drugset / Trial / NCT00832117

Phase I Combination Ixabepilone + Cisplatin

NCT00832117

Phase 1 Completed 30 enrolled R-Pharm
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the highest dose of ixabepilone that can be given safely with cisplatin without causing severe or life-threatening side effects and for some patients with non-small cell lung cancer, the effects (good or bad) on your cancer will also be studied

Timeline

Start
2009-05
Primary completion
2011-01
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cisplatin Other / unclassified 60 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 80 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 100 mg/m2 Intravenous
Subject Ixabepilone Small molecule 32 mg/m2 Intravenous
Subject Ixabepilone Small molecule 40 mg/m2 Intravenous