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NCT Number: NCT07821112

Phase II Elderly/Frail Pts With Newly Diagnosed or Recurrent Malignant Glioma Tx Treated With Cesium-131 GammaTile®

This is a phase 2, open-label clinical trial determining feasibility, safety, and tolerability of GammaTile® in elderly or frail subjects with newly diagnosed or recurrent malignant gliomas.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Chao Family Comprehensive Cancer Center, University of California, Irvine

Orange, California, 92868, United States

Location contact

Carlen Yuen, MD

CONTACT

[email protected]

877-827-8839

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Supratentorial
  • A bi-dimensionally measurable lesion of at least 10 mm, visible on two or more axial slices 5 mm apart.
  • The pre-operative tumor planned for resection is ≤ 7 cm in maximal dimension.
  • Tumor, which in the opinion of the enrolling neurosurgeon, is amenable to attempted gross total resection (GTR) or near total resection (NTR).
  • Anticipated GT placement (i.e., closest aspect of post resection tumor bed anticipated to receive GT placement) that is > 15mm from the optic chiasm or brainstem.
  • If multifocal, must be fully resectable in one operative bed. Surgical protocol will follow current institutional standards.
  • Able to receive 5-aminolevulinic acid (5-ALA, Gleolan) or other institutionally standard immunofluorescent-guidance such as fluorescein, prior to surgery to optimize GTR or NTR of enhancing tumor.
  • Karnofsky Performance Scale (KPS)
  • Elderly GBM: baseline KPS score of ≥ 60.
  • Frail GBM: baseline (pre-GBM diagnosis) is <70 and surgical management is expected to improve KPS to ≥ 60.

Exclusion criteria

  • Staged surgery planned (prior biopsy allowed).
  • Bilateral tumors, or multi-focal tumors that cannot be encompassed in one operative field.
  • Spinal tumors are excluded.
  • Enhancing extension into brainstem or thalamus, or significant invasion into the corpus callosum that would preclude a high likelihood of GTR or NTR.
  • Leptomeningeal disease not expected to be encompassed by the surgical resection.
  • Evidence of diffuse leptomeningeal disease that requires whole brain irradiation are excluded from this trial.

Treatment and study plan

GammaTile®

Device

GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.

Other names: GammaTile

Primary outcomes

  1. Percentage of Participants who were able to receive the GammaTile Implant

    Time frame: 28 days

    Feasibility is defined by proportion of participants who were able to be treated with GammaTile

  2. Number of Participants with Treatment-related Adverse Events

    Time frame: 24 months

    Safety and tolerability will be determined by the proportion, nature, and severity of treatment-related adverse events in accordance with the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 5.0.

    Adverse events (AEs) are reported based on clinical laboratory tests, vital sign and weight measurements, physical examinations, performance status evaluations, magnetic resonance imaging, and any other medically indicated assessments.

Secondary outcomes

  1. Progression-Free Survival (PFS)

    Time frame: 24 months

    Progression-Free Survival (PFS) as measured by Response Assessment in Neuro-Oncology (RANO) 2.0 on brain MRI with and without contrast.

  2. Overall Survival (OS)

    Time frame: 24 months

    Overall Survival (OS) as measured by time from registration to death of any cause as documented dates of registration and death within the electronic medical system.

Study contacts

Contact information is provided by the study sponsor or research team.

Chao Family Comprehensive Cancer Center University of California, Irvine

CONTACT

[email protected]

1-877-827-8839

University of California Irvine Medical

CONTACT

Sponsors and collaborators

Lead sponsor

University of California, Irvine

Other

Collaborators

  • GT Medical Technologies, Inc.

Registry information

Official study title

A Phase II Study of Elderly and Frail Patients With Newly Diagnosed or Recurrent Malignant Glioma Treated With Cesium-131 GammaTile® (ENDURANCE Trial)

Acronym: ENDURANCE

Important dates

Study start
2026
Primary completion
2027
Study completion
2029
First posted
Sep 15, 2026
Registry last updated
Sep 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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