Monday, December 18, 2017

Teva Says FDA Accepts BLA For Fremanezumab - Quick Facts

Teva Pharmaceutical Industries Ltd. (TEVA) said that the U.S. Food and Drug Administration has accepted for review the company's Biologics License Application or BLA for fremanezumab, an anti-calcitonin gene-related peptide or anti-CGRP monoclonal antibody for the preventive treatment of migraine.

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