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 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.
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
Where this trial is recruiting
Primary endpoints
Progression free survival (PFS)
Can't join this trial?
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.