products to amputees throughout the United States, Canada and Western Europe
through its Motion Control division. Motion Control's principal products were
the Utah Artificial Arm and the ProControl II, advanced myoelectric prostheses
for above and below the elbow amputees.
In December 1996, the Company sold the assets of the Motion Control
division for $1.0 million and granted the purchaser an exclusive, worldwide
license and sublicense to the patents, trademarks, know-how and other
intellectual property of the Company relating to the Motion Control products.
Under the terms of that sublicense agreement, the Company will receive license
fees and royalties on future sales of the Motion
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Control products. There was no significant gain or loss recognized on the sale.
The results of operations of the Motion Control division, exclusive of any
corporate allocations, are reported as discontinued operations in the
consolidated financial statements for all periods presented. See Note 4 of the
Notes to the Consolidated Financial Statements.
IMPACT OF THE YEAR 2000
Many computer systems experience problems handling dates beyond the year
1999. The Company has evaluated its primary operating systems (including its
financial systems, material requirements planning, and production lot tracking
systems) and believes, based upon its evaluation as well as representations from
its software suppliers, that its operating systems are substantially year 2000
compliant. To the extent that any software applications are not fully year 2000
compliant, the Company expects that software upgrades made in the normal course
of business will either minimize, isolate or possibly eliminate any substantive
risks associated with software or system failure.
To date, the Company has not incurred any significant costs associated with
the evaluation or modification of its systems relating to year 2000 compliance
and does not anticipate the need to incur any costs outside the normal course of
business. In the event that any of the Company's systems should fail due to a
failure to identify and address a year 2000 exposure, the Company believes that
the size and scope of its operations would allow the Company to revert to manual
operating systems on a timely basis.
The custom circuitry and software utilized in the Company's iontophoretic
dose controllers do not include any date driven functions and therefore will not
exhibit any change in performance due to the arrival of the year 2000. The
Company has initiated procedures designed to evaluate the year 2000 exposure of
its significant suppliers and other vendors whose systems may impact the
Company's operations. To date, the Company has not identified any compliance
deficiencies that might have a significant impact on the Company if not
rectified by such supplier or vendor on a timely basis. There can be no
assurance that such a deficiency will not be discovered or arise in the future
or that the Company would be able to identify and validate an alternative source
for any service or material which may be affected by such deficiency.
ADDITIONAL RISK FACTORS
Future results could differ materially from those currently anticipated by
the Company due to a number of factors, including those identified in this
section and elsewhere in this Form 10-K, any of which could have a material
adverse impact on the Company's business, financial condition or results of
operations.
Continuing Operating Losses; Uncertainty of Future Profitability. Since
1991, the Company has sustained losses in each fiscal year, except fiscal year
1996. The Company had an accumulated deficit of $22.6 million as of June 30,
1998. The Company intends to expand its product lines, research and development,
business development and marketing efforts in the near future and, therefore,
does not anticipate being profitable in the near term. The Company's ability to
achieve and sustain profitability will depend on its ability to achieve market
acceptance, and successfully expand sales of its existing products, as well as
successfully complete the development of, receive regulatory approvals for, and
successfully manufacture and market, its products under development, as to which
there can be no assurance.
Uncertainty of Market Acceptance and Limited Market Penetration. The
Company has generated only limited revenues, primarily from sales to physical
therapists of its drug delivery system for delivery of Dexamethasone for the
treatment of acute local inflammation. The Company began marketing a local
dermal anesthetic product that uses Iontocaine, in January 1997 and has
generated only limited revenues from that product to date. For the Company to be
successful, its products will need to achieve broad market acceptance by the
medical profession. The Company's products use a method of active transdermal
drug delivery which, to date, has not gained significant market penetration, and
no assurance can be given that the Company's current or future products will
ever achieve broad market acceptance.
Uncertainties Related to Product Development. Two of the primary components
of the Company's business strategy are to develop and commercialize
iontophoretic drug delivery systems for new and existing
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drugs and to develop additional applications for its existing products. The
Company will be required to undertake time-consuming and costly development
activities and seek regulatory approval for these new products and applications.
Product revenues may not be realized from the sale of any such products for
several years, if at all. The Company can give no assurance that its product
development efforts, either alone or in collaboration with other parties, will
ever be successfully completed, that it can obtain required regulatory approvals
of its products, that products under development can be manufactured at
acceptable cost or with appropriate quality, or that its products can meet
market needs or achieve market acceptance.
Reliance on Collaborative Partners. The Company's strategy is to enter into
arrangements with corporate partners, licensors, licensees and other parties for
the development, clinical testing, manufacture, marketing or commercialization
of certain of its products or products in development. The Company currently has
a collaborative arrangement with Novartis.
A significant portion of the Company's research and development resources
has been devoted to its contractual research and development efforts with
Novartis. Since 1995, Novartis has funded a substantial portion of the total
research and development costs of the Company. Although the Company met all of
the essential development objectives under the R&D Agreements, in July 1998,
Novartis advised the Company that it would not renew the R&D Agreements beyond
the scheduled December 31, 1998, expiration date. Novartis will continue to fund
research through December 31, 1998, in accordance with the terms of the R&D
Agreements. In addition, in connection with this collaboration, the Company
granted Novartis a perpetual, non-exclusive, royalty bearing license to certain
of the Company's iontophoretic technology which will survive the termination of
the collaboration. The license to Novartis, though non-exclusive, may make it
more difficult for the Company to enter into new collaborations. There can be no
assurance that pursuant to the royalty-bearing license, Novartis will not
independently develop products using the licensed technology, including products
which may compete directly with those currently marketed or under development by
the Company. After December 31, 1998, and until the Company enters into
additional collaborative agreements, the Company will be required to internally
fund all of its research and development expenditures. The failure to enter into
such arrangements on a timely basis could have a material adverse effect on the
Company's product development efforts, business, financial condition and results
of operations.
Although the Company anticipates it will enter into additional
collaborative arrangements with other parties in the future, there can be no
assurance the Company will be able to negotiate any such additional
collaborative arrangements on terms which are acceptable to the Company, if at
all. To the extent the Company chooses not, or is not able, to establish such
collaborations, it could experience significantly increased business risk and
capital requirements in the development, clinical testing, manufacturing,
marketing and commercialization of its products. The Company could also
encounter significant delays in introducing products into markets or find that
the development, manufacture or sale of proposed products in such markets is
adversely affected by the absence of those collaborative arrangements.
Intense Competition and Rapid Technological Change. The drug delivery,
pharmaceutical and biotechnology industries are highly competitive and rapidly
evolving, with significant developments expected to continue at a rapid pace.
The first pharmaceutical product to reach the market in a therapeutic area or
using a certain drug delivery technology generally obtains and maintains a
significant market share relative to later entrants to the market. The Company's
success will depend on its ability to maintain a competitive position and
develop new products and technologies for efficient and cost effective drug
delivery. The Company's products will compete with other formulations of drugs
and with other drug delivery systems, including other iontophoretic delivery
systems. There can be no assurance any of the Company's products will have
advantages that will be significant enough to cause medical professionals to
prefer or even use them. New drugs or further development of alternative drug
delivery methods may provide greater therapeutic benefits for a specific drug or
indication, or may offer comparable performance at lower cost, than that offered
by the Company's iontophoretic drug delivery systems, which could have a
material adverse effect on the Company's business, financial condition and
results of operations.
Many competitors, including public and private corporations, academic
institutions, governmental agencies and other public and private research
organizations, are involved in the development of drug delivery
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systems, including competing electrotransport-related drug delivery
technologies. Many of these competitors have substantially greater financial and
other resources, are more experienced, and are larger, more established
organizations than the Company. There can be no assurance the Company's
competitors will not succeed in more rapidly developing or marketing products
that are more effective or commercially attractive than the Company's current or
future products, or that would render the Company's products obsolete or
noncompetitive. There can also be no assurance the Company will have the
financial resources, technical or management expertise or manufacturing or
support capability to compete in the future.
The Company has licensed certain rights to its iontophoretic drug delivery
technologies to other parties, including Alza, Laboratoires Fournier and
Novartis, that may become or are direct competitors of the Company. These
companies could compete with the Company for contracts with the Company's
collaborative partners and could also develop iontophoretic drug delivery
systems that will compete directly with many of those currently marketed or
being developed by the Company.
Reliance on Third Party Distribution. The Company presently markets its
drug delivery systems for the treatment of acute local inflammation primarily to
physical therapists through a nationwide system of dealers. The Company is
currently marketing its local dermal anesthesia products in the United States
hospital market through a limited number of sales personnel who work directly
for the Company and independent manufacturers representatives.
In order to achieve broad distribution and market penetration of its
current and future products, the Company intends to enter into arrangements with
collaborative marketing partners or distributors that have national or
market-specific marketing capabilities. There can be no assurance that the
Company will be able to maintain its existing, or establish new, marketing
arrangements on terms favorable to the Company, if at all. The Company's
collaborative marketing partners and distributors may not be contractually
committed to make future purchases of the Company's products and could,
therefore, discontinue carrying the Company's products at any time or for any
reason.
If the Company's marketing resources fail to perform in accordance with the
Company's expectations, the Company may be required to obtain or develop
alternate marketing, sales and distribution capabilities or seek other methods
of distributing its products.
Dependence on Patents and Proprietary Technology. The Company's ability to
commercialize many of the products it has under development will depend, in
part, on its or its licensors' ability, both in the United States and in other
countries, to obtain patents, enforce those patents, preserve trade secrets and
operate without infringing on the proprietary rights of third parties.
The patent positions of drug delivery, pharmaceutical and biotechnology
companies are highly uncertain and involve complex legal and factual questions.
There can be no assurance the patents currently owned and licensed by the
Company, or any future patents, will prevent other companies from developing
similar or therapeutically equivalent products, or that other companies will not
be issued patents that may prevent the sale of Company products or require
licensing and the payment of significant fees or royalties by the Company.
Furthermore, there can be no assurance any of the Company's products or methods
will be patentable, will not infringe upon the patents of third parties, or that
the Company's patents or future patents will give the Company an exclusive
position in the subject matter claimed by those patents. The Company may be
unable to avoid infringement of third party patents and may have to obtain
licenses, defend infringement actions or challenge the validity of those patents
in court. There can be no assurance a license will be available to the Company,
if at all, on terms and conditions acceptable to the Company, or that the
Company will prevail in any patent litigation. There can be no assurance the
Company's pending patent applications will result in issued patents, patent
protection will be secured for any particular technology, any patents that have
been or may be issued to the Company or its licensors will be valid or
enforceable or that the Company's patents will provide meaningful protection to
the Company.
The Company also relies on trade secrets and other unpatented proprietary
information in its product development activities. To the extent the Company
relies on confidential information to maintain its
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competitive position, there can be no assurance other parties may not
independently develop the same or similar information.
In August 1993, the PTO issued a patent to Alza covering the iontophoretic
delivery of fentanyl. A similar patent application in Europe has thus far been
rejected, although the Company believes Alza has appealed that rejection. The
United States patent was the subject of a reexamination by the PTO and all of
the substantive claims within the patent were also rejected, but Alza has
appealed that rejection to the United States Board of Patent Appeals and
Interferences. There can be no assurance Alza will not be successful in one or
both of its appeals. Therefore, if the Company develops a drug delivery system
for fentanyl and if Alza is successful in its appeal, the Company would be
required to obtain a license from Alza to market any iontophoretic drug delivery
system it develops for fentanyl in the United States. There can be no assurance
such a license would be available on terms acceptable to the Company, if at all.
If the Company cannot obtain such license, the Company will be required to
discontinue its product development programs using fentanyl.
Need to Manage Expanding Operations. If the Company is successful in
achieving market acceptance of its products, it will be required to expand its
operations, particularly in the areas of research and development, sales and
marketing and manufacturing. As the Company expands its operations in these
areas, those expansions will likely result in new and increased responsibilities
for management personnel and place significant strain on the Company's
management, operating and financial systems and other resources. To accommodate
any such growth and compete effectively, the Company will be required to
implement improved information systems, procedures and controls, and to expand,
train, motivate and manage its work force. The Company's future success will
depend to a significant extent on the ability of its current and future
management personnel to operate effectively both independently and as a group.
There can be no assurance the Company's personnel, systems, procedures and
controls will be adequate to support the Company's future operations.
Future Capital Needs; Uncertainty of Additional Funding. The further
development and commercialization of the Company's products and technology will
require a commitment of substantial funds to conduct research and development
activities, including preclinical and clinical studies, to expand distribution
and hire additional sales and marketing personnel and to expand and develop
manufacturing capabilities. The Company believes that existing cash balances and
cash generated from operations will be sufficient to fund the operations of the
Company for at least the next 12 months; however, the Company's actual capital
requirements will depend on many factors, and the Company may be required or
elect to raise additional capital before that time.
To satisfy its capital requirements, the Company may seek to raise funds
through public or private financings, collaborative relationships or other
arrangements. Any additional equity financing may be dilutive to shareholders
and debt financing may involve significant restrictive covenants. Collaborative
arrangements to raise additional funds may require the Company to relinquish its
rights to certain of its technologies, products or marketing territories. There
can be no assurance that any such financing, if required, will be available on
terms satisfactory to the Company, if at all.
Uncertainty of Government Regulation. The research, development,
manufacture and marketing of the Company's products are extensively regulated by
the FDA, which requires its approval of drugs and medical devices before they
can be marketed in the United States. Similar approvals are also required from
other regulatory bodies in foreign countries. The regulatory processes
established by these government agencies are lengthy, expensive and uncertain.
In addition, once approval is obtained, that approval may be withdrawn. The
regulations applicable to the Company's products may change as the presently
limited number of approved iontophoretic drug delivery products increases and
regulators acquire additional experience in this area. The FDA has broad
authority to enforce the medical devices and drug regulations and laws, and
noncompliance can result in a variety of regulatory responses ranging from
warning letters and mandatory product recalls to civil or criminal actions and
penalties.
The Company has received approval from the FDA on its NDA for Iontocaine,
and the FDA has allowed the Company to market its electrical dose controllers
and electrode products for use with ions of soluble salts or other drugs under
the FDA's 510(k) regulations governing medical devices. However, the FDA has
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publicly stated that it intends to require manufacturers of iontophoretic
devices to obtain PMA of marketed devices currently used with drugs not
specifically labeled for iontophoretic delivery, which would include the
Company's dose controller for use with ions of soluble salts or other drugs,
such as Dexamethasone. The FDA's 1994 strategy document states that the
enactment of the modified regulatory procedure was a "high priority" and that
the agency intended to publish a proposed regulation requiring such PMAs in
1996. The agency to date has not published such a regulation.
If the FDA calls for PMAs for preamendment class III iontophoresis devices,
the Company would be required to have a PMA accepted for filing by the FDA
within 90 days after the date of the final regulation calling for PMAs. There
can be no assurance that the Company would be able to complete necessary
clinical studies and otherwise prepare and file a PMA within the prescribed time
period, or that any data and information submitted in a PMA would be adequate to
support approval. The Company's failure to submit a PMA and have it accepted for
filing by the FDA within the required timeframe could result in the Company
being required to cease commercial distribution of the Phoresor for use with
ions of soluble salts and other drugs, including Dexamethasone. Upon timely
filing of a PMA, the Company believes (based on FDA's announced position as to
certain other preamendment class III medical devices) that the FDA would permit
continued commercial distribution of the Phoresor for use with Dexamethasone
during the time necessary to review the PMA. There can be no assurance, however,
that the FDA would permit such continued commercial distribution pending review
of a PMA for the device, nor can any assurance be given that the FDA would
approve a PMA filed by the Company. The FDA also could condition PMA approval
upon approval of an NDA permitting Dexamethasone to be labeled for use with the
Phoresor. If the Company were required for any length of time to cease
commercial distribution of the Phoresor System for use with Dexamethasone, the
Company's business, financial condition and results of operations would be
materially and adversely affected pending approval of a PMA or NDA.
The Company will be required to obtain further FDA approvals before it may
promote or otherwise market or label any of its present or future drug delivery
products for use with other named drugs. There can be no assurance that such
approvals will be granted, and the process of obtaining them could be extensive,
time-consuming and costly. The time required to obtain FDA approval after filing
an NDA is uncertain and frequently takes several years. Further, the Company has
not yet filed NDAs on any drug other than Iontocaine. In the course of the
practice of medicine, medical practitioners legally can use the Company's
iontophoretic devices for the delivery of Dexamethasone even though the Company
has not filed an NDA for that therapeutic indication and even though the Company
is not permitted to label or promote its device for use with Dexamethasone. The
FDA may require that the Company conduct clinical trials and obtain NDA approval
for the iontophoretic delivery of Dexamethasone using the Company's dose
controllers and electrodes for the treatment of acute local inflammation in
order for the Company to continue to market its products for that therapeutic
indication. There can be no assurance that such clinical trials, if conducted,
would be successful in establishing safety and efficacy or that NDA approval
could be obtained.
There can be no assurance any future products developed by the Company will
prove to be safe and effective or meet all of the applicable regulatory
requirements necessary to be marketed. Data obtained from testing activities can
be susceptible to varying interpretations which could delay, limit or prevent
required regulatory approvals. In addition, the Company may encounter delays or
denials of approval based on a number of factors, including future legislation,
administrative action or changes in FDA policy made during the period of product
development and FDA regulatory review. The Company may encounter similar delays
in foreign countries. Furthermore, approval may entail ongoing requirements for,
among other things, post-marketing studies. Even if a product developer obtains
regulatory approval, a marketed product, its manufacturer and its manufacturing
facilities and pertinent operations are subject to extensive regulation and
periodic inspections. Discovery of previously unknown problems with a product,
manufacturer or facility could result in FDA sanctions, restrictions on a
product or manufacturer, or an order to withdraw and/or recall a specific
product from the market. There can also be no assurance that changes in the
legal or regulatory framework or other subsequent developments will not result
in the limitation, suspension or revocation of regulatory approvals granted to
the Company. Such events, were they to occur, could have a material adverse
effect on the Company's business, financial condition and results of operations.
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The Company is also required to comply with FDA regulations for
manufacturing practices, which mandate procedures for extensive control and
documentation of product design, control and validation of the manufacturing
process and overall product quality. Foreign regulatory agencies have similar
manufacturing standards. Ongoing compliance with these standards and with
labeling, adverse event reporting and other applicable regulatory requirements
is monitored through periodic inspections and market surveillance by federal,
state and local government agencies and by comparable agencies in other
countries. Any third parties manufacturing the Company's products or supplying
materials or components for such products may also be subject to the foregoing
requirements. If the Company, its management or its third party manufacturers
fail to comply with applicable regulations regarding these manufacturing
practices, the Company could be subject to a number of sanctions, including
fines, injunctions, civil penalties, delays, suspensions or withdrawals of
market approval, seizures or recalls of products, operating restrictions and, in
some cases, criminal prosecutions.
Under the FDA's regulations, when a manufacturer changes or modifies a
device for which it has received a 510(k) clearance, it is required to obtain an
additional 510(k) clearance for the modified device if the modification
significantly affects the safety or efficacy of the device, or if the
modification results in a major change in intended use. In such cases, the
manufacturer is expected to make the initial determination as to whether the
modification is of a kind that would require a new 510(k) clearance. The FDA's
regulations provide only limited guidance in making this determination. The FDA
has cleared the Company's electrical dose controller and electrode kits for
marketing under a 510(k) clearance. Since obtaining its 510(k) clearances, the
Company has made modifications to its products. Based on the checklist developed
by the FDA to assist manufacturers in determining whether they are required to
obtain a 510(k) clearance for a modified device, the Company has determined that
a new 510(k) submission was not required in connection with the commercial
introduction of such products. However, there can be no assurance that the FDA
will not require the Company to obtain additional 510(k) clearances with respect
to those products. If the FDA requires the Company to submit a new 510(k) notice
for any device modification, the Company may be prohibited from marketing the
modified device until the 510(k) notice is cleared by the FDA.
Because of the known safety and efficacy profile of Dexamethasone and other
approved drugs for which the Company may seek NDA approval for iontophoretic
delivery, the clinical trials and other studies may not be as lengthy or
extensive as would be required for unapproved new drugs that are subject to full
NDA requirements. This strategy, however, depends upon the Company's ability to
obtain a contractual right to reference the safety and efficacy data for such
drugs contained in approved NDAs held by other entities. The Company has
obtained a right to reference safety and efficacy data for Dexamethasone. There
can be no assurance that the Company will be able to obtain a right of reference
for all unapproved drugs that may be used for iontophoretic delivery. The
Company's failure to obtain a right of reference to safety and efficacy data for
any drug for which the Company would like to obtain approval for iontophoretic
delivery could result in the Company being required to independently satisfy any
requirements regulatory agencies may impose with respect to such references,
which could delay the Company's use of such drug or increase the Company's
costs.
Dependence on Single Sources of Supply. A key material used in many of the
Company's current electrode products is available only from a single supplier.
In addition, the Company obtains Iontocaine from Abbott Laboratories under a
contract expiring in December 1998. The Company also has the right to obtain
Dexamethasone from Luitpold Pharmaceuticals, Inc./American Regent Laboratories,
Inc. under a contract expiring in January 2005. The Company believes that, if
necessary, alternative sources can be developed or alternate materials can be
substituted for each of these single-sourced materials. Although the Company has
not experienced difficulty acquiring these materials on commercially reasonable
terms and in sufficient quantities to maintain required production levels, no
assurance can be given that price increases or interruptions in the supply of
these materials will not occur in the future or that the Company will not have
to seek alternate suppliers or obtain substitute materials, which may require
additional product validations and regulatory submissions. Any significant price
increase, interruption of supply, inability to secure an alternate source or
qualify a substitute material could have a material adverse effect on the
Company's ability to manufacture its products or to obtain or maintain
regulatory approval of its products.
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The Company's current dose controllers are manufactured under a contract
with a third party electronics manufacturer. There can be no assurance that its
present supplier can manufacture sufficient quantities of dose controllers that
meet quality and performance standards on a timely basis. If the supplier cannot
meet the Company's requirements, or in the event of an interruption of its
supply, the Company would be required to identify, qualify and validate an
alternate source of supply within a reasonable period of time.
Limited Manufacturing Experience. The Company manufactures its
iontophoretic drug delivery electrodes in quantities sufficient to satisfy its
current level of product sales. To meet anticipated increases in sales, the
Company may need to increase its production significantly beyond its present
manufacturing capacity. Accordingly, the Company may be required to increase its
manufacturing capacities or to contract with another party to manufacture its
products. There can be no assurance the Company can successfully increase its
capacity on a profitable basis, or contract with another party on terms
acceptable to the Company, if at all.
Significant increases in production volume will likely require changes in
the Company's product and manufacturing process in order to facilitate increased
automation of the Company's production. There can be no assurance such changes
in products or processes or efforts to automate the Company's manufacturing
process will be successful.
The Company believes its facilities operate in accordance with the Quality
System Regulation currently prescribed by the FDA and in substantial compliance
with ISO 9001 and CE Mark standards. The Company has GMP audits conducted by a
qualified, independent organization on a regular basis and is ISO 9001 and CE
Mark certified. There can be no assurance the Company will be able to maintain
such compliance, particularly if the scale of the Company's manufacturing
operations increases.
Uncertainty of Health Care Reimbursement. The Company's ability to
commercialize its products successfully will depend in part on the extent to
which reimbursement for the costs of those products and related treatments will
be available from government health administration authorities, private health
insurers and other organizations in the United States and in foreign markets
where the Company's products will be sold and used. Third party payors can
affect the pricing or relative attractiveness of the Company's products by
regulating the reimbursement they provide on the Company's or competing products
or therapies. There can be no assurance such reimbursement will continue at
present levels, if at all. Some insurance carriers do not reimburse health care
providers for use of the Company's products in certain applications.
Furthermore, significant uncertainty exists as to the reimbursement status of
new health care products.
Effective October 1, 1991, the Health Care Financing Administration adopted
new regulations providing for the treatment of capital related costs for medical
products. The Company is unable to predict what adverse impact on the Company,
if any, these or any additional government regulations, legislation or
initiatives or changes by other payors affecting reimbursement or other matters
that may influence decisions to obtain medical devices may have.
Retention and Attraction of Key Employees. The Company is highly dependent
on its ability to continue to attract and retain qualified scientific,
managerial, manufacturing and sales and marketing personnel. There is intense
competition for qualified personnel in the Company's area of activity, and there
can be no assurance the Company will be able to continue to attract and retain
the qualified personnel necessary for the development of its business. The
Company does not carry key-man insurance with respect to any of its executives
or employees.
Risk of Product Liability, Product Recalls and Warranty Claims;
Availability of Insurance. The testing, marketing and sale of drug delivery and
related pharmaceutical products for use in humans involves unavoidable risks.
The use of the Company's products in clinical trials and the sale of its
products upon approval may expose the Company to potential product liability
resulting from the use of such products. In addition, the existence of a product
liability claim, a product recall or excessive warranty claims (in any such
case, whether arising from defects in design or manufacture or otherwise) could
have an adverse effect on the Company's sales of that product or require a
change in the indications for which it may be used.
Product liability insurance in the Company's industry is expensive and
difficult to obtain. Although the Company currently has product liability
insurance with an annual limit of $2.0 million in the aggregate and per
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occurrence, there can be no assurance the existing coverage is adequate. The
Company will seek to maintain and appropriately increase its insurance coverage
as its product sales increase and the clinical development of its new product
applications progress. There can be no assurance, however, that the Company will
be able to maintain its current levels of insurance on acceptable terms, will be
able to secure increased coverage as the commercialization of its products
proceeds or that any particular level of insurance will provide adequate
protection against potential liabilities.
Anti-Takeover Provisions of Certain of the Company's Agreements. Certain
provisions of a cross-license agreement between the Company and Alza may have
the effect of deferring, delaying or preventing a change in control of the
Company, a merger involving the Company or the assignment or transfer of certain
technologies of the Company. Under the agreement, the Company and Alza, among
other things, exchanged non-exclusive, royalty free rights to certain patented
technologies which each party believed to be of significant strategic importance
to the potential technological success of many iontophoretic drug delivery
applications. Both parties are prohibited from assigning their rights under the
agreement to certain named companies or any other entity that derives more than
50 percent of its income from the development, licensing and/or sale of drug
delivery systems to other pharmaceutical companies without first receiving the
consent of the other party. Restrictions imposed on the Company's ability to
assign its rights under this agreement may have the effect of prohibiting a sale
of the Company to such named companies or entities, or may otherwise limit the
Company's ability to capitalize on the commercial and other economic potential
of these technologies through a technology license, asset sale, merger,
combination or similar transaction.
Environmental Matters. The Company's research and development activities
involve the controlled use of hazardous materials, chemicals and various
radioactive compounds. These materials, and their use, disposal and handling,
are extensively regulated by federal, state and local government authorities.
Although the Company believes its safety procedures for handling and disposing
of such materials comply in all material respects with the standards prescribed
by state and federal regulations, the risk of accidental environmental
contamination or personal injury from these materials cannot be completely
eliminated. In the event of such an accident, the Company could be held liable
for any damages and any such liability could exceed the resources of the
Company. There can be no assurance the Company will not be required to incur
significant costs to comply with such environmental and health and safety laws
and regulations in the future, particularly if the Company develops additional
manufacturing or research facilities and capacity.
ITEM 7A. QUANTITATIVE AND QUALITATIVE INFORMATION ABOUT MARKET RISK
Not applicable.
ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA
The consolidated financial statements of the Company and its subsidiary are
included elsewhere in this Report.
ITEM 9. CHANGES AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL
DISCLOSURE
None.
33
<PAGE> 35
(This page intentionally left blank)
34
<PAGE> 36
CONSOLIDATED FINANCIAL STATEMENTS
IOMED, INC.
JUNE 30, 1998
35
<PAGE> 37
INDEX TO CONSOLIDATED FINANCIAL STATEMENTS
IOMED, INC.
<TABLE>
<CAPTION>
PAGE
----
<S> <C>
AUDITED CONSOLIDATED FINANCIAL STATEMENTS:
Report of Independent Auditors.............................. 35
Consolidated Balance Sheets at June 30, 1997 and 1998....... 36
Consolidated Statements of Operations for the Years Ended
June 30, 1996, 1997 and 1998.............................. 37
Consolidated Statements of Shareholders' Equity (Deficit)
for the Years Ended June 30, 1996, 1997 and 1998.......... 38
Consolidated Statements of Cash Flows for the Years Ended
June 30, 1996, 1997 and 1998.............................. 39
Notes to Consolidated Financial Statements.................. 40
</TABLE>
36
<PAGE> 38
REPORT OF INDEPENDENT AUDITORS
The Board of Directors and Shareholders
IOMED, Inc.
We have audited the accompanying consolidated balance sheets of IOMED, Inc. and
subsidiary as of June 30, 1997 and 1998, and the related consolidated statements
of operations, shareholders' equity (deficit), and cash flows for each of the
three years in the period ended June 30, 1998. These financial statements are
the responsibility of the Company's management. Our responsibility is to express
an opinion on these financial statements based on our audits.
We conducted our audits in accordance with generally accepted auditing
standards. Those standards require that we plan and perform the audit to obtain
reasonable assurance about whether the financial statements are free of material
misstatement. An audit includes examining, on a test basis, evidence supporting
the amounts and disclosures in the financial statements. An audit also includes
assessing the accounting principles used and significant estimates made by
management, as well as evaluating the overall financial statement presentation.
We believe that our audits provide a reasonable basis for our opinion.
In our opinion, the financial statements referred to above present fairly, in
all material respects, the consolidated financial position of IOMED, Inc. and
subsidiary at June 30, 1997 and 1998, and the consolidated results of their
operations and their cash flows for each of the three years in the period ended
June 30, 1998, in conformity with generally accepted accounting principles.
ERNST & YOUNG LLP
Salt Lake City, Utah
August 4, 1998
35
<PAGE> 39
IOMED, INC.
CONSOLIDATED BALANCE SHEETS
ASSETS
<TABLE>
<CAPTION>
JUNE 30,
---------------------------
1997 1998
------------ ------------
<S> <C> <C>
Current assets:
Cash and cash equivalents................................. $ 6,346,000 $ 16,709,000
Accounts receivable, less allowance for doubtful accounts
of $28,000 in 1997 and $54,000 in 1998................. 1,189,000 1,570,000
Inventories............................................... 714,000 876,000
Prepaid expenses.......................................... 12,000 53,000
------------ ------------
Total current assets.............................. 8,261,000 19,208,000
Equipment and furniture, net................................ 385,000 783,000
Other assets................................................ 18,000 210,000
------------ ------------
Total assets...................................... $ 8,664,000 $ 20,201,000
============ ============
LIABILITIES AND SHAREHOLDERS' EQUITY (DEFICIT)
Current liabilities:
Trade accounts payable.................................... $ 171,000 $ 626,000
Accrued liabilities....................................... 944,000 687,000
Current portion of long-term obligations.................. 2,000 50,000
------------ ------------
Total current liabilities......................... 1,117,000 1,363,000
Commitments
Long-term obligations....................................... -- 187,000
Minority interest........................................... 898,000 --
Redeemable, convertible preferred shares; issued and
outstanding 36,000 Series C shares in 1997................ 900,000 --
Subordinated, convertible debt.............................. 15,240,000 --
Shareholders' equity (deficit):
Common shares, no par value; 100,000,000 shares
authorized; issued and outstanding 3,134,392 shares in
1997 and 6,499,518 shares in 1998...................... 12,047,000 34,408,000
Convertible preferred shares, no par value; 10,000,000
shares authorized; issued and outstanding of all series
893,801 shares in 1998................................. -- 6,881,000
Accumulated deficit....................................... (21,538,000) (22,638,000)
------------ ------------
Total shareholders' equity (deficit).............. (9,491,000) 18,651,000
------------ ------------
Total liabilities and shareholders' equity
(deficit)...................................... $ 8,664,000 $ 20,201,000
============ ============
</TABLE>
See accompanying notes.
36
<PAGE> 40
IOMED, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
<TABLE>
<CAPTION>
YEAR ENDED JUNE 30,
---------------------------------------
1996 1997 1998
---------- ------------ -----------
<S> <C> <C> <C>
Revenues:
Product sales......................................... $6,829,000 $ 7,483,000 $ 8,489,000
Contract research revenue, royalties and license
fees............................................... 2,409,000 1,800,000 1,788,000
---------- ------------ -----------
Total revenues................................ 9,238,000 9,283,000 10,277,000
Operating costs and expenses:
Cost of products sold................................. 3,138,000 3,338,000 3,890,000
Research and development.............................. 1,099,000 1,488,000 1,559,000
Selling, general and administrative................... 3,283,000 3,501,000 5,389,000
Non-recurring charges................................. 430,000 15,059,000 --
---------- ------------ -----------
Total costs and expenses...................... 7,950,000 23,386,000 10,838,000
---------- ------------ -----------
Income (loss) from operations........................... 1,288,000 (14,103,000) (561,000)
Interest expense........................................ 9,000 242,000 930,000
Interest income and other, net.......................... 167,000 291,000 402,000
---------- ------------ -----------
Income (loss) from continuing operations before income
taxes and minority interest........................... 1,446,000 (14,054,000) (1,089,000)
Minority interest....................................... (17,000) 23,000 11,000
Income tax expense (benefit)............................ (79,000) 5,000 --
---------- ------------ -----------
Income (loss) from continuing operations................ 1,542,000 (14,082,000) (1,100,000)
Income from discontinued operations, net of income
taxes................................................. 201,000 44,000 --
---------- ------------ -----------
Net income (loss)....................................... $1,743,000 $(14,038,000) $(1,100,000)
========== ============ ===========
Basic income (loss) per common share:
Income (loss) from continuing operations................ $ .49 $ (4.52) $ (.29)
Income from discontinued operations..................... .06 .01 --
---------- ------------ -----------
Net income (loss)....................................... $ .55 $ (4.51) $ (.29)
========== ============ ===========
Diluted income (loss) per common share:
Income (loss) from continuing operations................ $ .42 $ (4.52) $ (.29)
Income from discontinued operations..................... .05 .01 --
---------- ------------ -----------
Net income (loss)....................................... $ .47 $ (4.51) $ (.29)
========== ============ ===========
</TABLE>
See accompanying notes.
37
<PAGE> 41
IOMED, INC.
CONSOLIDATED STATEMENTS OF SHAREHOLDERS' EQUITY (DEFICIT)
<TABLE>
<CAPTION>
COMMON SHARES CONVERTIBLE
----------------------- PREFERRED ACCUMULATED
SHARES AMOUNT SHARES DEFICIT TOTAL
--------- ----------- ----------- ------------ ------------
<S> <C> <C> <C> <C> <C>
BALANCE AT JUNE 30, 1995.................. 2,049,051 $ 7,651,000 $ -- $ (9,243,000) $ (1,592,000)
Stock options exercised................. 43,974 23,000 -- -- 23,000
Conversion of redeemable, convertible
preferred shares..................... 494,193 895,000 -- -- 895,000
Conversion of subordinated debt......... 337,838 2,923,000 -- -- 2,923,000
Net income.............................. -- -- -- 1,743,000 1,743,000
--------- ----------- ---------- ------------ ------------
BALANCE AT JUNE 30, 1996.................. 2,925,056 11,492,000 -- (7,500,000) 3,992,000
Stock options exercised................. 6,483 5,000 -- -- 5,000
Conversion of redeemable, convertible
preferred shares..................... 165,651 300,000 -- -- 300,000
Sale of common shares for cash.......... 37,202 250,000 -- -- 250,000
Net loss................................ -- -- -- (14,038,000) (14,038,000)
--------- ----------- ---------- ------------ ------------
BALANCE AT JUNE 30, 1997.................. 3,134,392 12,047,000 -- (21,538,000) (9,491,000)
Stock options exercised................. 11,786 25,000 -- -- 25,000
Conversion of redeemable, convertible
preferred shares..................... 28,800 720,000 -- -- 720,000
Sale of common shares for cash.......... 1,850,000 11,445,000 -- -- 11,445,000
Conversion of subordinated, convertible
debt................................. 1,206,391 9,287,000 6,881,000 -- 16,168,000
Exchange of minority interest and
other................................ 268,149 884,000 -- -- 884,000
Net loss................................ -- -- -- (1,100,000) (1,100,000)
--------- ----------- ---------- ------------ ------------
BALANCE AT JUNE 30, 1998.................. 6,499,518 $34,408,000 $6,881,000 $(22,638,000) $ 18,651,000
========= =========== ========== ============ ============
</TABLE>
See accompanying notes.
38
<PAGE> 42
IOMED, INC.
CONSOLIDATED STATEMENTS OF CASH FLOWS
<TABLE>
<CAPTION>
YEAR ENDED JUNE 30,
---------------------------------------
1996 1997 1998
---------- ------------ -----------
<S> <C> <C> <C>
CASH FLOWS FROM OPERATING ACTIVITIES
Net income (loss)........................................... $1,743,000 $(14,038,000) $(1,100,000)
Adjustments to reconcile net income (loss) to net cash
provided by (used in) operating activities:
Depreciation and amortization............................. 400,000 267,000 289,000
Write-off of in-process research and development.......... -- 15,059,000 --
Non-cash interest expense................................. -- 240,000 928,000
Minority interest and other non-cash charges.............. (9,000) 34,000 11,000
Changes in assets and liabilities:
Accounts receivable.................................... (122,000) (444,000) (381,000)
Inventories............................................ 186,000 (196,000) (162,000)
Prepaid expenses and other assets...................... 9,000 (6,000) (34,000)
Trade accounts payable................................. (41,000) 53,000 455,000
Other current liabilities.............................. 83,000 25,000 (257,000)
---------- ------------ -----------
Net cash provided by (used in) operating activities......... 2,249,000 994,000 (251,000)
CASH FLOWS FROM INVESTING ACTIVITIES
Proceeds from sale of discontinued operations............... -- 1,000,000 --
Purchases of equipment and furniture........................ (316,000) (231,000) (670,000)
Purchase of patent license.................................. -- -- (214,000)
---------- ------------ -----------
Net cash provided by (used in) investing activities......... (316,000) 769,000 (884,000)
CASH FLOWS FROM FINANCING ACTIVITIES
Proceeds from issuance of common shares..................... 23,000 255,000 11,470,000
Proceeds from sale of minority interest..................... 892,000 -- --
Proceeds from long-term obligations......................... -- -- 240,000
Payments on long-term obligations........................... (132,000) (39,000) (5,000)
Redemptions of redeemable preferred shares.................. (70,000) (70,000) (180,000)
Other....................................................... -- (70,000) (27,000)
---------- ------------ -----------
Net cash provided by (used in) financing activities......... 713,000 76,000 11,498,000
Net increase (decrease) in cash and cash equivalents........ 2,646,000 1,839,000 10,363,000
Cash and cash equivalents at beginning of year.............. 1,861,000 4,507,000 6,346,000
---------- ------------ -----------
Cash and cash equivalents at end of year.................... $4,507,000 $ 6,346,000 $16,709,000
========== ============ ===========
SUPPLEMENTAL DISCLOSURES OF CASH FLOW INFORMATION
Cash paid for interest...................................... $ 9,000 $ 2,000 $ 2,000
Cash paid for income taxes.................................. $ -- $ 61,000 $ --
SUPPLEMENTAL SCHEDULE OF NON-CASH INVESTING AND FINANCING
ACTIVITIES
Issuance of subordinated, convertible debt for purchase of
in-process research and development....................... $ -- $ 15,000,000 $ --
Preferred shares converted to common shares................. $ 895,000 $ 300,000 $ 720,000
Subordinated debt converted to common and preferred
shares.................................................... $2,923,000 $ -- $16,168,000
Minority interest converted to common shares................ $ -- $ -- $ 909,000
</TABLE>
See accompanying notes.
39
<PAGE> 43
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
1. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Description of Business
IOMED, Inc., a Utah corporation (the "Company"), develops, manufactures and
commercializes controllable drug delivery systems using iontophoresis
technology.
Discontinued Operations
On December 31, 1996, the Company sold the assets of its Motion Control
Division, which was engaged in the research, development, manufacture and sale
of advanced myoelectric prosthetic devices. The results of operations of the
Motion Control Division prior to its sale have been classified as discontinued
operations in the accompanying consolidated statements of operations.
Principles of Consolidation
The consolidated financial statements include the accounts of the Company
and its wholly-owned subsidiary Dermion, Inc. ("Dermion"). Dermion was formed in
April 1996 to conduct advanced research and development of iontophoretic systems
on its own behalf and on behalf of third party clients. All significant
intercompany transactions and accounts have been eliminated. Prior to November
1997, Novartis Pharmaceuticals, Inc. owned a 20% interest in Dermion which is
reflected as minority interest in the accompanying financial statements.
Cash Equivalents
The Company considers all highly-liquid investments with maturities of
three months or less, when purchased, to be cash equivalents.
Concentrations of Credit Risk
The Company's financial instruments that are exposed to concentrations of
credit risk consist primarily of cash, cash equivalents and trade accounts
receivable. Cash and cash equivalents are held in federally insured financial
institutions or invested in high grade short-term commercial paper issued by
major United States corporations. The Company sells its products primarily to,
and has trade accounts receivable with, independent durable medical equipment
dealers in the United States and abroad. Less than 10% of product sales are to
foreign customers. As a general policy, collateral is not required for accounts
receivable; however, the Company maintains an allowance for losses based upon
expected collections of accounts receivable. Additionally, customers' financial
condition and credit worthiness are regularly evaluated and historical losses
have not been material. During the periods presented, none of the Company's
customers accounted for more than 10% of net product sales. Accordingly, the
Company considers concentrations of credit risk with respect to trade accounts
receivable to be low.
40
<PAGE> 44
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
Inventories
Inventories are stated at the lower of cost or market. Cost is determined
using the first-in, first-out method. Inventories consisted of the following:
<TABLE>
<CAPTION>
JUNE 30,
-------------------
1997 1998
-------- --------
<S> <C> <C>
Raw materials........................................ $568,000 $687,000
Work-in-progress..................................... 31,000 30,000
Finished goods....................................... 115,000 159,000
-------- --------
$714,000 $876,000
======== ========
</TABLE>
Equipment and Furniture
Equipment and furniture are stated at cost. Depreciation and amortization
is computed using the straight-line method over estimated useful lives of three
to five years. Leasehold improvements are amortized over the term of the lease
or the useful life of the improvements, whichever is shorter. Equipment and
furniture consisted of the following:
<TABLE>
<CAPTION>
JUNE 30,
-----------------------
1997 1998
---------- ----------
<S> <C> <C>
Manufacturing equipment........................... $1,896,000 $2,035,000
Office and research and development equipment..... 1,381,000 1,571,000
Leasehold improvements............................ 608,000 825,000
---------- ----------
3,885,000 4,431,000
Less accumulated depreciation and amortization.... (3,500,000) (3,648,000)
---------- ----------
$ 385,000 $ 783,000
========== ==========
</TABLE>
Revenue Recognition
Revenues on product sales are generally recognized upon shipment. Contract
research revenue and license fees are recognized as earned.
Patent Development Costs
In connection with its research and development efforts, the Company incurs
certain costs in the preparation, application, filing, maintenance and defense
of patents and trademarks. Where such costs primarily relate to patents and
trademarks covering technologies or products which are under development or in
the early stages of commercialization, the Company expenses such costs as
incurred.
Stock Options
The Company has elected to follow Accounting Principles Board Opinion No.
25, "Accounting for Stock Issued to Employees" (APB 25) and related
Interpretations in accounting for its employee stock options rather than
adopting the alternative fair value accounting provided for under FASB Statement
No. 123, Accounting for Stock-Based Compensation (SFAS 123). Under APB 25,
because the exercise price of the Company's stock options equals the market
price of the underlying shares on the date of grant, the Company does not
recognize any compensation expense.
41
<PAGE> 45
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
Income Taxes
The Company accounts for income taxes using the asset and liability method.
Under the asset and liability method, deferred tax assets and liabilities are
recognized for the future tax consequences attributable to differences between
the financial statement carrying amounts of existing assets and liabilities and
their respective tax bases, operating loss and tax credit carryforwards.
Deferred tax assets and liabilities are measured using enacted tax rates
expected to apply to taxable income in the years in which those temporary
differences are expected to be recovered or settled. The effect on deferred tax
assets and liabilities of a change in tax rates is recognized in income in the
period that includes the enactment date.
Earnings (Loss) Per Share
The Company's net income (loss) per share has been calculated in accordance
with SFAS No. 128-Earnings Per Share and accordingly includes a computation of
both basic and diluted earnings per share. Earnings (loss) from continuing
operations as presented in the statements of operations represents the numerator
used in computing earnings per share and the following table sets forth the
computation of the weighted average shares used in determining basic and diluted
earnings per share:
<TABLE>
<CAPTION>
1996 1997 1998
----- ----- -----
(IN THOUSANDS)
<S> <C> <C> <C>
Denominator for basic earnings per share -- weighted average
shares.................................................... 3,170 3,109 3,821
Dilutive securities: preferred stock, convertible debt,
warrants and stock options................................ 540 -- --
----- ----- -----
Denominator for diluted earnings per share -- adjusted
weighted average shares and assumed conversions........... 3,710 3,109 3,821
===== ===== =====
</TABLE>
At June 30, 1998, the following securities were outstanding but were not
included in the computation of diluted earnings per share due to their
anti-dilutive effect: options to purchase 331,337 common shares at a weighted
average exercise price of $4.96 per share; warrants to purchase 339,792 common
shares at a weighted average price of $13.70 per share; and 893,801 convertible
Series D preferred shares convertible on a share-for-share basis into common
shares.
Estimates
Preparation of financial statements in conformity with generally accepted
accounting principles requires management to make estimates and assumptions that
affect the reported amounts of assets and liabilities at the date of the
financial statements and the reported amounts of revenue and expenses during the
reporting period. Actual results could differ from those estimates.
Reclassifications
Certain reclassifications have been made to prior year balances to conform
to the financial statement presentation included herein.
2. PURCHASE OF IN-PROCESS RESEARCH AND DEVELOPMENT
In March 1997, the Company entered into agreements with Elan Corporation,
plc ("Elan"), an international developer of advanced drug delivery systems, to
obtain an exclusive, worldwide license for the commercial development of certain
of Elan's in-process research and development in the field of iontophoretic drug
delivery, including both issued and pending patents, know-how and clinical data.
Pursuant to the agreements, the Company paid Elan a one time fee of $15,000,000,
issued warrants to purchase up to 104,167 common shares at a price of $21.60 per
share and agreed to pay Elan certain royalties on net revenues derived
42
<PAGE> 46
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
from sales of its iontophoretic drug delivery products. Payment of the fee was
funded by the issuance of two subordinated convertible notes to Elan in an
aggregate principal amount of $15,000,000 (the "Elan Notes").
3. NON-RECURRING CHARGES
The intended clinical applications, as well as alternative future
applications, of the technologies purchased from Elan (see Note 2) are in the
early stages of research, design and clinical development, subject to numerous
technological, regulatory, and commercial risks and, therefore, represent
in-process research and development. Accordingly, during fiscal 1997, the
Company recorded a non-recurring charge of $15,059,000 reflecting the write-off
of the in-process research and development purchased, including the fee paid and
related transaction costs.
During fiscal 1996, a suit was filed against the Company by a competitor
alleging, among other things, that a recently introduced product of the Company
infringed upon the competitor's trade dress. In February 1996, a federal court
granted the plaintiff's request for a preliminary injunction. Thereupon, the
Company entered into a settlement agreement with the plaintiffs. The total costs
incurred in connection with the suit were approximately $430,000, which amount
includes legal fees, court costs and damages paid to the plaintiff, legal fees
incurred by the Company and inventory rework costs. The settlement agreement has
not had any material impact on the Company's ability to manufacture and sell its
products, including the product which gave rise to the litigation.
4. DISCONTINUED OPERATIONS
In December 1996, the Company sold the assets of its Motion Control
Division, which was engaged in the research, development, manufacture and sale
of myoelectric prosthetic devices. In addition, the Company granted a worldwide,
exclusive license to certain patent rights covering the products manufactured by
the division to the purchaser. Proceeds from the sale, which closed in January
1997, were $1,000,000. No significant gain or loss was recognized on the sale.
Additionally, the Company is entitled to receive royalties on future product
sales of the purchaser. The results of operations of the Motion Control Division
prior to its sale have been classified as discontinued operations in the
accompanying statements of operations. No interest expense has been allocated to
discontinued operations and income taxes have been allocated based upon
statutory rates. A summary of the results of discontinued operations is as
follows:
<TABLE>
<CAPTION>
FISCAL YEARS ENDED JUNE 30,
--------------------------------
1996 1997 1998
---------- -------- --------
<S> <C> <C> <C> <C>
Net product sales..................... $2,186,000 $957,000 --
Income taxes.......................... 120,000 26,000 --
Income from discontinued operations... 201,000 44,000 --
</TABLE>
5. INVESTMENTS IN MARKETABLE DEBT SECURITIES
Debt securities are classified as held-to-maturity when the Company has the
intent and ability to hold the security to maturity. Held-to-maturity securities
are stated at amortized cost, adjusted for amortization of premiums and
accretion of discounts to maturity, which approximates quoted fair market
values. Such amortization as well as interest earned is included in interest
income. As of June 30, 1997 and 1998, all investments were classified as
held-to-maturity and consisted primarily of United States corporate securities
totaling $4,635,000 and $16,502,000, respectively, and are included with cash
and cash equivalents.
43
<PAGE> 47
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
6. ACCRUED LIABILITIES
Accrued liabilities consisted of the following:
<TABLE>
<CAPTION>
JUNE 30,
-------------------
1997 1998
-------- --------
<S> <C> <C>
Payroll and related benefits......................... $436,000 $371,000
Professional fees.................................... 126,000 134,000
Warranty............................................. 10,000 10,000
Other................................................ 372,000 142,000
-------- --------
$944,000 $657,000
======== ========
</TABLE>
7. SUBORDINATED, CONVERTIBLE DEBT
In connection with the purchase of in-process research and development from
Elan (see Note 2), the Company issued the Elan Notes, an A Note and a B Note,
each bearing interest at 9.5%, in the amount of $10,000,000 and $5,000,000,
respectively. On April 28, 1998, concurrent with the closing of the initial
public offering of the Company's common shares, the Elan Notes, including
accrued interest thereon, were converted at $7.50 per share into an aggregate of
1,206,391 common shares and 893,801 Series D preferred shares of the Company.
In June 1993, the Company entered into a research and development agreement
with Laboratoires Fournier, a French pharmaceutical company ("Fournier") to
collaborate in the joint development and commercialization of certain drug
delivery systems. In connection with this transaction, in July 1993, the Company
borrowed $3,000,000 ($2,923,000, net of debt issuance costs) from Fournier
pursuant to a subordinated, convertible note. In March 1996, the companies
reached a mutual agreement to terminate their collaborative development efforts.
Among other things, the agreement provided for the conversion of the $3,000,000
subordinated, convertible note into 337,838 common shares. Pursuant to
anti-dilution provisions in the agreement, the Company issued an additional
29,697 shares to Fournier in connection with the closing of the initial public
offering of the Company's common shares.
8. COMMITMENTS
Operating Leases
The Company leases space and certain equipment under noncancellable
operating lease agreements that expire at various dates through June 2002.
Rental expense for such leases was $227,000, $218,000 and $239,000 for the years
ended June 30, 1996, 1997 and 1998, respectively. It is generally expected that,
in the normal course of business, operating leases that expire will be renewed
or replaced by other leases with similar terms. Future minimum lease payments
under noncancellable operating leases at June 30, 1998 were $388,000. These
obligations mature as follows: fiscal 1999 -- $247,000; fiscal 2000 and
thereafter $141,000.
Long-Term Obligations
The Company has acquired various equipment and furniture under capital
lease agreements. The capitalized cost of such equipment is $240,000 and
accumulated amortization was $22,000 at June 30, 1998.
44
<PAGE> 48
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
Future minimum payments under capital leases consisted of the following at
June 30, 1998:
<TABLE>
<S> <C>
YEAR ENDING JUNE 30:
1999...................................................... $ 70,000
2000...................................................... 72,000
2001...................................................... 72,000
2002...................................................... 67,000
2003...................................................... 3,000
--------
Total minimum lease payments................................ 284,000
Amounts representing interest............................... 47,000
--------
Present value of net minimum lease payments................. 237,000
Less current portion of capital lease obligations........... 50,000
--------
Noncurrent portion of capital lease obligations............. $187,000
========
</TABLE>
Royalty Agreements
The Company is the licensee under royalty agreements which provide for the
payment of royalties to the licensor based upon net sales of the products under
royalty. Royalty expense in each of the three years in the period ended June 30,
1998 was not material.
9. SHAREHOLDERS' EQUITY
Reverse Stock Split
On November 7, 1997, pursuant to a vote of the shareholders, the Company
effected a one for 4.8 reverse share split for each common and preferred share
then outstanding and amended and restated its Articles of Incorporation and
Corporate Bylaws. Among other things, these amendments changed the par value of
the Company's common shares from $0.001 per share to no par value common shares;
increased the number of authorized common shares from 40,000,000 shares to
100,000,000 shares; and increased the number of authorized preferred shares from
4,215,618 shares to 10,000,000 shares. For comparative purposes, all share
amounts in the accompanying financial statements and related footnotes have been
retroactively restated to reflect the effects of the reverse stock split and the
increases in the authorized shares of the Company's common and preferred shares.
Initial Public Offering
During fiscal 1998, the Company consummated an initial registered public
offering pursuant to which the Company issued 1,850,000 common shares and raised
approximately $11,445,000, net of underwriters' discounts and estimated
expenses.
In other transactions related to the initial public offering, (i) the
Company granted warrants to purchase 170,000 common shares to the underwriters,
exercisable after April 23, 1999, at an initial exercise price of $9.38 per
share; (ii) Elan converted the amounts outstanding under the Elan Notes,
including accrued interest thereon, into 1,206,391 common shares and 893,901
shares of newly created Series D preferred shares, at the initial public
offering price of $7.50 per share; (iii) the 28,800 Series C preferred shares of
the Company which were outstanding immediately prior to the offering were
automatically converted, on a share for share basis, into common shares; and
(iv) the Company issued an additional 29,697 common shares to Laboratoires
Fournier, pursuant to the anti-dilution provisions of a prior stock purchase
agreement between the companies.
45
<PAGE> 49
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
Redeemable, Convertible Preferred Shares
In connection with a reorganization of the Company in fiscal 1988, the
Company issued 878,254 shares of $.001 par value redeemable convertible
preferred shares in three series; Series A, Series B and Series C. Pursuant to
the terms of such preferred shares, the 14,000 Series A shares were redeemed in
five equal annual installments beginning in July 1992 through July 1996 for an
aggregate redemption price of $350,000 and the Series B shares (828,254 shares
with a carrying value of $1,500,000) were converted prior to July 15, 1996 into
common shares on a share for share basis at the equivalent of $1.81 per share.
The Series C preferred shares were comprised of 36,000 shares with an
aggregate redemption value of $900,000. Pursuant to mandatory redemption
requirements, 7,200 Series C preferred shares were redeemed in July 1997 for an
aggregate redemption price of $180,000. The remaining 28,800 Series C preferred
shares were subject to mandatory conversion, on a share-for-share basis, into
common shares upon the closing of the initial public offering of the Company.
Series D Convertible Preferred Shares
In April 1998, the Company issued 893,801 Series D preferred shares to Elan
in connection with the conversion of the Elan Notes. The Series D preferred
shares are convertible at the option of the holder into common shares, on a
share-for-share basis, subject to adjustment for certain corporate transactions.
Further, the Series D preferred shares are non-voting and have no dividend,
liquidation or similar preferences over common shares but are entitled to a pro
rata share of any such distribution as if the Series D preferred shares had been
converted into common shares.
Warrants
The Company has issued five warrants which entitle the holders thereof to
acquire common shares of the Company. In April 1998, the Company issued a
warrant to Everen Securities to acquire up to 170,000 shares for an initial
exercise price of $9.38 per share. In November 1997, the Company issued a
warrant to Novartis Pharmaceuticals Corporation to acquire up to 18,750 shares
for an exercise price of $21.60 per share. In March 1997, the Company issued a
warrant to Elan to acquire up to 104,167 shares for an exercise price of $21.60
per share. In December 1996, the Company issued a warrant to the Alliance of
Children's Hospitals, Inc. to acquire up to 44,792 shares for an exercise price
of $8.88 per share. In June 1995, the Company issued a warrant to the Silicon
Valley Bank to acquire up to 2,083 shares for an exercise price of $4.80 per
share. The warrants expire in April 2003, November 2002, April 2002, December
2003, and June 2002, respectively.
46
<PAGE> 50
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
Stock Options
The Company has adopted and approved two incentive compensation plans. The
Company's 1988 Stock Option Plan was approved by the shareholders in November
1988 and Company's 1997 Share Incentive Plan was approved by the shareholders in
November 1997. The 1988 Stock Option Plan expires in August 1998 and no further
grants were made under the Plan following the adoption of the 1997 Share
Incentive Plan. Options remaining available for grant under the plans as of the
beginning and end of the current fiscal year were 54,911 and 308,400,
respectively. A summary of the activity under the Plans during each of the three
years ended June 30, 1996, 1997 and 1998 is as follows:
<TABLE>
<CAPTION>
OUTSTANDING STOCK OPTIONS
-------------------------- WEIGHTED-
NUMBER OF PRICE AVERAGE
SHARES PER SHARE EXERCISE PRICE
---------- ------------ --------------
<S> <C> <C> <C>
Balance at June 30, 1995................... 293,620 $0.38-$4.80 $3.41
Options granted.......................... 84,271 $4.80-$6.72 $6.20
Options exercised........................ (44,078) $0.38-$4.80 $0.48
Options canceled......................... (5,203) $0.72-$4.80 $4.38
------- ----------- -----
Balance at June 30, 1996................... 328,610 $0.38-$6.72 $4.51
Options granted.......................... 15,417 $6.72 $6.72
Options exercised........................ (5,519) $0.72-$4.80 $1.01
Options canceled......................... (8,127) $2.16-$4.80 $4.18
------- ----------- -----
Balance at June 30, 1997................... 330,381 $0.38-$6.72 $4.70
Options granted.......................... 15,758 $8.88-$9.00 $8.91
Options exercised........................ (11,786) $0.38-$8.88 $2.09
Options canceled......................... (3,016) $4.80-$8.88 $6.58
------- ----------- -----
Balance at June 30, 1998................... 331,337 $0.72-$9.00 $4.96
======= =========== =====
</TABLE>
The weighted average fair value of options granted in the years ended June
30, 1996, 1997 and 1998 were $1.97, $2.11 and $1.24, respectively. Additional
information regarding the options outstanding at June 30, 1998 follows:
<TABLE>
<CAPTION>
OPTIONS OUTSTANDING OPTIONS EXERCISABLE
- -------------------------------------------------- ----------------------
WEIGHTED
AVERAGE WEIGHTED WEIGHTED
RANGE OF REMAINING AVERAGE AVERAGE
EXERCISE NUMBER CONTRACTUAL EXERCISE NUMBER EXERCISE
PRICES OUTSTANDING LIFE PRICE EXERCISABLE PRICE
-------- ----------- ----------- -------- ----------- --------
<S> <C> <C> <C> <C> <C>
$0.72 12,807 1.40 years $0.72 12,807 $0.72
$2.16 27,062 2.77 years $2.16 27,062 $2.16
$3.60-$4.80 201,894 5.31 years $4.67 185,610 $4.65
$6.72-$9.00 89,574 8.24 years $7.10 33,046 $7.10
- ----------- ------- ---------- ----- ------- -----
$0.72-$9.00 331,337 5.74 years $4.96 258,525 $4.51
=========== ======= ========== ===== ======= =====
</TABLE>
Pro forma information regarding net income and earnings per share is
required by SFAS 123, and has been determined as if the Company had accounted
for its employee stock options under the fair value method. The effect on the
Company's pro forma results for each of the fiscal years 1996, 1997 and 1998 was
not material (less than $0.01 per share).
For purposes of pro forma disclosures, the estimated fair value of the
options is amortized over the options' vesting period and was estimated at the
date of grant using a Minimum Value option pricing model
47
<PAGE> 51
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
based on the following assumptions for fiscal years ended June 30, 1996, 1997
and 1998, respectively: risk-free interest rates of 6.4%, 6.3% and 5.7%;
dividend yield of zero; volatility factors of the expected market price of the
Company's common stock of zero; and a weighted-average expected life of the
option of 6 years. Because the effect of SFAS 123 is prospective, the current
effect on pro forma net income (loss) may not be representative of such
compensation expense in future years.
10. RESEARCH & DEVELOPMENT
In July 1995, the Company entered into a research and development agreement
with Novartis Pharmaceuticals ("Novartis"), a Swiss pharmaceutical company, to
evaluate the feasibility of delivering certain Novartis compounds using the
Company's iontophoretic drug delivery technologies. Research funding payments
and license fees paid pursuant to the agreement with Novartis totaled
$2,409,000, $1,750,000 and $1,640,000, respectively, in fiscal years ended June
30, 1996, 1997 and 1998. As of June 30, 1997 and 1998, the Company had
receivables, in the amount of $301,000 and $360,000, respectively, due from
Novartis, for research services rendered, which is included in accounts
receivable in the accompanying balance sheet.
The term of the research and development agreement ends on December 31,
1998, and Novartis has informed the Company that it does not intend to renew the
agreement beyond that date. Dermion is currently devoting the majority of its
research and development capabilities to the development of these systems for
Novartis and will continue to do so through the term of the agreement.
In March 1996, in connection with the research and development agreement,
the Company formed Dermion, a wholly-owned subsidiary established to conduct
advanced iontophoretic drug delivery systems development. The Company
contributed cash, fixed assets and non-exclusive licenses to certain technology,
valued at a historical cost of approximately $1,300,000 to Dermion, in exchange
for common shares. Concurrently, Novartis acquired a 20% equity interest in
Dermion for $1,000,000 in cash. Effective November 1, 1997, the Company entered
into an Exchange Agreement with Novartis. Among other things, the Exchange
Agreement provided for the exchange of Novartis' 20% minority interest in
Dermion, the Company's research and development subsidiary, for 238,541 common
shares of the Company and warrants to purchase, under certain conditions,
through November 1, 2002 an additional 18,750 common shares at an exercise price
equal to $21.60 per share, making Dermion a wholly owned subsidiary of IOMED,
Inc.
11. EMPLOYEE BENEFIT PLAN
The Company has established a 401(k) savings plan for its full-time
employees. The Company makes a matching contribution based on a percentage of
the contributions of participating employees. The Company contributed
approximately $24,000, $19,000 and $21,000 over the years ended June 30, 1996,
1997 and 1998, respectively.
12. INCOME TAXES
Deferred taxes result from differences in the carrying value of various
assets and liabilities between income tax reporting and financial reporting
purposes. These differences arise from differing depreciation methods, and other
reserves that are deductible in different periods for tax and financial
reporting purposes.
48
<PAGE> 52
IOMED, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (CONTINUED)
The approximate tax effect of temporary differences, net operating loss
carryforwards and tax credit carryforwards as of June 30, 1997 and 1998 is as
follows:
<TABLE>
<CAPTION>
1997 1998
----------- -----------
<S> <C> <C>
Deferred tax assets:
Net operating loss carryforwards.......... $ 1,515,000 $ 2,312,000
Book in excess of tax depreciation........ 264,000 210,000
Book in excess of tax amortization........ 5,502,000 5,134,000
Tax credit carryforwards.................. 577,000 520,000
Reserves.................................. 265,000 261,000
Other..................................... -- --
----------- -----------
Total deferred tax assets................... 8,123,000 8,437,000
Valuation allowance......................... (8,123,000) (8,437,000)
----------- -----------
Net deferred tax assets..................... $ -- $ --
=========== ===========
</TABLE>
There were no significant deferred tax liabilities in 1997 or 1998. The
valuation allowance increased by $314,000 during the fiscal year.
There were no net deferred income tax provisions in any of the years
presented. Significant components of the provision for income taxes attributable
to continuing operations are as follows:
<TABLE>
<CAPTION>
1996 1997 1998
-------- ------ ------
<S> <C> <C> <C>
Current:
Federal................................. $(72,000) $5,000 $ --
State................................... (7,000) -- --
-------- ------ ------
Total current provision................... $(79,000) $5,000 $ --
======== ====== ======
</TABLE>
The reconciliation of income taxes at the statutory United States federal
income tax rate and the Company's effective income tax rate attributable to
continuing operations is as follows:
<TABLE>
<CAPTION>
1996 1997 1998
------ ------ ------
<S> <C> <C> <C>
United States statutory rate (percentage)... 34.0% (34.0)% (34.0)%
State tax, net of federal tax benefit....... 3.3% (3.3)% (3.3)%
Non-deductible interest and other
expenses.................................. 0.3% 0.2% 15.3%
Credits..................................... (1.7)% (0.4)% --%
Effect of NOL carryforward and valuation
allowance................................. (42.0)% 37.3% 22.2%
Other....................................... 0.6% 0.2% (0.2)%
------ ------ ------
Effective income tax rate (percentage)...... (5.5)% --% --%
====== ====== ======
</TABLE>
As of June 30, 1998, the Company had approximately $6,284,000 in federal
and state net operating loss carryforwards, and $488,000 in federal tax credit
carryforwards, that expire from 2001 through 2012. Utilization of the Company's
net operating loss and credit carryforwards is limited to the future taxable
income of the Company. Under the "change of ownership" provisions of the
Internal Revenue Code, utilization of these net operating loss and credit
carryforwards may be subject to substantial annual limitation.
49
<PAGE> 53
PART III
ITEM 10. DIRECTORS AND EXECUTIVE OFFICERS OF THE COMPANY
The information required by this item is included under "Election of
Directors," "The Board of Directors and Committees," and "Executive Officers" in
the Company's Proxy Statement to be filed in connection with its Annual Meeting
of Shareholders, to be held on November 20, 1998, and is incorporated herein by
reference.
ITEM 11. EXECUTIVE COMPENSATION
The information required by this item is included under "Compensation of
Directors and Executive Officers" in the Company's Proxy Statement to be filed
in connection with its Annual Meeting of Shareholders, to be held on November
20, 1998, and is incorporated herein by reference.
ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT
The information required by this item is included under "Security Ownership
of Certain Beneficial Owners and Management" in the Company's Proxy Statement to
be filed in connection with its Annual Meeting of Shareholders, to be held on
November 20, 1998, and is incorporated herein by reference.
ITEM 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS
The information required by this item is included under "Certain
Relationships and Related Transactions" in the Company's Proxy Statement to be
filed in connection with its Annual Meeting of Shareholders, to be held on
November 20, 1998, and is incorporated herein by reference.
PART IV
ITEM 14.EXHIBITS, FINANCIAL STATEMENT SCHEDULES, AND REPORTS ON FORM 8-K
FINANCIAL STATEMENTS
The consolidated financial statements of the Company and its subsidiary are
included elsewhere in this Report.
FINANCIAL STATEMENT SCHEDULES
No schedules are required in connection with the filing of this Report as
amounts are either immaterial or are otherwise disclosed in the financial
statements.
50
<PAGE> 54
EXHIBITS
<TABLE>
<CAPTION>
NUMBER DESCRIPTION
------ -----------
<S> <C>
3.1** Amended and Restated Articles of Incorporation of the
Company
3.2* Amended and Restated Bylaws of the Company
4.1* Reference is made to Exhibit 3.1
4.2* Specimen of Common Share Certificate
10.1* Lease between the Company and Hayter Properties, Inc., dated
September 1, 1997
10.2* License Agreement between the Company and Elan International
Services, Ltd., dated April 14, 1997
10.3* License Agreement between the Company and Drug Delivery
Systems, Inc., dated April 14, 1997
10.4* Promissory Note issued by the Company to Elan International
Management, Ltd., in the principal amount of $10,000,000,
dated April 14, 1997
10.5* Promissory Note issued by the Company to Elan International
Management, Ltd., in the principal amount of $5,000,000,
dated April 14, 1997
10.6* Note Purchase and Warrant Agreement among the Company, Elan
International Services, Ltd. And Elan International
Management, Ltd. dated April 14, 1997
10.7* Warrant issued to Elan International Services, Ltd., dated
April 14, 1997
10.8* Registration Rights Agreement between the Company and Elan
International Services, Ltd., dated April 14, 1997
10.9* Asset Acquisition Agreement between the Company and
Fillauer, Inc., dated December 27, 1996
10.10* License Agreement between the Company and Fillauer, Inc.,
dated December 26, 1996
10.11* Warrant issued to Alliance of Children's Hospitals, Inc.,
dated December 1, 1996
10.12* Stock Purchase Agreement between the Company and Child
Health Investment Corporation, dated November 29, 1996
10.13* Manufacturing Agreement between the Company and KWM
Electronics Corporation, dated November 1, 1996
10.14* Contribution Agreement between the Company and Dermion,
Inc., dated March 29, 1996
10.15* Patent License Agreement between the Company and Dermion,
Inc., dated March 29, 1996
10.16* Research and Development Agreement among the Company,
Dermion, Inc. and Ciba-Geigy Corporation, dated March 29,
1996
10.17* Stock Purchase Agreement among the Company, Dermion, Inc.
and Ciba-Geigy Corporation, dated March 29, 1996
10.18* Stockholders' Agreement among the Company, Dermion, Inc. and
Ciba-Geigy Corporation, dated March 29, 1996
10.19* Agreement between the Company and Laboratoires Fournier
S.C.A., dated February 20, 1996
10.20* Agreement between the Company and ALZA Corporation, dated
July 28, 1993
10.21* Supply Agreement between the Company and Abbot Laboratories,
Inc., dated April 27, 1993
10.22* Stock Purchase Agreement between the Company and The CIT
Group/Venture Capital, Inc., dated March 8, 1993
10.23* Stock Purchase Agreement between the Company and certain
investors, dated February 19, 1993
10.24* License Agreement between the Company and the University of
Utah Research Foundation, dated October 1, 1992
10.25* Warrant issued to Silicon Valley Bank, dated June 25, 1992
10.26* Company 1997 Share Incentive Plan
10.27* Preferred Stock Purchase Agreement between the Company,
Newtek Ventures, MBW Venture Partners, Michigan Investment
Fund, Utah Ventures, Cordis Corporation, Ian R.N. Bund,
James R. Weersing and Robert J. Harrington, dated August 4,
1987
</TABLE>
51
<PAGE> 55
<TABLE>
<CAPTION>
NUMBER DESCRIPTION
------ -----------
<S> <C>
10.28* Exchange Agreement among the Company, Novartis
Pharmaceuticals Corporation and Dermion, Inc., dated
November 1, 1997
10.29* Warrant to Purchase Shares of Common Stock in favor of
Novartis Pharmaceuticals Corporation, dated November 1, 1997
10.30* First Amendment of Research & Development Agreement among
the Company, Novartis Pharmaceuticals Corporation and
Dermion, Inc. dated November 1, 1997
10.31* Supply Agreement between the Company and Luitpold
Pharmaceuticals, Inc./American Regent Laboratories, Inc.
dated December 4, 1994
11.1*** Statement re computation of earnings per share
21.1* Schedule of Subsidiaries
27.1** Financial Data Schedule
</TABLE>
- ---------------
* Filed as an exhibit to the Registration Statement on Form S-1, filed by the
Company on April 23, 1998.
** Filed herewith.
*** Information included in consolidated financial statements.
REPORTS ON FORM 8-K
On July 2, 1998, the Company filed a report on Form 8-K with regard to the
decision by Novartis Pharmaceuticals Corporation not to renew the collaborative
research and development agreement between the Company, Dermion, Inc., the
Company's wholly owned subsidiary, and Novartis beyond its scheduled December
31, 1998, expiration date.
52
<PAGE> 56
INDEX TO EXHIBITS
<TABLE>
<CAPTION>
NUMBER DESCRIPTION PAGE
- ------ ----------- ----
<C> <S> <C>
3.1 Amended and Restated Articles of Incorporation dated April 59
28, 1998....................................................
27.1 Financial Data Schedule..................................... 64
</TABLE>
53
<PAGE> 57
SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) of the Securities
Exchange Act of 1934, the Registrant has duly caused this report to be signed on
its behalf by the undersigned thereunto duly authorized.
IOMED, INC.
By: /s/ JAMES R. WEERSING
------------------------------------
James R. Weersing
Date: September 28, 1998 Chairman
By: /s/ ROBERT J. LOLLINI
------------------------------------
Robert J. Lollini
Vice President, Finance and
Date: September 28, 1998 Chief Financial Officer
SIGNATURES
In accordance with the Securities Exchange Act of 1934, this report has
been signed below by the following persons on behalf of the Company and in the
capacities and on the dates indicated.
<TABLE>
<CAPTION>
SIGNATURE CAPACITY DATE
--------- -------- ----
<C> <S> <C>
/s/ JAMES R. WEERSING Chairman September 28, 1998
- ---------------------------------------------
James R. Weersing
/s/ JOHN W. FARA, PH.D. Director September 28, 1998
- ---------------------------------------------
John W. Fara, Ph.D.
/s/ STEVEN P. SIDWELL Director September 28, 1998
- ---------------------------------------------
Steven P. Sidwell
/s/ PETER J. WARDLE Director September 28, 1998
- ---------------------------------------------
Peter J. Wardle
/s/ WARREN WOOD Director September 28, 1998
- ---------------------------------------------
Warren Wood
</TABLE>
54
<PAGE> 1
EXHIBIT 3.1
ARTICLES OF AMENDMENT
OF THE ARTICLES OF INCORPORATION OF IOMED, INC.
Pursuant to the provisions of the provisions of the Utah Revised Business
Corporation Act (the "Act"), the undersigned corporation adopts the following
Articles of Amendment to its Articles of Incorporation:
FIRST: The name of the corporation is IOMED, Inc.
SECOND: Article II of the corporation's Articles of Incorporation is hereby
amended by adding thereto a new paragraph D, which shall read in its entirety as
set forth on Exhibit "A" to these Articles of Amendment, which by this reference
is incorporated herein as though set forth herein in full.
THIRD: The foregoing amendment to the corporation's Articles of
Incorporation do not provide for an exchange, reclassification or cancellation
of issued shares of the corporation.
FOURTH: Pursuant to the Act, the foregoing amendment to the corporation's
Articles of Incorporation was adopted by the Board of Directors of the
corporation on the 28th day of April, 1998.
FIFTH: Pursuant to the Act, the foregoing amendment to the corporation's
Articles of Incorporation was adopted by the Board of Directors of the
corporation without shareholder action, and no such shareholder action was
required under the Act or the corporation's Articles of Incorporation.
IN WITNESS WHEREOF, the undersigned has executed these Articles of
Amendment as of this 28th day of April, 1998.
IOMED, INC.
By: /s/ ROBERT J. LOLLINI
Robert J. Lollini
Vice President and Chief
Financial Officer
<PAGE> 2
EXHIBIT A
"D. SERIES D NON-VOTING PREFERRED SHARES. A total of 1,000,000 Preferred
Shares shall be designated as "Series D Non-Voting Preferred Shares", and
shall have the following preferences, limitations and relative rights:
1. VOTING RIGHTS. Except as otherwise expressly provided by law, the
holders of Series D Non-Voting Preferred Shares shall not have the right to vote
upon matters submitted to the shareholders of the corporation for consideration
and vote; provided, however, that such holders shall be entitled to notice of
any shareholders' meeting in accordance with the Bylaws of the Corporation.
2. LIQUIDATION RIGHTS. The Series D Non-Voting Preferred Shares shall not
have any liquidation or similar preference over the Common Stock in the event of
any voluntary or involuntary liquidation, dissolution or winding up of the
affairs of the Corporation. Upon any such liquidation, dissolution or winding
up, and after payment or provision for payment of the debt and other liabilities
of the Corporation, the holders of Series D Non-Voting Preferred Shares then
outstanding shall be entitled to receive, for each Common Share into which a
Series D Non-Voting Preferred Share is then convertible, the same amounts, if
any, as are received by the holders of Common Shares as the result of or in
connection with such liquidation, dissolution or winding up.
3. DIVIDENDS. The holders of shares of Series D Non-Voting Preferred
Shares shall be entitled, when and if declared by the Board of Directors, to
receive dividends and distributions out of any assets legally available
therefor. No dividend or distribution of cash, securities of other persons,
assets, or options or rights (not referred to in section 4(c) hereof) may be
declared or paid on the Common Shares unless at the same time an equivalent
dividend or distribution, as the case may be, is declared or paid on all
outstanding Series D Non-Voting Preferred Shares. No dividend or distribution of
cash, securities of other persons, assets or options or rights (not referred to
Section 4(c) hereof) may be declared or paid on the Series D Non-Voting
Preferred Shares unless at the same time an equivalent dividend or distribution,
as the case may be, is declared or paid on all outstanding Common Shares. In the
event a dividend or distribution is declared on the Common Shares, the dividend
or distribution on each Series D Non-Voting Preferred Share shall be paid at the
same rate per share based upon the number of Common Shares into which such share
of Series D Non-Voting Preferred Shares is convertible immediately prior to the
record date for such dividend or distribution. The right to dividends or
distributions on Series D Non-Voting Preferred Shares shall not be cumulative,
and no right shall accrue to holders of Series D Non-Voting Preferred Shares by
reason of the fact that dividends on said shares are not declared in any period.
4. CONVERSION. The holders of Series D Non-Voting Preferred Shares shall
have conversion rights as follows (the "Conversion Rights"):
(a) Conversion. Subject to the adjustments set forth in subsection (c)
below, each Series D Non-Voting Preferred Share shall be convertible, at
the option of the holder thereof and at any time after the date of issuance
of such share, at the office of the corporation or any transfer agent for
the Series D Non-Voting Preferred Shares, into one fully paid and
non-assessable Common Share (the "Conversion Rate").
(b) Mechanics of Conversion. Before any holder of the Series D
Non-Voting Preferred Shares shall be entitled to convert the same into
Common Shares, such holder shall surrender the certificate or certificates
therefor, duly endorsed, at the office of the Corporation or of any
transfer agent for the Series D Non-Voting Preferred Shares, and shall give
written notice by mail, postage prepaid, to the Corporation at its
principal corporate office. The written notice shall state the holder's
election to convert Series D Non-Voting Preferred Shares and shall state
therein the name or names in which the certificate or certificates for
Common Shares are to be issued. The Corporation shall, as soon as
practicable thereafter, issue, or cause to be issued, and deliver at such
office to such holder, or to the nominee or nominees of such holder, a
certificate or certificates for the number of Common Shares to which such
holder shall be entitled. Such conversion shall be deemed to have been made
immediately prior to the close of business on the date of the surrender of
the shares to be converted, and the person or persons
<PAGE> 3
entitled to receive the Common Shares issuable upon such conversion shall
be treated for all purposes as the record holder or holders of such Common
Shares as of such date.
(c) Adjustment Upon Split, Subdivision, Etc.
(i) In the event the Corporation should, at any time or from time
to time after the date on which any Series D Non-Voting Preferred Shares
are issued, fix a record date for the effectuation of a split or
subdivision of the outstanding Common Shares or the determination of
holders of Common Shares entitled to receive a dividend or other
distribution payable in additional Common Shares or in other securities
or rights convertible or exercisable into, or exchangeable for,
additional Common Shares (such other securities or rights hereinafter
referred to as "Common Share Equivalents") without payment of any
consideration by such holder for the additional Common Shares or the
Common Share Equivalents (including the additional Common Shares
issuable upon conversion, exercise or exchange thereof), then, as of
such record date (or the date of such dividend, distribution, split or
subdivision if no record date is fixed), the Conversion Rate of the
Series D Non-Voting Preferred Shares shall be appropriately adjusted so
that the number of Common Shares issuable on conversion of each Series D
Non-Voting Preferred Share shall be increased in proportion to such
increase of outstanding Common Shares (including Common Shares
represented by Common Share Equivalents in the manner of (ii) below).
(ii) In the case of a dividend or other distribution payable in
Common Share Equivalents, the following provisions shall apply for
purposes of subparagraph (c)(i):
A. The aggregate maximum number of Common Shares deliverable
upon the conversion or exercise of, or in exchange for, such Common
Share Equivalents shall be deemed to have been issued and to be
outstanding as of the record date therefor (or the date of such
dividend or distribution if no record date is fixed), but no further
adjustment shall be made for the actual issuance of Common Shares
upon the conversion, exercise or exchange of such Common Share
Equivalents.
B. In the event of any change in the number of Common Shares
deliverable upon the conversion or exercise of, or in exchange for,
such Common Share Equivalents, including without limitation a change
resulting from the antidilution provisions thereof, the Conversion
Rate then in effect for the Series D Non-Voting Preferred Shares
shall forthwith be readjusted to such Conversion Rate as would have
been obtained had the adjustment which was made in connection with
such Common Share Equivalents which were not converted, exercised or
exchanged prior to such change been made upon the basis of such
change, but no further adjustment shall be made for the actual
issuance of Common Shares upon the conversion, exercise or exchange
of such Common Share Equivalents.
C. Upon the expiration or termination of any Common Share
Equivalents, the Conversion Rate for the Series D Non-Voting
Preferred Shares shall forthwith be readjusted to such Conversion
Rate as would have been obtained had the adjustment which was made in
connection with such Common Share Equivalents been made upon the
basis of the issuance of only the number of Common Shares actually
issued upon the conversion, exercise or exchange of such Common Share
Equivalents.
(iii) If the number of Common Shares outstanding at any time after
the date on which any Series D Non-Voting Preferred Shares are issued is
decreased by a combination of the outstanding Common Shares, then,
following the record date of such combination, the Conversion Rate for
the Series D Non-Voting Preferred Shares shall be appropriately
decreased in proportion to such decrease in outstanding shares.
(d) Recapitalizations. If at any time or from time to time there
shall be a recapitalization of the Common Shares (other than a subdivision,
combination or merger or sale of assets transaction provided for elsewhere
in this Section 4), provision shall be made so that the holders of the
Series D Non-Voting Preferred Shares shall thereafter be entitled to
receive, with respect to each Common Share acquired
2
<PAGE> 4
upon conversion of the Series D Non-Voting Preferred Shares, the number of
shares of stock or other securities or property of the Corporation or
otherwise, to which a holder of Common Shares would have been entitled on
such recapitalization. In any such case, appropriate adjustment shall be
made in the application of the provisions of this Section 4 with respect to
the rights of the holders of the Series D Non-Voting Preferred Shares after
the recapitalization to the end that the provisions of this Section 4 shall
be applicable after the recapitalization in a manner which is, as nearly
equivalent as may be practicable, equivalent to the manner in which this
Section 4 applied prior to the recapitalization.
(e) No Impairment. The Corporation will not, by amendment of its
Articles of Incorporation or Bylaws or through any reorganization,
recapitalization, transfer of assets, consolidation, merger, dissolution,
issuance or sale of securities, agreement or any other voluntary action,
avoid or seek to avoid the observance or performance by the Corporation of
its obligations hereunder, but will, at all times and in good faith, take
such actions as may be necessary to carry out the intent of the provisions
of this Section 4.
(f) No Fractional Shares and Certificates as to Adjustments.
(i) No fractional shares shall be issued upon conversion of the
Series D Non-Voting Preferred Shares, and the number of Common Shares to
be issued shall be rounded to the nearest whole share, determined on the
basis of the total number of Series D Non-Voting Preferred Shares which
the holder is at the time converting into Common Shares and the number
of Common Shares issuable upon such aggregate conversion.
(ii) Upon the occurrence of each adjustment or readjustment of the
Conversion Rate of the Series D Non-Voting Preferred Shares pursuant to
this Section 4, the Corporation, at its expense, shall promptly compute
such adjustment or readjustment in accordance with he terms hereof and
prepare and furnish to each holder of Series D Non-Voting Preferred
Shares a certificate setting forth such adjustment or readjustment and
showing in detail the facts upon which such adjustment or readjustment
is based. The Corporation shall, upon the written request of any holder
of Series D Non-Voting Preferred Shares, furnish or cause to be
furnished to such holder a like certificate setting forth (A) such
adjustment and readjustment, (B) the Conversion Rate at the time in
effect, and (C) the number of Common Shares and the amount, if any, of
other property which at the time would be received upon the conversion
of a Series D Non-Voting Preferred Share.
(g) Notice of Record Date. In the event of any taking by the
Corporation of a record of the holders of any class of securities for the
purpose of determining the holders thereof who are entitled to receive any
dividend (other than a cash dividend) or other distribution, any right to
subscribe for, purchase or otherwise acquire any shares of any class or any
other securities of property, or to receive any other right, the
Corporation shall mail to each holder of Series D Non-Voting Preferred
Shares, at least 10 days prior to the date specified therein, a notice
specifying the date on which any such record is to be taken for the purpose
of such dividend, distribution or right, and the amount and character of
such dividend, distribution or right.
(h) Reservation of Common Shares Issuable Upon Conversion. The
Corporation shall at all times reserve and keep available out of its
authorized but unissued Common Shares, solely for the purpose of effecting
the conversion of the Series D Non-Voting Preferred Shares, such number of
its Common Shares as shall from time to time be sufficient to effect the
conversion of all outstanding Series D Non-Voting Preferred Shares. If at
any time the number of authorized but unissued Common Shares shall not be
sufficient to effect the conversion of all then outstanding Series D
Non-Voting Preferred Shares, the Corporation will take such corporate
action as may, in the opinion of its counsel, be necessary to increase its
authorized but unissued Common Shares to such number of shares as shall be
sufficient for such purposes.
(i) Notices. Any notice required by the provisions of this Section 4
to be given to the holders of Series D Non-Voting Preferred Shares shall be
deemed given if deposited in the United States mail, postage prepaid, and
addressed to each holder of record at his, her or its address, as such
address then appears on the books of the Corporation."
3
<TABLE> <S> <C>
<ARTICLE> 5
<LEGEND>
THIS SCHEDULE CONTAINS SUMMARY FINANCIAL INFORMATION EXTRACTED FROM THE
IOMED, INC. CONDENSED CONSOLIDATED BALANCE SHEETS AND STATEMENTS OF OPERATIONS
FOR THE TWELVE MONTHS ENDED JUNE 30, 1998 AND IS QUALIFIED IN ITS ENTIRETY BY
REFERENCE TO SUCH FINANCIAL STATEMENTS.
</LEGEND>
<S> <C>
<PERIOD-TYPE> 12-MOS
<FISCAL-YEAR-END> JUN-30-1998
<PERIOD-START> JUL-01-1997
<PERIOD-END> JUN-30-1998
<CASH> 16,709,000
<SECURITIES> 0
<RECEIVABLES> 1,624,000
<ALLOWANCES> 54,000
<INVENTORY> 876,000
<CURRENT-ASSETS> 19,208,000
<PP&E> 4,431,00
<DEPRECIATION> 3,648,000
<TOTAL-ASSETS> 20,201,000
<CURRENT-LIABILITIES> 1,363,000
<BONDS> 187,000
0
6,881,000
<COMMON> 34,408,00
<OTHER-SE> (22,638,000)
<TOTAL-LIABILITY-AND-EQUITY> 20,201,000
<SALES> 8,489,000
<TOTAL-REVENUES> 10,277,000
<CGS> 3,890,000
<TOTAL-COSTS> 10,838,000
<OTHER-EXPENSES> (391,000)
<LOSS-PROVISION> 0
<INTEREST-EXPENSE> 930,000
<INCOME-PRETAX> (1,100,000)
<INCOME-TAX> 0
<INCOME-CONTINUING> (1,100,000)
<DISCONTINUED> 0
<EXTRAORDINARY> 0
<CHANGES> 0
<NET-INCOME> (1,100,000)
<EPS-PRIMARY> (0.29)
<EPS-DILUTED> (0.29)
</TABLE>
