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OncoMatch/Clinical Trials/NCT06649851

G-CSF After Chemo-radiation in Patients With Glioblastoma

Is NCT06649851 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Granulocyte Colony Stimulating Factor (G-CSF) for mgmt-methylated glioblastoma.

Phase 2RecruitingMassachusetts General HospitalNCT06649851Data as of May 2026

Treatment: Granulocyte Colony Stimulating Factor (G-CSF)This research study involves the study of granulocyte colony stimulating factor (G-CSF) in patients with MGMT-methylated glioblastoma multiforme (GBM) that are undergoing standard chemoradiation. The study aims to evaluate G-CSF's effects on brain health and cognitive function. The name of the study drugs involved in this study are: * G-CSF (also called Filgrastim) * Temozolomide (TMZ), a standard of care chemotherapy drug

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Extracted eligibility criteria

Cancer type

Glioblastoma

Biomarker criteria

Required: MGMT promoter methylation (positive)

Molecular analysis needs to confirm a positive MGMT promoter methylation status using standard institutional testing methods

Required: IDH1 wild-type

IDH wildtype

Disease stage

Required: Stage WHO GRADE 4 (WHO)

Grade: 4 (WHO)

World Health Organization (WHO) grade 4

Prior therapy

No prior treatment (treatment-naive required)

Cannot have received: cranial irradiation

Lab requirements

Blood counts

leukocytes ≥2,500/mcL; absolute neutrophil count ≥1,500/mcL; platelets ≥100,000/mcL

Kidney function

creatinine ≤ institutional ULN OR GFR ≥60 mL/min/1.73 m2 unless data exists supporting safe use at lower kidney function values, no lower than 30 mL/min/1.73 m2

Liver function

total bilirubin ≤ institutional ULN (≤3xULN for Gilbert's syndrome); AST(SGOT)/ALT(SGPT) ≤3 × institutional ULN

Participants must have adequate organ and bone marrow function (as defined below) to be able to receive standard chemoradiation therapy: * leukocytes ≥2,500/mcL * absolute neutrophil count≥1,500/mcL * platelets ≥100,000/mcL * total bilirubin≤ institutional upper limit of normal (ULN) * AST(SGOT)/ALT(SGPT)≤3 × institutional ULN creatinine≤ institutional ULN OR * glomerular filtration rate (GFR) ≥60 mL/min/1.73 m2 unless data exists supporting safe use at lower kidney function values, no lower than 30 mL/min/1.73 m2. For patients with Gilbert's syndrome, total bilirubin can be ≤ 3xULN.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Massachusetts General Hospital · Boston, Massachusetts

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