Thursday, September 11, 2008

Glenmark files IND application with US FDA for GBR 500 molecule phase-I trials

Glenmark Pharmaceuticals Ltd. (India) has filed its molecule GBR 500 for phase-I trials with the US FDA. The filing of this crucial IND (Investigational New Drug Application) signifies the successful completion of a substantial number of pre-clinical studies for its humanized biologic molecule. GBR 500, a monoclonal antibody, is an antagonist of the VLA-2 (Alpha2 ?eta1) integrin.

The details can be read here.

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