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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 Oct 26, 2026, 4:39 PM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this clinical trial is to study Edotecarin in patients with the brain tumor glioblastoma multiforme (GBM) who have progression or first recurrence following initial treatment with surgery, radiation and 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

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 2003 (Type not available)
Primary completion
Not listed
Completion
Mar 2006 (Type not available)
Last update posted
Apr 1, 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 Apr 1, 2008 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00068952 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →