Phase 2 Brain Cancer Trial, Recruiting NCT07501156 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Brain Cancer
Back to Brain Cancer

Phase 2 Brain Cancer Trial, Recruiting

NCT07501156
Recruiting Phase 2

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 are able to understand the study and are willing to sign a written consent form
  • People aged 2 to 70 years old
  • People diagnosed with a returning or treatment-resistant brain tumour called diffuse midline glioma or diffuse intrinsic pontine glioma, confirmed to have a specific genetic change (H3K27M mutation), who have already received standard treatments such as surgery and radiation/chemotherapy
  • People who are either not taking a steroid medication called dexamethasone, or are taking only a low dose (4 mg per day or less) at a specific point in the process
  • People whose general health and ability to function meets a minimum level, as measured by a standard scoring tool (confirm with trial site)
  • People with a life expectancy of more than 3 months
  • People whose bone marrow, liver, and kidney are working well enough to meet specific blood test results (confirm with trial site for exact values)
  • People whose blood contains enough of a certain type of immune cell (lymphocytes) to meet a minimum level
  • People with satisfactory heart function
  • People willing to follow the medical team's instructions throughout the study; women of childbearing age must have a negative pregnancy test within 7 days of starting, and both male and female participants of reproductive age must agree to use contraception during the study and for 3 months after it ends

Who may not be able to join:

  • People who have had a specific type of chemotherapy wafer (gliadel) implanted within the 4 weeks before the study starts, or who are currently receiving antibody-based treatments
  • People who are HIV positive
  • People with tuberculosis that is not currently under control
  • People with a history of an autoimmune disease, or any condition requiring long-term use of steroids or immune-suppressing medications
  • People with a history of severe allergic disease, or known allergy to immune cells or the study treatment
  • People already actively taking part in another immune cell clinical trial, or people the investigators believe may not be suitable or able to follow the study requirements

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 16 July 2026
Phase 2: approximately ~30% 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

Phone: +86 0755-86573763

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 2
Sponsor
Shenzhen Geno-Immune Medical Institute
Registry
ClinicalTrials.gov
Start date
18 March 2026
Est. completion
31 December 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Percentage of adverse effects after H3K27M-EIE injection

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: 16 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