Glenmark receives Orphan Drug Designation for GBR 1324

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Last Updated : Sep 17 2019 | 11:04 AM IST

A bispecific antibody candidate under evaluation for treatment of multiple myeloma

Glenmark Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation to its bispecific antibody candidate GBR 1342 for the treatment of patients with multiple myeloma who have received prior therapies. Derived from the company's proprietary BEAT (Bispecific Engagement by Antibodies based on the T cell receptor) technology, GBR 1342 is being investigated for the treatment of multiple myeloma. The candidate is one of five clinical-stage assets in the pipeline of Glenmark's new innovation company.

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First Published: Sep 17 2019 | 9:58 AM IST

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