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:
- Adults aged 18 or older with a brain tumour called glioblastoma that has come back after previous surgery, and who are planned for another surgery to remove tumour tissue
- People whose tumour tests positive for a protein called GPC3, with a significant amount of the tumour cells (more than 25%) showing a moderate-to-strong presence of this protein (as measured by a lab test on tumour tissue)
- People with a general health and functioning score of 60% or higher on a standard medical scale called the Karnofsky Performance Scale, meaning they are able to care for themselves and carry out some normal activities
- People whose neurological symptoms (such as movement, speech, or thinking) have been stable for at least 7 days before joining the treatment part of the trial
- People who have been on a stable or reducing dose of steroid medication (up to a maximum of 0.1 mg/kg of dexamethasone or an equivalent steroid per day) for at least 7 days before surgery and treatment
- People whose kidneys, liver, and blood are functioning adequately based on lab tests — including kidney filtering rate, liver function, blood clotting, white blood cell count, platelet count, haemoglobin level, and blood oxygen level (confirm specific values with trial site)
- People who have recovered from the side effects of any previous chemotherapy or other investigational treatments before joining
- People who are sexually active and are willing to use effective contraception for 3 months after receiving the T-cell treatment
- People (or their legal guardian) who have read, understood, and signed a consent form agreeing to take part, and have been given a copy of that form
Who may not be able to join:
- People who have had allergic reactions to products containing mouse-derived proteins, or who have developed antibodies against mouse proteins (known as HAMA) — this applies to those who have previously been treated with mouse-derived antibodies
- People who have had an organ transplant at any point
- People who are known to be HIV positive
- People who currently have an active bacterial, fungal, or viral infection (active Hepatitis B or Hepatitis C may be considered separately — confirm with trial site)
- People who are pregnant or breastfeeding
- People with an uncontrolled infection
- People where the treating doctor considers participation to not be in their best interest due to other health risk factors
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: Ganesh Rao, MD, Baylor College of Medicine
Phone: (713) 798-4696
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
Number of Patients with Dose Limiting Toxicity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.