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NCT05303467 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study of Glioblastoma Multiforme and Recurrent Glioblastoma, sponsored by Boston Scientific Corporation.

Recruiting
Registry status
Phase 1
Development phase
36
Enrollment target
9
Study locations

NCT05303467 is a Phase 1 study of Glioblastoma Multiforme and Recurrent Glioblastoma that is actively recruiting participants, run by Boston Scientific Corporation. The registered enrollment target is 36 participants, below the 96-participant average among 88 other Glioblastoma Multiforme trials with a reported enrollment target (62% lower). The trial reports 9 study locations across 8 states.

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The verdict

NCT05303467, a Phase 1 study of Glioblastoma Multiforme and Recurrent Glioblastoma, is actively recruiting participants, sponsored by Boston Scientific Corporation.

RECRUITING
Registry status
Phase 1
Development phase
36 participants
Enrollment target
9
Study locations

Study Summary

The 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.

Interventions

  • DEVICE TheraSphere GBM

Study Locations (9)

California

  • University of California San Diego - San Diego
  • University of California San Francisco - San Francisco

Alabama

  • University of Alabama Birmingham - Birmingham

Florida

  • Mayo Jacksonville - Jacksonville

Illinois

  • Northwestern Univerity - Chicago

Maryland

  • Johns Hopkins Interventional Radiology Center - Baltimore

Missouri

  • Washington University School of Medicine - St Louis

New York

  • Lenox Hill Hospital - New York

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2022-07-30
Est. Completion 2027-01-31
Phase Phase 1

Sponsor

Boston Scientific Corporation

280 total trials

What the Registry Record Tells You About NCT05303467

The ClinicalTrials.gov registry entry for NCT05303467 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 96-participant average among 88 other Glioblastoma Multiforme trials with a reported enrollment target (62% lower). The listed sponsor is Boston Scientific Corporation, which has 280 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Glioblastoma Multiforme appearing as the primary indexed condition, and to 1 intervention - of which TheraSphere GBM is the first listed.

NCT05303467 reports 9 study locations spanning 8 distinct geographic areas - top geographies include California, Alabama, Florida.

Frequently Asked Questions

What is clinical trial NCT05303467 about?

NCT05303467 is a clinical study titled "A Feasibility Study to Evaluate the Safety of the TheraSphere Glioblastoma (GBM) Device in Patients With Recurrent GBM". The 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.

What is the current status of trial NCT05303467?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2022-07-30. Estimated completion is 2027-01-31.

What conditions does trial NCT05303467 study?

This clinical trial studies the following conditions: Glioblastoma Multiforme, Recurrent Glioblastoma.

What interventions are being tested in trial NCT05303467?

The interventions under investigation include: TheraSphere GBM (DEVICE).

Who is sponsoring clinical trial NCT05303467?

This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05303467 being conducted?

This trial has 9 study locations across Alabama, California, Florida, Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.