drugset / Trial / NCT00069264

Study of E7389 in Patients With Advanced Solid Tumors

NCT00069264

Phase 1 Completed 33 enrolled Eisai Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To determine the maximum tolerated dose of E7389 in patients with advanced solid tumors that have progressed following standard therapy or for which no standard therapy exists.

Timeline

Start
2003-09
Primary completion
2005-03
Completion
2005-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Eribulin Small molecule 0.25 mg/m2 Intravenous

Indications