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Completed Phase 2 Interventional Results available

Temozolomide Alone or in Combination With Thalidomide and/or Isotretinoin and/or Celecoxib in Treating Patients Who Have Undergone Radiation Therapy for Glioblastoma Multiforme

ClinicalTrials.gov ID: NCT00112502

Public ClinicalTrials.gov record NCT00112502. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 12:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Factorial-Design, Phase II Trial of Temozolomide Alone and in Combination With Possible Permutations of Thalidomide, Isotretinoin and/or Celecoxib as Post-Radiation Adjuvant Therapy of Glioblastoma Multiforme

Study identification

NCT ID
NCT00112502
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
M.D. Anderson Cancer Center
Other
Enrollment
178 participants

Conditions and interventions

Interventions

  • Celecoxib Drug
  • Isotretinoin Drug
  • Temozolomide Drug
  • Thalidomide Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2005
Primary completion
Aug 31, 2014
Completion
Aug 31, 2014
Last update posted
Oct 17, 2021

2005 – 2014

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Hembree Mercy Cancer Center at St. Edward Mercy Medical Center Fort Smith Arkansas 72913
University of Texas MD Anderson Cancer Center at Orlando Orlando Florida 32806-2134
CCOP - Atlanta Regional Atlanta Georgia 30342-1701
CCOP - Central Illinois Decatur Illinois 62526
CCOP - Wichita Wichita Kansas 67214-3882
CCOP - Grand Rapids Grand Rapids Michigan 49503
CCOP - Kalamazoo Kalamazoo Michigan 49007-3731
CCOP - Kansas City Kansas City Missouri 64131
Cancer Research for the Ozarks Springfield Missouri 65804
Arthur G. James Cancer Hospital and Richard J. Solove Research Institute at Ohio State University Comprehensive Cancer Center Columbus Ohio 43210-1240
CCOP - Upstate Carolina Spartanburg South Carolina 29303
University of Texas MD Anderson Cancer Center Houston Texas 77030-4009

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00112502, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 17, 2021 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00112502 live on ClinicalTrials.gov.

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