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OncoMatch/Clinical Trials/NCT05303467

A Feasibility Study to Evaluate the Safety of the TheraSphere Glioblastoma (GBM) Device in Patients With Recurrent GBM

Is NCT05303467 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies TheraSphere GBM for glioblastoma multiforme.

Phase 1RecruitingBoston Scientific CorporationNCT05303467Data as of May 2026

Treatment: TheraSphere GBMThe FRONTIER Study is a prospective, interventional, single-arm, multi-center, study to assess the safety and technical feasibility of TheraSphere GBM in patients with recurrent GBM.

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Extracted eligibility criteria

Cancer type

Glioblastoma

Performance status

WHO 0–2

Prior therapy

Max 2 prior lines

Must have received: surgery

Prior surgery

Must have received: radiation therapy

treatment with combination of radiotherapy and chemotherapy ± Tumor Treating Fields (Optune®)

Must have received: chemotherapy

treatment with combination of radiotherapy and chemotherapy ± Tumor Treating Fields (Optune®)

Cannot have received: cranial radiotherapy

Exception: no more than 1 course of prior cranial radiotherapy (EBRT)

Have received more than 1 course of prior cranial radiotherapy (EBRT)

Cannot have received: radiosurgery

Have received radiosurgery

Cannot have received: brachytherapy

Have received...brachytherapy

Cannot have received: hypofractionated radiotherapy

Have received...hypofractionated radiotherapy

Cannot have received: systemic therapy

Exception: no more than 2 systemic treatment protocols (lines of treatment), not including maintenance temozolomide

Have received more than 2 systemic treatment protocols (lines of treatment), not including maintenance temozolomide

Cannot have received: intra-arterial cerebral infusion therapy

Have received prior intra-arterial cerebral infusion therapy

Cannot have received: surgery

Exception: no more than 2 surgical GBM-related procedures

Have received more than 2 surgical GBM-related procedures

Cannot have received: thoracic radiation therapy

Have received prior thoracic radiation therapy

Lab requirements

Blood counts

platelets ≥ 100,000/l; absolute neutrophil count ≥1.5 x 10^9/l; hemoglobin ≥9.0 g/dl

Kidney function

creatinine ≤1.5 mg/dl

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

US trial sites

  • University of Alabama Birmingham · Birmingham, Alabama
  • University of California San Diego · San Diego, California
  • University of California San Francisco · San Francisco, California
  • Mayo Jacksonville · Jacksonville, Florida
  • Northwestern Univerity · Chicago, Illinois

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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