drugset / Trial / NCT00794781

A Phase 1, Multicenter, Open-Label, Dose-Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of E6201 in Subjects With Advanced Solid Tumors

NCT00794781

Phase 1 Completed 55 enrolled Eisai Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the maximum tolerated dose (MTD), safety, tolerability, pharmacokinetics, pharmacodynamics and preliminary anti-tumor activity of E6201 in subjects with advanced solid tumors.

Timeline

Start
2008-06-22
Primary completion
2011-08-01
Completion
2015-10-15

Drugs

EvaluationDrugModalityDoseRoute
Subject E6201 Small molecule 20 mg/m2 Intravenous

Indications