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Lumiliximab

Alternative Names: lumiliximab
Latest Update: 2015-10-02
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: CD23 Inhibitor

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: N/A

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Biogen
Company Location: CAMBRIDGE MA 02142
Company CEO: Michel Vounatsos
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Lumiliximab

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Chronic Lymphoid Leukemia|Lymphocytic Chronic B-Cell Leukemia

Phase 1: Chronic Lymphoid Leukemia|Lymphocytic Chronic B-Cell Leukemia|Lymphoma, B-Cell

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
Lumiliximab in combination with FCR in the treatment of relapsed CLL

P2

Completed

Chronic Lymphoid Leukemia

2010-12-25

LUCID

P2

Terminated

Chronic Lymphoid Leukemia|Lymphocytic Chronic B-Cell Leukemia

2010-07-01

152CL202

P2

Terminated

Lymphocytic Chronic B-Cell Leukemia|Chronic Lymphoid Leukemia

2010-06-01

2008-002204-25

P2

Terminated

Chronic Lymphoid Leukemia

2010-03-22

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