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Phase II Study of Oxaliplatin and Navelbine for Second-Line Treatment of Advanced NSCLC. Summary The purpose of this study is to determine the response rate to treatment with oxaliplatin and Navelbine in patients with previously treated NSCLC. Oxaliplatin and Navelbine have not been clinically evaluated yet. However, Navelbine has been safely administered with other platinum compounds.
View Full Description Full Description This is a non-randomized trial for patients with previously treated Non-small cell lung cancer . Each patient will receive 6 cycles of chemotherapy consisting of Oxaliplatin and Navelbine. Oxaliplatin is given intravenously every 21 days and Navelbine is administered Intravenously on day 1 and day 8 every 21 days.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Locally advanced or metastatic non-small cell lung cancer that has recurred, progressed, or failed to respond to previous systemic chemo. Measurable disease Good performance status (ECOG 0,1 or 2) Exclusion Criteria: Previously treated with Oxaliplatin or Navelbine Symptomatic CNS metastases
Check Your Eligibility
Let’s see if you might be eligible for this study.
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There are 2 Locations for this study
Integrated Community Oncology Network Jacksonville Florida, 32256, United States
More Info
Integrated Community Oncology Network Orange Park Florida, 32073, United States
More Info How clear is this clinincal trial information?
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