Trial Information
Phase I Alimta Combination With BMS-275183 (Oral Taxane)
Inclusion Criteria:
- Advanced or metastatic pretreated NSCLC
- Measurable disease
- Adequate hematologic, hepatic and renal functions.
- ECOG Performance Status 0-2
Exclusion Criteria:
- Inability to swallow capsules
- Recent significant cardiovascular disease
- Women who are pregnant or breastfeeding
Type of Study:
Interventional
Study Design:
Endpoint Classification: Safety/Efficacy Study, Primary Purpose: Treatment
Authority:
United States: Food and Drug Administration
Study ID:
CA165-021
NCT ID:
NCT00103831
Start Date:
Completion Date:
Related Keywords:
- Non-Small Cell Lung Cancer
- NSCLC - non-small cell lung cancer
- Carcinoma, Non-Small-Cell Lung
- Lung Neoplasms
Name | Location |
Local Institution |
Aurora, Colorado |
Local Institution |
Duluth, Minnesota |