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NCT01822275 · ClinicalTrials.gov registry record · Phase 2

Phase II Trial of Low-Dose Whole Brain Radiotherapy With Concurrent Temozolomide and Adjuvant Temozolomide in Patients With Newly-Diagnosed Glioblastoma Multiforme

A Phase 2 study, sponsored by University of Maryland, Baltimore.

Terminated
Registry status
Phase 2
Development phase
24
Enrollment target

NCT01822275: Clinical Trial Phase 2 study, sponsored by University of Maryland, Baltimore.

NCT01822275 is a Phase 2 study that was terminated before completion, run by University of Maryland, Baltimore. The registered enrollment target is 24 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01822275, a Phase 2 study, was terminated before completion, sponsored by University of Maryland, Baltimore.

TERMINATED
Registry status
Phase 2
Development phase
24 participants
Enrollment target

Study Summary

In the current proposed trial the role of the low-dose WBRT (0.15 Gy) would be to safely treat the microscopic distant GBM cells outside of the high dose RT region and sensitize the gross tumor, while the focal radiation dose (1.85 Gy) to the gross tumor will bring the total tumor dose of 2 Gy per fraction which is the standard of care. Radiotherapy (RT) has been integral in the treatment of GBM since the 1970s when Walker et al. showed that post-operative whole brain radiotherapy (WBRT) offered significant improvements in median survival time, and even more so when given with concomitant BCNU chemotherapy. Ensuing dose escalation studies found the optimal dose to be 60 Gy. Patients could not tolerate escalation to higher doses than 60 Gy with WBRT due to unacceptable toxicity. Even with WBRT of 60 Gy, a huge volume of healthy brain tissue was unnecessarily treated with high-dose radiation; recurrences with WBRT remained overwhelmingly local. Hochberg and Pruitt (1980) found that after WBRT only 3% of recurrences were outside 2 cm of the margins of the primary tumor. With the rise of the CT scan in the 1980s and the MRI in the 1990s, along with subsequent improvements in three-dimensional conformal radiation, partial brain RT (PBRT) became practical since tumor margins could be visualized and irradiated more accurately. - Subsequently, WBRT was shown to provide no survival benefit over PBRT at the same dosage; - thus, the latter took over as the standard of care.

Primary Outcome

Median survival (in months from time of diagnosis to date of death) was calculated and reported below. It is very difficult to draw efficacy outcomes for outcome measure #1 and #2 because of incomplete enrollment.

Interventions

  • RADIATION Radiation therapy
  • DRUG Chemotherapy with Temodar.

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2013-05
Est. Completion 2019-09
Phase Phase 2
University of Maryland, Baltimore

560 total trials

Why NCT01822275 stopped before completion

NCT01822275 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 2 interventions - of which Radiation therapy is the first listed.

NCT01822275 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01822275 about?

NCT01822275 is a clinical study titled "Phase II Trial of Low-Dose Whole Brain Radiotherapy With Concurrent Temozolomide and Adjuvant Temozolomide in Patients With Newly-Diagnosed Glioblastoma Multiforme". In the current proposed trial the role of the low-dose WBRT (0.15 Gy) would be to safely treat the microscopic distant GBM cells outside of the high dose RT region and sensitize the gross tumor, while the focal radiation dose (1.85 Gy) to the gross tumor will bring the total tumor dose of 2 Gy per f...

What is the current status of trial NCT01822275?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2013-05. Estimated completion is 2019-09.

What interventions are being tested in trial NCT01822275?

The interventions under investigation include: Radiation therapy (RADIATION), Chemotherapy with Temodar. (DRUG).

Who is sponsoring clinical trial NCT01822275?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01822275's enrollment target sits among peer trials

24 1756th of 2000 higher than 217 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01822275, the US trial registry maintained by the National Library of Medicine. NCT01822275 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.