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Terminated Phase 2 Interventional Results available

Phase II Trial of BIBW 2992 (Afatinib) in Genetically Pre-screened Cancers With EGFR and/or HER2 Gene Amplification.

ClinicalTrials.gov ID: NCT00748709

Public ClinicalTrials.gov record NCT00748709. 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 22, 2026, 8:05 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

An Open Label Phase II Trial of BIBW 2992 (Afatinib) in Genetically Pre-screened Cancers With EGFR and/or HER2 Gene Amplification or EFGR Activating Mutations.

Brief summary

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

This is a Phase II open-label exploratory trial of BIBW 2992 administered to patients with tumors of various histologies found to possess EGFR and/or HER2 gene amplification, or EGFR activating mutations.

Study identification

NCT ID
NCT00748709
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
20 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
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 1, 2008 (Actual)
Primary completion
Nov 1, 2010 (Actual)
Completion
Not listed
Last update posted
Feb 11, 2025

Started 2008

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
1200.26.3 Boehringer Ingelheim Investigational Site Los Angeles California — —
1200.26.11 Boehringer Ingelheim Investigational Site Denver Colorado — —
1200.26.9 Boehringer Ingelheim Investigational Site Indianapolis Indiana — —
1200.26.1 Boehringer Ingelheim Investigational Site Boston Massachusetts — —
1200.26.13 Boehringer Ingelheim Investigational Site Las Vegas Nevada — —
1200.26.4 Boehringer Ingelheim Investigational Site Albany New York — —
1200.26.2 Boehringer Ingelheim Investigational Site New York New York — —
1200.26.7 Boehringer Ingelheim Investigational Site Kettering Ohio — —
1200.26.12 Boehringer Ingelheim Investigational Site Dallas Texas — —
1200.26.8 Boehringer Ingelheim Investigational Site Tyler Texas — —
1200.26.6 Boehringer Ingelheim Investigational Site Norfolk Virginia — —
1200.26.10 Boehringer Ingelheim Investigational Site Vancouver 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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00748709, 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 11, 2025 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00748709 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →