Phase 3 Endometrial Cancer Trial, Recruiting
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 diagnosed with locally advanced cervical cancer at a specific stage (FIGO 2018 stages IB3, IIA2, or IIB with a tumour larger than 4 cm), confirmed by two qualified doctors using physical examination and imaging.
- People who have at least one tumour that can be measured on scans, particularly MRI, at the start of the trial.
- People whose cervical cancer has been confirmed by tissue testing as one of these types: squamous cell carcinoma, adenocarcinoma (common type), or adenosquamous carcinoma.
- People whose tumour tests positive for a protein called PD-L1, with a Combined Positive Score (CPS) of 1 or higher (confirm with trial site).
- People aged 18 to 70 years old.
- People who are generally well enough to carry out daily activities with little or no limitation, based on a standard health performance scale called ECOG (score of 0 or 1).
- People whose blood test results fall within acceptable ranges, showing healthy levels of white blood cells, platelets, liver function, and kidney function, as assessed by the trial team.
- People who are willing and able to attend follow-up appointments and follow the trial requirements.
- People who are willing to sign a consent form agreeing to the trial's conditions.
- People who agree to use effective contraception during the trial and for at least 5 months after the last dose of the immunotherapy drug, or 6 months after chemotherapy ends — whichever period is longer.
Who may not be able to join:
- People who currently have, or have a history of, an active autoimmune disease that has required treatment — such as autoimmune liver disease, lung inflammation, eye inflammation, bowel inflammation, thyroid problems, or asthma requiring certain medications, among others.
- People who have previously been treated with immune checkpoint inhibitor drugs (such as anti-PD-1 or anti-PD-L1 medicines), or who are known to have an allergy to any component of the study drugs or similar medicines.
- People with a known HIV infection, active hepatitis B, or active hepatitis C.
- People who have taken immune-suppressing medications, including steroid medicines above a certain dose, within the 2 weeks before starting the trial.
- People who have been diagnosed with another cancer (other than cervical cancer) within the past 5 years.
- People who have taken part in another clinical drug trial or received an experimental treatment within the 4 weeks before joining (observational studies without treatment are generally allowed).
- People who are pregnant or currently breastfeeding.
- People with serious uncontrolled health conditions, including certain heart problems, a heart attack within the past 6 months, uncontrolled high blood pressure, a stroke or brain condition within the past 6 months, serious blood clotting or bleeding disorders, significant kidney or liver abnormalities, or an active infection requiring treatment within 14 days before starting the trial.
- People who have received a live or weakened (attenuated) vaccine within the 4 weeks before starting the trial (standard inactivated flu vaccines are generally permitted).
- People who have previously had a bone marrow transplant or a solid organ transplant from a donor.
- People with a current problem with drug or alcohol misuse.
- People who the trial doctors believe are unlikely to be able to follow the trial's procedures and 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.
Contact this trial
Principal Investigator: Ding Ma, Tongji Hospital
Phone: 086-027-8362
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
Where this trial is recruiting
Primary endpoints
Progression-free survival, PFS; Objective Response Rate, ORR
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.