Takeda Pharmaceutical Co Ltd
PDUFA AI-extracted
Oveporexton (TAK-861)
narcolepsy type 1
Countdown
86days
FDA decision · ~ Sep 30, 2026 estimated
What's at stake The FDA's approval decision on Oveporexton (TAK-861) for narcolepsy type 1 is due ~ Sep 30, 2026. A green light opens the market; a complete response letter (CRL) usually sinks the stock.
“The Prescription Drug User Fee Act (PDUFA) Target Action Date is the Third Quarter of this Calendar Year”

Provenance

1 source on file.

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