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OncoMatch/Clinical Trials/NCT03830151

Hyperpolarized Carbon C 13 Pyruvate in Diagnosing Glioma in Patients With Brain Tumors

Is NCT03830151 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies Hyperpolarized Carbon C 13 Pyruvate for primary brain neoplasm.

Phase 1RecruitingM.D. Anderson Cancer CenterNCT03830151Data as of Jun 2026

Treatment: Hyperpolarized Carbon C 13 PyruvateThis trial studies how an imaging agent, hyperpolarized carbon C 13 pyruvate, works in diagnosing glioma in patients with brain tumors. Giving hyperpolarized carbon C 13 pyruvate before an advanced imaging technique called a magnetic resonance spectroscopic imaging (MRSI) scan may help researchers better diagnose glioma in patients with brain tumors.

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Extracted eligibility criteria

Treatments studied

Other

Hyperpolarized Carbon C 13 Pyruvate

Cancer type

Glioblastoma

Demographics

Ages ≥ 19

Prior therapy

No prior treatment (treatment-naive required)

Cannot have received: surgical resection

Exception: previous biopsy permitted

Prior brain tumor treatment, including surgical resection, radiation therapy or chemotherapy for a primary brain neoplasm. Previous biopsy will not disqualify the patient from participation.

Cannot have received: radiation therapy

Exception: previous biopsy permitted

Prior brain tumor treatment, including surgical resection, radiation therapy or chemotherapy for a primary brain neoplasm. Previous biopsy will not disqualify the patient from participation.

Cannot have received: cytotoxic chemotherapy

Exception: previous biopsy permitted

Prior brain tumor treatment, including surgical resection, radiation therapy or chemotherapy for a primary brain neoplasm. Previous biopsy will not disqualify the patient from participation.

Lab requirements

Kidney function

GFR > 60. In patients with moderate renal failure (GFR 30-60), alternate injection with 2 times half-dose multihance (gadobenate dimeglumine) or gadovist (gadobutrol) will be considered, if a contrast exam is deemed clinically necessary.

Patient has a GFR > 60. In patients with moderate renal failure (GFR 30-60), an alternate injection with 2 times half-dose multihance (gadobenate dimeglumine) or gadovist (gadobutrol) will be considered, if a contrast exam is deemed clinically necessary.

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

US trial sites

  • M D Anderson Cancer Center · Houston, Texas

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Frequently asked questions

Is NCT03830151 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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Related pages

Glioblastoma trials