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Corcept获得FDA批准用于癌症治疗
2026-03-25 22:55
- Shares of Corcept Therapeutics (CORT) surged before a trading halt in the morning hours on Wednesday after the U.S. Food and Drug Administration (FDA) approved its cancer therapy, relacorilant.
- Specifically, the FDA has approved the drug under the brand name Lifyorli in combination with chemotherapy nab-paclitaxel as a late-line option for adults with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer.
- In September, the FDA accepted Corcept’s (CORT) New Drug Application (NDA) for relacorilant, assigning July 11 as the target action date.
- The NDA was based on data from the company’s Phase 3 ROSELLA and Phase 2 trials in which patients on relacorilant plus nab-paclitaxel witnessed an improvement in progression-free and overall survival compared to those who received nab-paclitaxel monotherapy.
More on Corcept Therapeutics
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- Corcept Therapeutics Incorporated (CORT) Q4 2025 Earnings Call Transcript
- Corcept Therapeutics: The Bad News Is Priced In; The Ovarian Cancer Upside Is Not
- Corcept rises after insider buy worth over $3M
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