Overview

An Open Label Phase I Dose Escalation Study of E7080 Administered to Patients With Solid Tumors

Status:
Completed
Trial end date:
2008-11-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to determine the maximum tolerable dose (MTD) and the related effects of E7080 administered to patients with solid tumors that are resistant to approved existing anti-tumor therapies, or for which no appropriate treatment is available.
Phase:
Phase 1
Details
Lead Sponsor:
Eisai Inc.
Treatments:
Lenvatinib