Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers

This is a Phase 2, open-label, global, multi-arm study to evaluate efficacy and safety of relacorilant in combination with other treatments in patients with gynecological cancers.

Trial Details

NCT ID
NCT06906341
Phase
PHASE2
Sponsor
Corcept Therapeutics
Status
RECRUITING
Cancer Type
Ovarian Cancer
Interventions
  • Relacorilant 150 mg once daily (QD)
  • Nab-paclitaxel 80 mg/m^2
  • Bevacizumab 10 mg/kg
Locations (sample)
  • Birmingham, Alabama, United States|33.52066,-86.80249
  • Palo Alto, California, United States|37.44188,-122.14302
  • San Francisco, California, United States|37.77493,-122.41942
  • Fort Myers, Florida, United States|26.62168,-81.84059
  • Miami Beach, Florida, United States|25.79065,-80.13005

Key Eligibility Criteria

  • Arms A and B
  • Histologic diagnosis of epithelial ovarian, primary peritoneal, or fallopian-tube carcinoma
  • Arm A Only: Platinum-resistant disease
  • Arm B Only: Platinum-sensitive disease who had progression while receiving treatment with a poly(ADP-ribose) polymerase (PARP) inhibitor

For full eligibility, visit ClinicalTrials.gov.

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