Phase 3 Ovarian Cancer Trial, Recruiting NCT06791460 Sponsor: Obstetrics & Gynecology Hospital of Fudan University Condition: Ovarian Cancer
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Phase 3 Ovarian Cancer Trial, Recruiting

NCT06791460
Recruiting Phase 3

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:

  • People who have signed a formal consent form agreeing to participate in the study.
  • People who are generally well enough to carry out daily activities with little to no limitation (rated 0 or 1 on a standard medical fitness scale).
  • People who have been diagnosed with a specific type of cancer confirmed by laboratory testing — ovarian cancer, fallopian tube cancer, or primary peritoneal cancer — that started in the lining of these organs (called epithelial cancer).
  • People who have already received a first course of platinum-based chemotherapy (given by drip or directly into the abdomen) after surgery, and whose cancer has since come back.
  • People whose cancer returned within 12 months of finishing their last chemotherapy treatment (platinum-based or otherwise).
  • People who have measurable tumours visible on scans at the start of the study, based on standard measurement guidelines.
  • People with a life expectancy of at least 12 weeks.
  • People who can provide a tumour tissue sample — either from a previous surgery or a newly collected sample taken during the screening period.
  • People whose major organ systems (such as liver, kidneys, and bone marrow) are functioning at an adequate level.
  • People who have not yet fully recovered from side effects of a previous treatment (confirm with trial site).

Who may not be able to join:

  • People whose ovarian, peritoneal, or fallopian tube cancer is of certain specific types, including non-epithelial, borderline, mucinous, predominantly mucinous seromucinous, malignant Brenner's tumour, or undifferentiated carcinoma.
  • People who have previously been treated with certain immune checkpoint therapies that target specific proteins on immune cells (such as PD-1, PD-L1, PD-L2, CTLA-4, OX-40, or CD137), or who have taken part in a previous study involving adebrelimab.
  • People who have received any systemic cancer treatment, radiation therapy, or maintenance therapy within 4 weeks before joining the study.
  • People who have had a severe allergic reaction (Grade 3 or higher) or have uncontrolled high blood pressure related to any of the study drugs or their ingredients.
  • People who have had major surgery within 3 weeks before joining the study, or who are still recovering from complications of surgery.
  • People who have had another type of cancer in the last 5 years that was growing or required active treatment.
  • People who are pregnant or currently breastfeeding.
  • People who have received a transplant of tissue or a solid organ from another person.
  • People who have a history of blood clotting disorders, significant bleeding, coughing up blood, or active gastrointestinal bleeding within the past 6 months.
  • People with a history of active autoimmune disease (a condition where the immune system attacks the body's own tissues).
  • People who currently have an active infection that requires treatment throughout the body (such as intravenous or oral antibiotics or antivirals).
  • People who have a history of HIV infection.
  • People who have a history of Hepatitis B or Hepatitis C infection.
  • People with any other medical condition, history, or circumstance that the trial team determines could interfere with the study results (confirm with trial site).
  • People with a known mental health condition or substance use disorder that could make it difficult to follow the study requirements.

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 27 July 2026
Phase 3: approximately ~65% 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

Phone: 86 13301971027

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 3
Sponsor
Obstetrics & Gynecology Hospital of Fudan University
Registry
ClinicalTrials.gov
Start date
18 March 2025
Est. completion
14 February 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective response rate (ORR)

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: 27 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