An Open Label Dose Escalation Study Of E7080
NCT00121719 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 82
Last updated 2023-06-22
Summary
The purpose of this study is to determine the maximum tolerated dose (MTD) of lenvatinib in patients with solid tumors or lymphomas.
Conditions
- Solid Tumor or Lymphoma
Interventions
- DRUG
-
Lenvatinib tablets taken orally, once daily.
Sponsors & Collaborators
-
Eisai Inc.
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-07-01
- Primary Completion
- 2009-06-19
- Completion
- 2019-03-01
Countries
- Netherlands
- United Kingdom
Study Locations
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