Phase 2 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 between 18 and 70 years
- People who have been diagnosed with cervical cancer (confirmed by a tissue or cell sample) at a specific stage of disease — FIGO stage IB3 or IIA2
- People whose scans show that the lymph nodes in the pelvis and near the main abdominal artery are below a certain size (less than 1.5 cm in a specific measurement)
- People whose cervical cancer has been identified as one of three specific types: squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma
- People who have not previously received any cancer treatment
- People who are generally well enough to carry out daily activities, meeting a standard health and activity measure known as ECOG performance status 0 or 1 (confirm with trial site)
Who may not be able to join:
- People who have another type of cancer at the same time
- People who are pregnant or have recently given birth
- People with a history of heart attack, stroke, unstable chest pain, severe heart failure, or blood clots in a deep vein
- People with certain heart rhythm problems of a moderate or serious level, including any degree of atrial fibrillation, or other significant rhythm problems that require treatment (confirm with trial site)
- People with active, unresolved hepatitis — meaning ongoing symptoms such as loss of appetite, weakness, nausea, or jaundice — or, for hepatitis B specifically, a virus level above a certain threshold in blood tests
- People whose liver is not functioning well enough, based on specific blood test results being more than 2.5 times the normal upper limit
- People whose kidneys are not functioning well enough, based on a specific blood test result being more than twice the normal upper limit
- People with a history of long-term lung disease that limits breathing capacity
- People who have had a major organ transplant or have an autoimmune disease
- People with a history of severe mental illness or significant brain-related conditions affecting function
- People with a history of substance abuse or drug addiction
- People who have been taking immune-suppressing medications or steroid medicines (above a certain dose) within the two weeks before joining, and are still taking them
- People with blood clotting problems, a tendency to bleed, or who are currently on blood-thinning or clot-dissolving therapy (note: low-dose aspirin and a specific type of low-dose heparin are generally permitted — confirm with trial site)
- People with an immune system deficiency, whether present from birth or developed — for example, those with HIV infection
- People who have received an inactivated (non-live) vaccine within 30 days before the first study treatment
- People who are unable or unwilling to give written consent to participate, or who are unable to follow the requirements of the study
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
Phone: +86 20 87341779
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
Pathological Complete Response (pCR) Rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.