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SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
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FORM 10-K/A
AMENDMENT NO. 2
(Mark One)
X Annual report pursuant to section 13 or 15(d) of the Securities
Exchange Act of 1934 for the fiscal year ended December 31, 1998, or
___ Transition report pursuant to section 13 or 15(d) of the Securities
Exchange Act of 1934 for the transition period ended
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Commission File Number: 2-93277-D
MEDIZONE INTERNATIONAL, INC.
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(Exact name of registrant as specified in its charter)
Nevada 87-0412648
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(State or other jurisdiction (I.R.S. Employer Identification No.)
of incorporation or organization)
144 Buena Vista, P.O. Box 742, Stinson Beach, California 94970
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(Address of principal executive offices) (Zip code)
Registrant's telephone number (including area code): (415) 868-0300
Securities registered pursuant to Section 12(b) of the Act: None
Securities registered pursuant to Section 12(g) of the Act: None
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. Yes X No __
Indicate by check mark if disclosure of 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 hereto. Yes __ No X
The aggregate market value of voting common stock held by non-affiliates of
the Registrant was $5,388,427 on December 31, 1998, based on the average bid and
asked prices of such stock as reported in the OTC Electronic Bulletin Board and
the "pink sheets" of the National Daily Quotation Bureau.
On January 8, 1999, the Company had 148,926,434 shares of common stock, par
value $.001 per share issued and outstanding.
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TABLE OF CONTENTS
PART I
Page
Item 1. Business..........................................................1
Item 2. Properties.......................................................18
Item 3. Legal Proceedings................................................19
Item 4. Submission of Matters to a Vote of Security Holders..............19
PART II
Item 5. Market for Registrant's Common Equity and Related Stockholder
Matters..........................................................20
Item 6. Selected Financial Data..........................................21
Item 7. Management's Discussion and Analysis
of Financial Condition and Results of Operations.................21
Item 8. Financial Statements and Supplementary Data......................22
Item 9. Changes in and Disagreements with
Accountants on Auditing and Financial Disclosure.................23
PART III
Item 10. Directors and Executive Officers of the Registrant...............24
Item 11. Executive Compensation...........................................25
Item 12. Security Ownership of Certain
Beneficial Owners and Management..............................26
Item 13. Certain Relationships and Related Transactions...................27
PART IV
Item 14. Exhibits, Financial Statement
Schedules, and Reports on Form 8-K...............................29
Signatures................................................................34
Exhibits Index...........................................................E-1
Financial Statements and Schedules.......................................F-1
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PART I
Item 1. Business
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General
Medizone International, Inc., a Nevada corporation (the "Company")
organized in 1986, is a development stage company. To date its principal
business has been limited to(i)seeking regulatory approval for its drug, a
precise mixture of ozone and oxygen called MEDIZONE(R)(sometimes referred to in
this report as the "Drug"), and its process of inactivating lipid enveloped
viruses for the intended purpose of decontaminating blood and blood products and
assisting in the treatment of certain diseases; and (ii) developing or acquiring
the related technology and equipment for the medical application of its
products, including its drug production and delivery system (the "Medizone
Technology").
The Drug is intended to be used as a therapeutic drug in humans to
inactivate certain viruses, and thereby afford a treatment for certain
virally-based diseases (including Human Immunodeficiency Virus ["HIV"], the AIDS
related virus, Hepatitis B, Hepatitis C, Epstein-Barr, herpes and
cytomegalovirus), and to decontaminate blood and blood products. Applications of
these uses are covered under the Company's patent (U.S. Patent No. 4,632,980).
The Medizone Technology was developed for the production of the Drug and is the
basis for the design of equipment for which a patent has been issued in the
United States (Patent No. 5,052,382). The Company has also obtained several
foreign patents based on these patents.
Patents
The Company owns two key patents. The first is a United States process
patent (U.S. Patent No. 4,632,980) entitled, "Ozone Decontamination of Blood
and Blood Products" (the "Patent"). The second patent is a related United
States equipment patent (U.S. Patent No. 5,052,382) entitled "Approaches for
the Control Generation and Administration of Ozone" (the "Equipment Patent").
The Patent, which covers a procedure for ozone decontamination of blood
and blood products through the treatment of blood and blood components, is the
Company's principal asset. It was purchased, together with rights to other
ozone-related inventions, from Immunologics Limited Partnership, L.P. ("ILP") in
1987, for 6,000,000 shares of the Company's common stock (the "Patent Purchase
Agreement"). John M. Kells, the general partner of ILP, was Chairman of the
Company's Board of Directors from November 1992 through September 1993.
The Patent Purchase Agreement requires the Company to pay to ILP an
annual royalty equal to 3% of the net receipts (i.e., net receipts after all
credits, returns and customary deductions, and exclusive of all taxes) of the
Company received in connection with the sale of any product, device, or
apparatus embodying the Patent. The method covered by the Patent is the
principal use of ozone under study by the Company and is the method incorporated
in its regulatory applications. In June 1990, pursuant to the Company's request
for re-examination of the Patent, the U.S. Patent Office issued a re-examination
certificate, confirming the patentability of the claims covered by the Patent.
The Patent will expire in 2003, subject to
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extension based upon the length of time required to bring the Patent to
commercial fruition. The Company has been granted patents (based on the
Patent)in Canada and the European Patent Community, Australia, Malaysia, Hong
Kong and Japan, with applications pending in Singapore. The foreign patents
began to be issued in 1990 and will expire 17 years after their respective dates
of issuance.
The Equipment Patent, which covers apparatus for the controlled
generation, monitoring and dosage of a precise admixture of ozone and oxygen
i.e., the Drug, was developed by a consultant engineer to the Company and issued
and assigned to the Company in 1991. The Equipment Patent was developed to
provide the physical means to deploy the Patent. The foreign patent coverage of
the Equipment Patent parallels the coverage of the Patent.
In late 1996, the Company became aware that a United States patent had
been issued to a Canadian corporation, which it believes infringes on the
Medizone patent. The Company contacted its patent attorneys who took appropriate
steps to protect the Company's patent rights. While the Company never received a
response to its protests, it has been reported the Canadian company did stop
working with ozone.
On July 30, 1998, the Company was given recorded assignment US. Serial
No. 09/126,504 for a new patent application, External Application of
Ozone/Oxygen For Pathogenic Conditions. The Company believes that this
application, if granted, would strengthen the Company's existing equipment
patents as it addresses advanced developments with ozone generating equipment.
Research and Development
The Company does not own laboratories or other clinical research or
testing facilities. The Company's research and development activities have been
conducted by contract laboratories and clinicians. Research and Development
activities are directed by Gerard V. Sunnen, MD. Dr. Sunnen is a member of the
Board of Directors and also serves as President and Director of Research of the
Company.
Pre-clinical Studies
Pre-clinical Studies are non-human studies of the Drug and related
equipment. Since 1988, the Company has both sponsored and been the beneficiary
of research, among other things, (i) to determine whether the use of ozone,
either alone or with other modalities, is efficacious in the treatment of
certain diseases and (ii) to establish additional scientific evidence that
ozone, through the use of the patents or applications of scientific
methodologies of a similar nature can decontaminate blood or lipid enveloped
viruses and thereby significantly diminish the degree of transfusion related
disease.
Pre-clinical projects sponsored by the Company include: (1) studies to
test ozone's ability to inactivate HIV, conducted at the State University of New
York ("SUNY") Health Science Center at Syracuse; (2) a pilot animal study of the
potential toxicity of ozone, conducted by the Arnold & Marie Schwartz College of
Pharmacy and Health Science at Long Island University; and (3) studies
investigating the effects of ozone/oxygen admixtures on human
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peripheral blood, including whole blood, serum and plasma, conducted by the
Blood Bank of Mt. Sinai Medical Center, New York City.
In 1990, the Canadian Blood Forces Program (under the aegis of the
Canadian Department of Defense and Agriculture and the Canadian Red Cross)
requested that the Company add the Medizone Technology to the other proprietary
technology being investigated as an experimental arm of an ozone-based blood
sterilization investigative program. The program was an attempt to develop an
effective technology for sterilizing whole blood and blood products. This
program, which was to study the Medizone Technology as it relates to the
inactivation of Simian Immunodeficiency Virus ("SIV"), included a live primate
model. The program continued until 1994, completing two out of the three
proposed stages, when the funding of the Canadian Blood Forces Program was
discontinued. The Company's management learned in late 1997 that the program
suffered difficulties with the ozone/bioserum interface that was used in the
study, which resulted in an inconsistent, difficult to accurately measure,
dosage of ozone. As a result, from a regulatory perspective the study yielded
results that could not be used due to the inability to specifically identify
dosage. From a practical standpoint, the Company vies this study of the Drug as
a success, in that the treated simians never became ill through the entire
course of the trial period.
Governmental Regulation
The Drug, the Medizone Technology and related products derived
therefrom are regulated under the Federal Food, Drug and Cosmetic Act and the
regulations promulgated thereunder (the "FDC Act") by the Food and Drug
Administration (the "FDA"). The FDA exercises broad and extensive authority in
regulating the development, production, importation, distribution and promotion
of "new drug" products and "investigational devices" pursuant to the FDC.
Because ozone generation for purposes of interfacing with blood and
blood products is regarded as a new drug delivery, the Company is precluded from
selling or distributing the Drug or the Medizone Technology until after FDA
approval has been granted. In order to obtain FDA approval, the Company will be
required to submit medical and scientific evidence sufficient to demonstrate
that the Drug and the Medizone Technology have been successfully used in
pre-clinical studies followed by well-controlled clinical studies using human
volunteer subjects. The FDA will not grant a "new drug application" or NDA
unless it contains sufficient medical evidence and data to permit a body of
qualified and experienced scientists to conclude that the new drug product is
safe and effective for its recommended and proposed medical uses. Historically,
the FDA has had a bias against treating humans with ozone, citing issues of
safety.
In order to initiate the first phase (Phase I) of human clinical
studies required as part of a NDA, an applicant must submit to the FDA an
application for an Investigational New Drug Exemption ("IND"), which contains
adequate information to satisfy the FDA that human clinical studies can be
conducted without exposing the volunteer human subjects to an unreasonable risk
of illness or injury. The Company submitted an IND application to the FDA on
October 6, 1985, and requested FDA approval to commence human clinical trials
using ozone-oxygen to inactivate HIV. The FDA deemed the IND application to be
incomplete and required the Company to conduct additional animal studies prior
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to commencing a large animal study and human trials. In September 1994, the FDA
inactivated the Company's IND. The Company has no present plans to commence a
large animal study, which would require, as a precursor, additional small animal
and laboratory work. Accordingly, there can be no assurance that the Company's
IND application will ever be re-opened. Until an NDA has been granted to the
Company, it may not distribute ozone-generating devices, except to researchers
who agree to follow FDA guidelines, and provided the devices are labeled as
"Investigational Devices."
Because ozone has been used to treat humans in Europe for at least 30
years, the European Union (the "EU") is more accepting than the United States of
human clinical trials of ozone therapies. Accordingly, management believes the
Company should pursue foreign Phase I human toxicity trials, as well as early
stage efficacy trials.
It is the Company's intention to pursue future trials in Canada as soon
as funding allows. The Company believes trials successfully completed in Canada
should be acceptable to both the United States FDA and the Regulatory Agencies
of the EU.
Clinical Studies
The Italian Initiative
To date the Company has not performed any human clinical studies. In
late 1992, the Italian Ministry of Health suspended the clinical use of ozone
until such time as sufficient scientific evidence was available to support its
use as a human therapeutic treatment. The Italian Ministry of Health designated
the Italian Scientific Society for Ozone-Oxygen Therapy in Bergamo, Italy
("ISSOT") as the agency to select those treatment protocols utilizing ozone as
worthy of investigation and to provide those protocols to the Italian Ministry
of Health for review and approval. By letter agreement dated March 23, 1993,
with ISSOT, the Company entered into a collaborative arrangement to research and
examine the efficacy of the Medizone Technology in the treatment of various
blood-related human diseases. The research is to be supervised by ISSOT in
Italy, under the direction of a research group assembled by the Italian Ministry
of Health. The research is to be conducted in accordance with protocols that
will meet EU Standards for human clinical trials (to be furnished by the
Company) at university-based hospitals, which will enter into agreements with
the Company on a site-by-site basis. The ISSOT letter agreement requires the
Company to furnish ozone-generating instruments for use in the trials and to pay
for laboratory tests performed by each testing institution that are outside the
scope of the normal realm of clinical analyses performed by the testing
institutions. There can be no assurance that any of the data generated from the
ISSOT research will be permitted to be utilized in connection with the Company
efforts to re-open the FDA IND (see "Governmental Regulation").
While the ethics committees at certain university hospitals have stated
their approval for the Company to conduct Phase II trials, they would require
the Company to have either completed a large animal study and Phase I trials or
to have these requirements waived. The Company has never performed a large
animal study or Phase I clinical trials and does not possess the necessary data
with respect to its ozone therapy to commence Phase II study. However, there
does exist a broad use and understanding of ozone therapy throughout Europe and
there have been numerous scientific articles published in European
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medical journals describing the use of ozone on humans. The Company has held
discussions with an Italian Contract Research Organization (the "ICRO")with a
view to having the ICRO act as an intermediary on behalf of the Company with the
Italian Ministry of Health and prepare a written submission to the Italian
Ministry of Health regarding the data in the public domain on ozone therapy with
a view to having the Italian Ministry of Health accept this material as proof of
safety, toxicity and tolerance of the use of the Company's ozone technology on
humans in lieu of having the Company perform a large animal study and possibly
even a Phase I clinical study. The ICRO would also design a research program and
protocols for clinical trials which would meet the standards of the EU and FDA,
monitor the clinical terms and collect and prepare analyses of the data produced
by the trials.
The Company will not be able to enter into a formal contract with ICRO
unless it obtains additional funding. If the Italian Ministry of Health does not
accept the published evidence on the use of ozone therapy on humans, the Company
will be required to perform its own Phase I clinical trials and possibly a large
animal study. In late 1997, the Company entered into discussion with Italian and
Belgium clinicians to perform Phase I clinical studies. However, no formal
agreements with these clinicians can be signed and the studies will not begin
until the Company obtains additional funding. The Company estimates that it
would require approximately $1.5 million to advance these research initiatives
through the completion of a Phase III study and submission of the data for
approval to the Italian Ministry of Health.
Instrument Development
On October 17, 1996, the Company executed an agreement with
Multiossigen, S.r.L., an Italian corporation located in Bergamo, Italy (the
"Manufacturer"), dated as of September 13, 1996 (the "Equipment Contract"),
providing for the manufacture of ozone generating devices to be used in human
trials.
In November 1997, the Company's President & CEO, Director of Research
and Italian Liaison, met in Italy with the Company's proposed Italian research
partners and the Company's ozone generating equipment manufacture, Multiossigen,
S.r.L. At that time they determined that the equipment did not produce an
acceptable level of ozone concentration, nor did it allow a consistent dosage
required to satisfy the Company's goals relative to therapeutic treatment and
regulatory approval.
An agreement was made to manufacture equipment to the new standard. The
new equipment was originally to be delivered in late January of 1998, that date
was then extended to late March of 1998. When it appeared that it might be
difficult for Multiossigen to meet the Company's requirements, Dr. Guenter
Moldzio, President of Biozone Corporation of Englewood, Colorado was contracted
to build a prototype of the required equipment. The Biozone prototype was
delivered to Medizone in 60 days. Following extensive testing by Dr. Sunnen, the
Company's Director of Research, the prototype was accepted. Used in the
veterinary research program investigating the deactivation of viruses in serum
products, the Biozone equipment appears to meet all of the Company's development
goals.
By September of 1998, Multiossigen had not delivered the new equipment
to Medizone and the agreement with Multiossigen was terminated. The Company
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entered into an agreement with Biozone Corporation, under which Biozone was
granted world wide manufacturing rights for Medizone Ozone Generating Equipment.
Medizone has exclusive world wide marketing rights for Biozone manufactured
equipment intended for scientific research and medical applications, to be
marketed under the Medizone label. Biozone Corporation expects to relocate to
California in the future, so the manufacturing facility can be located near
Medizone's corporate headquarters. Under this agreement, Biozone retains the
right to market its other industrial applications, such as water treatment
plants. Once Medizone has obtained regulatory approvals for its technology and
protocols, and is in production mode, Biozone will phase out its other business
to concentrate on its work with Medizone. As part of this licensing agreement
the Company issued 100,000 shares of restricted stock Biozone Corporation.
International Activities
Medizone Canada Limited
-----------------------
To maximize both research opportunities and the potential market for
its products, the Company intends to establish subsidiary or affiliated
corporations in other countries. The organization of these subsidiaries may
initially require the Company to incur significant expenses; thereafter, it is
intended that the subsidiaries would be responsible for organizing research
programs and generating possible sources of financing, from which the Company
would benefit directly or indirectly. It is anticipated that the Company would
also enter into license agreements with all subsidiary companies.
In June 1998, the Company sold its interest in Medizone Canada Limited,
a Utah corporation ("MCL")for $125,000 cash in a private transaction. The
Company retained ownership of all of the issued and outstanding stock of MCL
Medizone Canada, Ltd., a Canadian corporation("MedCan"). MedCan was a
participant in the Canadian Blood Forces Program's SIV Study.
The Canadian government requires that research accepted under the
auspices of the Health Canada must be performed by a Canadian Company. Future
research in Canada will be pursued through MedCan. Future staffing of MedCan
will be with Canadian citizens and MedCan will be operated from Canada.
Furthermore, unlike US Law, under Canadian law, a for profit corporation can own
a non-profit. The Company also intends to establish under the structure of
Medizone Canada, Ltd., a non-profit corporation in the future. The future
business of the non-profit will be to aid the economically underdeveloped third
world countries in the acquisition of Medizone equipment, training of doctors,
and funding of programs for hepatitis and aids, at greatly discounted prices in
those countries.
Medizone New Zealand Limited
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On June 22, 1995, the Company entered into a series of contracts
(collectively the "Transaction Documents") which resulted in the formation of a
joint venture subsidiary incorporated in New Zealand, Medizone New Zealand
Limited ("MNZ"). MNZ,is owned equally under the name by the Company and Solwin
Investments Limited ("Solwin"), a New Zealand corporation which is an affiliate
of Richard G. Solomon ("Solomon"),a former director of the Company.
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MNZ is a research and development stage company formed to obtain regulatory
approval for the distribution of the Company's patented technology in New
Zealand, Australia, South East Asia and the South Pacific Islands.
Pursuant to the Transaction Documents, the Company purchased 100% of
MNZ from Solomon, who had caused the formation of MNZ. Contemporaneously with
this transaction, the Company sold 50% of MNZ to Solwin, a corporation owned by
Solomon, for $150,000, of which $50,000 was loaned by the Company to MNZ on a
demand basis and repaid on October 26, 1995. On October 26, 1995, the Company
loaned MNZ $50,000 on a demand basis, which has not been repaid as of the date
of this report.
Contemporaneous with the creation of the above share structure, the
Company and MNZ entered into a Licensing Agreement (the "Licensing Agreement")
and a Managing Agent Agreement (the "Managing Agent Agreement") with MNZ.
Under the Licensing Agreement, the Company granted an exclusive license
to MNZ for the Patent and the Equipment Patent and the Company's trademark in
New Zealand. MNZ has agreed to apply for corresponding patent protection for
these patents in New Zealand and to use its best effort to exploit the rights
granted in the Licensing Agreement. The Licensing Agreement will terminate on
the expiration date of the last patent obtained in New Zealand, or, if no
patents are obtained, on June 22, 2010. The Company will receive a guaranteed
minimum royalty, in an amount to be agreed to by the Company and MNZ, commencing
in the third year after all necessary regulatory approvals requisite to the
license, use or distribution of the Company's proprietary technology have been
obtained in New Zealand. If the Company and MNZ are unable to agree upon the
amount of the guaranteed minimum royalty, the Company may terminate the
Licensing Agreement. Commencing on the first sale to a user by MNZ, the Company
will receive a sales royalty of MNZ's gross annual sales under the Licensing
Agreement.
Under the Managing Agent Agreement, MNZ will act as the Company's agent
to find licensees of the Medizone Technology in Australia, New Zealand, the
South Pacific Islands and South East Asia (including the Philippines, Indonesia
and Vietnam). Licensing fees will be divided between the Company and MNZ on a
sliding scale as set forth below:
<TABLE>
<CAPTION>
The Company MNZ
----------- ---
<S> <C> <C>
Initial license 50% 50%
Subsequent license
fees up to $500,000 50% 50%
Subsequent license
fees between $500,000
and $750,000 75% 25%
Subsequent license
fees in excess of
$750,000 85% 15%
</TABLE>
MNZ and the Company will also divide any net royalties paid to the
Company under any license entered into pursuant to the Managing Agent Agreement,
with MNZ being paid 10% of the net royalties and the Company
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receiving 90% of the net royalties.
The Managing Agent Agreement expires on the termination or expiration
of the last of the licenses obtained under the agreement, subject to earlier
termination by the Company under certain circumstances.
Competition
The market in which the Company intends to do business is extremely
competitive. The Company is aware of several domestic companies that have
commenced research into the use of ozone as a virucide in the treatment of HIV
and other diseases, or that have announced the intention to do so. Other
companies, foundations, research laboratories or institutions may also be
conducting similar investigations into the use of ozone as a virucide or as a
decontaminant for blood or blood products. The Company is also aware that
another company has provided ozone-generating equipment to departments of the
Canadian government conducting studies in Canada for the purposes of comparison
of technologies.
Employees
As of December 31, 1998, the Company had four employees. Gerard V.
Sunnen, MD. the Director of Research since June 12, 1997 and President of
Medizone since April 15, 1998; Edwin G. Marshall, Chairman of the Board since
June 12, 1997 and Chief Executive Officer since April 15, 1998; Jill C.
Marshall, ND, Chief Operating Officer since April 15, 1998 and Corporate
Secretary since August 6, 1998; and Kevin R. Andersen, CPA, M.S., Chief
Financial Officer since November 2, 1998.
Status of the Company's Research
--------------------------------
The Company has entered into a research agreement with a multi national
research partner interested in the possibility of viral deactivation of serum
products by using ozone. Serum products are used to make a media base that is
then used in the manufacture of vaccines for humans and animals. Under the terms
of the agreement, if the research proves successful, Medizone will then enter
into a licensing agreement for the use of its technology in the viral
deactivation of commercial vats of serum product.
At the Company's 1998 Annual meeting of Shareholders, it was announced
that a human pilot trial into the deactivation of hepatitis C had begun. The
pilot trial, using Medizone ozone generating equipment constructed by Biozone
Corporation, was conducted by a Company associate, Dr. William Hitt, in the
course of his regular medical practice. Dr. Hitt is a member of the Board of
Directors and operates the William Hitt Center in Tijuana, Mexico. The initial
results, with the first four patients, showed significant reductions in viral
load and the normalization of previously elevated liver enzyme levels as
measured by SGOT and SGPT tests. While the therapy, consisting of an out-patient
daily treatment protocol, averaging 21 days in duration, was done in Mexico, the
laboratory tests were evaluated at FDA reference laboratories in the United
States. The pilot trial was not conducted as a double blind, or under conditions
that would allow for peer review, journal published research as required by the
FDA. However, as a proof of concept human trial for the Company's proposed
hepatitis protocols, we view the study as a very positive
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development.
RISK FACTORS
The Company's business, particularly in the development stage, is
subject to a number of risks, including, but not limited to the following:
Development Stage Company/Net Losses
------------------------------------
The Company is in the development stage and has not yet commenced full
operations, nor has it earned any revenues. No assurance can be given that its
business activities will ever generate revenues. As indicated in the Company's
financial statements, it has experienced substantial losses throughout its
history. Losses can be expected to continue for the foreseeable future.
Need for Additional Financing
-----------------------------
The Company has had no source of funds other than through the sale of
its common stock and will require substantial additional capital, which will
most likely be obtained through sales of its common stock, to continue the
research program outlined above, pay its administrative and operating expenses,
meet its filing and disclosure obligations as a public company, and repay
certain outstanding indebtedness. No assurances can be given that the Company
will be able to obtain sufficient additional capital for it to continue its
research program, or that any additional financing will be sufficient to satisfy
the Company's administrative and operating expenses for any significant period
of time.
Production Identification & Development
---------------------------------------
The Company believes that its proprietary technology offers benefits
which are not currently found in existing purification, disinfection and
sterilization systems. To date, the Company has not brought to market any
products which incorporate the technology and has not conducted other than
preliminary clinical, engineering or other tests to determine the feasibility of
products which could incorporate the technology, although it believes that the
technology may be incorporated into other products and devices. The Company has
conducted proof-of-concept tests of the technology, but there can be no
assurance that the Company will be able to develop or market any products, or
that the Company's technology may be successfully incorporated into any existing
or future products.
Early Stage of Development; Technological Uncertainty
-----------------------------------------------------
The Company is at an early stage of development it has not received any
required governmental approvals for the use or application of its Medizone
Technology in any medical or other clinical product or device, and it has not
yet realized any revenues from the sale or license of any products. Product
revenues may not be realized from the sale or licensing of any products (if they
are identified and developed) for several years, if at all. Many of the products
and applications the Company is currently evaluating will require significant
research and development efforts prior to any commercial use, and
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those additional research and development efforts may include pre-clinical and
clinical testing, as well as a lengthy regulatory approval process. There can be
no assurance the Company's research and development efforts will be successful,
that the Company's potential products will prove to be safe and effective in any
required clinical trial or other governmental tests, or that any commercially
successful products will ultimately be developed by the Company.
Potential Dependence On Strategic Alliances
-------------------------------------------
The Company's strategy for the identification, development, testing,
manufacture, marketing and commercialization of its technology includes entering
into various collaborations with corporate partners, licensors, licensees and
others. There can be no assurance that the Company will be able to negotiate
strategic alliances on acceptable terms, if at all, or that these collaborative
arrangements will be successful. To the extent the Company chooses not, or is
not able, to establish such arrangements, it could experience increased capital
requirements as a result of its undertaking such activities at its own risk and
expense. In addition, the Company may encounter significant delays in
introducing products or product applications currently under development into
the marketplace or find that the development, manufacture or sale of its
proposed products are adversely affected by the absence of such collaborative
agreements.
Under typical collaborative relationships, the collaborative partners have the
right to pursue parallel development of other products which may compete with
the products of the other collaborative partner, and to terminate the agreements
without significant penalty under certain conditions. Any parallel development
by a collaborative partner of the Company of competing products, or the failure
by a collaborative partner to devote sufficient resources to the development and
commercialization of the Company's products, could have a material adverse
effect on the Company's business, financial condition or results of operations.
The Company's success may depend upon, among other things, the skills,
experience and efforts of the Company's collaborative partners, employees who
are responsible for the collaborative project, such partners' commitment to the
collaborative arrangement, and the financial condition of such partners, all of
which are beyond the control of the Company. If one or more of the Company's
collaborative partners defaulted on their obligations under their collaborative
arrangements, the Company could be forced to engage in litigation to enforce
those obligations (which could be time consuming and costly) or seek to enter
into agreements with other parties upon similar terms.
Future Capital Needs; Uncertainty of Additional Funding
-------------------------------------------------------
The identification, development and commercialization of the Company's
products and technology will require a commitment of substantial funds to
conduct research and development activities, including possible preclinical and
clinical studies, to create and expand distribution and marketing capabilities
and to acquire and expand manufacturing capacity. Although the Company believes
that the net proceeds of the Offering, together with existing cash balances,
will be sufficient to fund the operations of the Company for
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approximately the next two years, 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, including but not limited to, the costs and timing
of the Company's research and development activities, the number and type of
clinical or other tests the Company may be required to conduct in seeking
approval of its products from governmental or other agencies, the success of the
Company's development efforts, the cost and timing of establishing or expanding
the Company's sales and marketing and/or manufacturing activities, the extent to
which the Company's products (if any) gain market acceptance, the Company's
ability to establish and maintain collaborative relationships, competing
technological and market developments, the progress of the Company's
commercialization efforts and the commercialization efforts of the Company's
marketing partners, the costs involved in preparing, filing, prosecuting,
maintaining and enforcing and defending patent claims and other intellectual
property rights, developments related to regulatory issues, and other factors.
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 stockholders,
and debt financing, if available, may involve significant restrictive covenants.
Collaborative arrangements, if necessary to raise additional funds, may require
the Company to relinquish its rights to certain of its technologies, products or
marketing territories. The Company's failure to raise capital when needed could
also have a material adverse effect on the Company's business, financial
condition and results of operations. There can be no assurance that any such
financing, if required, will be available on terms satisfactory to the Company,
if at all.
Governmental Regulation
-----------------------
The research, development, manufacture and marketing of the Company's
products which constitute medical devices or products will be extensively
regulated by a number of governmental agencies, including the United States Food
& Drug Administration ("FDA"). The FDA requires governmental clearance of all
medical devices and drugs before they can be marketed in the United States.
Similar approvals are required from other regulatory bodies in virtually every
foreign country. The regulatory processes established by these government
agencies are lengthy, expensive, uncertain and may require extensive and
expensive clinical trials. There can be no assurance that any future products
developed by the Company and which are subject to the FDA's authority will prove
to be safe and effective and meet all of the applicable regulatory requirements
necessary to be marketed. The results the Company obtains from its testing
activities could be susceptible to varied 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 facility are subject to on-going regulation
and inspections. Discovery of previously unknown problems with a product,
manufacturer or facility could result in FDA sanctions, restrictions on a
11
<PAGE>
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 limitation, suspension or revocation of regulatory approvals granted to the
Company. Any such events, were they to occur, could have a material adverse
effect on the Company's business, financial condition and results of operations.
The Company may also be 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. Any third parties manufacturing the Company's products
or supplying materials or components for such products may also be subject to
these manufacturing practices and mandatory procedures. If the Company, its
management or its third party manufacturers fail to comply with applicable
regulations regarding these manufacturing practices, it could be subject to a
number of sanctions, including fines, injunctions, civil penalties, delays,
suspensions or withdrawals of market approval, seizures or recalls of product,
operating restrictions and, in some cases, criminal prosecutions.
The Company's products may also be subject to regulation, inspection
and licensing by other governmental agencies, including the Environmental
Protection Agency ("EPA"), state agencies similar to the FDA and EPA and the
Occupational Health and Safety Administration ("OSHA"). In addition, if the
Company engages in contract sterilization services, the Company's products and
operations may be subject to the infection control or other requirements of the
Joint Commission on Accreditation of Health Care Organizations, the Center for
Disease Control, the Association for Advancement of Medical Instrumentation and
other federal and state agencies that have established or maintain testing
methods or sterilization process monitoring.
Uncertainty Associated with Clinical Trials and Other Tests
-----------------------------------------------------------
Certain of the Company's products may constitute medical devices within
the meaning of the Food, Drug and Cosmetic Act (the "FDA Act") and, therefore,
may be subject to the FDA's regulations governing medical devices. 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 approval or clearance 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 ss.
510(k) of the FDA Act. In order for a device to qualify under that procedure,
the manufacturer must, among other things, establish that the product is
substantially equivalent in intended use, safety and effectiveness to another
legally marketed class I or class II device or to a "pre-amendment" class III
device for which the FDA has not called for preliminary market approval ("PMA").
Medical class III is the class reserved for devices deemed by the FDA to pose
the greatest risk. Manufacturers of class III devices must file a PMA under ss.
515 of the FDA Act. PMA applications generally require a much more complex
submission than a 510(k) notification and typically require a showing that the
device is safe and effective based on extensive and costly clinical and other
testing. There can
12
<PAGE>
be no assurance that any product developed by the Company which is deemed to be
a medical device for FDA Act purposes will qualify for approval under the 510(k)
notification process or that any such products will be deemed to be safe and
effective if required to be qualified under a PMA.
The time required to obtain FDA approval is uncertain, and frequently
takes several years or more, if approval is ever granted. There can be no
assurance that any future products developed or identified by the Company alone
or in conjunction with others will prove to be safe and efficacious in any
required clinical trials, or that they will meet the applicable regulatory
requirements necessary for their marketing, including the receipt of a marketing
clearance, should such be required. Further, if regulatory approval is granted,
that approval would generally be limited to the uses for which the product has
been demonstrated through clinical studies and other means to be safe and
effective. Furthermore, approval may entail ongoing requirements for, among
other things, post-marketing studies. Even if regulatory approval is obtained, a
marketed product, its manufacturer and its manufacturing facilities and
pertinent operations are subject to extensive regulation and periodic
inspections. The regulatory requirements pertinent to medical device
manufacturing and related activities are stringently applied and enforced by the
FDA and similar governmental agencies in other countries.
If the Company is required to conduct clinical or other testing or
trials of its products, any such testing will need to made in compliance with
regulations promulgated by the FDA under the authority granted it under the FDA
Act. In other countries, governmental agencies similar to the FDA also regulate
the sale of medical devices and products, generally in a manner similar to the
FDA's regulation of those products. Sales of any products to Europe also require
a "CE" mark, which shows that the product has been manufactured in accordance
with required standards. The Company's sterilization technology has not been
approved for use in connection with or as part of any device, and there can be
no assurance that the Company will not encounter problems in the conduct of any
clinical trials or tests it is required to complete which will cause the FDA, or
any other regulatory agencies to delay or suspend the tests or otherwise not
approve the sale of the Company's products. If any of the Company's products
under development are not shown to be safe and effective in any required
clinical trials, the resulting delays in developing other products or conducting
related preclinical testing and clinical trials, as well as the need for
financing to complete any such testing and trials, could have a material adverse
effect on the Company's business, financial condition and results of operations.
No Manufacturing Capability
---------------------------
The Company has no manufacturing capability or capacity to produce any
products utilizing its sterilization technology, including any products to be
used in any required clinical or other tests. The Company initially intends to
develop relationships with other companies to manufacture those components
and/or products, with the Company being primarily in the role of specification
developer and final assembly manufacturer for selected products only. The two
products currently being developed by the Company have never been manufactured
on a commercial scale and there can be no assurance that such products can be
manufactured at a cost or in quantities necessary to make them commercially
viable. Any delay in availability of products may result in a delay in the
submission of products for any required regulatory approval or market
13
<PAGE>
introduction, subsequent sales of such products, which could have a material
adverse effect on the Company's and business, financial condition, or results of
operations. The Company's manufacturing processes may be labor intensive and, if
so, significant increases in production volume would likely require changes in
both product and process design in order to facilitate increased automation of
the Company's then-current production processes. There can be no assurance that
any such changes in products or processes or efforts to automate all or any
portion of the Company's manufacturing processes would be successful, or that
manufacturing or quality problems will not arise as the Company initiates
production of any products it might develop.
In addition, some or all of the Company's potential products, or
products in which the Company's sterilization technology may be incorporated,
may be required to be manufactured in accordance with current FDA or other
governmental agency manufacturing regulations. If the manufacturing facilities
cannot pass a plant inspection by the FDA, the manufacturer's ability to
manufacture the products will be adversely affected. There can be no assurance
the Company can successfully acquire manufacturing capacity on a profitable
basis, or contract with another party on terms acceptable to the Company, if at
all.
No Sales or Marketing Capability
--------------------------------
The Company has no experience in sales, marketing or distribution. To
market any of its products directly, the Company would be required to develop a
marketing and sales force with technical expertise and with supporting
distribution capability. Alternatively, the Company may obtain the assistance of
other companies with an established distribution and sales force. To this end,
the Company would be required to enter into agreements with such parties
regarding the use and maintenance of such distribution systems and sales forces.
There can be no assurance the Company will be able to establish sales and
distribution capabilities, or that it will be successful in gaining market
acceptance for its products through the use of the efforts of third parties.
The Company intends to develop and maintain a marketing and sales
organization for its products with a portion of the proceeds of the Offering.
There can be no assurance the Company will be able to recruit, train and
maintain successfully any such sales and marketing personnel, or that the
efforts of such personnel will be successful.
Uncertainty of Protection of Patents or Proprietary Rights
-----------------------------------------------------------
The Company's success will depend, in large part, on its ability to
obtain and enforce patents, maintain its trade secrets and operate without
infringing on the proprietary rights of others, both in the United States and in
other countries. The patent positions of companies can be uncertain to some
extent and involve complex legal and factual questions, and, therefore, the
scope and enforceability of claims allowed in patents are not systematically
predictable with absolute accuracy. The Company's license rights in the patents
depends, in part, upon the breadth and scope of protection provided by the
patents and the validity of the patents. Any failure to maintain the issued
patents could adversely affect the Company's business. The Company intends to
file additional patent applications (both United States and
14
<PAGE>
foreign), when appropriate, relating to its technologies, improvements to its
technologies and for specific products it develops. There can be no assurance
that any issued patents or pending patent applications of the Company will not
be challenged, invalidated or circumvented. There can also be no assurance that
the rights granted thereunder will provide proprietary protection or competitive
advantages to the Company.
The commercial success of the Company will also depend, in part, on the
Company not infringing patents issued to others and not breaching any technology
licenses upon which the Company's products and services are based. It is
uncertain whether any third party patents will require the Company to alter its
products or processes, obtain licenses or cease certain activities. In addition,
if patents have been issued to others which contain competitive or conflicting
claims and such claims are ultimately determined to be valid, the Company may be
required to obtain licenses to those patents or to develop or obtain alternative
technology. If any licenses are required, there can be no assurance the Company
will be able to obtain any such licenses on commercially favorable terms, if at
all. The Company's breach of an existing license or its failure to obtain a
license to any technology that it may require in order to commercialize its
products may have a material adverse impact on the Company's business, results
of operations and financial condition. Further, litigation, which could result
in substantial costs to the Company, may also be necessary to enforce patents
licensed or issued to the Company or to determine the scope or validity of third
party proprietary rights. If competitors of the Company prepare and file patent
applications in the United States that claim technology also claimed by the
Company, the Company may have to participate in interference proceedings
declared by the U.S. Patent and Trademark Office to determine priority of
invention, which could result in substantial cost to the Company, even if the
eventual outcome is favorable to the Company. An adverse outcome could subject
the Company to significant liabilities to third-parties, require disputed rights
to be licensed from third-parties or require the Company to cease using such
technology.
The Company also relies on secrecy to protect portions of its
technology for which patent protection has not yet been pursued or which is not
believed to be appropriate or obtainable in addition to any information of a
confidential and proprietary nature relating to the Company, including but not
limited to its know-how, trade secrets, methods of operation, names and
information relating to the Company's vendors or suppliers and customer names
and addresses. This technology includes technology which the Company acquired
from two parties in connection with, but separate from, the patented technology
from Biozone, a portion of which the Company has acquired and a portion of which
it has obtained a license to use. There can be no assurance that the Company's
undivided ownership and/or license rights in such technology is enforceable.
The Company intends to protect this unpatentable and unpatented
proprietary technology and processes, in addition to other confidential and
proprietary information in part, by confidentiality agreements with its
employees, collaborative partners, consultants and certain contractors. There
can be no assurance that these agreements will not be breached, that the Company
will have adequate remedies for any breach, whether the Company's trade secrets
and other confidential and proprietary information will not otherwise become
known or be independently discovered or reverse-engineered by competitors.
15
<PAGE>
Intense Competition; Rapid Technological Change
-----------------------------------------------
There can be no assurance the Company's technology will have advantages
over those of its competitors, which will be significant enough to cause users
to adopt its use. The products in which the Company's technology may be
incorporated will compete with products currently marketed, and competition from
such products is expected to increase.
Most of the companies currently producing products or using techniques
have significantly greater financial resources and expertise in research and
development, marketing, manufacturing, pre-clinical and clinical testing,
obtaining regulatory approvals and marketing than the Company. Smaller companies
may also prove to be significant competitors, particularly through collaborative
arrangements with large third-parties. Academic institutions, governmental
agencies and public and private research organizations also conduct research,
seek patent protection and establish collaborative arrangements for product and
clinical development and marketing. Many of these competitors have products or
techniques approved or in development and operate large, well funded research
and development programs. Moreover, these companies and institutions may be in
the process of developing technology that could be developed more quickly or
ultimately proved safer or more effective than the Company's technology.
The Company faces competition based on product efficacy, safety, the
timing and scope of regulatory approvals, availability of supply, marketing and
sales capability, reimbursement coverage, price and patent position. There can
be no assurance the Company's competitors will not develop more effective or
more affordable products, or achieve earlier patent protection or product
commercialization than the Company.
Product Liability
-----------------
The testing, marketing and sale of medical or clinical products and
other products which may utilize the Company's technology involves unavoidable
risks. The use of any of the Company's potential products in clinical or other
tests or as a result of the sale of its products, or the use of its technology
in products, may expose the Company to potential liability resulting from the
use of such products. Such liability may result from claims made directly from
consumers or by regulatory agencies, companies or others selling such products.
The Company currently has no clinical trial or product liability insurance
coverage, although it anticipates obtaining and maintaining appropriate
insurance coverage as clinical or other development of its product candidates
progresses and if and when its products are ready to be commercialized. There
can be no assurance the Company will be able to obtain such insurance or, if it
obtains such insurance, that such insurance can be acquired at a reasonable cost
or in sufficient amounts to protect the Company against such liability. The
obligation to pay any product liability claim in excess of whatever insurance
the Company is able to acquire, or the recall of any of its products (or the
products incorporating the Company's technology), could have a material adverse
effect on the Company's business, financial condition and future prospects.
Hazardous or Toxic Materials
----------------------------
16
<PAGE>
The Company's research and development activities, and the application
of the Company's technology, may involve the controlled use of materials,
substances or electro-magnetic radiation which may, if used or employed
improperly, prove hazardous. The Company believes, however, that its technology
employs such potentially hazardous or toxic materials and substances in a manner
which minimizes their adverse effects. Further, where such hazards are employed,
the Company intends to utilize appropriate detection equipment and take
appropriate countermeasures in design, or in the test lab environment.
Need to Attract and Retain Key Employees and Consultants
--------------------------------------------------------
The Company is dependent on the principal members of its scientific and
management staff. In addition, the Company anticipates that it will rely upon
consultants and advisors to assist it in formulating its research and
development strategies and operations. Retaining and attracting qualified
personnel, consultants and advisors will be critical to the Company's success.
In order to pursue its product development and marketing plans, the Company will
be required to hire additional qualified scientific personnel, as well as
personnel with expertise in clinical testing, governmental regulation,
manufacturing and marketing. Expansion of product development and marketing are
also expected to require the addition of management personnel and the
development of additional expertise by existing management personnel. The
Company faces competition for qualified individuals from numerous medical and
clinical companies, universities and other research institutions. There can be
no assurance the Company will be able to attract and retain such individuals on
acceptable terms, when needed, and to the degree required.
The Company anticipates that any clinical development or other approval
tests in which it participates will be augmented by agreements with universities
and/or medical institutions or other personnel. It is likely the Company's
academic collaborators will not be employees of the Company. As a result, the
Company will have limited control over their activities and can expect that only
limited amounts of their time will be dedicated to the Company's activities. The
Company's academic collaborators may have relationships with other commercial
entities, some of which could compete with the Company.
Uncertainty of Health Care Reform Measures and Third Party Reimbursement
------------------------------------------------------------------------
The Company currently anticipates that one or more of its potential
products may constitute medical products. Recently, a series of legislative and
regulatory proposals has been initiated with the aim of changing the United
States health care system. While the Company cannot predict whether any such
legislative or regulatory proposals will be adopted, or the effect such
proposals may have on its business if they are adopted, the pendency of such
proposals could have a material adverse effect on the Company's ability to raise
capital, and the adoption of such proposals could have a material adverse effect
on the Company's business, financial condition and results of operations.
Furthermore, the Company's ability to develop, identify or commercialize its
potential product portfolio (which includes medical and clinical applications)
may be adversely affected to the extent that such proposals have a material
adverse effect on the business, financial condition
17
<PAGE>
and profitability of other companies that are prospective collaborators for
certain of the Company's proposed products.
Forward-looking Statements
--------------------------
Certain statements in this report constitute "forward-looking
statements" within the meaning of the rules and regulations promulgated by the
Securities and Exchange Commission. Such forward-looking statements involve
known and unknown risks, uncertainties and other factors which may cause the
actual results, performance or achievements of 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 Company's
unprofitability and the continuing uncertainty of its profitability, the
Company's ability to develop and introduce new products, the Company's lack of
sales, marketing and distribution experience and anticipated dependence on third
parties for such matters, the risks associated with obtaining governmental
approval of the Company's products, the highly competitive industry in which the
Company intends to operate and the rapid pace of technological change within
those industries, the uncertainty of patent and proprietary technology
protection and the Company's reliance on such patent 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
above.
Forward-Looking Information May Prove Inaccurate
------------------------------------------------
This report contains forward-looking statements and information that
are based on management's beliefs as well as assumptions made by and information
currently available to management. When used in this report, the words
"anticipate," "believe," "estimate," and "expect," and similar expressions are
intended to identify forward-looking statements. Such statements reflect the
Company's current views with respect to future events and are subject to certain
risks, uncertainties and assumptions, including the specific risk factors
described above. Should one or more of these risks or uncertainties materialize,
or should underlying assumptions prove incorrect, actual results may vary
materially from those anticipated, believed, estimated or expected. The Company
does not intend to update these forward-looking statements and information.
Item 2. Properties
----------
On September 23, 1997, the Company entered into a three-year lease with
an unaffiliated third party for its offices at 4505 South Wasatch Boulevard, in
Salt Lake City, Utah, comprising approximately 1400 square feet, at an annual
rental of $22,984.56. The office space was used for executive offices and
administrative purposes. Following the re-organization of April 15, 1998, the
Company's offices were moved to Stinson Beach, California. The offices are
located temporarily in the home of the Company's CEO, Ed Marshall. When
financial resources permit, the Company intends to remain in the San Francisco
Bay Area and lease office space that will allow for additional staffing. The
18
<PAGE>
current, temporary offices are located at 144 Buena Vista Ave. in Stinson Beach
and are provided to the Company without any charge. The Company pays $100 a
month for an adjacent storage area for the Company's archives and pays or
reimburses all telephone and related expenses incurred by or for the Company.
Item 3. Legal Proceedings
-----------------
In November 1992, the Company consented to the entry of a final
judgment of permanent injunction (S.E.C. v. Medizone International, Inc., Civil
Action 93-2761, D.D.C.), pursuant to which the Company was permanently enjoined
from failing to timely file the reports required to be filed pursuant to the
Securities Exchange Act of 1934. The Company's report for the year ended
December 31, 1998 is being filed late. There is no assurance that the failure of
the Company to file this, or any future report in a timely manner will not lead
to additional sanctions or actions against the Company by the SEC or others.
Item 4. Submission of Matters to a Vote of Security Holders.
-----------------------------------------------------
At its Annual Meeting of Shareholders held September 17, 1998, the
following actions were submitted and approved by vote of the majority of the
shares present in person and by proxy:
1. Election of three directors;
2. Approval of the adoption of amended and restated bylaws of the
Company; and
3. Approval of the selection of Andersen, Andersen & Strong, LC
as the Company's independent public accountants.
A total of 144,323,804 shares of common stock were issued and
outstanding as of August 3, 1998, the date set by the Board of Directors of the
Company for notice of and eligibility to vote at the Annual Meeting. At the
meeting, there were present or represented by proxy a total of 63,722,706 shares
(approximately 44%) of the issued and outstanding shares of the Company. Under
the Company's bylaws as then in effect, a quorum of 33% of the issued and
outstanding shares was required for the purpose of establishing a quorum and
proceeding with the business of the meeting. A majority of the votes present and
cast at the meeting voted in favor of the actions proposed by the Board of
Directors. The details of the voting results were as follows:
For the Directors:
<TABLE>
<CAPTION>
Name of Nominee Number of Shares Number of Shares Number of Shares
for Director for Nominee Against Nominee Abstaining/Withheld
- --------------- ----------------- ----------------- --------------------
<S> <C> <C> <C>
Edwin G. Marshall 63,470,842 251,864 0
Gerard V. Sunnen, M.D 63,486,342 236,364 0
William Hitt, Ph.D., MD 63,418,342 241,364 0
</TABLE>
For the adoption of Amended and Restated Bylaws, a total of 44,317,651
shares were voted for the ratification, 299,865 shares were voted against this
proposal, and 132,928 shares abstained or were withheld. Broker non-votes were
not counted in the voting on this proposal.
19
<PAGE>
For the ratification of Andersen, Andersen & Strong, LC as the
independent public accountants of the Company, a total of 65,519,773 shares were
voted in favor of ratification, 128,250 shares were voted against this proposal,
and 74,683 shares abstained or were withheld. This vote is not binding on the
Board of Directors and the Board may, in its discretion, appoint other
independent public accountants.
Part II
Item 5. Market for Registrant's Common Equity and Related
Stockholder Matters.
-------------------------------------------------
Prices/Trading Market Information
The Company's shares are traded in the over-the-counter market, with
price quotes listed on the OTC Electronic Bulletin Board under the trading
symbol "MZEI," and in the "pink sheets" published by the National Quotation
Bureau.
The following table summarizes data from the National Quotation Bureau,
indicating the high and low bid prices for a share of the Company's common stock
during each of the four calendar quarters of fiscal 1997 and 1998. These prices
reflect interdealer prices without retail markup, markdown or commission; are
not necessarily representative of actual transactions, or of the value of the
Company's securities; and are, in all likelihood, not based upon any recognized
criteria of securities valuation as used in the investment banking community.
<TABLE>
<CAPTION>
Bid Price
---------
Calendar Period High Low
--------------- ---- ---
<S> <C> <C> <C> <C>
1998 First Quarter .09 .045
Second Quarter .06 .037
Third Quarter .095 .035
Fourth Quarter .102 .047
1997 First Quarter .085 .01
Second Quarter .0825 .05
Third Quarter .105 .085
Fourth Quarter .10 .065
</TABLE>
Number of Holders
On January 8, 1999, according to the Company's transfer agent, there
were approximately 3839 holders of record of the Company's common stock, and
approximately 4511 beneficial owners.
Dividends
The Company has never paid cash dividends on its common stock. Payment
of cash dividends is subject to the discretion of the Board of Directors and
20
<PAGE>
is dependent upon various factors, including the Company's earnings, capital
needs and general financial condition. The Company does not believe that it has
any immediate prospect of earnings. However, the Company anticipates that in the
foreseeable future, it will follow a policy of retaining earnings, if any, to
finance research and development.
Item 6. Selected Financial Data.
-----------------------
<TABLE>
<CAPTION>
Year Ended
1998 1997 1996 1995 1994
---- ---- ---- ---- ----
Operations Data:
<S> <C> <C> <C> <C> <C>
Revenues $ 125,000 $ -0- $ -0- $ -0- $ -0-
Net income (507,761) (775,559) (1,329,395) (1,081,027) (1,126,315)
(loss) before
minority interest
Net income (loss) (507,761) (775,559) (1,329,395) (1,081,027) (1,126,315)
Net income (loss) (.00) (.01) (.01) (.01) (.01)
per common share
Weighted average 142,645,000 133,568,000 118,022,000 111,306,000 98,292,000
common shares
outstanding
Balance Data
Sheet:
Working capital (1,031,586) (945,859) (949,254) (538,102) (576,101)
(deficiency)
Total assets 15,255 307,019 74,368 124,653 87,230
Long-term -0- -0- -0- -0- -0-
liabilities
Accumulated (13,720,439) (13,217,678) (12,442,119) (11,112,724) (10,103,503)
(deficit)
Stockholders' (1,023,974) (886,167) (885,241) (432,880) (558,679)
equity
deficiency
</TABLE>
Item 7. Management's Discussion and Analysis of
Financial Condition and Results of Operations.
----------------------------------------------
Results of Operations
General
- -------
From its inception (January 1986), the Company has been a development
stage company primarily engaged in research into the medical uses of ozone. The
Company has not generated, and cannot predict when or if it will generate,
revenues or sufficient cash flow to fund its continuing operations. Since its
inception, the Company expended $2,332,853 for research and development,
including $13,218 in 1998, compared to $116,950 in 1997.
21
<PAGE>
Years Ended December 31, 1997 and 1996.
- --------------------------------------
There were no sales during either year. In 1998, the Company had
revenues of $125,000 from the sale of a subsidiary.
Expenditures for research and development, including work performed by
independent contractors was $13,218 in 1998, compared to $116,950 in 1997.
The decrease was due to lack of capital.
General and administrative expenses were $524,929 in 1998, compared to
$633,187 in 1997. These expenses include professional fees, payroll, insurance
costs and travel expenses.
Notes payable in 1998 of $280,491 and in 1997 of $354,115 at rates
averaging from 6% to 8%.
Years Ended December 31, 1997 and 1996
- --------------------------------------
There were no sales during either year.
Expenditures for research and development including work performed by
independent contractors were $116,950 in 1997, compared to $25,000 in 1996.
General and administrative expenses were $633,187 in 1997, compared to
$1,291,082 in 1996. These expenses include professional fees, payroll, insurance
costs and travel expenses. The reduction in 1997 is due to the termination of
its former CEO, Mr. Latino.
Notes payable in 1997 totaled $354,115 and in 1996 $332,315. Interest
accrues at rates ranging from 8% to 10%.
Liquidity and Capital Resources
- -------------------------------
At December 31, 1998, the Registrant had a working capital deficiency
of $1,031,586 and a stockholders' deficiency of $1,023,974 compared to a working
capital deficiency of $945,859 and a stockholders' deficiency of $886,167.
During 1998, the Company sold its interest in a subsidiary, Medizone
Canada Ltd., a Utah Corporation for $125,000.
The Company will continue to require additional funding to enable it to
fund research necessary to make the appropriate regulatory application and
continue operations. It is expected that these funds will be generated by the
sale of the Company's securities.
Item 8. Financial Statements and Supplementary Data.
-------------------------------------------
The financial statements and supplementary data are listed under Item
14 in this Annual Report and commence on page F-1.
22
<PAGE>
Item 9. Changes in and Disagreements with Accountants
on Accounting and Financial Disclosure.
---------------------------------------------
Subsequent to the end of the period covered by this report, on January
18, 2000, the Company appointed Jones Jensen & Co. ("Jones Jensen") to replace
Andersen & Andersen LLP ("Andersen") as independent public accountants of the
Company.
The former accountant, Andersen, was dismissed June 30, 1998. This
change was required because Kevin R. Andersen, a principal in Andersen, accepted
the position of Chief Financial Officer of the Company in June 1998.
The report of Andersen on the Company's consolidated financial
statements for the years ended December 31, 1996 and 1997 contained no adverse
opinion or disclaimer of opinion and was not qualified or modified as to
uncertainty, audit scope or accounting principle, except that such report on the
consolidated financial statements included an explanatory paragraph with respect
to the Company being in the development stage and its having suffered recurring
losses which raise substantial doubt about its ability to continue as a going
concern.
The decision to engage Jones Jensen as the Company's independent
auditors was approved by the Company's board of directors.
In connection with the audits for the years ended December 31, 1997 and
1996, and through June 30, 1998, the Company has had no disagreements with
Andersen on any matter of accounting principles or practices, financial
statement disclosure, or auditing scope or procedure, which disagreements if not
resolved to the satisfaction of Andersen would have caused it to make reference
thereto in its report on the consolidated financial statements for 1997 and
1996.
During the years ended December 31, 1997 and 1996, and through June 30,
1998, there have been no reportable events (as defined in Item 304(a)(1)(v) of
Regulation S-K).
Andersen has provided to the Company a letter addressed to the
Securities and Exchange Commission stating that it has reviewed the disclosure
provided in this section of this report on Form 10-K, as amended, and has no
disagreement with the relevant portions of this disclosure, pursuant to the
requirements of Item 304(a)(3) of Regulation S-K. A copy of such letter, dated
February 29, 2000, is filed as an Exhibit to this report, as amended.
23
<PAGE>
PART III
Item 10. Directors and Executive Officers of Registrant.
----------------------------------------------
The following table sets forth certain information concerning the
directors and executive officers of the Company , as of December 31, 1998.
<TABLE>
<CAPTION>
Director Officer Positions with
Name Age Since Since Registrant
- ----- --- -------- ------- --------------
<S> <C> <C> <C> <C>
Edwin G. Marshall 56 1997 1998 Chairman of the Board, CEO
Gerard V. Sunnen 56 1997 1997 Director, President
William M. Hitt 72 1997 Director
Jill C. Marshall 48 N/A 1998 Chief Operating Officer,
Corporate Secretary
Kevin R. Andersen 48 N/A 1998 Chief Financial Officer
</TABLE>
Edwin G. Marshall, became Chairman of the Board & Chief Executive
Officer in April 1998 and has been with the Company since June 1997. Mr.
Marshall attended Santa Rosa Junior College and the College of Marin, studying
fire science and business administration. From 1964 to 1978, Mr. Marshall worked
in the fire service in a city with a major chemical industrial complex, leaving
with the rank of Captain. A private investor since 1973, he went to work in the
real estate business in 1978. From 1978 until 1995, Mr. Marshall pursued various
business interests in real estate brokerage, a vacuum forming business in the
plastics industry, an industrial computer controls company, and an automobile
and truck dealership. Since 1992 he has concentrated on his own investments, and
since 1997 devoted substantially all of his time to management responsibilities
with Medizone.
Gerard V. Sunnen, M.D. became a Director of the Company in June 1997,
Director of Research in 1997 and President in 1998. He graduated from Rutgers
University in 1963 and from the medical school of the State University of New
York, Downstate, in 1967. Dr. Sunnen has practiced psychiatric medicine since
his graduation from medical school and has taught clinical psychiatry at New
York University Medical Center since 1977, where he is now an Associate Clinical
Professor of Psychiatry. He is currently a consultant to several organizations
and companies, including the Institute for Behavior Therapy and the Training
Institute for Mental Health Practitioners in New York. He is a member of the
American Psychiatric Association, the American Society of Clinical Hypnosis, the
International Association of Emergency Psychiatry, of which he is Honorary
President, and the World Psychiatric Association, where he is currently Vice
President of the Section for Emergency Psychiatry. He received the Chevalier de
l'Ordre du Merite from the French government in 1990 for his work in assisting
members of the French community in New York. Dr. Sunnen has written and lectured
extensively on psychiatric medicine and medical hypnosis. He have also written
on the medical applications of ozone.
William M. Hitt became a Director of the Company in June 1997. He
received a Bachelor's of Science degree from the University of Denver in 1946
and a Ph.D. from Colorado A&M University in 1948. He received a medical degree
from the University of Colorado in 1952 and did post-medical school studies at
Duke University and Washington University School of Medicine. Dr. Hitt has
taught and conducted research at several institutions in the United States and
24
<PAGE>
Mexico, culminating with his work at the World Health Organization in Mexico
City from 1989 to 1994. He was the recipient of the Eli Lily Award from the
National Institute of Health in 1953, the Leovenhoek Award in 1960, the
Cientifico Destacado in 1990 and 1992, and the Bioethics International Award of
Merit in 1993. Dr. Hitt was a member of the Board of Directors of Physicians
Against Nuclear War, which organization was awarded the Nobel Peace Prize in
1985. Dr. Hitt is currently the Director of the William Hitt Center, which
conducts clinical immunology and addiction recovery programs, has operated since
1986 and now has seven locations in Central and South America, with headquarters
in Tijuana, Mexico.
Jill C. Marshall, N.D., has been the Chief Operating Officer and
Corporate Secretary of Medizone since April 1998. Dr. Marshall is the recipient
of a Doctor of Naturopathy degree from The Southern College of Naturopathy and a
Bachelor of Arts degree from Long Beach State majoring in Sociology and Health
Education. She brings a successful background in Naturopathic healing, teaching,
sales training and marketing to Medizone with 20 years experience working in
corporate environments. Dr. Marshall's previous sales and marketing clients
include: Foundation Health, Plus Financial, Principal Financial Group, Paul
Revere Companies, Discovery Toys, Lotus Development, Pacific Bell, PG&E and Blue
Shield of California. Dr. Marshall is the wife of Ed Marshall, the Company's
CEO.
Kevin R. Andersen, CPA, M.S., was appointed Chief Financial Officer in
November 1998. Mr. Andersen is a partner in Andersen, Andersen & Strong L.C.,
Certified Public Accountants, who previously served as the Company's auditors
for the past four years ended December 31, 1997. Mr. Andersen has a Master of
Science in Taxation (graduating Phi Kappa Phi) from UNLV and a Bachelor of
Science in Accountancy from the University of Utah. His professional experience
includes work as a Senior Tax Manager with the national accountancy firm of
Laventhol & Horwath, working in their Las Vegas office and National Tax
Department in Washington, D.C.
Item 11. Executive Compensation.
----------------------
Directors Compensation
During 1998, each Director received a grant of restricted stock as
follows: Mr. Marshall, 1,500,000 shares, Dr. Sunnen, 1,500,000 shares, Dr.
Hitt, 250,000 shares. In addition, a former director, Kenneth Gropper, was
issued 50,000 shares.
Executive Compensation
The following table sets forth the compensation of all individuals
serving as the CEO of the Company during the year ended December 31, 1998 and
the Company's executive officers (other than the CEO) who were serving as
executive officers at December 31, 1998 (the "Named Officers") and whose
compensation exceeded $100,000 during the year:
25
<PAGE>
<TABLE>
<CAPTION>
Summary Compensation Table
-------------------------
Long Term
Annual Compensation Compensation
------------------- ------------
Other
Name and Annual Restricted
Principal Compensa- Stock
Position Year Salary Bonus tion Awards
- --------- ---- ------ ----- -------- ---------
<S> <C> <C> <C> <C>
Edwin G. Marshall 1998 75,000 (1) 1,500,000
</TABLE>
(1)Mr. Marshall's $75,000 salary was paid in the form of 1,500,000 shares of the
Company's common stock. Each shares was valued at $.05.
Compensation Committee Interlocks and Insider Participation
The Company does not have a compensation committee. Matters concerning
the compensation of executive officers are determined by the Company's Board of
Directors.
Item 12. Security Ownership of Certain Beneficial Owners and Management.
---------------------------------------------------------------
The following table sets forth certain information as of January 8,
1999, pertaining to the beneficial ownership of Common Stock, by (i) persons
known to the Company to beneficially own 5% or more of the outstanding Common
Stock, (ii) each director and executive officer of the Company in office at
December 31, 1998, and (iii) all such directors and executive officers of the
Company as a group.
<TABLE>
<CAPTION>
Number of Shares Percentage of
Name and Address Beneficially Owned Total Outstanding
- ----------------- ------------------ -----------------
<S> <C> <C>
Edwin G. Marshall 76,098,333(1) 51.09%
P.O. Box 342
Stinson Beach, CA 94970
Jill C. Marshall 76,098,333(2) 51.09%
P.O. Box 342
Stinson Beach, CA 94970
Dr. Gerard V. Sunnen 3,000,005 2.01%
200 East 23rd Street
New York, NY 10016
Dr. William M. Hitt 250,000 *
4248 Palm Avenue
San Diego, CA 92154
Kevin R. Andersen 50,000 *
8760 Hidden Oak Drive
Salt Lake City, UT 84121
</TABLE>
26
<PAGE>
<TABLE>
<CAPTION>
<S> <C> <C>
All directors and 79,398,338 53.31%
executive officers
as a group (5 persons)
- -------------------
</TABLE>
(1) Includes: (i) an aggregate of 351,000 shares owned by Mr. Marshall's
wife and son; (ii) 6,571,428 shares owned by Sand Dollar, of which Mr.
Marshall is the general partner; and (iii) options to purchase
66,761,905 shares owned by Sand Dollar.
(2) Includes shares beneficially owned by Ed Marshall, the husband of Mrs.
Marshall.
Item 13. Certain Relationships and Related Transactions.
-----------------------------------------------
Private Sales of Shares
During the past three years the Company has issued the following
securities without registration under the Securities Act:
1996
- ------
The Company entered into an employment agreement with its former
president, Joseph S. Latino, effective January 1, 1995, pursuant to which the
Company agreed to employ Mr. Latino as its Chief Executive Officer and Director
of Research, at a salary of $180,000 per annum, for a one year period; provided,
however, that the agreement was to remain in effect until terminated by either
of the parties in accordance with its terms. Mr. Latino received fringe
benefits, including the use of an automobile and health and life insurance and
was granted an option to purchase 3,000,000 shares of the Company's common
stock, par value $.001, at a per share price of $.20. These options were to vest
in annual increments of 1,000,000 shares, on and after January 1 of each of
1996, 1997 and 1998, provided that Mr. Latino continued to be employed by the
Company at the time. The Company has since taken the position that this
Agreement was not validly authorized and is nonenforceable. The agreement, if it
was enforceable, terminated for cause in May 1997.
The Company agreed to employ Arthur P. Bergeron, effective January 1,
1995, as its Chief Financial Officer, at a salary of $72,000 per annum, plus
monthly expenses, for a one year period; provided, however, that the agreement
was to remain in effect until terminated by either party in accordance with its
terms. Mr. Bergeron was permitted to continue his private accounting practice.
Mr. Bergeron also received health insurance from the Company and was granted an
option to purchase 1,500,000 shares of the Company's common stock, par value
$.001, at a per share price of $.20, provided that Mr. Bergeron continued to be
employed by the Company at that time. The agreement also provided for certain
bonuses to be paid if the Company achieves certain financial results. Mr.
Bergeron was terminated for cause in November 1998.
27
<PAGE>
1997
- ----
In May 1997, the Company issued 500,000 shares of the Company's common
stock to each of Arthur P. Bergeron and Kenneth Gropper in consideration of
their services as officers of the Company and 750,000 to George Handel in
consideration of his services as the Company's Secretary. In December 1997, the
Company awarded Dr. Gerard Sunnen 100,000 shares of common stock in
consideration of his services as the Company's Director of Science. In December
1997, the Board of Directors voted to establish the Option Plan, which was
approved by the shareholders at the Annual Meeting. Pursuant to the Option Plan,
options to purchase shares of the Company's common stock were granted to Milton
G. Adair (3,000,000 shares), Gerard V. Sunnen (300,000 shares) and Kenneth
Gropper (100,000). On September 23, 1997, Sand Dollar purchased 5,714,285 shares
of the Company's common stock pursuant to the Sand Dollar Warrant, at a per
share price of $.07, an aggregate of $400,000.
In June 1997, the Company issued warrants to purchase 73,333,333 shares
of its common stock to The Sand Dollar Solution ("Sand Dollar"), a California
limited partnership, whose general partner is Edwin G. Marshall, the Chairman of
the Company's Board of Directors (the "Sand Dollar Warrants").
The Sand Dollar Warrants have the following exercise prices and
expiration dates:
<TABLE>
<CAPTION>
Shares Exercise Price Termination Dates
- ------- -------------- -----------------
<S> <C> <C>
15,000,000 $.07 per share Originally
September 7, 1997, then
extended until ten
days after the Company
becomes current in its
filings with
Securities and
Exchange Commission.
33,333,333 $.15 per share Originally June 9, 1998,
extended to March 30, 1999.
25,000,000 $.20 per share Originally June 9, 1999
</TABLE>
On September 23, 1997, Sand Dollar purchased 5,714,285 shares of the
Company's common stock by exercise of the Sand Dollar Warrant, paying $.07 a
share, or aggregate consideration of $400,000.
In March and May 1997, the Company issued an aggregate of 2,716,600
shares of common stock to Kenneth Gropper (500,000 shares), Arthur P. Bergeron
(500,000 shares), George Handel (750,000 shares), counsel to the Company (an
aggregate of 666,666 shares), an employee (50,000 shares), and its public
relations firm (250,000 shares) in consideration of services rendered, relying
on the private offering exemption under the Securities Act. In December 1997,
the Company authorized the issuance of 100,000 shares of common stock to Dr.
Gerard Sunnen in consideration of his services as the Company's Director of
Science. The Company issued 103,200 shares of its common stock to an employee
28
<PAGE>
of its New Zealand subsidiary, pursuant to Regulation S promulgated under the
Securities Act, as consideration for services rendered.
1998
- ----
In March 1998, Sand Dollar purchased 857,143 shares of the Company's
common stock pursuant to the Sand Dollar Warrant, paying $.07 a share, or
$60,000. The Company relied on the private offering exemption from registration
under the Securities Act of 1933 (the "Securities Act") in issuing the Sand
Dollar Warrants and for the sale of shares pursuant to the exercise of the Sand
Dollar Warrants.
On March 4, 1998 the Company issued 864,747 shares of common stock to
Mark Peterson, a principal with Alpine Securities Corporation. The issued stock
was for repayment of the principal and interest of a $40,000 loan made to the
Company on Oct. 2, 1996. Alpine Securities is a market maker in our stock.
On May 27, 1998 the Sand Dollar Warrants due to expire on May 31, 1998
were extended to Oct. 30, 1998 with the Company retaining the previously adopted
right of cancellation with 10 days notice should other funding be obtained.
August 6, 1998 Grants of stock for uncompensated work and other
contributions by members of the Board of Directors were made as follows: Dr.
Gerard Sunnen, 1.5 million shares; Edwin G. Marshall, 1.5 million shares; Dr.
William Hitt, 250,000 shares; and Kenneth Gropper, 50,000 shares. In addition,
grants of 150,000 shares of common stock to Medizone's former President and
Chief Executive Officer, Milton Adair, and 15,000 shares to former employee, Joy
Erickson, were made as final settlement of their employment.
PART IV
Item 14. Exhibits, Financial Statement Schedules,
Reports on Form 8-K
----------------------------------------
(a) See Index to Consolidated Financial Statements and
Schedule on Page F-1.
(b) See Index to Exhibits on page E-1.
(c) None.
(d) Exhibits and Financial Statement Schedules. The
following Exhibits form a part of this Annual Report
on Form 10-K:
Exhibit
Number Description of Exhibit
- ------- ----------------------
2 Agreement and Plan of Reorganization dated March 12, 1986.(2)
3(a) Articles of Incorporation of Registrant.(2)
29
<PAGE>
3(b) By-laws of Registrant.(2)
3(c) Articles of Amendment to Registrant's Articles of Incorporation.(3)
10(a) Patent Agreement, dated February 26, 1987.(5)
10(b) Assignment of Distributor Agreement by Terrence O. McGrath to
Medizone Delaware, dated February 4, 1986, and Distributor Agreement
between Terrence O. McGrath and Dr. J. Hansler GmbH, dated
September 25, 1985.(3)
10(c) Letter confirmation and Protocol, dated June 2, 1986, by Registrant
with regard to research to be conducted by the State University of New
York at Syracuse.(2)
10(d) Consulting Agreement between P.J. Watrous & Co., Inc. and the
Registrant.(2)
10(f) Consulting Agreement between Jeffrey Freed, MD, PC and the
Registrant.(2)
10(g) Consulting Agreement between Joseph Latino and the Registrant.(2)
10(h) Consulting Agreement between Susan Golden, RN and the Registrant.(2)
10(i) Stock Option of Joseph Latino.(2)
10(j) Stock Option of Jeffrey Freed.(2)
10(k) Stock Option of Susan Golden.(2)
10(l) Stock Option of Hubert Weinberg.(2)
10(m) Agreement dated June 16, 1987, between Registrant and Oliver
Grace.(5)
10(n) Agreement dated June 26, 1987, between Registrant and John Grace.(5)
10(o) Agreement dated June 26, 1987, between Registrant and Oliver
Grace.(5)
10(p) Agreement dated June 30, 1987, by and among Registrant and John C.
Black, Dr. Gerard V. Sunnen and Dr. Priyakant S. Doshi.(5)
10(q) License Agreement with MCL Medizone Canada Ltd. dated November 18,
1987.(5)
10(r) Agreement dated October 1988 by and among Immunologics, Limited
Partnership, John M. Kells, Y. C. Zee, David C. Bolton and Medizone
International, Inc.(6)
10(s) Form of Stock Purchase Agreement between Registrant and individuals
who purchased Shares from Registrant.(7)
10(t) Letter agreement between Registrant and Rebus Oil Co., Ltd. dated
July 28, 1992.(8)
30
<PAGE>
10(u) Letter of understanding between Registrant and the RMB Group of
Boston dated August 10, 1992.(8)
10(v) Agreement between Registrant and Rebus Oil Company, Ltd., dated as
of October 20, 1992.(9)
10(w) Letter agreement among Messrs. McGrath, Watrous, Melera, Chou,
Kells, Handel and Pealer, dated as of November 10, 1992.(9)
10(x) Loan agreement with Messrs. McGrath and Watrous dated as of November
16, 1992.(9)
10(y) Settlement agreement with former consultant dated February 12,
1993.(9)
10(z) Consulting Agreement with Joseph S. Latino dated as of January 1,
1993.(9)
10(aa) Consulting Agreement with Arthur P. Bergeron dated as of January 1,
1993.(9)
10(bb) Employment Agreement with Katherine M. Kalinowski dated as of
January 1, 1993.(9)
10(cc) Consulting Agreement with Roger Shelley dated as of January 1,
1993.(9)
10(dd) Consulting Agreement with Jeannette Arsenault dated as of January 1,
1993.(9)
10(ee) Loan Agreements between Registrant and John Kells, George Handel and
John Pealer, executed as of June 11, 1993 (and promissory notes).(9)
10(ff) Promissory Note to Joseph S. Latino dated as of October 26, 1993 and
Acceptance Form dated as of November 26, 1993.(9)
10(gg) Letter Agreement dated March 23, 1993 between Registrant and the
Italian Scientific Society.(10)
10(hh) Contract between Registrant and Capmed USA.(10)
10(ii) Agreement made as of May 18, 1994, among Medizone International,
Inc., Medizone Canada Ltd., John M. Kells, George Handel, John
Pealer, Joseph S. Latino, Terrence O. McGrath and Philip J.
Watrous.(11)
10(jj) Agreement made as of January 1, 1995, between Medizone
International, Inc. and Joseph S. Latino.(11)
10(kk) Agreement made as of January 1, 1995 between Medizone
International, Inc. and Arthur P. Bergeron.(11)
10(ll) Agreement made as of January 1, 1995 between Medizone International,
Inc. and Giacomo C. DiGiorgio, M.D.(11)
10(mm) Lease Agreement between Medizone International, Inc. and Benabi
31
<PAGE>
Realty, made on September 27, 1991, as extended, January 17,
1995.(11)
10(nn) Agreement for Sale and Purchase of Shares in Medizone New Zealand
Limited between Richard G. Solomon and Medizone International, Inc.,
dated June 22, 1995.(12)
10(oo) Shareholders' Agreement relating to Medizone New Zealand Limited
between and among Solwin Investments Limited, Medizone
International, Inc. and Medizone New Zealand Limited, dated June 22,
1995.(12)
10(pp) Licensing Agreement between Medizone International, Inc. and
MNZ, dated June 22, 1995.(12)
10(qq) Managing Agent Agreement between Medizone International, Inc. and
Medizone New Zealand Limited, dated June 22, 1995.(12)
10(rr) Lease Agreement between Medizone International, Inc. and Linmar
L.P., dated January 17, 1996.(13)
10(ss) Agreement between Medizone International, Inc. and Multiossigen
S.r.l., dated as of September 13, 1996.(14)
10(tt) Agreement between Medizone International, Inc. and JRH Biosciences,
Inc., dated April 17, 1997.(15)
10(uu) Lease Agreement between Medizone International Inc. and Eagle
Overlook, L.C., made on September 23, 1997.(16)
16 Letter re: change in certifying accountants.(1)
- --------------------
(1) Filed herewith.
(2) Incorporated by reference to the Registrant's registration statement
on Form S-18 (Registration No. 2-93277-D), effective May 14, 1985.
(3) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1986.
(4) Incorporated by reference to the Registrant's current report on Form
8-K, filed March 13, 1987.
(5) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1987.
(6) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1988.
(7) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1989.
(8) Incorporated by reference to the Registrant's annual report on Form
32
<PAGE>
10-K for the period ended December 31, 1990.
(9) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1992.
(10) Incorporated by reference to the Registrant's current annual report
on Form 8-K dated September 8, 1993.
(11) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1994.
(12) Incorporated by reference to the Registrant's current annual report
on Form 8-K, dated June 22, 1995.
(13) Incorporated by reference to the Registrant's annual report on Form
10-K for the period ended December 31, 1995.
(14) Incorporated by reference to the Registrant's current report on Form
8-K, dated October 17, 1996.
(15) Incorporated by reference to the Registrant's current report on Form
8-K, dated May 5, 1997.
(16) Incorporated by reference to the Registrant's current report on Form
8-K dated September 24, 1997.
33
<PAGE>
SIGNATURES
-----------------
Pursuant to the requirements of Section 13 or 15(d) of the Securities
Exchange Act of 1934, the Company has duly caused this Annual Report to be
signed on its behalf by the undersigned, thereunto duly authorized.
MEDIZONE INTERNATIONAL, INC.
By: /s/ Edwin G. Marshall
-------------------------------------
Edwin G. Marshall
President and Chief Executive Officer
Date: February 7, 2000
Pursuant to the requirements of Section 13 or 15(d) of the Securities
Exchange Act of 1934, this Annual Report has been signed below by the following
persons on behalf of the Company, in the capacities shown and on the date
indicated:
Date: February 7, 2000 /s/ Edwin G. Marshall
------------------------------------
Edwin G. Marshall, President
Chief Executive Officer and Director
Date: February 7, 2000 /s/Gerard V. Sunnen
------------------------------------
Gerard V. Sunnen, Director
Date: February 7, 2000 /s/ William M. Hitt
------------------------------------
William M. Hitt, Director
Date: February 7, 2000 /s/ Kevin R. Andersen
------------------------------------
Kevin R. Andersen, Chief Financial
Officer (and Principal Accounting Officer)
34
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
CONSOLIDATED FINANCIAL STATEMENTS
December 31, 1998 and 1997
<PAGE>
C O N T E N T S
Independent Auditors' Report...................................................3
Consolidated Balance Sheets....................................................4
Consolidated Statements of Operations..........................................6
Consolidated Statements of Stockholders' Equity (Deficit) .....................7
Consolidated Statements of Cash Flows.........................................14
Notes to the Consolidated Financial Statements................................16
<PAGE>
INDEPENDENT AUDITORS' REPORT
The Board of Directors
Medizone International, Inc. and Subsidiary
(A Development Stage Company)
Stinson Beach, California
We have audited the accompanying consolidated balance sheet of Medizone
International, Inc. and Subsidiary (a development stage company) as of December
31, 1998, and the related consolidated statements of operations, stockholders'
equity (deficit), and cash flows for the year ended December 31, 1998 and for
the period January 31, 1986 (date of inception) through December 31, 1998. These
consolidated financial statements are the responsibility of the Company's
management. Our responsibility is to express an opinion on these consolidated
financial statements based on our audit. The consolidated financial statements
of Medizone International, Inc. and Subsidiary (a development stage company) as
of December 31, 1997, for the years ended December 31, 1997 and 1996 and the
period January 31, 1986 (date of inception) through December 31, 1997 were
audited by other auditors, whose report, dated March 19, 1998 included an
explanatory paragraph related to the Company's ability to continue as a going
concern. The consolidated financial statements for the period January 31, 1986
(date of inception) through December 31, 1998 include total revenues,
stockholders' equity and net loss of $133,349, $(1,023,974) and $(13,783,439),
respectively. Our opinion on the consolidated statements of operations,
stockholders' equity (deficit) and cash flows for the period January 31, 1986
(date of inception) through December 31, 1998, insofar as it relates to amounts
for prior periods through December 31, 1997, is based solely on the report of
other auditors.
We conducted our audit in accordance with generally accepted auditing standards.
Those standards require that we plan and perform the audit to obtain reasonable
assurance about whether the consolidated financial statements are free of
material misstatement. An audit includes examining, on a test basis, evidence
supporting the amounts and disclosures in the consolidated financial statements.
An audit also includes assessing the accounting principles used and significant
estimates made by management, as well as evaluating the overall consolidated
financial statement presentation. We believe that our audit provides a
reasonable basis for our opinion.
In our opinion, based on our audit and the report of other auditors, the
consolidated financial statements referred to above present fairly, in all
material respects, the consolidated financial position of Medizone
International, Inc. and Subsidiary (a development stage company) as of December
31, 1998, and the consolidated results of their operations and their cash flows
for the year ended December 31, 1998 and for the period January 31, 1986 (date
of inception) through December 31, 1998, in conformity with generally accepted
accounting principles.
The accompanying consolidated financial statements have been prepared assuming
the Company will continue as a going concern. As discussed in Note 10 to the
consolidated financial statements, the Company has incurred significant losses
which have resulted in an accumulated deficit and a deficit in stockholders'
equity, raising substantial doubt about its ability to continue as a going
concern. Management's plans in regard to these matters are also described in
Note 10. The consolidated financial statements do not include any adjustments
that might result from the outcome of this uncertainty.
Jones, Jensen & Company
Salt Lake City, Utah
January 24, 2000
<PAGE>
Andersen Andersen & Strong, L.C. 941 East 3300 South, Suite 202
Certified Public Accountants Salt Lake City, Utah 84106
and Business Consultants
Member SEC Practice Section of the AICPA Telephone 801 486-0096
Fax 801-486-0098
REPORT OF INDEPENDENT CERTIFIED PUBLIC ACCOUNTANTS
The Board of Directors and Stockholders
Medizone International, Inc.
We have audited the consolidated balance sheet of Medizone International, Inc.
and subsidiaries (a development stage company) as of December 31, 1997, and the
related statements of operations, stockholders' equity and cash flows for the
years ended December 31, 1997, and 1996, and the period January 31, 1986 (date
of inception) through December 31, 1997. 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 audit in accordance with generally accepted auditing standards.
Those standards require that we plan and perform the audits 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 audit provides a reasonable basis for our opinion.
In our opinion, the financial statements referred to above present fairly, in
all material respects, the financial position of Medizone International, Inc.
and subsidiaries as of December 31, 1997, and the results of their operations
and their cash flows for the years ended December 31, 1997 and 1996, and the
period January 31, 1986 (date of inception) through December 31, 1997, in
conformity with generally accepted accounting principles.
The accompanying financial statements have been prepared assuming that the
Company will continue as a going concern. As discussed in Note 3 to the
financial statements, the Company has suffered recurring losses from operations
and has a net capital deficiency that raise substantial doubt about its ability
to continue as a going concern. Management's plans in regard to these matters
are also described in Note 3. The financial statements do not include any
adjustments that might result from the outcome of this uncertainty.
/s/ Andersen Andersen & Strong, L.C.
Salt Lake City, Utah
February 4, 2000
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Balance Sheets
ASSETS
<TABLE>
<CAPTION>
December 31,
1998 1997
CURRENT ASSETS
<S> <C> <C>
Cash and cash equivalents $ 7,643 $ 138,173
Prepaid expenses and advances - 9,154
----------------- -----------------
Total Current Assets 7,643 147,327
----------------- -----------------
PROPERTY AND EQUIPMENT (Net) (Notes 1 and 2) 7,612 8,268
----------------- -----------------
OTHER ASSETS
Receivable from affiliate, net (Note 1) - 48,947
Deposits - 2,477
----------------- -----------------
Total Other Assets - 51,424
----------------- -----------------
TOTAL ASSETS $ 15,255 $ 207,019
================= =================
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
4
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Balance Sheets (Continued)
LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT)
<TABLE>
<CAPTION>
December 31,
1998 1997
----------------- -----------------
CURRENT LIABILITIES
<S> <C> <C>
Accounts payable $ 470,132 $ 517,011
Accrued expenses (Note 3) 288,606 222,060
Notes payable (Note 6) 280,491 354,115
----------------- -----------------
Total Current Liabilities 1,039,229 1,093,186
----------------- -----------------
Total Liabilities 1,039,229 1,093,186
----------------- -----------------
COMMITMENTS AND CONTINGENCIES (Note 4)
STOCKHOLDERS' EQUITY (DEFICIT)
Common stock; 250,000,000 shares authorized
of $0.001 par value, 148,926,434 and 136,887,629
shares issued and outstanding, respectively 148,926 136,888
Common stock subscribed (Note 5) - 5,714
Additional paid-in capital 12,610,539 12,188,909
Deficit accumulated during the development stage (13,783,439) (13,217,678)
----------------- -----------------
Total Stockholders' Equity (Deficit) (1,023,974) (886,167)
----------------- -----------------
TOTAL LIABILITIES AND STOCKHOLDERS'
EQUITY (DEFICIT) $ 15,255 $ 207,019
================= =================
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
5
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Operations
<TABLE>
<CAPTION>
From
Inception on
January 31,
For the Years Ended 1986 Through
December 31, December 31,
1998 1997 1996 1998
---------------- ----------------- ------------------ ------------------
<S> <C> <C> <C> <C>
REVENUE $ - $ - $ - $ 133,349
---------------- ----------------- ------------------ ------------------
EXPENSES
Cost of sales - - - 103,790
Research and development 13,218 116,950 25,000 2,332,853
General and administrative 562,729 631,491 1,288,175 11,130,564
Bad debt expense 48,947 - - 48,947
Depreciation and amortization 2,673 1,696 2,907 25,453
---------------- ----------------- ------------------ ------------------
Total Expenses 627,567 750,137 1,316,082 13,641,607
---------------- ----------------- ------------------ ------------------
Loss from Operations (627,567) (750,137) (1,316,082) (13,508,258)
---------------- ----------------- ------------------ ------------------
OTHER INCOME (EXPENSE)
Minority interest in loss - - - 26,091
Other income 420 3,342 - 19,780
Gain on sale of subsidiary (Note 1) 108,417 - - 208,417
Interest expense (47,031) (28,764) (13,313) (820,697)
---------------- ----------------- ------------------ ------------------
Total Other Income (Expense) 61,806 (25,422) (13,313) (566,409)
---------------- ----------------- ------------------ ------------------
LOSS BEFORE EXTRAORDINARY
ITEMS (565,761) (775,559) (1,329,395) (14,074,667)
---------------- ----------------- ------------------ ------------------
EXTRAORDINARY ITEMS
Debt forgiveness - - - 291,228
---------------- ----------------- ------------------ ------------------
Total Extraordinary Items - - - 291,228
---------------- ----------------- ------------------ ------------------
NET LOSS $ (565,761) $ (775,559) $ (1,329,395) $ (13,783,439)
================ ================= ================== ==================
BASIC LOSS PER SHARE $ (0.00) $ (0.01) $ (0.01)
================ ================= ==================
WEIGHTED AVERAGE NUMBER
OF SHARES OUTSTANDING 142,645,000 133,568,000 118,022,000
================ ================= ==================
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
6
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
----------------------------------------------- Paid-in Development
Shares Amount Subscribed Capital Stage
-------------- --------------- --------------- --------------- ---------------
<S> <C> <C> <C> <C> <C>
Balance, January 31, 1986 (inception) - $ - $ - $ $ -
Initial capitalization of Medizone -
Nevada at $0.03 per share 5,500,000 5,500 - 150,128 -
Common shares issued in acquisition
of Medizone - Delaware (Note 1) 37,500,000 37,500 - (37,500) -
Common stock issued for services
rendered in July 1986 at $0.10
per share 50,000 50 - 4,950 -
Common stock issued in conversion
of warrants during 1986 at $0.10
per share 7,814,600 7,815 - 773,645 -
Stock issuance costs - - - (105,312) -
Net loss for the year ended
December 31, 1986 - - - - (796,068)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1986 50,864,600 50,865 - 785,911 (796,068)
Common stock issued upon exercise
of warrants in January 1987 at $0.10
per share 2,600 2 - 257 -
Common stock issued for patent in
March 1987 at $0.69 per share 1,000,000 1,000 - 692,750 -
Common stock issued for cash in
June 1987 at an average price of
$0.16 per share 950,000 950 - 149,050 -
Common stock issued for services
in June and July 1987 at an
average price of $0.12 per share 203,167 203 - 24,314 -
Common stock issued through
exercise of options in August 1987
at $1.75 per share 250,000 250 - 437,250 -
Net loss for the year ended
December 31, 1987 - - - - (2,749,400)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1987 53,270,367 $ 53,270 $ - $ 2,089,532 $ (3,545,468)
--------------- --------------- ---------------- --------------- ---------------
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
7
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
------------------------------------------- Paid-in Development
Shares Amount Subscribed Capital Stage
---------- --------------- -------------- --------------- -----------------
<S> <C> <C> <C> <C> <C>
Balance, December 31, 1987 53,270,367 $ 53,270 $ - $ 2,089,532 $ (3,545,468)
Common stock issued through exercise
of options in January 1988 at $0.50
per share 200,000 200 - 99,800 -
Common stock issued for cash in
September 1988 at $0.08 per share 1,000,000 1,000 - 79,000 -
Common stock issued for services
at an average price of $0.23
per share 35,000 35 - 7,965 -
Additional capital contributed - - - 174,126 -
Net loss for the year ended
December 31, 1988 - - - - (714,347)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1988 54,505,367 54,505 - 2,450,423 (4,259,815)
Common stock issued for services
at an average price of $0.18 per
share 261,889 262 - 46,363 -
Common stock issued for cash at
an average price of $0.05 per share 5,790,000 5,790 - 285,710 -
Common stock issued for services
and in lieu of outstanding debt at
an average price of $0.12 per share 4,749,532 4,750 - 578,978 -
Common stock issued upon exercise
of options at $0.16 per share 375,000 375 - 59,125 -
Net loss for the year ended
December 31, 1989 - - - - (862,051)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1989 65,681,788 $ 65,682 $ - $ 3,420,599 $ (5,121,866)
--------------- --------------- ---------------- --------------- ---------------
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
8
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
------------------------------------------------ Paid-in Development
Shares Amount Subscribed Capital Stage
--------------- --------------- -------------- --------------- -----------------
<S> <C> <C> <C> <C> <C>
Balance, December 31, 1989 65,681,788 $ 65,682 $ - $ 3,420,599 $ (5,121,866)
Common stock issued for services
at $0.10 per share 880,000 880 - 87,120 -
Common stock issued for cash at an
average price of $0.04 per share 4,250,000 4,250 - 175,250 -
Common stock issued for services
and in lieu of outstanding debt at
an average price of $0.06 per share 2,422,727 2,423 - 137,577 -
Additional capital contributed - - - 100,000 -
Net loss for the year ended
December 31, 1990 - - - - (606,309)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1990 73,234,515 73,235 - 3,920,546 (5,728,175)
Common stock issued for cash at an
average price of $0.07 per share 4,366,667 4,366 - 305,634 -
Common stock issued for services
at an average price of $0.17 per
share 425,000 425 - 72,075 -
Common stock issued through
exercise of options at an average
price of $0.45 per share 450,000 450 - 204,050 -
Additional capital contributed - - - 5,000 -
Net loss for the year ended
December 31, 1991 - - - - (1,220,152)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1991 78,476,182 $ 78,476 $ - $ 4,507,305 $ (6,948,327)
--------------- --------------- ---------------- --------------- ---------------
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
9
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
------------------------------------------------ Paid-in Development
Shares Amount Subscribed Capital Stage
--------------- --------------- -------------- --------------- -----------------
<S> <C> <C> <C> <C> <C>
Balance, December 31, 1991 78,476,182 $ 78,476 $ - $ 4,507,305 $ (6,948,327)
Common stock issued for services
at $0.20 per share 151,500 152 - 30,148 -
Common stock issued in lieu of
debt at $0.15 per share 250,000 250 - 37,250 -
Common stock issued for cash at
an average price of $0.16 per share 2,702,335 2,702 - 427,648 -
Common stock issued through
exercise of options at $0.50
per share 250,000 250 - 124,750 -
Additional capital contributed - - - 81,100 -
Net loss for the year ended
December 31, 1992 - - - - (649,941)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1992 81,830,017 81,830 - 5,208,201 (7,598,268)
Common stock issued for services
at an average price of $0.10
per share 5,347,219 5,347 - 542,859 -
Common stock issued for cash at
an average price of $0.18 per share 1,471,666 1,472 - 269,528 -
Common shares subscribed for
at $0.10 per share - - 2,619 259,296 -
Net loss for the year ended
December 31, 1993 - - - - (1,598,342)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1993 88,648,902 $ 88,649 $ 2,619 $ 6,279,884 $ (9,196,610)
--------------- --------------- ---------------- --------------- ---------------
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
10
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
------------------------------------------------ Paid-in Development
Shares Amount Subscribed Capital Stage
--------------- --------------- -------------- --------------- -----------------
<S> <C> <C> <C> <C> <C>
Balance, December 31, 1993 88,648,902 $ 88,649 $ 2,619 $ 6,279,884 $ (9,196,610)
Common stock issued for services
at $0.10 per share 1,431,590 1,431 - 141,727 -
Common shares subscribed for at
$0.10 per share - - 9,552 945,682 -
Common shares subscribed for as
cancellations of indebtedness at
$0.10 per share - - 417 41,234 -
Common shares subscribed for as
cancellation of indebtedness at
$0.18 per share - - 11,250 2,022,379 -
Issuance of subscribed stock 10,384,900 10,385 (10,385) - -
Issuance of shares in recognition
of disparity in purchase price in
offering 1,125,834 1,126 - (1,126) -
Prior period adjustment (Note 8) - - - - 219,422
Net loss for the year ended
December 31, 1994 - - - - (1,126,315)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1994 101,591,226 $ 101,591 $ 13,453 $ 9,429,780 $ (10,103,503)
--------------- --------------- ---------------- --------------- ---------------
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
11
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
------------------------------------------------ Paid-in Development
Shares Amount Subscribed Capital Stage
--------------- --------------- -------------- --------------- -----------------
<S> <C> <C> <C> <C> <C>
Balance, December 31, 1994 101,591,226 $ 101,591 $ 13,453 $ 9,429,780 $ (10,103,503)
Redeemable common shares
converted to common stock (Note 9) 200,000 200 - 39,800 -
Common stock issued for services
at $0.10 per share 2,050,000 2,050 - 202,950 -
Issuance of subscribed stock 17,524,860 17,524 (17,524) - -
Cancellation of common shares (1,242,727) (1,242) - (70,563) -
Common shares subscribed for at
$0.10 per share - - 9,118 902,707 -
Prior period adjustment (Note 8) - - - - 71,806
Additional capital contributed - - - 50,000 -
Net loss for the year ended
December 31, 1995 - - - - (1,081,027)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1995 120,123,359 120,123 5,047 10,554,674 (11,112,724)
Common stock issued for cash
at $0.10 per share 100,000 100 - 9,900 -
Common stock issued for services
at $0.10 per share 1,415,875 1,416 - 140,171 -
Issuance of subscribed stock 8,412,379 8,413 (8,413) - -
Common shares subscribed for
at $0.11 per share - - 6,456 718,991 -
Net loss for the year ended
December 31, 1996 - - - - (1,329,395)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1996 130,051,613 $ 130,052 $ 3,090 $ 11,423,736 $ (12,442,119)
--------------- --------------- ---------------- --------------- ---------------
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
12
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)
<TABLE>
<CAPTION>
Deficit
Accumulated
Common Stock Additional During the
------------------------------------------------ Paid-in Development
Shares Amount Subscribed Capital Stage
--------------- --------------- -------------- --------------- -----------------
<S> <C> <C> <C> <C> <C>
Balance, December 31, 1996 130,051,613 $ 130,052 $ 3,090 $ 11,423,736 $ (12,442,119)
Issuance of subscribed stock 3,089,680 3,090 (3,090) - -
Common shares subscribed for
at $0.10 per share - - 5,714 394,287 -
Common stock issued for services
at $0.10 per share 3,746,336 3,746 - 370,886 -
Net loss for the year ended
December 31, 1997 - - - - (775,559)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1997 136,887,629 136,888 5,714 12,188,909 (13,217,678)
Common stock issued through
exercise of warrants at $0.07
per share 857,142 857 - 59,143 -
Common stock issued in lieu of
debt at $0.05 per share 864,747 865 - 42,372 -
Issuance of subscribed stock 5,714,286 5,714 (5,714) - -
Cancellation of common shares (630,000) (630) - 630 -
Common stock issued for services
at $0.05 per share 3,465,000 3,465 - 169,786 -
Common stock issued for services
at $0.09 per share 750,000 750 - 63,785 -
Common stock issued in lieu of
debt at $0.09 per share 967,630 967 - 82,214 -
Common stock issued for services
at $0.08 per share 50,000 50 - 3,700 -
Net loss for the year ended
December 31, 1998 - - - - (565,761)
--------------- --------------- ---------------- --------------- ---------------
Balance, December 31, 1998 148,926,434 $ 148,926 $ - $ 12,610,539 $ (13,783,439)
=============== =============== ================ =============== ===============
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
13
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Cash Flows
<TABLE>
<CAPTION>
From
Inception on
For the Years Ended January 31,
December 31, 1986 Through
-------------------------------------------------- December 31,
1998 1997 1996 1998
--------------- --------------- --------------- ---------------
CASH FLOWS FROM OPERATING ACTIVITIES
<S> <C> <C> <C> <C>
Net loss $ (565,761) $ (775,559) $ (1,329,395) $ (13,783,439)
Adjustments to reconcile net loss to net cash
used by operating activities:
Depreciation and amortization 2,673 1,696 2,907 25,453
Stock issued for services 241,536 374,632 141,587 2,867,416
Bad debt expense 48,947 - - 48,947
Minority interest in loss - - - (26,091)
Loss on disposal of assets - - - 693,752
Changes in assets and liabilities:
(Increase) decrease in prepaid expenses
and deposits 11,631 1,143 60,959 (48,947)
Increase (decrease) in accounts payable (18,698) 61,126 139,913 704,502
Increase (decrease) in accrued expenses 69,783 50,651 79,423 348,628
--------------- --------------- --------------- ---------------
Net Cash Used by Operating Activities (209,889) (286,311) (904,606) (9,169,779)
--------------- --------------- --------------- ---------------
CASH FLOWS FROM INVESTING ACTIVITIES
Organization costs - - - (8,904)
Purchase of fixed assets (2,017) (895) (10,002) (24,159)
--------------- --------------- --------------- ---------------
Net Cash Used by Investing Activities (2,017) (895) (10,002) (33,063)
--------------- --------------- --------------- ---------------
CASH FLOWS FROM FINANCING ACTIVITIES
Principle payments on notes payable (3,624) - - (192,774)
Cash received from notes payable 25,000 21,800 184,500 1,106,518
Capital contributions - - - 421,847
Stock issuance costs - - - (105,312)
Increase in minority interest - - - 14,470
Issuance of common stock for cash 60,000 400,000 735,447 7,965,736
--------------- --------------- --------------- ---------------
Net Cash Provided by Financing Activities 81,376 421,800 919,947 9,210,485
--------------- --------------- --------------- ---------------
NET INCREASE (DECREASE) IN CASH (130,530) 134,594 5,339 7,643
CASH AT BEGINNING OF PERIOD 138,173 3,579 (1,760) -
--------------- --------------- --------------- ---------------
CASH AT END OF PERIOD $ 7,643 $ 138,173 $ 3,579 $ 7,643
=============== =============== =============== ===============
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
14
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Consolidated Statements of Cash Flows (Continued)
<TABLE>
<CAPTION>
From
Inception on
For the Years Ended January 31,
December 31, 1986 Through
-------------------------------------------------- December 31,
1998 1997 1996 1998
--------------- --------------- --------------- ---------------
SUPPLEMENTAL CASH FLOW INFORMATION
CASH PAID FOR:
<S> <C> <C> <C> <C>
Interest $ - $ - $ - $ 26,483
Income taxes $ - $ - $ - $ -
NON-CASH FINANCING ACTIVITIES:
Stock issued for services $ 241,536 $ 374,632 $ 141,587 $ 2,867,416
Stock issued in conversion of debt to common stock $ 126,418 $ - $ - $ 3,776,293
Stock issued for license agreement and patent $ - $ - $ - $ 693,752
</TABLE>
The accompanying notes are an integral part of these consolidated financial
statements.
15
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
a. Organization
The consolidated financial statements presented are those of
Medizone International, Inc. (Medizone-Nevada) and its
wholly-owned subsidiaries, Medizone International, Inc.
(Medizone-Delaware) and Medizone Canada, Ltd. (MedCan).
Collectively, they are referred to herein as the "Company".
Medizone-Nevada was incorporated under the name of Madison
Funding, Inc. on August 27, 1984 under the laws of the State of
Nevada for the purpose of investing in, acquiring, operating and
disposing of businesses or assets of any nature. Effective Match
26, 1986, Medizone-Nevada issued 37,500,000 shares of its common
stock in exchange for the issued and outstanding common stock of
Medizone-Delaware.
Medizone-Delaware was incorporated on January 31, 1986 under the
state laws of Delaware. Medizone-Delaware was organized to seek
regulatory approval for a MEDIZONE (R) drug, a precise mixture of
ozone and oxygen for the purpose of inactivating lipid enveloped
viruses for the intended purpose of decontaminating blood and
blood products and assisting in the treatment of certain diseases.
It is also trying to develop or acquire the related technology and
equipment for the medical application of the products, including
the drug production and delivery system.
At the time of the acquisition of Medizone-Delaware,
Medizone-Nevada was essentially inactive, with no operations and
minimal assets. Additionally, the exchange of Medizone-Nevada's
common stock for the common stock of Medizone-Delaware resulted in
the former stockholders of Medizone-Delaware obtaining control of
Medizone-Nevada. Accordingly, Medizone-Delaware became the
continuing entity for accounting purposes, and the transaction was
accounted for as a recapitalization of Medizone-Delaware with no
adjustment to the basis of Medizone-Delaware's assets acquired or
liabilities assumed. For legal purposes, Medizone-Nevada was the
surviving entity.
On November 18, 1987, Medizone Canada Ltd. (MedCan) was
incorporated under the laws of the Province of British Columbia.
Shortly thereafter, MedCan entered into a license agreement with
the Company wherein the Company transferred to MedCan the licenses
and rights necessary to permit MedCan to hold substantially the
same rights with respect to the medical applications of ozone in
Canada as the Company does in the United States. As consideration
for the transfer, the Company received 3,000,000 shares of MedCan
and, in addition, purchased 1 share for the sum of $1.00. Under a
separate agreement among the Company, MedCan and Australian Gold
Mines Corporation (AGMC), (which later changed its name to
International Blue Sun Resource Corporation), AGMC purchased
130,000 shares of MedCan for $100,000. On December 23, 1988,
MedCan was recapitalized in a transaction in which the majority of
its shares were exchanged for shares of KPC Investments, (a Utah
corporation) (KPC). Following this transaction, the Company owned
25,029,921 shares of KPC, representing 72% of the outstanding
shares. KPC then changed its name to Medizone Canada, Ltd. (MCL).
MedCan acquired all of the assets of MCL, consisting solely of
cash in the amount of approximately $89,000.
16
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
a. Organization (Continued)
In June 1998, the Company sold its interest in MCL for $125,000
cash debt assumed of $8,417 less fees of $25,000 in a private
transaction which resulted in a gain of $108,417 for the year
ended December 31, 1998. The Company retained ownership, however,
of all of the issued and outstanding stock of MedCan, the Canadian
subsidiary.
b. Formation of Joint Venture
On June 22, 1995, the Company entered into a series of contracts
which resulted in the formation of a joint venture subsidiary
incorporated in New Zealand, Medizone New Zealand Limited (MNZ).
MNZ, a privately held corporation equally owned by the Company and
Solwin Investments Limited (Solwin), a New Zealand corporation, is
a research and development stage company whose objective is to
obtain regulatory approval for the distribution of the Company's
patented technology in New Zealand, Australia, South East Asia and
the South Pacific Islands.
Pursuant to the contracts, the Company purchased 100% of MNZ from
Richard G. Soloman (Solomon), a New Zealand citizen, who became a
director of the Company in January 1996 and who caused the
formation of MNZ on June 22, 1995. Contemporaneously with this
transaction, the Company sold 50% of MNZ to Solwin, a corporation
owned by Solomon, for $150,000, of which $50,000 was thereupon
loaned by the Company to MNZ on a demand basis (see Note 1(i)).
Contemporaneous with the creation of the above share structure,
the Company and MNZ entered into a Licensing Agreement (the
Licensing Agreement) and a Managing Agent Agreement (the Managing
Agent Agreement).
Pursuant to the Licensing Agreement, the Company granted an
exclusive license to MNZ for its process and equipment patents and
trademark in New Zealand. MNZ has agreed to apply for
corresponding patent protection for the patents in New Zealand and
to use its best effort to exploit the rights granted in the
agreement. The License Agreement shall terminate on the date of
the expiration of the last to expire of any patent obtained in New
Zealand, or, if no such patents are obtained, on June 22, 2010.
The Company is to receive a guaranteed minimum royalty (the
Guaranteed Minimum Royalty) in an amount to be agreed to by the
Company and MNZ, commencing in the third year after all necessary
regulatory approvals requisite to the license, use or distribution
of the Company's proprietary technology have been obtained in New
Zealand. If the Company and MNZ are unable to agree upon the
amount of the Guaranteed Minimum Royalty, the Company may
terminate the license on thirty days notice. Commencing on the
first sale to a user by MNZ, the Company shall receive a sales
royalty in an amount equal to 10% of MNZ's gross annual sales
under the License Agreement.
17
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
b. Formation of Joint Venture (Continued)
Pursuant to the Managing Agent Agreement, MNZ will act as the
Company's agent in the finding of other licensees of the Company's
patents and trademark in the following countries: Autralasia
(including Australia and New Zealand), the South Pacific Islands
and South East Asia (including the Philippines, Indonesia and
Vietnam). Licensing fees obtained as a result of the Managing
Agent Agreement shall be divided between the Company and MNZ on a
sliding scale as set forth below:
<TABLE>
<CAPTION>
Medizone Medizone
International, New Zealand
Inc. Limited
<S> <C> <C>
Initial license 50% 50%
Subsequent license fees up to $500,000 50% 50%
Subsequent license fees between $500,000
and $750,000 75% 25%
Subsequent license fees in excess of $750,000 85% 15%
</TABLE>
MNZ and the Company will also divide any net royalties paid to the
Company pursuant to any license obtained pursuant to the Managing
Agent Agreement, with MNZ being paid 10% of the net royalties and
the Company receiving 90% of the net royalties.
The Managing Agent Agreement shall expire on the termination or
expiration of the last of the licenses obtained pursuant thereto,
subject to earlier termination by the Company upon an occurrence
of certain events.
Pursuant to Emerging Issued Task Force Statement No. 89-7, the
Company recognized a $100,000 gain on the sale of MNZ to Solwin.
The investment in the joint venture has been recorded under the
equity method of accounting as the Company does not have ultimate
control of the joint venture. The investment is recorded at $-0-
as of December 31, 1998.
c. Business Activities
The Company's objective is to gain regulatory approval for the
medical uses of ozone to inactivate certain viruses and to assist
in the treatment of certain diseases and to develop, promote and
distribute ozone-generating equipment and related products for
medical applications.
18
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
c. Business Activities (Continued)
By letter agreement with the Italian Scientific Society for
Oxygen-Ozone Therapy (ISSOT) in Bergamo, Italy, dated March 23,
1993, the Company entered into a collaborative arrangement to
research and examine the efficacy of ozone therapy and the
Company's technology in the treatment of various blood-related
human diseases. The research is to be conducted by ISSOT in Italy,
under the direction of a research group assembled by the Italian
Ministry of Health.
On May 16, 1994, the Company announced that human trials were to
commence at the University of Naples ("Naples"). However, after
the termination of the Company's former President, the Company's
inquiry into the conduct of its operations during the former
President's tenure, that disclosed that human clinical trials of
the Company's ozone therapy on patients infected with either
Acquired Immunodeficiency Syndrome (AIDS) or Hepatitis B (chronic
active) has not been authorized by Naples or commenced at that
institution. The Company also learned that the Italian Ministry of
Health had not issued approvals for human clinical trials to
commence at certain sites as previously disclosed. While the
ethics committees at certain university hospitals have stated
their approval for the Company to conduct Phase II trials, they
would require the Company to have either completed a large animal
study and Phase I human clinical trials or to have these
requirements waived. The Company has never performed a large
animal study or Phase I human clinical trials and does not possess
the necessary data with respect to its ozone therapy to commence
Phase II study. However, there does exist a broad use and
understanding of ozone therapy throughout Europe and there have
been numerous scientific articles published in European medical
journals describing the use of ozone on humans.
19
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
c. Business Activities (Continued)
The Company has held discussions with an Italian Contract Research
Organization (the ICRO) with a view to having the ICRO act as an
intermediary on behalf of the Company with the Italian Ministry of
Health and prepare a written submission to the Italian Ministry of
Health regarding the data in the public domain on ozone therapy
with a view to having the Italian Ministry of Health accept this
material as proof of safety, toxicity and tolerance of the use of
the Company's ozone technology on humans in lieu of having the
Company perform a large animal study and possibly even Phase I
human clinical trials. The ICRO would also design a research
program and protocols for human clinical trials which would meet
the standards of the European Union (EU) and Food and Drug
Administration (FDA), monitor the clinical terms and collect and
prepare analyses of the data produced by the trials. The Company
will not be able to enter into a formal contract with the ICRO
unless it obtains additional funding. If the Italian Ministry of
Health does not accept the published evidence on the use of ozone
therapy on humans, the Company will be required to perform its own
Phase I human clinical trials and possibly a large animal study.
In late 1997, the Company entered into discussions with Italian
and Belgium clinicians with regard to them performing Phase I
human clinical trials. However, assuming the Italian Ministry of
Health did not grant the Company's request for waiver, no formal
agreements with these clinicians would be signed and the studies
would not begin until the company obtains additional funding. The
Company estimates that it would require an infusion of
approximately $1.5 million to advance the above-described research
initiatives through the completion of a Phase III human clinical
trials and submission of the data for approval to the Italian
Ministry of Health.
d. Accounting Methods
The Company's consolidated financial statements are prepared using
the accrual method of accounting. The Company has elected a
December 31 year end.
e. Cash and Cash Equivalents
Cash equivalents include short-term, highly liquid investments
with maturities of three months or less at the time of
acquisition.
f. Basic Loss Per Share
The computations of basic loss per share of common stock are based
on the weighted average number of common shares outstanding during
the period of the consolidated financial statements as follows:
20
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
f. Basic Loss Per Share (Continued)
<TABLE>
<CAPTION>
For the Years Ended
December 31,
----------------------------------------------------------
1998 1997 1996
------------------ ------------------ ------------------
<S> <C> <C> <C>
Numerator (net loss) $ (565,761) $ (775,559) $ (1,329,395)
Denominator (weighted
average number of
shares outstanding) 142,645,000 133,568,000 118,022,000
Loss per share $ (0.00) $ (0.01) $ (0.01)
================== ================== ==================
</TABLE>
Common stock equivalents, consisting of warrants and options, have
not been included in the calculation as their effect is
antidilutive for the periods presented.
g. Change in Accounting Principle
The Financial Accounting Standards Board has issued Statement of
Financial Accounting Standards ("SFAS") No. 128, "Earnings Per
Share" and Statement of Financial Accounting Standards No. 129
"Disclosures of Information About an Entity's Capital Structure."
SFAS No. 128 provides a different method of calculating earnings
per share than was previously used in accordance with APB Opinion
No. 15 "Earnings Per Share." SFAS No. 128 provides for the
calculation of "Basic" and "Dilutive" earnings per share. Basic
earnings per share includes no dilution and is computed by
dividing income (loss) available to common shareholders by the
weighted average number of common shares outstanding for the
period. Diluted earnings per share reflects the potential dilution
of securities that could share in the earnings of an entity,
similar to fully diluted earnings per share. SFAS No. 129
establishes standards for disclosing information about an entity's
capital structure. SFAS No. 128 and SFAS No. 129 are effective for
financial statements issued for periods ending after December 15,
1997. In fiscal 1998, the Company adopted SFAS No. 128, which did
not have a material impact on the Company's financial statements.
In addition, the implementation of SFAS No. 129 did not have a
material effect on the Company's financial statements.
21
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
g. Change in Accounting Principle (Continued)
The Financial Accounting Standards Board has also issued SFAS No.
130, "Reporting Comprehensive Income" and SFAS No. 131,
"Disclosures about Segments of an Enterprise and Related
Information." SFAS No. 130 establishes standards for reporting and
display of comprehensive income, its components and accumulated
balances. Comprehensive income is defined to include all changes
in equity except those resulting from investments by owners and
distributions to owners. Among other disclosures, SFAS No. 130
requires that all items that are required to be recognized under
current accounting standards as components of comprehensive income
be reported in a financial statement that displays with the same
prominence as other financial statements. SFAS No. 131 supersedes
SFAS No. 14 "Financial Reporting for Segments of a Business
Enterprise." SFAS No. 131 establishes standards on the way that
public companies report financial information about operating
segments in annual financial statements and requires reporting of
selected information about operating segments in interim financial
statements issued to the public. It also establishes standards for
disclosure regarding products and services, geographic areas and
major customers. SFAS No. 131 defines operating segments as
components of a company about which separate financial information
is available that is evaluated regularly by the chief operating
decision maker in deciding how to allocate resources and in
assessing performance. The adoption of these statements did not
have a material impact on the Company's financial statements.
In February 1998, the Financial Accounting Standards Board
("FASB") has issued Statement of Financial Accounting Standard
("SFAS") No 132. "Employers' Disclosures about Pensions and other
Postretirement Benefits" which standardizes the disclosure
requirements for pensions and other Postretirement benefits and
requires additional information on changes in the benefit
obligations and fair values of plan assets that will facilitate
financial analysis. SFAS No. 132 is effective for years beginning
after December 15, 1997 and requires comparative information for
earlier years to be restated, unless such information is not
readily available. The adoption of this statement had no material
impact on the Company's financial statements.
22
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
g. Change in Accounting Principle (Continued)
In June 1998, the FASB issued SFAS No. 133, "Accounting for
Derivative Instruments and Hedging Activities" which requires
companies to record derivatives as assets or liabilities, measured
at fair market value. Gains or losses resulting from changes in
the values of those derivatives would be accounted for depending
on the use of the derivative and whether it qualifies for hedge
accounting. The key criterion for hedge accounting is that the
hedging relationship must be highly effective in achieving
offsetting changes in fair value or cash flows. SFAS No. 133 is
effective for all fiscal quarters of fiscal years beginning after
June 15, 1999. Management believes the adoption of this statement
will have no material impact on the Company's financial
statements.
h. Property and Equipment
Property and equipment is recorded at cost. Major additions and
improvement are capitalized. The cost and related accumulated
depreciation of equipment retired or sold are removed from the
accounts and any differences between the undepreciated amount and
the proceeds from the sale are recorded as gain or loss on sale of
equipment. Depreciation is computed using the straight-line method
over a period of five years.
i. Receivable from Affiliate
The Company loaned $50,000 in 1996 to MNZ, the joint venture
company, on a demand basis. MNZ currently has minimal assets and
operations. Management has recorded an allowance for the full
amount of the loan as of December 31, 1998.
j. Provision for Taxes
At December 31, 1998, the Company has net operating loss
carryforwards of approximately $11,750,000 that may be offset
against future taxable income through 2018. No tax benefit has
been reported in the consolidated financial statements because the
Company believes there is a 50% or greater chance the net
operating loss carryforwards will not be used. Accordingly, the
potential tax benefits of the net operating loss carryforwards are
offset by a valuation allowance of the same amount.
k. Principles of Consolidation
The consolidated financial statements include those of Medizone
International, Inc. (Medizone-Nevada) and its wholly-owned
subsidiaries, Medizone International, Inc. (Medizone-Delaware) and
Medizone Canada, Ltd (MedCan).
All material intercompany accounts and transactions have been
eliminated.
23
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
l. Estimates
The 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 and disclosure of contingent assets and
liabilities at the date of the financial statements and the
reported amounts of revenues and expenses during the reporting
period. Actual results could differ from those estimates.
m. Advertising
The Company follows the policy of charging the costs of
advertising to expense as incurred.
n. Stock Based Compensation
In October 1995, the Financial Accounting Standards Board issued
Statement of Financial Accounting Standard No. 123, Accounting for
Stock-Based Compensation. The Company currently accounts for its
stock-based compensation plans using the accounting prescribed by
Accounting Principles Board Opinion No. 25, Accounting for Stock
Issued to Employees. Since the Company is not required to adopt
the fair value based recognition provisions prescribed under SFAS
No. 123, it has elected to comply with the disclosure requirements
set forth in the Statement, which includes disclosing proforma net
income (loss) as if the fair value based method of accounting had
been applied. (See Note 7.)
o. Patents
In March 1987, the Company acquired a patent from Immunologics
Limited Partnership (Immunologics) in exchange for 1,000,000
shares of the Company's common stock. In 1988, Immunologics
purchased for $25,000, 5,000,000 shares of the Company's common
stock from the former Chairman and Chief Executive Officer of the
Company.
The patent covers a procedure for "ozone decontamination of blood
and blood products" through the treatment of stored blood and
blood components. The Board of Directors assigned a value of
approximately $700,000 to the patent based upon the fair market
value of the stock on the date of acquisition together with
related legal costs. The Company charged the cost of the patent to
research and development expense at acquisition because the
technologies covered by the patent have not been approved by the
FDA. Additionally, the Company agreed to pay the seller a royalty
fee equal to 3% of the net receipts received by the Company in
connection with the sale of any product, device or apparatus which
embodies the patent. The Company's management considers the
acquisition and retention of the patent to be material in its
development and prospects. In 1992, the General Partner of
Immunologics became chairman of the Company's Board of Directors
and subsequently resigned from the Company's Board of Directors in
September 1993.
24
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 1 - ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
(Continued)
p. Revenue Recognition Policy
The Company currently ha no source of revenues. Revenue
recognition policies will be determined when principal operations
begin.
NOTE 2 - PROPERTY AND EQUIPMENT
Property and equipment consists of the following:
<TABLE>
<CAPTION>
December 31,
--------------------------------------
1998 1997
------------------ ------------------
<S> <C> <C>
Office equipment $ 4,318 $ 2,301
Furniture and fixtures 6,307 6,307
------------------ ------------------
10,625 8,608
Accumulated depreciation (3,013) (340)
------------------ ------------------
Net property and equipment $ 7,612 $ 8,268
================== ==================
</TABLE>
Depreciation expense for the years ended December 31, 1998, 1997
and 1996 was $2,673, $1,696 and $2,907, respectively.
NOTE 3 - ACCRUED EXPENSES
Accrued expenses consist of the following:
<TABLE>
<CAPTION>
December 31,
--------------------------------------
1998 1997
------------------ ------------------
<S> <C> <C>
Accrued payroll $ 162,000 $ 130,350
Accrued interest 126,606 90,310
Other - 1,400
------------------ ------------------
Total $ 288,606 $ 222,060
================== ==================
</TABLE>
NOTE 4 - COMMITMENTS AND CONTINGENCIES
The Company retains an investor relations firm to act as the
Company's liaison with the brokerage community. The agreement was
originally for a period of one year, but has been extended by the
parties for additional one year periods. It receives a monthly
payment of $2,000, plus expenses. As additional compensation in
1996, it received 250,000 shares of the Company's common stock,
restricted under the federal securities laws.
On September 23, 1997, the Company entered into a three-year lease
with an unaffiliated third party for offices in Salt Lake City at
an annual rent of approximately $23,000. The office was used for
executive offices and administrative purposes. Following the
Company's reorganization on April 15, 1998, the Company's offices
were moved to Stinson Beach, California, and the Salt Lake City
lease was terminated.
25
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 5 - ISSUANCE OF COMMON STOCK AND WARRANTS
Unless otherwise stated, all transactions shown below were with
unrelated parties and the securities issued were restricted.
Medizone-Nevada initially issued 5,500,000 shares in a private
transaction.
On March 26, 1986, Medizone-Nevada issued 37,500,000 shares of
common stock, representing 87.2% of the then outstanding shares,
to the stockholders of Medizone-Delaware, including two officers
and directors, in exchange for all of the shares of
Medizone-Delaware. The costs of the transactions were offset
against paid-in capital.
In July 1986, the Company issued 50,000 shares of common stock to
individuals for services rendered.
During the period from August 1986 through October 31, 1986, the
final expiration date for exercise, warrants to purchase 7,814,600
shares together with cash totaling $781,460 were received by the
Company which then issued 7,814,600 shares of new common stock. In
January 1987, an additional 2,600 shares were issued in exchange
for warrants and cash of $259.
In March 1987, the Company issued 1,000,000 shares of common stock
in exchange for a patent (see Note 1).
In June 1987, the Company issued 950,000 shares to individuals in
private transactions for aggregate proceeds of $150,000.
During the period from June 1987 through July 1987, the Company
issued 203,167 shares of common stock to various vendors and
individuals for services rendered in 1986 and 1987.
On August 26, 1987, an officer of the Company exercised options to
purchase 250,000 shares of common stock. In January 1988, two
holders exercised their options and acquired an aggregate of
200,000 shares of common stock.
On September 26, 1988, the Company sold, in a private placement,
1,000,000 shares of common stock at $0.08 per share to an
individual.
During 1988, the Company issued a total of 35,000 shares of common
stock for services.
During 1989, the Company issued 261,889 shares of common stock to
various vendors and individuals for services rendered in 1988 and
1989.
During 1989, the Company issued 5,790,000 shares to individuals in
private transactions for aggregate proceeds of $291,500.
26
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 5 - ISSUANCE OF COMMON STOCK AND WARRANTS (Continued)
Also during 1989, the Company satisfied obligations for notes
payable to and accrued interest due to unrelated individuals
totaling $377,539 by the issuance of 3,899,532 shares of common
stock. The Company issued 250,000 shares of common stock to an
officer and 600,000 shares of common stock to three advisors to
the Company as additional compensation for work done for the
Company. These issuances were ascribed values of $60,650 and
$145,539, respectively, by the Company. Also during 1989, two
holders exercised their options and acquired an aggregate of
375,000 shares of common stock.
During 1990, the following equity transactions occurred: The
Company issued 4,250,000 shares to individuals in private
transactions for aggregate proceeds of $179,500; the Company
satisfied obligations totaling $125,000 to the former vice
president, secretary and treasurer as well as director by issuing
2,272,727 shares of common stock at $0.55 per share; the Company
satisfied an outstanding account payable to an unrelated
individual totaling $15,000 by the issuance of 150,000 shares of
common stock at $0.10 per share; and the Company issued to an
employee and four other unrelated persons as compensation or
payment a total of 880,000 shares of common stock to which it
ascribed a value of $88,000.
During 1991, the following equity transactions occurred: The
Company issued 4,366,667 shares to individuals in private
transactions for aggregate proceeds of $310,000; the Company
issued a total of 425,000 shares of common stock for services and
accrued liabilities of which an aggregate of 100,000 shares were
issued to two directors; and three holders exercised their options
and acquired an aggregate of 450,000 shares of common stock.
During 1992, the following equity transactions occurred: The
Company issued 2,702,335 shares to individuals in private
transactions for aggregate proceeds of $430,350; the Company
issued a total of 401,500 shares of common stock for services and
accrued liabilities; holders exercised options and acquired an
aggregate of 250,000 shares of common stock.
During 1993, the following equity transactions occurred: The
Company issued 1,471,666 shares to individuals in private
transactions for aggregate proceeds of $271,000; the Company
issued a total of 5,347,219 shares of common stock for services.
Also, during 1993, a total of $261,915 was received in cash for
2,619,150 shares subscribed as a result of a private placement
offering. The offering commenced as of November 26, 1993, with a
maximum of $700,000 to be raised in gross proceeds from the sale
of up to 7,000,000 shares.
27
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 5 - ISSUANCE OF COMMON STOCK AND WARRANTS (Continued)
During 1994, the following equity transactions occurred: The
Company issued a total of 1,431,590 shares of common stock for
services; the Company issued a total of 1,125,834 shares of common
stock to certain prior purchasers of common stock in recognition
of disparity in purchase in contemporaneous offerings. Also during
1994, a total of $680,040 was received in cash for 6,800,499
shares subscribed as a result of the offering. Subsequent to the
offering, an additional $316,860 was received in cash from foreign
investors subscribing to 3,168,600 shares of common stock. On
December 28, 1994, the Company settled a dispute regarding the
validity of notes payable to former management in the amount of
$2,033,628 by agreeing to issue 11,250,000 common shares (recorded
as shares subscribed) in satisfaction of the total amount of the
debt.
Also in 1994, $40,000 of notes payable (a portion of loans
totaling $60,000) together with interest, was satisfied by issuing
416,500 shares of common stock.
During 1995, the following equity transactions occurred: The
Company issued a total of 2,050,000 shares of common stock for
services. $911,825 was received from investors subscribing to
9,118,260 shares of common stock. Also, 7,524,860 common shares,
previously recorded as shares subscribed, were issued, and
1,242,727 were retired in accordance with the settlement agreement
with former management. 200,000 of redeemable shares were
converted into common stock. The Company sold shares of its New
Zealand subsidiary for aggregate proceeds of $150,000.
During 1996, the Company received stock subscription agreements
for the purchase of 7,254,470 shares of its common stock, together
with proceeds totaling $725,447 from sales of its securities to
non-United States investors, outside of the United States pursuant
to Regulation S promulgated under the Securities Act of 1993.
Approximately $635,447 of these proceeds were from the sale of the
Company's common stock at a per share price of $0.10 (including
$37,500 for 375,000 shares from Richard G. Solomon, at the time a
director of the Company). The remaining $90,000 were from the sale
of 900,000 units, each unit consisting of one share of the
Company's common stock at a per share price of $0.10 to a director
pursuant to the non-public offering exemption from registration
under the Securities Act. In May 1996, the Company issued 600,000
shares of its common stock to employees and 250,000 shares of its
common stock to its public relations consultant as additional
compensation. The Company also issued 565,875 shares of its common
stock to various consultants for services rendered.
During 1997, the Company issued 3,089,680 previously subscribed
shares of its common stock and also issued 3,746,336 shares of its
common stock to various consultants for services rendered. Also in
1997, the Company received $400,000 for subscriptions to acquire
5,714,285 shares of its common stock and warrants to purchase
9,285,715 shares of common stock at $0.07 per share, 25,000,000
shares at $0.20 per share, and 33,333,333 shares at $0.15 per
share.
28
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 5 - ISSUANCE OF COMMON STOCK AND WARRANTS (Continued)
During 1998, the Company issued 5,714,286 previously subscribed
shares of its common stock and also issued a total of 4,265,000
shares of its common stock to various individuals for services
rendered. Also in 1998, the Company issued 857,142 shares of
common stock through exercise of outstanding warrants at $0.07 per
share for a total of $60,000, and issued 1,832,377 shares in lieu
of outstanding debt of $126,418. The Company also canceled 630,000
shares for services that were never performed.
As of December 31, 1998, the following warrants were outstanding:
<TABLE>
<CAPTION>
Warrants Exercise Price Termination Dates
---------------- ------------------------- ----------------------
<S> <C> <C> <C>
8,428,573 $ 0.07 April 30, 2000
33,333,333 $ 0.15 April 30, 2000
25,000,000 $ 0.20 April 30, 2000
</TABLE>
NOTE 6 - NOTES PAYABLE
Notes payable consisted of the following at December 31, 1998 and
1997:
<TABLE>
<CAPTION>
December 31,
---------------------------------------
1998 1997
------------------- ------------------
<S> <C> <C>
Notes payable to ten stockholders, due on demand, plus interest at
10% per annum (in arrears). The Company is obligated to accept
the rate at face value plus accrued interest as partial payment
for shares the lender may purchase from the Company upon exercise
of the lender's option to acquire shares from
the Company. $ 60,815 $ 60,815
Notes payable to directors totaling $28,000 and a note payable to
a third party in the amount of $9,000, due on April 22, 1995
(principal and accrued interest in arrears as of report date),
plus interest ranging from 8% to 9% per annum. Each lender has
the right to convert any portion of the principal and interest
into common stock at a price per share equal to the price per
share under the most
recent private placement transaction. 37,000 37,000
----------------- ------------------
Balance Forward $ 97,815 $ 97,815
----------------- ------------------
</TABLE>
29
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 6 - NOTES PAYABLE (Continued)
<TABLE>
<CAPTION>
December 31,
---------------------------------------
1998 1997
------------------- ------------------
<S> <C> <C>
Balance Forward $ 97,815 $ 97,815
Notes payable to directors and a family member of a director, due
at various dates in 1995, 1996 and 1997 (principal and accrued
interest in arrears as of report date), plus interest at 8% per
annum. The Company has the right to repay the loans with
restricted stock at $0.10
per share if alternative financings do not occur. 182,676 216,300
Note payable to individual, due on December 2, 1996 (principal and
accrued interest in arrears as of report date), plus interest at
6.07% per annum. The Company has the right, on or after the
payment due date, to repay the loan with
restricted shares valued at $0.05 per share. - 40,000
----------------- -----------------
Total Notes Payable 280,491 354,115
Less: Current Portion (280,491) (354,115)
----------------- -----------------
Long-Term Notes Payable $ - $ -
================= =================
</TABLE>
The aggregate principal maturities of notes payable are as
follows:
<TABLE>
<CAPTION>
Year Ended
December 31, Amount
<S> <C> <C>
1999 $ 280,491
2000 -
2001 -
2002 -
2003 -
2004 and thereafter -
-----------------
Total $ 280,491
=================
</TABLE>
30
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 7 - STOCK OPTIONS
All options are exercisable for a period of five years beginning
one year from the date of grant. Compensation expense, measured as
to the excess of the estimated fair value over the exercise price,
was accrued over the service period. If, on the date of exercise,
the estimated fair value of a share of the Company's common stock
exceeded the exercise price, the exercise price was decreased by a
like amount (but not below the par value of $0.001). At the end of
each fiscal period, total accrued compensation was recorded as the
difference between the adjusted exercise price and the fair market
value at the end of the period for all exercisable shares. The
total accrued compensation was adjusted each year for changes in
the fair market value of the Company's stock and for option
exercises and cancellations. The shares issued in connection with
the exercise of the options were restricted shares to be held for
investment purposes only.
In 1995, as part of their employment agreements, the Company's
president and chief executive officer, and vice-president and
chief financial officer and treasurer were granted options to
purchase an aggregate of 4,500,000 shares of the Company's common
stock at an exercise price of $0.20 per share, which vested fully
on January 1, 1998. The fair value of each option grant is
estimated on the grant date using an option-pricing model with the
following weighted-average assumptions used for grants in 1995:
risk-free interest rate of 6%, and expected lives of 3 years of
the options.
The following is a summary of option transactions:
<TABLE>
<CAPTION>
Weighted
Average
Exercise
Fixed Options Shares Price
-------------------------- ----------------- -----------------
<S> <C> <C> <C>
Balance - January 1, 1996 4,500,000 $ 0.20
Granted - -
Exercised - -
Forfeited - -
----------------- -----------------
Balance - December 31, 1996 4,500,000 0.20
Granted - -
Exercised - -
Forfeited (3,000,000) -
----------------- -----------------
Balance, December 31, 1997 1,500,000 0.20
Granted - -
Exercised - -
Forfeited - -
----------------- -----------------
Balance, December 31, 1998 1,500,000 $ 0.20
================= =================
</TABLE>
31
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 7 - STOCK OPTIONS (Continued)
The following table summarizes information about fixed stock
options outstanding at December 31, 1998:
<TABLE>
<CAPTION>
Outstanding Options Exercisable Options
----------------------------------------------------------------- ----------------------------------
Weighted
Average Weighted Weighted
Range of Number Remaining Average Number Average
Exercisable Outstanding Contractual Exercise Exercisable Exercise
Prices 12/31/98 Life Price at 12/31/98 Price
--------------- --------------- ------------ ---------------- -------------- -----------------
<S> <C> <C> <C> <C> <C> <C>
$ 0.20 1,500,000 3 years $ 0.20 1,500,000 $ 0.20
</TABLE>
If the Company had used the fair value based method of accounting
for its employee stock option plan, as prescribed by Statement of
Financial Accounting Standard No. 123, compensation cost in net
loss for the year ended December 31, 1998, 1997 and 1996 would
have increased by $-0-, $72,338 and $242,387, respectively, and
the Company's net loss and loss per share would have been reduced
to the proforma amounts indicated below:
<TABLE>
<CAPTION>
1998 1997 1996
----------------- ------------------ ----------------
<S> <C> <C> <C>
Net loss As reported $ (502,761) $ (775,559) $ (1,329,395)
Proforma $ (502,761) $ (703,221) $ (1,571,782)
Net loss per share As reported $ (0.00) $ (0.01) $ (0.01)
Proforma $ (0.00) $ (0.01) $ (0.01)
</TABLE>
NOTE 8 - PRIOR PERIOD ADJUSTMENTS
The Company has restated its financial statements to reflect
adjustments to write off liabilities which were accrued and
expensed in years prior to fiscal 1992. These adjustments
increased previously reported accumulated deficit and reduced
previously reported results of operations (for the period January
31, 1986, date of inception, through December 31, 1994) by
$219,422. During the first quarter of 1995, the Company recorded a
further reduction to accumulated deficit in the amount of $71,806
relating to the cancellation of shares previously issued to former
management.
NOTE 9 - REDEEMABLE COMMON STOCK
On February 12, 1993, per a settlement agreement, the Company
issued 200,000 shares of restricted common stock to an unrelated
third party. According to the agreement, if the Company files a
registration statement for an offering of its securities, it must
use its best efforts to include such shares in the registration
statement. If all, or any portion of the shares have not been
purchased by the Company or all the shares have not been covered
by an effective registration, then the Company shall be required
to pay, no later than April 13, 1995, an amount equal to the
lesser of $50,000 minus the aggregate purchase price amount
payable under the formula set forth in the agreement, or $25,000.
In September 1995, the Company paid $5,000 and issued 200,000
shares of restricted common stock in full and final settlement of
the agreement.
32
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 10 - GOING CONCERN
The Company's consolidated financial statements are prepared
using generally accepted accounting principles applicable to a
going concern which contemplates the realization of assets and
liquidation of liabilities in the normal course of business. The
Company has historically incurred significant losses which have
resulted in an accumulated deficit of $13,783,439 at December 31,
1998 which raises substantial doubt about the Company's ability
to continue as a going concern. The accompanying consolidated
financial statements do not include any adjustments relating to
the recoverability and classification of asset carrying amounts
or the amount and classification of liabilities that might result
from the outcome of this uncertainty.
Continuation of the Company as a going concern is dependent upon
obtaining additional capital, obtaining the requisite approvals
from the FDA and/or the EU for the marketing of ozone-related
products and equipment, and ultimately, upon the Company's
attaining profitable operations. The Company will require a
substantial amount of additional funds to complete the
development of its products, to establish manufacturing
facilities, to build a sales and marketing organization and to
fund additional losses which the Company expects to incur over
the next several years.
Because ozone-generation for the purposes of interfacing with
blood and blood products is regarded as a new drug delivery
system, the Company is precluded from selling or distributing its
drug or the Medizone Technology in the United States until after
FDA approval has been granted. In order to obtain FDA approval,
the Company will be required to submit a New Drug Application
("NDA") for review by the FDA and provide medical and scientific
evidence sufficient to demonstrate that the drug and the Medizone
Technology has been successfully used in pre-clinical studies
followed by three phases of well-controlled clinical studies
using human volunteer subjects. The FDA will not grant an NDA
unless it contains sufficient medical evidence and data to permit
a body of qualified and experienced scientists to conclude that
the new drug product is safe and effective for its recommended
and proposed medical uses. Historically, the FDA has held a
strong bias against treating humans with ozone, due largely to
issues of safety.
In order to initiate the first phase (i.e., Phase I) of human
clinical trials required as part of an NDA, an applicant must
submit to the FDA an application for an Investigational New Drug
Exemption ("IND"), which contains adequate information to satisfy
the FDA that human clinical trials can be conducted without
exposing the volunteer human subjects to an unreasonable risk of
illness or injury. The Company submitted an IND application
(assigned to the Company by its former president) to the FDA on
October 6, 1985, and requested FDA approval to commence human
clinical trials using ozone-oxygen to inactivate HIV. The FDA
deemed the IND application to be incomplete, and required the
Company to conduct additional animal studies prior to commencing
a large animal study and human trials. In September 1994, after
not receiving responses to requests for information from the
Company, the FDA inactivated the Company's IND. The Company has
no present plans to commence a large animal study, which would
require, as a precursor, additional small animal and laboratory
work. Accordingly, there can be no assurance that the Company's
IND application will ever be reopened. Until an NDA had been
granted to the Company, it may not distribute ozone-generating
devices, except to researchers who agree to follow FDA
guidelines, and provided the devices are labeled as
"Investigational Devices."
33
<PAGE>
MEDIZONE INTERNATIONAL, INC. AND SUBSIDIARY
(A Development Stage Company)
Notes to the Consolidated Financial Statements
December 31, 1998 and 1997
NOTE 10 - GOING CONCERN (Continued)
Because ozone has been used to treat humans in Europe for at
least 30 years, the EU is more accepting of human clinical trials
of ozone therapies being conducted than is the United States.
Accordingly, management believes that the Company should pursue
the option of conducting human clinical trials in Europe, using
stringent protocols that will meet EU standards, with a view to
utilizing the results of such a trial in an effort to obtain EU
approval, to market the product in Europe and to reopen the
Company's FDA file.
The management of the Company intends to seek additional funding
which will be utilized to fund additional research and continue
operations. The Company recognizes that, if it is unable to raise
additional capital, it may find it necessary to substantially
reduce or cease operations.
NOTE 11 - SUBSEQUENT EVENTS
Subsequent to December 31, 1998, the following events occurred:
1. On February 18, 1999, warrants to purchase 222,222 shares of
common stock were exercised at $0.07 per share for $15,556.
2. On November 4, 1999, warrants to purchase 714,285 shares of
common stock were exercised at $0.07 per share for $50,000.
3. The Board of Directors approved the following salaries: a)
$170,000 a year for the Company's C.E.O., b) $170,000 a year
for the Company's President and Director of Research, and c)
$95,000 a year for the Company's C.O.O. and Corporate
Secretary.
4. On January 27, 2000, warrants to purchase 3,142,857 shares
of common stock were exercised at $0.07 per share for
$220,000.
34
February 29, 2000
Securities and Exchange Commission 450 5th Street, N.W.
Washington, D.C. 20549
To Whom It May Concern:
We have been furnished with a copy of the amended response to Item 9 of the Form
10-K for the year ended December 31, 1998, filed by our former client Medizone
International, Inc. We agree with the statements made in response to that Item,
as amended, insofar as they relate to our firm.
Very truly yours,
/s/ Andersen Andersen & Strong, L.C.
Andersen Andersen & Strong, L.C.
<TABLE> <S> <C>
<ARTICLE> 5
<S> <C>
<PERIOD-TYPE> YEAR
<FISCAL-YEAR-END> DEC-31-1998
<PERIOD-END> DEC-31-1998
<CASH> 7,643
<SECURITIES> 0
<RECEIVABLES> 0
<ALLOWANCES> 0
<INVENTORY> 0
<CURRENT-ASSETS> 7,643
<PP&E> 10,626
<DEPRECIATION> 3,014
<TOTAL-ASSETS> 15,255
<CURRENT-LIABILITIES> 1,039,229
<BONDS> 280,491
0
0
<COMMON> 148,926
<OTHER-SE> (1,023,974)
<TOTAL-LIABILITY-AND-EQUITY> 15,255
<SALES> 0
<TOTAL-REVENUES> 0
<CGS> 0
<TOTAL-COSTS> 0
<OTHER-EXPENSES> 589,567
<LOSS-PROVISION> 0
<INTEREST-EXPENSE> 47,031
<INCOME-PRETAX> (502,761)
<INCOME-TAX> 0
<INCOME-CONTINUING> (502,761)
<DISCONTINUED> 0
<EXTRAORDINARY> 0
<CHANGES> 0
<NET-INCOME> (502,761)
<EPS-BASIC> 0
<EPS-DILUTED> 0
</TABLE>
