Corcept Therapeutics Reports 37% Revenue Growth Amid Cushing’s Syndrome Demand Surge

  • Corcept Therapeutics reported $761.4M in 2025 revenue, up 37% YoY, driven by record new prescriptions for Cushing’s syndrome treatments.
  • Fourth-quarter revenue hit $202.1M, up from $181.9M in Q4 2024, but net income fell to $24.3M from $30.7M due to operational disruptions.
  • FDA reviewing NDA for relacorilant in platinum-resistant ovarian cancer with PDUFA date of July 11, 2026.
  • Company plans Phase 3 trial for dazucorilant in ALS by mid-2026, following promising DAZALS study results.

Corcept’s growth reflects increasing physician recognition of hypercortisolism, positioning it as a leader in cortisol modulation therapies. The company’s pipeline diversification into oncology and metabolic diseases could drive long-term value, but regulatory and operational hurdles remain critical. With $532.4M in cash reserves, Corcept has financial flexibility to navigate these challenges while pursuing multiple high-impact clinical programs.

Regulatory Approval
Whether the FDA will approve relacorilant for Cushing’s syndrome following the Complete Response Letter and the July 2026 PDUFA date for ovarian cancer indication.
Clinical Trial Results
The pace at which Corcept delivers data from ongoing trials, including MOMENTUM in resistant hypertension and MONARCH in MASH, which could expand market opportunities.
Operational Execution
How Corcept manages post-transition demand fulfillment after fourth-quarter disruptions at its new specialty pharmacy partner.