Phase 2 Endometrial Cancer Trial, Recruiting NCT07646301 Sponsor: Sun Yat-sen University Condition: Endometrial Cancer
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Phase 2 Endometrial Cancer Trial, Recruiting

NCT07646301
Recruiting Phase 2

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.

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 26 July 2026
Phase 2: approximately ~30% 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

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

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
1 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological Complete Response (pCR) Rate

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: 26 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