High Grade Glioma (HGG)

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Review clinical trials related to High Grade Glioma (HGG). 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: Aug 18, 2026Locations: 17
Eligibility criteria

Participants must have histologically confirmed diagnosis of an LGG (WHO grade I... [+40]

Participants that have received prior therapy with a MEK inhibitor in combinatio... [+13]

Status: Not yet recruiting

Phase 1/2 Study Evaluating the Safety, PK/PD, and Clinical Activity of Oral JBI-778 in Patients With Brain Metastases, Leptomeningeal Disease, or Recurrent High Grade Glioma

This is a Phase 1/2, multicenter, open-label, dose-escalation and dose-expansion study evaluating the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), cerebrospinal fluid penetration, and preliminary antitumor activity of orally administered JBI-778, a selective PRMT5 inhibitor, in patients with brain metastases, leptomeningeal disease, or recurrent high-grade glioma. The study consists of a dose-escalation phase to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D), followed by expansion cohorts to evaluate preliminary efficacy at the RP2D.

Participants needed: 113
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Jubilant Therapeutics Inc.Updated: Aug 7, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma

This is a prospective, multicenter, single-arm, pilot clinical investigation, aimed at evaluating the safety and preliminary efficacy of the GlioHook implant in patients with high-grade glioma undergoing surgical resection followed by standard of care (SoC) treatment. GlioHook is a sterile medical device designed to be implanted after tumour resection surgery in suspected high grade glioma patients, covering the entire surface of the tumour resection margins, decreasing infiltration and focalizing the disease, while improving the effects of radiotherapy. Once implanted, GlioHook exerts a dual mechanism that combines tumour cell focalization and radiosensitization.

Participants needed: 15
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Batea OncologyUpdated: Jul 27, 2026Locations: 3
Eligibility criteria

Willing and able to provide written informed consent prior to the performance of... [+12]

Life expectancy <3 months, as estimated by the investigator. [+19]

Status: Not yet recruiting

A Safety and Efficacy Study of Combined Fianlimab + Cemiplimab in Children and Young Adults With Recurrent or Progressive High-Grade Glioma or Posterior Fossa-A Ependymoma

This study is researching an experimental drug called cemiplimab (called "study drug") and the combination of experimental drugs of fianlimab and cemiplimab (called "study drugs"). The study is focused on children and young adults with recurrent or progressive High-Grade Glioma (HGG) or ependymoma. "Recurrent" means that the cancer came back after treatment. "Progressive" means that the tumor has grown or spread. The aim of the study is to see how safe, tolerable, and effective cemiplimab and the combination of fianlimab and cemiplimab are. The study is looking at several other research questions, including: * What side effects may happen from receiving the study drug(s) * Do the study drug(s) help study participants live longer without their tumors growing or spreading * How much of the study drug(s) is in the blood at different times * Whether the body makes antibodies against the study drug(s) (which could make the study drug\[s\] less effective or lead to side effects)

Participants needed: 120
Trial details
Phase: Phase 1, Phase 2Age: 0-39Biological sex: AllType: InterventionalSponsor: Regeneron PharmaceuticalsUpdated: May 5, 2026
Eligibility criteria

Participant must be diagnosed with recurrent/progressive HGG or PF-A ependymoma... [+4]

Active autoimmune disease requiring systemic immunosuppressive therapy in the pa... [+6]