UNIGENE LABORATORIES INC
8-K, 1997-07-02
MEDICINAL CHEMICALS & BOTANICAL PRODUCTS
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                       SECURITIES AND EXCHANGE COMMISSION
                             Washington, D.C. 20549



                                    Form 8-K

                                 Current Report


                     Pursuant to Section 13 or 15(d) of the
                         Securities Exchange Act of 1934



         Date of Report (Date of earliest event reported): June 30, 1997 


                           UNIGENE LABORATORIES, INC.
             (Exact name of registrant as specified in its charter)

                
                                    Delaware
                 (State or other jurisdiction of incorporation)



         0-16005                                        22-2328609
(Commission File Number)                    (IRS Employer Identification Number)



                              110 Little Falls Road
                           Fairfield, New Jersey 07004
               (Address of Principal Executive Offices) (Zip Code)



                                 (973) 882-0860
              (Registrant's telephone number, including area code)



<PAGE>
Item 5.           Other Events.

                  On June 30,  1997,  the  Company  announced  the  signing of a
letter of intent for a worldwide  licensing  agreement for oral  calcitonin with
the Parke-Davis division of Warner-Lambert Company.


Item 7.           Financial Statements and Exhibits.

                  (c)      Exhibits.

                  99       Press Release dated June 30, 1997 regarding letter of
                           intent with Warner-Lambert.



                                   SIGNATURES


         Pursuant to the  requirements  of the Securities  Exchange Act of 1934,
the  Registrant  has duly  caused  this report to be signed on its behalf by the
undersigned, hereunto duly authorized.

                                                    UNIGENE LABORATORIES, INC.



                                                    By /S/WARREN P. LEVY
                                                       -----------------
                                                       Warren P. Levy, President


Date:    July 2, 1997
<PAGE>
FOR IMMEDIATE RELEASE                  Contact: Warren P. Levy, Ph.D., President
                                                Unigene Laboratories, Inc. 
                                                973/882-0860  

                                                Thomas Redington 
                                                203/222-7399 
                                                212/926-1733 
                                                                   
                                               
  

               UNIGENE AND WARNER-LAMBERT EXECUTE LETTER OF INTENT
                   TO DEVELOP ORAL CALCITONIN FOR OSTEOPOROSIS

         Fairfield,   NJ,   June  30,   1997  --  Unigene   Laboratories,   Inc.
(Nasdaq:UGNE)  announced today the signing of a letter of intent for a worldwide
licensing  agreement  for oral  calcitonin  with  the  Parke-Davis  division  of
Warner-Lambert Company. The parties are targeting mid-July as the execution date
for a definitive agreement.

         Under the terms of the proposed agreement,  Warner Lambert would assume
responsibility  for the  development  and marketing of the product while Unigene
would provide  analytical  support services and be the exclusive supplier of the
bulk active raw  material.  If the product is  successfully  developed,  Unigene
would receive up-front and milestone payments in excess of $50 million,  as well
as  royalties  on  commercial  sales.  Warner  Lambert  would also  purchase  an
undisclosed amount of Unigene common stock.

         "This  agreement  is a  part  of  our  ongoing  commitment  to  provide
healthcare  solutions to women  throughout  their lives," said Ronda Dean,  vice
president,  Parke-Davis/Women's  Healthcare Division. "With this partnership, we
hope to develop and  introduce a new dosage  form of  calcitonin  that is a more
acceptable, affordable and convenient treatment for the osteoporotic patient."

         "We  believe  that  oral  calcitonin  has the  potential  to  become  a
blockbuster  drug," commented Dr. Warren Levy,  President of Unigene.  "With the
development and marketing expertise and resources of Warner-Lambert,  we hope to
maximize the opportunity to achieve that goal."

         Calcitonin  is  a  leading   treatment  for  osteoporosis  with  annual
worldwide  sales of more than $700 million.  Available  only in  injectable  and
nasal forms, it is the only marketed osteoporosis  treatment that combines being
a natural hormone with pain killing  properties and no significant  side effects
or contraindications.  Consequently,  Unigene and Warner-Lambert believe that an
oral form of  calcitonin  would enjoy  significant  advantages  over many of the
other currently available therapeutic alternatives.

         Unigene  Laboratories,  Inc.  has  developed  a  proprietary  amidation
process capable of producing  peptide hormones for the treatment of a variety of
diseases and disorders, including osteoporosis,  hypertension and arthritis. The
Company is currently  producing the FORTICAL raw material in compliance with the
FDA's Good Manufacturing  Practice  guidelines at its manufacturing  facility in
Boonton, N.J.
<PAGE>
         Parke-Davis,  a  division  of  Warner-Lambert  Company,  is  devoted to
discovering,  developing,  manufacturing  and marketing  quality  pharmaceutical
products.   Its  central   research  focus  is  on  heart   disease,   diabetes,
anti-infectives,  central nervous system, and women's healthcare. Warner-Lambert
is a worldwide company  employing  approximately  38,000 people,  and along with
Parke-Davis is headquartered in Morris Plains, N.J.

         Except for  historical  information,  the  statements  made  herein are
forward looking statements  involving risks and  uncertainties.  These risks and
uncertainties,  including those relating to the timing or successful  completion
of the  Company's  product  commercialization  activities,  are  detailed in the
Company's filings with the Securities and Exchange Commission.


                                       ###


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