Overview

Study of TAK-901 in Adults With Advanced Solid Tumors or Lymphoma

Status:
Completed
Trial end date:
2011-11-01
Target enrollment:
Participant gender:
Summary
This study is being conducted to evaluate the safety profile and the Maximum Tolerated Dose (MTD) of TAK-901 in adult patients with advanced solid tumors or lymphoma. This study will help to identify the recommended phase 2 dose and infusion duration, and describe the pharmacokinetics of TAK-901.
Phase:
Phase 1
Details
Lead Sponsor:
Millennium Pharmaceuticals, Inc.