Lung Cancer Clinical Trial

A Comparison Between BMS-690514 and Erlotinib in Patients Who Were Previously Treated for NSCLC

Summary

The purpose of this study is to improve disease control and survival for patients who were treated with chemotherapy using BMS-690514 over erlotinib

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

ECOG PS of 0 or 1
Histologically confirmed NSCLC
Adequate amount of tumor (archived or fresh) for biomarker evaluation
Received one to two regimens of chemotherapy (with at least one platinum-containing)
Serum creatinine of less than 1.0 mg/dL or a 24 hour creatinine clearance of greater than 60 mL/min
Stable control of blood pressure on agents other than calcium channel blockers
Women of child-bearing potential must avoid pregnancy or maintain adequate contraception
Must be able to swallow pills and take the medications at the same time every day on an empty stomach

Exclusion Criteria:

ECOG PS 2 or greater
Women unwilling to avoid pregnancy or use adequate contraception
Symptomatic brain metastases
Recent history of TIA, CVA, or thrombotic/thromboembolic event (within 6 months)
History of hemoptysis greater than 10 mL/day
Significant cardiovascular disease
Uncontrolled diarrhea, Crohn's disease, ulcerative colitis, or any malabsorptive disease
History of use of other TKIs
Uncontrolled hypertension
HIV+

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

141

Study ID:

NCT00743938

Recruitment Status:

Completed

Sponsor:

Bristol-Myers Squibb

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There are 28 Locations for this study

See Locations Near You

Yale University School Of Medicine
New Haven Connecticut, 06520, United States
Hematology Oncology, P.C.
Stamford Connecticut, 06902, United States
Mass General Hospital
Boston Massachusetts, 02114, United States
Henry Ford Hospital
Detroit Michigan, 48202, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
Piedmont Hematology Oncology Associates, Pllc
Winston-salem North Carolina, 27103, United States
Oregon Health & Science University
Portland Oregon, 97239, United States
Hema/Oncology Assoc. Of Nepa
Dunmore Pennsylvania, 18512, United States
Cancer Center Of The Carolinas
Greenville South Carolina, 29605, United States
Local Institution
Bahia Blanca Buenos Aires, , Argentina
Local Institution
La Plata Buenos Aires, 1900, Argentina
Local Institution
Buenos Aires , , Argentina
Local Institution
Cordoba , X5000, Argentina
Local Institution
La Rioja , 5300, Argentina
Local Institution
Montreal Quebec, H3T 1, Canada
Local Institution
Sherbrooke Quebec, J1H 5, Canada
Local Institution
Lyon Cedex 08 , 69373, France
Local Institution
Marseille Cedex 20 , 13915, France
Local Institution
Strasbourg , 67000, France
Local Institution
Toulouse , 31052, France
Local Institution
Villejuif Cedex , 94800, France
Local Institution
Gyeonggi-do , 410-7, Korea, Republic of
Local Institution
Seoul , 135-7, Korea, Republic of
Local Institution
Seoul , 138-7, Korea, Republic of
Local Institution
Otwock , 05-40, Poland
Local Institution
Barcelona , 08035, Spain
Local Institution
Madrid , 28046, Spain
Local Institution
Vizcaya , 48903, Spain
Local Institution
Taipei , 100, Taiwan
Local Institution
Taipei , 112, Taiwan

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

141

Study ID:

NCT00743938

Recruitment Status:

Completed

Sponsor:


Bristol-Myers Squibb

How clear is this clinincal trial information?

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