The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) at its September 2018 meeting recommended 13 medicines for approval, including three orphan medicines that are covered in a separate article.
The CHMP recommended granting a marketing authorization for Emgality (galcanezumab), Eli Lilly’s (NYSE: LLY) monoclonal antibody for the prevention of migraine. Emgality belongs to a new class of medicines that work by blocking the activity of calcitonin gene-related peptide (CGRP), a molecule that is involved in migraine attacks.
Emgality is the second monoclonal antibody therapy for the prevention of migraine to be recommended for authorization, following the positive opinion for Amgen (Nasdaq: AMGN) and Novartis’s (NOVN: VX) Aimovig (erenumab) in May 2018.
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