Recurrent World Health Organization (WHO) Grade II Glioma

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Review clinical trials related to Recurrent World Health Organization (WHO) Grade II Glioma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Trametinib and Everolimus for Treatment of Pediatric and Young Adult Patients With Recurrent Gliomas (PNOC021)

This phase I trial studies the side effects and best dose of trametinib and everolimus in treating pediatric and young adult patients with gliomas that have come back (recurrent). Trametinib acts by targeting a protein in cells called MEK and disrupting tumor growth. Everolimus is a drug that may block another pathway in tumor cells that can help tumors grow. Giving trametinib and everolimus may work better to treat low and high grade gliomas compared to trametinib or everolimus alone.

Participants needed: 50
Trial details
Phase: Phase 1Age: 1-25Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Jun 17, 2026Locations: 17
Eligibility criteria

Participants must have histologically confirmed diagnosis of an LGG (WHO grade I... [+39]

Participants who are receiving any other investigational agent for treatment of... [+12]

Status: Recruiting

Serial MR Imaging and MR Spectroscopic Imaging for the Characterization of Lower Grade Glioma

This trial studies how well serial magnetic resonance (MR) imaging and MR spectroscopic imaging work in characterizing lower grade glioma. Diagnostic procedures, such as MR imaging and MR spectroscopic imaging, may detect serial changes in lower grade glioma. This study may help researchers learn more about practical ways of evaluating and standardizing treatment in patients with brain tumors.

Participants needed: 300
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Susan ChangUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

For patients in cohort 1: histologically proven lower grade glioma who are being... [+12]

Subjects will be excluded from participating in this study if they are unable to...