Nexviadyme (avalglucosidase alfa) approved by European Commission as a potential new standard of care for the treatment of Pompe disease

Sanofi

28 June 2022 - Approved for the treatment of the full spectrum of both late-onset Pompe disease and infantile-onset Pompe disease.

The European Commission has granted marketing authorisation for Nexviadyme (avalglucosidase alfa), an enzyme replacement therapy for the long-term treatment of both late-onset and infantile-onset Pompe disease, a rare, progressive and debilitating muscle disorder.

Read Sanofi press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe , Orphan drug