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NCT06906341
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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