Phase 2 Ovarian Cancer Trial, Recruiting NCT06906341 Sponsor: Corcept Therapeutics Condition: Ovarian Cancer
Back to Ovarian Cancer

Phase 2 Ovarian Cancer Trial, Recruiting

NCT06906341
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

For Arms A and B (ovarian, peritoneal, or fallopian tube cancer):

  • People who have been diagnosed with epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer, confirmed by tissue testing
  • (Arm A only) People whose cancer has stopped responding to platinum-based chemotherapy (called platinum-resistant disease)
  • (Arm B only) People whose cancer was responding to platinum-based chemotherapy but then got worse while being treated with a type of drug called a PARP inhibitor
  • People who are expected to live at least 3 months or more
  • People who are relatively well and able to carry out daily activities, as measured by a standard health scale (ECOG score of 0 or 1)
  • People who are able to swallow and keep down tablets or capsules
  • People who have received between 1 and 3 previous cancer drug treatments
  • People whose liver, kidneys, and other organs are working well enough (confirm with trial site for specific thresholds)
  • People who test negative for pregnancy (for those who could become pregnant)

For Arm C (endometrial cancer):

  • People who have been diagnosed with Stage III or IV, returned, or spread endometrial cancer
  • People who are expected to live at least 3 months or more
  • People who are relatively well and able to carry out daily activities (ECOG score of 0 or 1)
  • People who are able to swallow and keep down tablets or capsules
  • People who have previously been treated with a platinum-based chemotherapy and an approved immunotherapy drug targeting a protein called PD-L1
  • People who have received between 1 and 2 previous cancer drug treatments for endometrial cancer
  • People who are able to provide a stored tumour tissue sample or recently prepared tissue slides for testing
  • People whose liver, kidneys, and other organs are working well enough (confirm with trial site for specific thresholds)
  • People who test negative for pregnancy (for those who could become pregnant)

Who may not be able to join:

For Arms A and B:

  • (Arm A only) People whose cancer got worse while being treated with weekly paclitaxel or nab-paclitaxel chemotherapy
  • People who have previously taken part in a clinical trial of a drug called relacorilant
  • People who still have side effects from previous cancer treatments that have not cleared up to a mild level
  • People who have had surgery within the 4 weeks before joining the trial
  • People who have had large-area radiation treatment covering more than 25% of the body's bone marrow regions
  • People who have a medical condition that requires regular or long-term use of steroid medications (corticosteroids)
  • People who are currently taking a drug called mifepristone or similar drugs that affect a hormone receptor called the glucocorticoid receptor
  • People who have more than mild nerve damage (numbness, tingling, or pain in hands or feet), from any cause
  • People with high blood pressure reading of 150 or higher (top number) or 100 or higher (bottom number)
  • People with other uncontrolled health conditions that could affect the trial results or their safety (confirm with trial site)
  • People who had a bowel blockage within the 12 weeks before joining the trial
  • People who have fluid build-up in the abdomen or around the lungs that requires a procedure to drain it
  • People with cancer that has spread to the brain or spinal cord that is untreated or causing symptoms
  • People who have had another cancer diagnosis within the 3 years before joining the trial
  • People who have received a live vaccine within 30 days before the trial start date

For Arm C:

  • People whose cancer got worse while being treated with weekly paclitaxel or nab-paclitaxel chemotherapy
  • People who have previously taken part in a clinical trial of a drug called relacorilant
  • People who still have side effects from previous cancer treatments that have not cleared up to a mild level
  • People who have had surgery within the 4 weeks before joining the trial
  • People who have had large-area radiation treatment covering more than 25% of the body's bone marrow regions
  • People who have a medical condition that requires regular or long-term use of steroid medications (corticosteroids)
  • People who are currently taking a drug called mifepristone or similar drugs that affect a hormone receptor called the glucocorticoid receptor
  • People who have more than mild nerve damage (numbness, tingling, or pain in hands or feet), from any cause
  • People with other uncontrolled health conditions that could affect the trial results or their safety (confirm with trial site)
  • People who had a bowel blockage within the 12 weeks before joining the trial
  • People who have fluid build-up in the abdomen or around the lungs that requires a procedure to drain it
  • People who have had another cancer diagnosis within the 3 years before joining the trial
  • People who have received a live vaccine within 30 days before the trial start date
  • People with cancer that has spread to the brain or spinal cord — unless local treatment for it has been completed and steroid medications for that condition have been stopped for at least 4 weeks before starting the trial

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Danny Nguyen, MD, Corcept Therapeutics

Phone: 650-414-2314

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Corcept Therapeutics
Registry
ClinicalTrials.gov
Start date
11 April 2025
Est. completion
1 August 2026

Where this trial is recruiting

🇧🇪 Belgium 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy 🇵🇱 Poland 🇰🇷 South Korea 🇪🇸 Spain 🇺🇸 United States

Primary endpoints

Progression-Free Survival (PFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov