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Completed Phase 2 Interventional Results available

BIBW 2992 (Afatinib) With or Without Daily Temozolomide in the Treatment of Patients With Recurrent Malignant Glioma

ClinicalTrials.gov ID: NCT00727506

Public ClinicalTrials.gov record NCT00727506. 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 Sep 3, 2026, 8:38 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

Phase I/II Trial of BIBW 2992 (Afatinib) in Treating Patients With Recurrent Glioblastoma Multiforme

Brief summary

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

Phase I Part: To determine the maximum tolerated dose (MTD) and pharmacokinetics of BIBW 2992 administered in combination with TMZ in patients with recurrent malignant gliomas (WHO Grade III and IV). Phase II Part: To estimate the efficacy and safety of BIBW 2992 monotherapy and BIBW 2992 / TMZ combination therapy compared to TMZ monotherapy (three treatment arms) in patients with recurrent GBM. To evaluate molecular determinants of response to BIBW 2992.

Study identification

NCT ID
NCT00727506
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
151 participants

Conditions and interventions

Conditions

Interventions

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 13, 2008
Primary completion
May 11, 2011
Completion
May 24, 2016
Last update posted
Aug 14, 2017

2008 – 2016

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
1200.36.0016 Boehringer Ingelheim Investigational Site Birmingham Alabama
1200.36.0012 Boehringer Ingelheim Investigational Site Phoenix Arizona
1200.36.0005 Boehringer Ingelheim Investigational Site Duarte California
1200.36.0014 Boehringer Ingelheim Investigational Site Los Angeles California
1200.36.0019 Boehringer Ingelheim Investigational Site Orlando Florida
1200.36.0023 Boehringer Ingelheim Investigational Site Atlanta Georgia
1200.36.0008 Boehringer Ingelheim Investigational Site Louisville Kentucky
1200.36.0002 Boehringer Ingelheim Investigational Site Boston Massachusetts
1200.36.0003 Boehringer Ingelheim Investigational Site Detroit Michigan
1200.36.0009 Boehringer Ingelheim Investigational Site New York New York
1200.36.0001 Boehringer Ingelheim Investigational Site Durham North Carolina
1200.36.0007 Boehringer Ingelheim Investigational Site Charleston South Carolina
1200.36.0020 Boehringer Ingelheim Investigational Site Memphis Tennessee
1200.36.0017 Boehringer Ingelheim Investigational Site Dallas Texas
1200.36.0010 Boehringer Ingelheim Investigational Site Houston Texas
1200.36.0011 Boehringer Ingelheim Investigational Site Charlottesville Virginia
1200.36.0022 Boehringer Ingelheim Investigational Site Seattle Washington

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00727506, 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 Aug 14, 2017 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00727506 live on ClinicalTrials.gov.

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