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Bionumerik reports data on two novel supercomputer engineered anticancer agents

ased on historical studies of patients who were treated with the same chemotherapy drugs without BNP7787. These results also appear to indicate that while the toxic side effects of cisplatin and paclitaxel are alleviated , the tumor specific programmed cell death (apoptosis) associated with this therapy remains intact.

The Company plans to initiate Phase 3 trials later this year for BNP7787 which has been granted U.S. Food and Drug Administration "Fast Track" designation for the prevention or reduction of the nerve damage associated with paclitaxel.

Karenitecin
Additional data presented at AACR further indicates that BioNumerik's goal of being the first to discover, synthesize, formulate, patent and develop a new class of silicon containing semisynthetic camptothecins has been accomplished. Karenitecin BNP1350 is a member of a novel class of specifically developed lipophilic camptothecins. Antitumor activity of BNP1350 has been confirmed in in vitro models of human prostate, breast, lung, colon, melanoma, glioblastoma and ovarian cancer cell lines. Experimental observations suggest the presence of a BNP1350 dimer complex that is believed to be responsible for protecting a key chemical "lactone ring" on the camptothecin molecule. These findings were confirmed in the ongoing Phase 1 study where an impressive 90% or greater lactone ring stability has been measured in patients receiving doses ranging from 0.15- 1.2mg/m2 daily times five days of karenitecin.

Based on these encouraging results and scientific findings, BioNumerik is planning to proceed with Phase 2 clinical trials in gliomas and lung cancer later this year. Additionally, a pediatric Phase 1 study has been initiated and an oral formulation of karenitecin BNP1350 is expected to be introduced into the clinic in the coming months.


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Contact: Page Sargisson
p.sargisson@noonanrusso.com
415-677-4455 x 229
Noonan/Russo Communications
5-Apr-2000


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