Posted January 30, 2007

CeNeRx Prepares To Launch First Clinical Trial for Lead Drug

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RESEARCH TRIANGLE PARK, N.C. – CeNeRx BioPharma has received Food and Drug Administration approval to launch testing of its lead drug candidate on humans.

The drug, Tyrima, is targeted as a treatment for depression and anxiety. Tyrima is one of several candidates being developed by CeNeRx, which has already raised $25 million in venture capital. Among its investors is Pappas Ventures, which is based in RTP.

CeNeRx recently met with the FDA to discuss its new drug application.

Tyrima is based on reversible inhibitors of monoamine oxidase A, or RIMA. RIMA based antidepressants are already sold in Europe. RIMA drugs elevate levels of three neurotransmitters that affect mood and anxiety rather than other antidepressants that focus on one neurotransmitter.

"Initiation of human trials for Tyrima is an important milestone for CeNeRx, marking our transition to a clinical stage company," said Barry Brand, chief executive officer of CeNeRx, in a statement.

If the drug is approved it would be the first RIMA antidepressant available in the U.S. CeNeRx owns worldwide rights to Tyrima.

In the U.S. alone, nearly 15 million adults deal with what the National Institute of Mental Health calls “major depressive disorders.”Copyright 2010 by Capitol Broadcasting Company. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.
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