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Completed Phase 2 Interventional

Phase 2 Study of VELCADE Alone or VELCADE® Plus Docetaxel in Previously Treated Patients With Advanced Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00051974

Public ClinicalTrials.gov record NCT00051974. 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 21, 2026, 4:40 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

A Randomized, Multicenter, Open-Label, Phase 2 Study of VELCADE Alone or VELCADE Plus Docetaxel in Previously Treated Patients With Advanced Non-Small Cell Lung Cancer

Study identification

NCT ID
NCT00051974
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Millennium Pharmaceuticals, Inc.
Industry
Enrollment
155 participants

Conditions and interventions

Interventions

  • VELCADE™ (bortezomib) for Injection (formerly PS-341) 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
Nov 30, 2002
Primary completion
Aug 31, 2004
Completion
Not listed
Last update posted
Feb 10, 2008

Started 2002

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
U of Alambama at Birmingham Comprehensive Cancer Center Birmingham Alabama 35294
Cedars-Sinai Comprehensive Cancer Center Los Angeles California 90048
UCLA Medical Center Thoracic Malignancy Los Angeles California 90095
University of Colorado Health Sciences Center Aurora Colorado 80010
Yale University School Of Medicine New Haven Connecticut 06520
Univeristy of Florida Shands Cancer Center Gainesville Florida 32610
Sylvester Comprehensive Cancer Center Miami Florida 33136
Winship Cancer Institute Atlanta Georgia 30322
Atlanta VAMC Decatur Georgia 30033
Mass. General Hospital Hem/Onc. Associates Boston Massachusetts 02114
DBA Kansas City Cancer Centers Kansas City Missouri 64154
St. Louis University Health Sciences Center St Louis Missouri 63110
Washington University, Barnard Cancer Center St Louis Missouri 63110
Carolinas Hematology-Oncology Associates Charlotte North Carolina 28203
Duke University Medical Center Durham North Carolina 27710
Kimmel Cancer Center at Jefferson Philadelphia Pennsylvania 19107
Vanderbilt University-Clinical Trials Center Nashville Tennessee 37232
University of Texas MD Anderson Cancer Center Houston Texas 77030
Hunstman Cancer Institute-University of Utah Salt Lake City Utah 84112
University of Wisconsin Comprehensive Cancer Center Madison Wisconsin 53792

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 NCT00051974, 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 10, 2008 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00051974 live on ClinicalTrials.gov.

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