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Sanofi secures EC approval for two enzyme replacement treatments for rare diseases

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Abstract

French healthcare company Sanofi has received separate regulatory approvals from the European Commission (EC) for two of its enzyme replacement therapies to treat rare diseases. The European regulator approved Nexviadyme (avalglucosidase alfa) to treat the full spectrum of both infantile-onset Pompe disease (IOPD) and late-onset Pompe disease (LOPD). French healthcare company Sanofi has received separate regulatory approvals from the European Commission (EC) for two of its enzyme replacement therapies to treat rare diseases. The European regulator approved Nexviadyme (avalglucosidase alfa) to treat the full spectrum of both infantile-onset Pompe disease (IOPD) and late-onset Pompe disease (LOPD).
Key Data

  • Publication Date
    29 June 2022
  • Primary Author
    Amit Thadani
  • Source
    Practical Patient Care
  • Language
    English
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