PRINCETON, N.J., BOSTON, and STOCKHOLM, Sweden (PROTEXT) -
Bristol-Myers Squibb Company (NYSE: BMY) and OXiGENE, Inc.
(Nasdaq: OXGN; Sweden) today announced an exclusive licensing
agreement and research collaboration to develop and commercialize
combretastatin anti-tumor vascular targeting agents. Bristol-
Myers Squibb has obtained worldwide rights to develop compounds
in this new class of anticancer therapies, including the lead
compound, Combretastatin A4 Prodrug (CA4P).
Under the terms of the definitive agreement, Bristol-Myers
Squibb will provide up to $70 million in licensing fees,
including an upfront payment, development milestones and research
funding to OXiGENE for the development of combretastatin
compounds for systemic use in all indications. In addition,
OXiGENE will receive royalties from any systemic drugs resulting
from the collaboration and has retained the rights for non-
systemic use in all indications. Further financial details were
not disclosed.
Combretastatin compounds, including CA4P, may selectively
target existing blood vessels at tumor sites, thereby cutting off
the tumor's blood supply and depriving it of oxygen and nutrients
necessary for survival and growth. CA4P is being developed for
potential use either as a stand-alone therapy for solid tumors
that require blood vessels for survival, or in combination with
chemotherapy and radiation to enhance the effectiveness of these
traditional cancer treatments.
"As a world leader in oncology therapy, we are committed to
developing a variety of new approaches for treating cancer," said
Renzo Canetta, M.D., vice president, Clinical Oncology, Bristol-
Myers Squibb. "We believe the combretastatin technology shows
great promise for attacking the lifeline of tumors. We look
forward to working with OXiGENE to further develop this exciting
new approach."
Bjorn Nordenvall, Ph.D, M.D., OXiGENE's President and CEO,
said, "This definitive agreement with Bristol-Myers Squibb is a
strong validation of the potential significance of our
combretastatin compounds and makes us confident that we can
develop the first anti-tumor targeting agent to shutdown
bloodflow at the existing tumor site for patients with cancer.
Bristol-Myers Squibb is widely recognized as a global leader in
the field of oncology and historically has an excellent track
record for bringing anticancer therapies through the development
stages to market. CA4P's potential, combined with the commitment
from Bristol-Myers Squibb makes this an extraordinary event for
OXiGENE."
With the signing of this agreement, Bristol-Myers Squibb
assumes responsibility for the clinical development of CA4P, with
the exception of three ongoing Phase I/II clinical trials.
OXiGENE is funding and conducting two of these trials in the
United States, and one in the United Kingdom, in collaboration
with the Cancer Research Campaign. Interim data from two of these
studies were recently presented in London, New York and
Washington, DC.
OXiGENE's Phase I/II clinical trials have shown CA4P's ability
to reduce blood flow to the tumor measured by magnetic resonance
imaging, thus inhibiting the tumor's survival and growth. The
studies are the first demonstrations in human clinical trials of
an inhibitor that blocks the flow of blood within tumor-
associated blood vessels.
"In preclinical models, a single dose of CA4P could destroy up
to 95 percent of solid tumor cells. In addition, the interim
clinical results show that we can administer CA4P to humans
safely at doses that cause a significant decrease in bloodflow to
tumors," said Dr. Nordenvall.
OXiGENE is an international biopharmaceutical company
developing a diverse portfolio of innovative products to combat
cancer and other major diseases. The Company's mission is to
develop new therapeutics that will enhance the effectiveness of
traditional cancer treatments and to introduce therapies that
attack cancer in new ways.
Bristol-Myers Squibb is a diversified worldwide health and
personal care company whose principal businesses are
pharmaceuticals, consumer medicines, beauty care, nutritionals,
and medical devices. It is a leading maker of innovative
therapies for cardiovascular, metabolic and infectious diseases,
central nervous system and dermatological disorders, and cancer.
The company is a leader in consumer medicines, orthopaedic
devices, ostomy care, wound management, nutritional supplements,
infant formulas, and hair and skin care products.
Certain statements made in this press release related to
consummation of a definitive agreement between the two parties,
and success of the Company's business and technology goals are
forward-looking and are made pursuant to the safe harbor
provisions of the Securities Litigation Reform Act of 1995. Such
statements involve risks and uncertainties that may cause the
Company's (OXiGENE's) actual results or outcomes to be materially
different from those anticipated and discussed in this press
release. Factors that may cause such a difference include, but
are not limited to, those risks and uncertainties associated with
the regulatory approval of the Company's proprietary drugs, and
other risks included in the Company's Annual Report on Form 10-K
and in the Company's other filings with the Securities and
Exchange Commission during the past 12 months.
Visit OXiGENE's website at: www.oxigene.com
Visit Bristol-Myers Squibb on the World Wide Web at
http://www.bms.com
CONTACT: Sylvia D. Sharockman of Bristol-Myers Squibb, 609-
252-3390, or
sylvia.sharockman@bms.com; or Bjorn Nordenvall,
Ph.D., M.D., President and CEO, 46-8-678-87-20, or David Sherris,
Ph.D., COO and Director of Drug Development, 617-536-9500, both
of OXiGENE; or Judy Brenna (investors and media), Assistant Vice
President, 212-696-4455, Ext. 221, or Matthew Knight (media),
212-696-4455, Ext. 271, both of Noonan/Russo Communications, for
OXiGENE. ots Original Text Service: Bristol-Myers Squibb Company
Internet:
http://www.newsaktuell.de Contact: Sylvia D.
Sharockman of Bristol-Myers Squibb, 609-252-3390, or
sylvia.sharockman@bms.com; or Bjorn Nordenvall, Ph.D., M.D.,
President and CEO, 46-8-678-87-20, or David Sherris, Ph.D., COO
and Director of Drug Development, 617-536-9500, both of OXiGENE;
or Judy Brenna (investors and media), Assistant Vice President,
212-696-4455, Ext. 221, or Matthew Knight (media), 212-696-4455,
Ext. 271, both of Noonan/Russo Communications, for OXiGENE
Company News On-Call: Bristol-Myers Squibb press releases
available by fax, 800-758-5804, ext. BMYFAX, or 269329, or at
http://www.prnewswire.com/comp/269329.html Web site:
http://www.oxigene.com Web site:
http://www.bms.com
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