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 who have been newly diagnosed with a specific type of brain tumor called DIPG or DMG, confirmed either by biopsy or by brain imaging that meets specific criteria (confirm with trial site for details on imaging requirements)
- The tumor must have a confirmed histone mutation, shown on a pathology report (confirm with trial site)
- Children and young people aged 12 months to 18 years (note: for certain parts of the trial, the first three patients enrolled must be aged 12 years or older)
- People whose body surface area (a measurement based on height and weight) is at least 0.35 m² at the time of joining the trial
- People who meet a minimum physical functioning score, measured using standard scales used by doctors to assess daily activity and mobility — wheelchair users who cannot walk due to paralysis may still meet this criterion (confirm with trial site)
- People who are able to start radiation therapy within 42 days of their diagnostic scan, and begin the trial treatment between 6 and 10 weeks after finishing radiation
- People whose steroid medication (if prescribed) has been reduced to a low dose for at least 7 days before joining
- People whose tumor can be measured on scans
Who may not be able to join:
- People who received a chemotherapy drug called temozolomide during their radiation treatment
- People whose cancer has spread beyond the original tumor site (disseminated disease)
- People who have received any cancer treatment other than radiation therapy
- People with autoimmune conditions or immune system disorders
- People with an active breathing or respiratory condition or infection
- People with an active viral infection
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: Ashley Plant-Fox, MD, Ann and Robert H. Lurie Children's Hospital
Phone: 312-227-4847
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
Safety and Tolerability: Dose limiting toxicities of rHSC-DIPGVax; Safety and Tolerability: Dose limiting toxicities of rHSC-DIPGVax plus BALSTILIMAB; Safety and Tolerability: Dose limiting toxicities of rHSC-DIPGVax plus BALSTILIMAB and ZALIFRELIMAB
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.