Phase 1 Brain Cancer Trial, Recruiting NCT06815432 Sponsor: Baylor College of Medicine Condition: Brain Cancer
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Phase 1 Brain Cancer Trial, Recruiting

NCT06815432
Recruiting Phase 1

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
10 October 2025
Est. completion
5 December 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of Patients with Dose Limiting Toxicity

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov