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Zydus Lifesciences' Nulibry Receives EC’s Marketing Authorization for the Treatment of Molybdenum Cofactor Deficiency Type A

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Zydus Lifesciences' Nulibry Receives EC’s Marketing Authorization for the Treatment of Molybdenum Cofactor Deficiency Type A

Shots:

  • The EC has granted marketing authorization for Nulibry to treat MoCD Type A. The EC decision was based on the efficacy & safety data of the Nulibry vs natural history study
  • The EC’s centralized marketing authorization will be valid in all EU member states, Iceland, Liechtenstein, and Norway. The regulatory filing to the MHRA is expected in the coming months
  • Nulibry is a cPMP substrate replacement therapy & was approved in the US in 2021 to reduce the risk of mortality in patients with MoCD Type A. In Mar 2022, Sentynl holds the global rights to Nulibry and is responsible for the ongoing development and commercialization in the US and also for developing, manufacturing, and commercializing fosdenopterin globally

Ref: Hindu | Image: Zydus Lifesciences

Click here to­ read the full press release 

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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