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BioMarin submits NDA to FDA for vosoritide to treat children with achondroplasia.

Read time: 1 mins
Published:21st Aug 2020
BioMarin Pharmaceutical Inc. announced that it has submitted a New Drug Application (NDA) to the FDA for vosoritide, an investigational, once daily injection analog of C-type Natriuretic Peptide (CNP) for children with achondroplasia, the most common form of disproportionate short stature in humans. BioMarin recently announced that the European Medicines Agency (EMA) validated the Company's Marketing Authorization Application (MAA) for vosoritide on 13 August, 2020.
Condition: Achondroplasia
Type: drug

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