Relacorilant: First Approval
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Abstract:
Relacorilant (LIFYORLI™) is a non-steroidal, selective glucocorticoid receptor II (GR II) antagonist being developed by Corcept Therapeutics for the treatment of various solid tumours (including ovarian cancer, fallopian tube cancer, peritoneal cancer, pancreatic cancer and prostate cancer) and Cushing syndrome. Relacorilant received its first approval in the USA on 25 March 2026 for use in combination with nab-paclitaxel for the treatment of adults with platinum-resistant epithelial ovarian, fallopian tube or primary peritoneal cancer who have received 1-3 prior systemic treatment regimens, at least one of which included bevacizumab. This article summarizes the milestones in the development of relacorilant leading to this first approval for platinum-resistant ovarian, fallopian tube or peritoneal cancer.
Insights
Relacorilant is now approved for platinum-resistant ovarian cancer. This selective glucocorticoid receptor II antagonist offers a new treatment option for patients who have not responded to prior therapies.
Area of Science:
- Oncology
- Pharmacology
Background:
- Relacorilant (LIFYORLI™) is a novel non-steroidal, selective glucocorticoid receptor II (GR II) antagonist.
- It is under development by Corcept Therapeutics for treating solid tumors and Cushing syndrome.
Purpose of the Study:
- To summarize the development milestones of relacorilant.
- To highlight its first approval for platinum-resistant ovarian, fallopian tube, and peritoneal cancers.
Main Methods:
- Review of relacorilant's development pathway.
- Analysis of clinical trial data leading to regulatory approval.
Main Results:
- Relacorilant received its first US approval on March 25, 2026.
- Approved in combination with nab-paclitaxel for specific ovarian cancer patients.
Conclusions:
- Relacorilant's approval marks a significant advancement in treating platinum-resistant ovarian cancers.
- This milestone provides a new therapeutic option for patients with limited treatment alternatives.
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