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Not listed Phase 2 Interventional

BBR 3464 in Treating Patients With Metastatic Small Cell Lung Cancer That Has Not Responded to Previous Treatment

ClinicalTrials.gov ID: NCT00014547

Public ClinicalTrials.gov record NCT00014547. 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, 8:11 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

Phase II Study Of BBR 3464 As Treatment In Patients With Sensitive Or Refractory Small Cell Lung Cancer After One Prior Chemotherapy Regimen

Brief summary

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

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of BBR 3464 in treating patients who have metastatic small cell lung cancer that has not responded to previous treatment.

Study identification

NCT ID
NCT00014547
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Theradex
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

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
Nov 2000 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Jul 24, 2008

Started 2000

United States locations

U.S. sites
18
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
Clinical Research Consultants, Inc Hoover Alabama 35216 —
Highlands Oncology Group, P.A. Fayetteville Arkansas 72703 —
Alta Bates Comprehensive Cancer Center Berkeley California 94704 —
Office of Peter D. Byeff Southington Connecticut 06489 —
Robert H. Lurie Comprehensive Cancer Center, Northwestern University Chicago Illinois 60611-3013 —
Indiana Cancer Pavilion Indianapolis Indiana 46202 —
Michiana Hematology/Oncology P.C. South Bend Indiana 46617 —
University Hospital Lexington Lexington Kentucky 40536-0084 —
Louisiana Oncology Associates Lafayette Louisiana 70506 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Washington University Barnard Cancer Center St Louis Missouri 63110 —
Theradex Princeton New Jersey 08543 —
Lineberger Comprehensive Cancer Center, UNC Chapel Hill North Carolina 27599-7295 —
Cancer Services Columbus Ohio 43214 —
Oklahoma Oncology Inc. Tulsa Oklahoma 74104 —
University of Pennsylvania Cancer Center Philadelphia Pennsylvania 19104-4283 —
Cancer Center at the University of Virginia Charlottesville Virginia 22908 —
Massey Cancer Center Richmond Virginia 23298-0037 —

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 NCT00014547, 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 24, 2008 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00014547 live on ClinicalTrials.gov.

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