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Corcept asks FDA to OK experimental Cushing's therapy relacorilant

Summary by Cushing's Disease News
Corcept Therapeutics has asked the U.S. Food and Drug Administration (FDA) to approve relacorilant for people with endogenous Cushing’s syndrome. “Relacorilant’s combination of efficacy and safety give it the potential to become the standard of care for the medical treatment of patients with hypercortisolism,” Joseph Belanoff, MD, CEO of Corcept, said in a company press release. “Our commitment to the health of patients with hypercortisolism is …
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Cushing's Disease News broke the news in on Friday, January 3, 2025.
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