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Completed Phase 1Phase 2 Interventional

Efaproxiral Plus Carmustine in Treating Patients With Progressive or Recurrent Malignant Glioma

ClinicalTrials.gov ID: NCT00005855

Public ClinicalTrials.gov record NCT00005855. 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 23, 2026, 10:08 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 I/II Study to Evaluate the Safety and Tolerance of Escalating Doses of RSR13 Administered With a Fixed Dose of BCNU Every Six Weeks in Patients With Recurrent Malignant Glioma

Brief summary

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

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of efaproxiral when given with carmustine and to see how well they work in treating patients with progressive or recurrent malignant glioma.

Study identification

NCT ID
NCT00005855
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
48 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
Jul 2000 (Type not available)
Primary completion
Not listed
Completion
Oct 2006 (Actual)
Last update posted
Jun 21, 2013

2000 – 2006

United States locations

U.S. sites
9
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
University of Alabama at Birmingham Comprehensive Cancer Center Birmingham Alabama 35294 —
H. Lee Moffitt Cancer Center and Research Institute at University of South Florida Tampa Florida 33612-9497 —
Winship Cancer Institute of Emory University Atlanta Georgia 30322 —
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21231-2410 —
Massachusetts General Hospital Cancer Center Boston Massachusetts 02114 —
Josephine Ford Cancer Center at Henry Ford Hospital Detroit Michigan 48202 —
Wake Forest University Comprehensive Cancer Center Winston-Salem North Carolina 27157-1096 —
Abramson Cancer Center of the University of Pennsylvania Philadelphia Pennsylvania 19104-4283 —
University of Texas Health Science Center at San Antonio San Antonio Texas 78229-3900 —

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 NCT00005855, 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 Jun 21, 2013 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00005855 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →