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FDA Files Corcept's New Drug Application for Relacorilant as Treatment for Patients With Hypercortisolism

1. CORT announced FDA submission for relacorilant's New Drug Application. 2. This move is a significant step towards potential new revenue streams.

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FAQ

Why Bullish?

The FDA submission suggests progress for CORT's product pipeline, which historically leads to price increases in biotech stocks.

How important is it?

The FDA submission is crucial for CORT's growth, and such announcements typically have significant market implications.

Why Short Term?

The immediate market reaction may be positive due to investor sentiment towards FDA news, but sustained impact depends on clinical outcomes.

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REDWOOD CITY, Calif.--(BUSINESS WIRE)--Corcept Therapeutics Incorporated (NASDAQ: CORT), a commercial-stage company engaged in the discovery and development of medications to treat severe endocrinologic, oncologic, metabolic and neurologic disorders by modulating the effects of the hormone cortisol, today announced that the U.S. Food and Drug Administration (FDA) filed its New Drug Application (NDA) submission for its proprietary, selective cortisol modulator, relacorilant, to treat patients wi.

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