Early Phase 1 Brain 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 75 years old
- People who have been confirmed by tissue testing to have a primary, returned, or spread brain glioma (a type of brain tumour)
- People whose life expectancy is estimated to be more than 3 months
- People who have a reasonable level of general physical functioning, as assessed by their doctor using standard scoring tools (confirm with trial site)
- People whose standard treatment options have not worked, or for whom no standard treatments are available
- People who have a tumour area that a surgeon can sample or remove, or a body fluid from which immune cells can be collected
- People who have at least one measurable tumour that can be tracked during the trial
- People whose recent blood test results (taken within 7 days before joining) show that white blood cells, infection-fighting cells, immune cells, platelets, and haemoglobin are all at or above minimum levels, and that kidney, liver, and blood-clotting results are within acceptable ranges (confirm specific values with trial site)
- People who have no medical reason preventing them from having a biopsy or surgery
- People of childbearing potential who are willing to use highly effective contraception from the time of agreeing to join, and for one year after a specific part of the treatment is completed
- People who have stopped any cancer-targeting treatments — including radiotherapy, chemotherapy, or biological therapies — at least 28 days before immune cells are collected
- People who are able to understand and sign the consent form
- People who are able to attend follow-up visits and meet the other requirements of the trial
Who may not be able to join:
- People who need steroid medications (such as prednisone) at a daily dose above 15mg, or who need immune-suppressing treatment for an autoimmune condition
- People with significantly reduced lung function, based on specific breathing test measurements (confirm with trial site)
- People with serious heart conditions, such as severe heart failure, uncontrolled coronary artery disease, very low blood pressure, poor heart pumping function, or significant heart rhythm or electrical conduction problems
- People who have HIV infection or a positive HIV antibody test, active hepatitis B or C infection, or a syphilis infection
- People with serious physical or mental health conditions
- People who have an active infection throughout the body that requires treatment, or who have had a positive blood culture or imaging showing signs of infection
- People who have received or are currently receiving other medicines, biological therapy, chemotherapy, or radiotherapy within the past month
- People with a known allergy to substances similar to those used in cell-based therapies
- People who have previously received immunotherapy and experienced a serious immune-related side effect rated at level 3 or above
- People who still have significant side effects (above a mild level) from previous cancer treatments that have not resolved
- People who are pregnant or breastfeeding
- People who have previously had an organ transplant, a bone marrow or stem cell transplant from a donor, or kidney replacement therapy (such as dialysis)
- People who, in the opinion of the trial doctor, have other serious health conditions or circumstances that make participation unsuitable
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: Qing Lan, Second Affiliated Hospital of Soochow University
Phone: 086-18001759113
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
Adverse Events (AE); Objective Response Rate (ORR); Disease Control Rate (DCR); Duration of Response (DOR); Progression-Free Survival (PFS); Overall Survival (OS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.