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NCT04574856 · ClinicalTrials.gov registry record · Phase 2

Multiparametric MR-Guided High Dose Adaptive Radiotherapy With Concurrent Temozolomide in Patients With Newly Diagnosed Glioblastoma

A Phase 2 study of Glioblastoma, sponsored by University of Michigan Rogel Cancer Center.

Active
Registry status
Phase 2
Development phase
30
Enrollment target
1
Study location

NCT04574856 is a Phase 2 study of Glioblastoma that is active but no longer recruiting, run by University of Michigan Rogel Cancer Center. The registered enrollment target is 30 participants, below the 109-participant average among 199 other Glioblastoma trials with a reported enrollment target (72% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04574856, a Phase 2 study of Glioblastoma, is active but no longer recruiting, sponsored by University of Michigan Rogel Cancer Center.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

This study will investigate whether or not intensified radiation therapy adapted during the radiation treatment course to high-risk, treatment-resistant tumor regions will improve overall survival in patients with newly diagnosed glioblastoma (GBM) compared to conventional chemoradiotherapy.

Conditions Studied

Interventions

  • DRUG Temozolomide
  • RADIATION Dose-Intensified Radiotherapy
  • DRUG Adjuvant temozolomide

Study Locations (1)

Michigan

  • University of Michigan Rogel Cancer Center - Ann Arbor

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2020-11-04
Est. Completion 2026-10
Phase Phase 2

What the Registry Record Tells You About NCT04574856

The ClinicalTrials.gov registry entry for NCT04574856 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 109-participant average among 199 other Glioblastoma trials with a reported enrollment target (72% lower). The listed sponsor is University of Michigan Rogel Cancer Center, which has 292 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Glioblastoma appearing as the primary indexed condition, and to 3 interventions - of which Temozolomide is the first listed.

NCT04574856 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT04574856 about?

NCT04574856 is a clinical study titled "Multiparametric MR-Guided High Dose Adaptive Radiotherapy With Concurrent Temozolomide in Patients With Newly Diagnosed Glioblastoma". This study will investigate whether or not intensified radiation therapy adapted during the radiation treatment course to high-risk, treatment-resistant tumor regions will improve overall survival in patients with newly diagnosed glioblastoma (GBM) compared to conventional chemoradiotherapy.

What is the current status of trial NCT04574856?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2020-11-04. Estimated completion is 2026-10.

What conditions does trial NCT04574856 study?

This clinical trial studies the following conditions: Glioblastoma.

What interventions are being tested in trial NCT04574856?

The interventions under investigation include: Temozolomide (DRUG), Dose-Intensified Radiotherapy (RADIATION), Adjuvant temozolomide (DRUG).

Who is sponsoring clinical trial NCT04574856?

This trial is sponsored by University of Michigan Rogel Cancer Center, which has 292 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04574856 being conducted?

This trial has 1 study location across Michigan. 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

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