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NCT00805961 · ClinicalTrials.gov registry record · Phase 2

RT, Temozolomide, and Bevacizumab Followed by Bevacizumab/Everolimus in First-line Treatment of GBM

A Phase 2 study, sponsored by SCRI Development Innovations.

Completed
Registry status
Phase 2
Development phase
68
Enrollment target

NCT00805961: Completed Phase 2 study, sponsored by SCRI Development Innovations.

NCT00805961 is a Phase 2 study that has completed, run by SCRI Development Innovations. The registered enrollment target is 68 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (49% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00805961, a Phase 2 study, has completed, sponsored by SCRI Development Innovations.

COMPLETED
Registry status
Phase 2
Development phase
68 participants
Enrollment target

Study Summary

In this phase II trial the investigators plan to incorporate two targeted agents, bevacizumab and everolimus, into the first-line multimodality therapy of glioblastoma. In the first portion of the treatment, bevacizumab will be added to standard concurrent radiation therapy plus temozolomide. After completing radiation therapy, patients will continue treatment with the combination of bevacizumab and everolimus.

Primary Outcome

Progression-free survival is defined as the duration of time from start of treatment to time of progression or death, whichever comes first.

Interventions

  • DRUG Bevacizumab
  • DRUG Temozolomide
  • DRUG Everolimus
  • RADIATION Radiation therapy

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2009-01
Est. Completion 2013-05
Phase Phase 2
SCRI Development Innovations

146 total trials

What the finished NCT00805961 record still lists

NCT00805961 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (49% lower).

The record links to 0 conditions, and to 4 interventions - of which Bevacizumab is the first listed.

NCT00805961 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00805961 about?

NCT00805961 is a clinical study titled "RT, Temozolomide, and Bevacizumab Followed by Bevacizumab/Everolimus in First-line Treatment of GBM". In this phase II trial the investigators plan to incorporate two targeted agents, bevacizumab and everolimus, into the first-line multimodality therapy of glioblastoma. In the first portion of the treatment, bevacizumab will be added to standard concurrent radiation therapy plus temozolomide. After ...

What is the current status of trial NCT00805961?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 68 participants. The study started on 2009-01. Estimated completion is 2013-05.

What interventions are being tested in trial NCT00805961?

The interventions under investigation include: Bevacizumab (DRUG), Temozolomide (DRUG), Everolimus (DRUG), Radiation therapy (RADIATION).

Who is sponsoring clinical trial NCT00805961?

This trial is sponsored by SCRI Development Innovations, which has 146 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00805961's enrollment target sits among peer trials

68 967th of 2000 higher than 1,027 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 NCT00805961, the US trial registry maintained by the National Library of Medicine. NCT00805961 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.