Lung Cancer Clinical Trial

CPG 7909 Injection in Non-Small Cell Lung Cancer

Summary

Eligible patients will be randomized in a ratio of 2:1 to receive either chemotherapy (a taxane and a platinum compound) plus CPG 7909 Injection or chemotherapy alone. Protocol therapy will be administered until disease progression or intolerable toxicity. CpG 7909 Injection will be administered subcutaneously, on Weeks 2 and 3 of each three-week cycle (days 8 and 15) and chemotherapy will be administered on Week 1 (Day 1). Patients will undergo complete disease evaluation at the end of every other treatment cycle until disease progression.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically or cytologically confirmed non-small cell lung cancer that is beyond surgical cure or that is metastatic (Stage IIIB or IV according to AJCC).
Patients must have measurable disease according to the RECIST criteria.

Exclusion Criteria:

Prior treatment with chemotherapy; patients may have received prior radiotherapy.
Patients with suspected or known CNS metastases.

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

116

Study ID:

NCT00070629

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 23 Locations for this study

See Locations Near You

Office of Ronald Yanagihara
Gilroy California, 95020, United States
Kenmar Research Institute, LLC
Los Angeles California, 90057, United States
Comprehensive Cancer Center of the Dessert
Palm Springs California, 92262, United States
Florida Cancer Specialist
Fort Myers Florida, 33901, United States
Indiana Hematology and Oncology Associates
Indianapolis Indiana, 46202, United States
Medical Center Vincennes
Vincennes Indiana, 47591, United States
Kentucky Cancer Clinic
Hazard Kentucky, 41701, United States
University of Minnesota
Minneapolis Minnesota, 55455, United States
Southeast Nebraska Hematology Oncology Consultants, PC
Lincoln Nebraska, 68516, United States
VA New Jersey Health Care System
East Orange New Jersey, 07018, United States
HemOnCare
Brooklyn New York, 11212, United States
Cancer Care of Western North Carolina
Asheville North Carolina, 28801, United States
Providence Portland Medical Center
Portland Oregon, 97213, United States
Cancer Care Institute of Carolina
Aiken South Carolina, 29801, United States
Charleston Hematology/Oncology, PA
Charleston South Carolina, 29403, United States
The Family Cancer Center
Collierville Tennessee, 38017, United States
Marshfield Clinic
Marshfield Wisconsin, 54449, United States
Queen Elizabeth II Health
Halifax Nova Scotia, B3H 1, Canada
Ottawa Regional Cancer Center
Ottawa Ontario, K1H 1, Canada
McGill University
Montreal Quebec, H2W 1, Canada
Staedtisches Krankenhaus Martha-Maria
Halle-Dolau , D-061, Germany
Universitätsklinikum Mannheim der Universität Heidelberg
Heidelberg , , Germany
St. Vincentius-Kliniken gAG, Hamatologie-Onkologie
Karlsruhe , D7613, Germany
Klinikum Rechts der Isar
Munchen , 81675, Germany

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

116

Study ID:

NCT00070629

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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