Feasibility of Acquiring Hyperpolarized Imaging in Patients With Meningioma

Recruiting now · Phase 1

Conditions studied: Meningioma

In brief

This is a Pilot/Phase I clinical study of hyperpolarized 13C (HP 13C) pyruvate injection that includes the acquisition of magnetic resonance (MR) data performed on participants with meningioma to evaluate metabolism and aid in the non-invasive characterization of aggressive tumor behavior

Key facts

Study ID

NCT06014905

Run by

Javier Villaneuva-Meyer, MD

People needed

50

Starts

2023-09-01

Expected to finish

2027-09-30

Last updated by the study team

2026-06-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Known (histopathologically confirmed) or presumed meningioma based on imaging with measurable disease on MRI that shows gadolinium enhancement (at least one cm diameter) intracranially (e.g., not confined to skull base alone).
• a. Thirty of the participants plan to have surgical resection within 4 weeks
• Participants cannot have contraindication to MRI examinations.
• Age >=18 years.
• Have a life expectancy of >12 weeks.
• Karnofsky Performance Status > 60%.
• Participants must have adequate renal function (creatinine < 1.5 mg/dL) before imaging. This test must be performed within 60 days prior to hyperpolarized imaging scan.
• Participants must sign an informed consent indicating that they are aware of the investigational nature of this study.
• Participants must sign an authorization for the release of their protected health information.

You may not qualify if…

• Has any significant medical illnesses that in the investigator's opinion cannot be adequately controlled with appropriate therapy, would compromise the patient's ability to participate in this study or any disease that will obscure toxicity or dangerously impact response to the imaging agent.
• Uncontrolled blood pressure (Systolic BP≥140 mmHg or diastolic BP ≥>=90 mmHg) despite an optimized regimen of antihypertensive medication.
• Has a history of any other cancer (except non-melanoma skin cancer or carcinoma in-situ of the cervix), unless in complete remission and off of all therapy for that disease for a minimum of 3 years.
• Participants must not be pregnant or breast feeding. Women of childbearing potential are required to obtain a negative pregnancy test within 14 days of Hyperpolarized Imaging scan. Effective contraception (men and women) must be used in participants of child-bearing potential.
• Participants must be excluded from participating in the study if they are not able to comply with the study and/or follow-up procedures.

Where it is running

• University of California, San Francisco — San Francisco, California, United States (enrolling)

Full record on ClinicalTrials.gov

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