ADVISORY/OXiGENE -Nasdaq: OXGN, SSE: OXGN- Second-Quarter 2002 Conference Call.Business Editors & Health/Medical Writers ADVISORY ... for Thursday (July 25) --(BUSINESS WIRE) -O-
When: 10:00 a.m. ET, Thursday, July 25, 2002
Speakers: Fred Driscoll, president and chief executive officer
Dai Chaplin, Ph.D., chief scientific officer
Dial-in Number: 800-837-5450 (U.S.); (212) 676-5376 (international)
48-hour Replay: (800) 633-8284 (U.S.); or (402) 977-9140
(international) Res. #: 20775513
Audio Webcast: (Live and archived for one week)
http://www.corporate-ir.net/ireye/
ir_site.zhtml?ticker=OXGN&script=1000
Investment Highlights: -- Leading Technology Position: OXiGENE is a global biopharmaceutical company that is pioneering a novel technology platform -- vascular targeting -- for drug development in the fight against cancer. In contrast to anti-angiogenesis agents, which stop the formation of new tumor blood vessels Blood vessels Tubular channels for blood transport, of which there are three principal types: arteries, capillaries, and veins. Only the larger arteries and veins in the body bear distinct names. , OXiGENE's flagship vascular targeting agent, Combretastatin A4 Prodrug prodrug /pro·drug/ (-drug) a compound that, on administration, must undergo chemical conversion by metabolic processes before becoming an active pharmacological agent; a precursor of a drug. (CA4P), attacks existing tumor vasculature vasculature /vas·cu·la·ture/ (vas´ku-lah-chur) 1. circulatory system. 2. any part of the circulatory system. vas·cu·la·ture n. . --Clinical Development Milestones: OXiGENE has successfully completed Phase I U.S. clinical trials of CA4P, the first vascular targeting drug to be tested in a human trial in the United States United States, officially United States of America, republic (2005 est. pop. 295,734,000), 3,539,227 sq mi (9,166,598 sq km), North America. The United States is the world's third largest country in population and the fourth largest country in area. . The trials demonstrated CA4P's ability to reduce blood flow that feeds malignant tumors, without the presence of traditional cytotoxic cy·to·tox·ic adj. Of, relating to, or producing a toxic effect on cells. cy to·tox·ic side
effects Side effectsEffects of a proposed project on other parts of the firm. . OXiGENE has launched a Phase Ib clinical trial with CA4P in combination with chemotherapy, and also expects to initiate a Phase II clinical trial Noun 1. phase II clinical trial - a clinical trial on more persons than in phase I; intended to evaluate the efficacy of a treatment for the condition it is intended to treat; possible side effects are monitored phase II . --Strong Product Pipeline: OXiGENE's next-generation vascular targeting compound, Oxi-4503, induced complete regression of human breast cancer tumors grown in mice. Oxi-4503 has demonstrated the ability to block blood flow in all regions of the tumor, including the periphery. The company plans to begin Phase I clinical trials Noun 1. phase I clinical trial - a clinical trial on a few persons to determine the safety of a new drug or invasive medical device; for drugs, dosage or toxicity limits should be obtained phase I on Oxi-4503 in 2003. For questions regarding conference call logistics, contact: Scott Solomon, Investor Relations Investor relations The process by which the corporation communicates with its investors. , 617-542-5300 This conference call notice contains forward-looking statements including, but not limited to, those relating to relating to relate prep → concernant relating to relate prep → bezüglich +gen, mit Bezug auf +acc planned clinical trials of Combretastatin A4P and Oxi-4503 and the efficacy of these compounds. Any or all of the forward-looking statements in this notice may turn out to be wrong. They can be affected by inaccurate assumptions we might make or by known or unknown risks and uncertainties, including, but not limited to, the early stage of our product development; our ability to raise capital when needed and on reasonable terms; uncertainties as to the future success of ongoing and planned clinical trials; our dependence on others for much of the clinical development of our technology, as well as for obtaining regulatory approvals and conducting manufacturing and marketing of any products that might successfully reach the end of the development process; competition from other companies and other institutions pursuing alternative technologies; and uncertainties related to our ability to obtain adequate intellectual property protection for our technology and products. Consequently, no forward-looking statement can be guaranteed, and actual results may vary materially. Additional information concerning factors that could cause actual results to materially differ from those in the forward-looking statements are contained in our reports to the Securities and Exchange Commission including our 10-Q, 8-K and 10-K reports. However, we undertake no obligation to publicly update forward-looking statements, whether as a result of new information, future events or otherwise. |
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