FDA nimmt Zulassungsantrag für Oveporexton von Takeda zur Prüfung an
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The FDA has accepted Takeda Pharmaceutical Co. Ltd.'s application for Oveporexton (TAK-861) to treat Type 1 Narcolepsy and granted it Priority Review. The decision deadline under the Prescription Drug User Fee Act (PDUFA) is set for the third quarter of this calendar year.
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