Phase 1 Mesothelioma 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 willing to participate and have signed a consent form agreeing to take part
- You are 18 years old or older, any gender
- You have been diagnosed with an advanced solid tumour cancer that has caused a build-up of fluid around the lungs (malignant pleural effusion) confirmed by lab testing, whether the cancer started in the lungs or spread there from elsewhere
- Your cancer has not responded to standard treatments, or no standard treatments are available
- You have not received any medication injected into the chest cavity in the month before joining (routine diagnostic fluid removal is acceptable)
- You are willing to provide tumour tissue or fluid samples, and your cancer cells test positive for a protein called B7-H3
- Your general health and ability to carry out daily activities is rated at a reasonable level (ECOG score of 0, 1, or 2 — confirm with trial site)
- Your recent blood test results meet specific requirements, including: enough white blood cells, platelets, and red blood cells; liver, kidney, and blood clotting function within acceptable ranges (confirm exact values with trial site)
- Any side effects from previous cancer treatments have mostly resolved before starting this trial
- If you are able to have children, you agree to use reliable contraception from consent until 6 months after your last dose
Who may not be able to join:
- You have a known allergy to the study drug or any of its ingredients
- You have a medical reason that prevents chest drainage, or draining the fluid would not help you
- You are already receiving other anti-cancer treatments or anything that could affect the fluid around your lungs (other than diagnostic procedures)
- You have had radiation therapy within the 2 weeks before starting the trial
- You have had major surgery within 4 weeks before starting and have not fully recovered
- You are currently taking steroid medications or other immune-suppressing drugs within 1 week before starting
- You have taken part in another clinical drug trial within the past 4 weeks
- You have previously received a specific type of cell therapy that targets B7-H3 (CAR-T cell therapy)
- You have an active infection, serious blood clotting problems, or other significant ongoing illnesses
- You have severe heart, lung, liver, or kidney disease beyond specified thresholds (confirm details with trial site)
- You have a severe autoimmune disease
- You have previously received a transplant of an organ or tissue from another person
- You received a live vaccine within 2 weeks before starting, or plan to receive one during the study
- You have an active hepatitis B infection, active hepatitis C infection, HIV, or a positive syphilis test
- You have serious problems with memory, thinking, or understanding, as assessed by the study doctor
- You are pregnant or breastfeeding
- You have any other medical or personal circumstances that the study doctor believes would 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
Phone: 010-87788713
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) and serious adverse events (SAE); Dose Limiting Toxicity (DLT); GvHD; CRS; Immune effector cell-associated neurotoxicity syndrome (ICANs)
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.