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Terminated Phase 2 Interventional

A Phase II Study of Temozolomide and O6-Benzylguanine (O6-BG) in Patients With Temozolomide-Resistant Anaplastic Glioma

ClinicalTrials.gov ID: NCT00389090

Public ClinicalTrials.gov record NCT00389090. 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 18, 2026, 12:55 AM EDT

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

Brief summary

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

This is an open-label, multicenter, phase II trial, assessing the antitumor activity, and safety of temozolomide in combination with O6-BG in patients with temozolomide-resistant anaplastic glioma.

Study identification

NCT ID
NCT00389090
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
32 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
Oct 2006 (Type not available)
Primary completion
Jun 2008 (Actual)
Completion
Feb 2009 (Actual)
Last update posted
Feb 9, 2012

2006 – 2009

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
AOI Pharmaceuticals Investigative Site Los Angeles California 90033 —
AOI Pharmaceuticals Investigative Site Orlando Florida 32804 —
AOI Pharmaceuticals Investigative Site Chicago Illinois 60611 —
AOI Pharmaceuticals Investigative Site Evanston Illinois 60201 —
AOI Pharmaceuticals Investigative Site Lexington Kentucky 40536 —
AOI Pharmaceuticals Investigative Site Louisville Kentucky 40202 —
AOI Pharmaceuticals Investigative Site Minneapolis Minnesota 54407 —
AOI Pharmaceuticals Investigative Site Durham North Carolina 27710 —
AOI Pharmaceuticals Investigative Site Greenville South Carolina 29605 —
AOI Pharmaceuticals Investigative Site Dallas Texas 75246 —
AOI Pharmaceuticals Investigative Site Houston Texas 77024 —
AOI Pharmaceuticals Investigative Site Salt Lake City Utah 84132 —

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 NCT00389090, 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 Feb 9, 2012 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00389090 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →