HuMax-CD4 in Non-Cutaneous T-Cell Lymphoma
NCT00877656 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 21
Last updated 2024-03-18
Summary
The purpose of this study is to assess the safety and efficacy of treatment of non-cutaneous T-cell lymphoma with treatment with CD4.
Conditions
- T Cell Lymphoma
Interventions
- BIOLOGICAL
-
HuMax-CD4
Active treatment
Sponsors & Collaborators
-
Emergent BioSolutions
lead INDUSTRY
Principal Investigators
-
Abhay Patki, PhD · Genmab
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-08-31
- Primary Completion
- 2006-01-31
- Completion
- 2008-12-31
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