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Completed Phase 2 Interventional

A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00073151

Public ClinicalTrials.gov record NCT00073151. 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 2, 2026, 3:50 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 Phase II Study of ABT-751 in Patients With Non-Small Cell Lung Cancer Refractory to Taxane Regimens

Brief summary

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

The purpose of the study is to determine if ABT-751 will decrease tumors, and determine how long the tumor shrinkage can be maintained in patients with non-small cell lung cancer. Patients will receive ABT-751 by mouth daily for 21 days. Patients will be off drug for 7 days before starting the next cycle of drug.

Study identification

NCT ID
NCT00073151
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Abbott
Industry
Enrollment
30 participants

Conditions and interventions

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
Aug 31, 2003
Primary completion
Not listed
Completion
Dec 31, 2005
Last update posted
Nov 28, 2007

2003 – 2006

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Oncology Hematology Group of South Florida Miami Florida
Florida Cancer Institute New Port Richey Florida
University of Chicago Medical Center Chicago Illinois 60637-1460
University of Maryland Greenbaum Cancer Center Baltimore Maryland 21201-1595
Oncology & Hematology Associates of Kansas City, PA Kansas City Missouri 64111
Washington University School of Medicine St Louis Missouri 63110-1093
Albany Regional Cancer Center Albany New York
Raleigh Hematology Oncology Cary North Carolina
Dayton Oncology and Hematology Kettering Ohio
Cancer Care Associates Oklahoma City Oklahoma
Cancer Centers of the Carolinas Greenville South Carolina
West Cancer Clinic Memphis Tennessee 38120
Texas Oncology Dallas Texas
Texas Oncology Fort Worth Texas
Cancer Care Northwest Spokane Washington
Northwest Cancer Specialists Vancouver Washington
University of Wisconsin Comprehensive Cancer Center Madison Wisconsin 53792-5666

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 NCT00073151, 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 Nov 28, 2007 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00073151 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →