EMA
approval
· 2024-07-25
EMA Authorised: Nulibry (fosdenopterin hydrobromide dihydrate) — TMC Pharma (EU) Limited
Summary
The European Medicines Agency authorised Nulibry (fosdenopterin hydrobromide dihydrate) for the treatment of molybdenum cofactor deficiency, an inborn error of …
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Metal Metabolism, Inborn Errors. MAH: TMC Pharma (EU) Limited. Decision date: 24/07/2024. Orphan medicine