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:
- 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.
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
Where this trial is recruiting
Primary endpoints
Objective Response 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.