Phase 3 Endometrial Cancer Trial, Recruiting NCT05173272 Sponsor: Sichuan Cancer Hospital and Research Institute Condition: Endometrial Cancer
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Phase 3 Endometrial Cancer Trial, Recruiting

NCT05173272
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 aged 18 or older
  • People who have been diagnosed with cervical cancer (confirmed by laboratory tissue testing) of a specific type — adenocarcinoma, adenosquamous, or squamous cell — at a certain stage of the disease (FIGO 2018 stage Ib3 to IIIc2) (confirm with trial site for staging details)
  • People who have at least one tumour that can be measured using standard imaging criteria (RECIST 1.1)
  • People who have not yet received any treatment for this cancer
  • People with an expected survival of at least 3 months
  • People who are generally well enough to carry out light activity or normal daily tasks, based on a standard performance scale (ECOG score of 0 or 1)
  • People whose blood counts fall within acceptable ranges — including white blood cells, platelets, haemoglobin, and neutrophils — and who have no signs of bleeding problems
  • People whose liver and kidney function test results are within acceptable limits set by the trial
  • People whose heart is pumping blood effectively, with a heart function measurement (left ventricular ejection fraction) of 50% or above
  • People who have voluntarily agreed to take part and have signed a consent form

Who may not be able to join:

  • People who are pregnant or breastfeeding, or people of childbearing potential who are unwilling to use contraception during the trial (a negative pregnancy test within 7 days before the first dose is required)
  • People who have, or have had, another type of cancer — except for certain fully cured skin cancers or non-invasive cancers (carcinoma in situ)
  • People who have a bone marrow disorder or another condition affecting how the body produces blood cells
  • People who have an active infection, HIV, or hepatitis that requires ongoing treatment
  • People who already have nerve damage in their hands or feet (peripheral neuropathy), even at a mild level (Grade 1 or above)
  • People who have experienced a serious heart or blood vessel problem within the past 6 months — such as a stroke, heart attack, uncontrolled high blood pressure, unstable chest pain, heart failure, or a heart rhythm problem requiring medication
  • People with a known allergy to any of the study drugs or their ingredients
  • People who have a significant thyroid condition at the time of enrolment
  • People who have taken part in another cancer treatment clinical trial within the 30 days before starting this trial
  • People with a known history of dementia, significant changes in mental state, or a mental health condition that would make it difficult to understand or consent to the study
  • People whom the trial investigators consider unsuitable for participation for any other reason

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 23 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: Guonan Zhang, Sichuan Cancer Hospital and Research Institute

Phone: 86-13881866599

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
Sichuan Cancer Hospital and Research Institute
Registry
ClinicalTrials.gov
Start date
24 July 2023
Est. completion
28 December 2027

Where this trial is recruiting

🇨🇳 China

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: 23 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