Zolgensma and Seven Other Products Get CHMP Thumbs Up

Zolgensma should receive a conditional approval, says the European Medicines Agency’s drug evaluation committee, the CHMP.

Gene editing genes therapy concept with nurse and DNA lab technician medical laboratory
A gene therapy for spinal muscular atrophy has moved closer to the EU market • Source: Shuuterstock

The European Medicines Agency has recommended that eight new medicines be awarded pan-EU marketing authorization, including Zolgensma, AveXis/Novartis’s one-off gene replacement therapy for treating spinal muscular atrophy in babies and young children.

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