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Zevra Therapeutics已向欧洲药品管理局提交上市许可申请,以评估Arimoclomol治疗C型尼曼皮克病
2025-07-28 18:06
- The EMA will review the application under the centralized marketing authorization procedure. If a marketing authorization is granted by the European Commission, the authorization is valid in all EU Member States as well as in the European Economic Area (EEA) countries Iceland, Liechtenstein and Norway.
- Arimoclomol is marketed in the U.S. under the brand name MIPLYFFA
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