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Phase II Study Of BBR 3464 As Treatment In Patients With Sensitive Or Refractory Small Cell Lung Cancer After One Prior Chemotherapy Regimen
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.
OBJECTIVES: I. Determine the efficacy of BBR 3464 in terms of response rate in patients with sensitive or refractory metastatic small cell lung cancer. II. Determine the duration of response and time to progression in patients treated with this drug. III. Determine the overall survival of patients treated with this drug. IV. Determine the incidence and severity of toxic effects of this drug in this patient population. V. Determine the pharmacokinetics of this drug in this patient population. OUTLINE: This is a multicenter study. Patients are stratified according to disease (refractory vs sensitive). Patients receive BBR 3464 IV over 1 hour on day 1. Treatment repeats every 21 days for at least 3 courses in the absence of disease progression or unacceptable toxicity. Patients with complete or partial response or stable disease may receive up to 6 courses of therapy. Patients without progressive disease after 6 courses may continue treatment at the investigator's discretion. Patients are followed every 9 weeks for 3 years. PROJECTED ACCRUAL: A total of 24-74 patients (12-37 per stratum) will be accrued for this study.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Clinical Research Consultants, Inc
Hoover, Alabama, United States
Highlands Oncology Group, P.A.
Fayetteville, Arkansas, United States
Alta Bates Comprehensive Cancer Center
Berkeley, California, United States
Office of Peter D. Byeff
Southington, Connecticut, United States
Robert H. Lurie Comprehensive Cancer Center, Northwestern University
Chicago, Illinois, United States
Indiana Cancer Pavilion
Indianapolis, Indiana, United States
Michiana Hematology/Oncology P.C.
South Bend, Indiana, United States
University Hospital Lexington
Lexington, Kentucky, United States
Louisiana Oncology Associates
Lafayette, Louisiana, United States
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States
Start Date
November 1, 2000
Last Updated
July 24, 2008
BBR 3464
DRUG
Lead Sponsor
Theradex
NCT06066138
NCT07485114
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