Phase 2 Endometrial Cancer Trial, Recruiting NCT05910177 Sponsor: Fujian Cancer Hospital Condition: Endometrial Cancer
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Phase 2 Endometrial Cancer Trial, Recruiting

NCT05910177
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:

  • You are a woman between 18 and 75 years old
  • You have been diagnosed with cervical neuroendocrine carcinoma (a specific type of cervical cancer) confirmed by a tissue or cell sample — if it is a mixed cancer type, at least 60% must be the neuroendocrine type
  • Your cancer is at an early stage (FIGO Stage I or II) and a specialist doctor has assessed that surgery is possible for you
  • You have at least one tumour that can be measured on a scan, meeting specific size requirements (confirm with trial site)
  • You are generally well and able to carry out everyday activities with little or no limitation (confirm with trial site)
  • Your doctors expect you to survive for more than 3 months after surgery
  • Your blood counts are within acceptable levels — including healthy levels of red blood cells, white blood cells, and platelets (no blood transfusions in the past 14 days)
  • Your liver and kidney function test results are within acceptable ranges (confirm with trial site)
  • You are not currently taking part in any other clinical trial
  • If you are of childbearing age, you must have a negative pregnancy blood test within 7 days before starting treatment, and you must agree to use contraception from signing the consent form until 24 weeks after the last dose
  • You are willing to take part, can follow the study requirements, and agree to attend follow-up appointments

Who may not be able to join:

  • You have previously had chemotherapy, radiotherapy, targeted therapy, or immunotherapy for this condition
  • You are not suitable for surgery or chemotherapy due to your physical condition or organ function
  • Your cancer has spread to distant parts of the body (distant metastasis)
  • You have an active autoimmune disease or a history of one (such as certain types of lung, eye, bowel, liver, or heart inflammation, or thyroid conditions) — some exceptions may apply, such as vitiligo, stable thyroid replacement therapy, or controlled Type 1 diabetes (confirm with trial site)
  • You have a weakened immune system, including HIV/AIDS, other immune deficiency conditions, or a history of organ or bone marrow transplant
  • You have serious heart, lung, liver, or kidney disease; a neurological or mental health condition; jaundice; bowel obstruction; or a severe infection
  • You are pregnant or breastfeeding
  • You have a heart condition such as coronary heart disease, irregular heartbeat (including a specific abnormality on a heart trace), or reduced heart function
  • Your blood clotting results are outside the acceptable range (confirm with trial site)
  • You have heart failure, unstable chest pain, a heart attack within the past year, or poorly controlled heart rhythm problems
  • You have a history of interstitial lung disease or non-infectious lung inflammation
  • You have had an allergic reaction to Camrelizumab (the study drug) or any of its ingredients
  • The research team considers you unsuitable for the trial 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 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: 13805056536

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
Sponsor
Fujian Cancer Hospital
Registry
ClinicalTrials.gov
Start date
28 December 2023
Est. completion
31 August 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective Response 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