A Phase I/Ib, Multicenter, Open-Label, Dose Escalation Study of E7080 in

Clinical Trial Summary

The purpose of this study is to study the safety of E7080 administered to patients with solid tumors or lymphomas.

Please note: this study is now recruiting patients with advanced and/or metastatic melanoma only.

In the current phase of this study, To determine the MTD and the pharmacokinetic profile of E7080 when given as continuous daily (qd) dosing in combination with temozolomide.

See also
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NCT number	NCT00121680
Study type	Interventional
Source	Eisai Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	July 2005
Completion date	May 2015

A Phase I/Ib, Multicenter, Open-Label, Dose Escalation Study of E7080 in Patients With Solid Tumors and in Combination With Temozolomide in Patients With Advanced and/or Metastatic Melanoma

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms