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Completed Phase 2 Interventional Results available

BIBW 2992 (Afatinib) in Head & Neck Cancer

ClinicalTrials.gov ID: NCT00514943

Public ClinicalTrials.gov record NCT00514943. 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 Jul 24, 2026, 7:53 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 Randomized, Open-label Phase II Study of BIBW 2992 Versus Cetuximab (Erbitux) in Patients With Metastatic or Recurrent Head and Neck Squamous Cell Carcinoma (HNSCC) After Failure of Platinum-containing Therapy With a Cross-over Period for Progressing Patients

Study identification

NCT ID
NCT00514943
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
124 participants

Conditions and interventions

Interventions

  • BIBW 2992 Drug
  • Cetuximab Drug

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 31, 2007
Primary completion
Feb 28, 2010
Completion
Jun 30, 2013
Last update posted
Jul 25, 2016

2007 – 2013

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
1200.28.0010 Boehringer Ingelheim Investigational Site Stanford California
1200.28.0001 Boehringer Ingelheim Investigational Site Chicago Illinois
1200.28.0005 Boehringer Ingelheim Investigational Site Chicago Illinois
1200.28.0011 Boehringer Ingelheim Investigational Site Harvey Illinois
1200.28.0022 Boehringer Ingelheim Investigational Site Indianapolis Indiana
1200.28.0024 Boehringer Ingelheim Investigational Site Baltimore Maryland
1200.28.0012 Boehringer Ingelheim Investigational Site Ann Arbor Michigan
1200.28.0021 Boehringer Ingelheim Investigational Site Saint Joseph Michigan
1200.28.0016 Boehringer Ingelheim Investigational Site Rochester Minnesota
1200.28.0002 Boehringer Ingelheim Investigational Site Jackson Mississippi
1200.28.0006 Boehringer Ingelheim Investigational Site Omaha Nebraska
1200.28.0008 Boehringer Ingelheim Investigational Site New Hyde Park New York
1200.28.0017 Boehringer Ingelheim Investigational Site Chapel Hill North Carolina
1200.28.0004 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina
1200.28.0013 Boehringer Ingelheim Investigational Site Charleston South Carolina
1200.28.0007 Boehringer Ingelheim Investigational Site Houston Texas
1200.28.0009 Boehringer Ingelheim Investigational Site Madison Wisconsin
1200.28.0020 Boehringer Ingelheim Investigational Site Milwaukee Wisconsin

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00514943, 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 Jul 25, 2016 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00514943 live on ClinicalTrials.gov.

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