Phase 3 Endometrial Cancer Trial, Recruiting NCT06288373 Sponsor: Tongji Hospital Condition: Endometrial Cancer
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Phase 3 Endometrial Cancer Trial, Recruiting

NCT06288373
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 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.

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 14 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

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

Status
Recruiting
Phase
Phase 3
Sponsor
Tongji Hospital
Registry
ClinicalTrials.gov
Start date
22 April 2024
Est. completion
1 March 2031

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free survival, PFS; 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: 14 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