ClinicalTrials.gov record
Completed Phase 3 Interventional

Study of IV Edotecarin Vs Temozolomide or Carmustine (BCNU) or Lomustine (CCNU) in Patients With Glioblastoma Multiforme

ClinicalTrials.gov ID: NCT00068952

Public ClinicalTrials.gov record NCT00068952. 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 6, 2026, 8:24 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 Phase III, Randomized, Open-Label Study Of IV Edotecarin Vs Temozolomide Or Carmustine (BCNU) Or Lomustine (CCNU) In Patients With Glioblastoma Multiforme At First Relapse After Alkylator-Based (NEO) Adjuvant Chemotherapy

Study identification

NCT ID
NCT00068952
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
118 participants

Conditions and interventions

Conditions

Interventions

  • Carmustine (BCNU) Drug
  • Edotecarin Drug
  • Lomustine (CCNU) Drug
  • Temozolomide 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
Jul 31, 2003
Primary completion
Not listed
Completion
Feb 28, 2006
Last update posted
Mar 31, 2008

2003 – 2006

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Pfizer Investigational Site Phoenix Arizona
Pfizer Investigational Site Little Rock Arkansas
Pfizer Investigational Site New Haven Connecticut
Pfizer Investigational Site Orlando Florida
Pfizer Investigational Site Atlanta Georgia
Pfizer Investigational Site Chicago Illinois
Pfizer Investigational Site Evanston Illinois
Pfizer Investigational Site Edgewood Kentucky
Pfizer Investigational Site Edgweood Kentucky
Pfizer Investigational Site Lexington Kentucky
Pfizer Investigational Site Boston Massachusetts
Pfizer Investigational Site Lebanon New Hampshire
Pfizer Investigational Site Edison New Jersey
Pfizer Investigational Site Summit New Jersey
Pfizer Investigational Site Cincinnati Ohio
Pfizer Investigational Site Philadelphia Pennsylvania
Pfizer Investigational Site Pittsburgh Pennsylvania
Pfizer Investigational Site Dallas Texas
Pfizer Investigational Site Charlottesville Virginia

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 33 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00068952, 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 Mar 31, 2008 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00068952 live on ClinicalTrials.gov.

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