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Completed Phase 2 Interventional

A Phase II Study of Epothilone Analog BMS-247550 in Patients With Non-Small Cell Lung Cancer Who Have Failed First Line Platinum Based Chemotherapy

ClinicalTrials.gov ID: NCT00035516

Public ClinicalTrials.gov record NCT00035516. 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, 2:09 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

The purpose of this clinical research study is to learn if BMS-247550 can shrink or slow the growth of the cancer in patients with non-small cell lung cancer who have failed first-line platinum based chemotherapy. The safety of this treatment will also be studied.

Study identification

NCT ID
NCT00035516
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
R-Pharm
Industry
Enrollment
Not listed

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
Jan 31, 2001
Primary completion
Mar 31, 2004
Completion
Mar 31, 2004
Last update posted
Feb 9, 2016

2001 – 2004

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Un of California Davis Cancer Center Sacramento California 958177
Mount Sinai Medical Center Miami Beach Florida 33140
H Lee Moffitt Cancer Center Tampa Florida 33612
Rush Presbyterian St Lukes ME Chicago Illinois 60612-3828
Consultants in Blood Disorders Louisville Kentucky 40207
Ochsner Cancer Institute New Orleans Louisiana 70121
University of Maryland Greenbaum Cancer Center Baltimore Maryland 21201
Lahey Clinic Burlington Massachusetts 01805
University of Missouri/Ellis Fischel Cancer Center Columbia Missouri 65203
Dartmouth-Hitchcock /Norris Cotton Cancer Center Lebanon New Hampshire 03756
Cancer Institute of New Jersey New Brunswick New Jersey 08901
Unviversity of North Carolina Chapel Hill North Carolina 27599
Sarah Cannon Cancer Center Nashville Tennessee 37203
Vanderbilt University Med School Div of Medical Oncology Nashville Tennessee 37232-5536
University of Wisconsin Hospital 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 NCT00035516, 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 9, 2016 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00035516 live on ClinicalTrials.gov.

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