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 have been diagnosed with untreated stage IB2 cervical cancer (confirmed by two senior doctors using examination and imaging)
- You have at least one tumour that can be measured on a scan (mainly MRI)
- Your cervical cancer has been confirmed by a tissue sample (biopsy) and is one of these types: squamous cell carcinoma (any grade), usual type adenocarcinoma (certain grades), or adenosquamous carcinoma (certain grades)
- Your tumour tests positive for a protein called PD-L1, with a score of 1 or higher
- You are between 18 and 70 years old
- You are generally well enough to carry out light activity or desk work (your performance score shows you are mostly active)
- Your blood counts, liver, and kidney results are within acceptable ranges as shown by recent lab tests
- You are willing and able to attend follow-up appointments and follow the trial schedule
- You are willing to sign a consent form agreeing to the trial's requirements
Who may not be able to join:
- You have, or have had, an autoimmune disease (where your immune system attacks your own body), unless it is a mild condition such as vitiligo, hair loss, certain skin conditions not needing ongoing treatment, well-controlled thyroid conditions, stable type 1 diabetes, or childhood asthma that has fully resolved
- You have previously been treated with immune checkpoint inhibitor drugs (a type of cancer immunotherapy, such as anti-PD-1 or anti-PD-L1 medicines)
- You have a known allergy to any ingredient in the trial medication
- You have taken strong immune-suppressing medicines or high-dose steroid tablets within the past 2 weeks (certain steroid creams, eye drops, nasal sprays, or inhalers are allowed)
- You have taken certain herbal or immune-boosting treatments within the past 2 weeks
- You currently have a serious infection that requires treatment
- You had a serious infection (such as sepsis or severe pneumonia requiring hospitalisation) within the past 4 weeks
- You have untreated or poorly controlled hepatitis B, or active hepatitis C (stable, treated cases may be eligible — confirm with trial site)
- You have active tuberculosis (TB)
- You have a weakened immune system or are HIV positive
- You have active or past inflammatory bowel disease (such as Crohn's disease or ulcerative colitis), or severe problems swallowing or absorbing medicines
- You have a known lung condition causing scarring or inflammation (interstitial lung disease) that could interfere with treatment
- You have received a live or weakened (attenuated) vaccine within the past 4 weeks (standard inactivated flu vaccines are allowed)
- You have previously had a bone marrow transplant or a solid organ transplant
- You have been diagnosed with another cancer within the past 5 years
- You have had major surgery or serious injury within the past 28 days
- You have a history of a hole in your gut (gastrointestinal perforation), a gut fistula, or a fistula in the female genital area
- You have serious uncontrolled heart or blood vessel problems, including recent heart attack, stroke, blood clots, or severe heart failure within the past 6 months
- You have had significant bleeding (such as from your stomach or gut) within the past month, or currently have active coughing of blood, bowel blockage, or uncontrolled fluid build-up in the body
- You have abnormal liver or kidney development, or a related surgical history (confirm with trial site)
- You are pregnant, breastfeeding, or are of childbearing age and unwilling to use contraception during the treatment period
- You are currently taking part in another clinical trial that involves a treatment or intervention
- Your doctor feels that joining the trial would not be safe or suitable for you 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: Ding Ma, Tongji Hospital
Phone: 086-027-8362
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
Percentage of patients meeting ConCerV criteria
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.