drugset / Trial / NCT00374660

Study of Irofulven in Combination With Oxaliplatin in Patients With Advanced Solid Tumors

NCT00374660

Phase 1/2 Completed 63 enrolled Eisai Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the maximum tolerated dose (MTD) and to investigate the efficacy, safety and pharmacokinetics of irofulven combined with oxaliplatin in patients with advanced solid tumors.

Timeline

Start
2003-06
Primary completion
2007-04
Completion
2007-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxaliplatin Small molecule 40 mg/m2
Subject Oxaliplatin Small molecule 50 mg/m2
Subject Oxaliplatin Small molecule 60 mg/m2
Subject Oxaliplatin Small molecule 70 mg/m2
Subject Oxaliplatin Small molecule 80 mg/m2
Subject irofulven Small molecule 0.3 mg/kg
Subject irofulven Small molecule 0.4 mg/kg

Indications