OncoMatch/Clinical Trials/NCT07501156
H3K27M-specific Immune Effector Cells Targeting DMG/DIPG
Is NCT07501156 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies H3K27M-EIEs for diffuse midline glioma or diffuse intrinsic pontine glioma.
Treatment: H3K27M-EIEs — The purpose of this study is to assess the feasibility, safety and efficacy of H3K27M-specific engineered immune effector (EIE) therapy in patients with high-risk, H3K27M-positive diffuse midline glioma/diffuse intrinsic pontine glioma. Another goal of the study is to learn more about the function of the anti-H3K27M EIE cells and their persistency in patients.
Check if I qualifyExtracted eligibility criteria
Cancer type
Diffuse Intrinsic Pontine Glioma
Glioblastoma
Biomarker criteria
Required: H3-3A K27M
confirmed H3K27M mutation
Prior therapy
Must have received: standard care of medication, such as gross total resection with concurrent radio-chemotherapy (~54 - 60 Gy, TMZ) (temozolomide)
Patients have received standard care of medication, such as gross total resection with concurrent radio-chemotherapy (~54 - 60 Gy, TMZ)
Cannot have received: gliadel implantation
Exception: within 4 weeks before study start
A prior history of gliadel implantation 4 weeks before this study start
Cannot have received: antibody based therapies
Exception: currently receiving
currently receiving antibody based therapies
Lab requirements
Blood counts
absolute neutrophile count ≥ 1500/mm^3; hemoglobin > 10 g/dL; platelets > 100000 /mm^3; Peripheral blood absolute lymphocyte count must be above 0.8×10^9/L
Kidney function
creatinine < 1.5×ULN
Liver function
Bilirubin < 1.5×ULN; ALT or AST < 2.5×ULN
Cardiac function
Satisfactory heart functions
Satisfactory bone marrow, liver and kidney functions as defined by the following: absolute neutrophile count ≥ 1500/mm^3; hemoglobin > 10 g/dL; platelets > 100000 /mm^3; Bilirubin < 1.5×ULN; alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 2.5×ULN; creatinine < 1.5×ULN; Peripheral blood absolute lymphocyte count must be above 0.8×10^9/L; Satisfactory heart functions
Structured fields extracted by AI. May contain errors — verify against the official protocol.
Could you qualify for this trial?
Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.
Check if I qualify