Migraine drug BLA accepted for review by FDA

21 July 2017

US biotech Amgen (Nasdaq: AMGN) has had its Biologics License Application (BLA) for the migraine treatment Aimovig (erenumab) accepted by the US Food and Drug Administration (FDA).

If approved, Aimovig is expected to be the first-and-only monoclonal antibody targeting the calcitonin gene-related peptide (CGRP) receptor, specifically designed for the prevention of migraine.

Sean Harper, executive vice president of research and development at Amgen, said: “Migraine is a serious neurological disease that has a substantial economic burden for both patients and the healthcare system, yet it continues to be under recognized and under treated.

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