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.
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.
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There are 23 Locations for this study
Gilroy California, 95020, United States
Los Angeles California, 90057, United States
Palm Springs California, 92262, United States
Fort Myers Florida, 33901, United States
Indianapolis Indiana, 46202, United States
Vincennes Indiana, 47591, United States
Hazard Kentucky, 41701, United States
Minneapolis Minnesota, 55455, United States
Lincoln Nebraska, 68516, United States
East Orange New Jersey, 07018, United States
Brooklyn New York, 11212, United States
Asheville North Carolina, 28801, United States
Portland Oregon, 97213, United States
Aiken South Carolina, 29801, United States
Charleston South Carolina, 29403, United States
Collierville Tennessee, 38017, United States
Marshfield Wisconsin, 54449, United States
Halifax Nova Scotia, B3H 1, Canada
Ottawa Ontario, K1H 1, Canada
Montreal Quebec, H2W 1, Canada
Halle-Dolau , D-061, Germany
Heidelberg , , Germany
Karlsruhe , D7613, Germany
Munchen , 81675, Germany
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