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

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

Lymphocytic Chronic B-Cell Leukemia|Chronic Lymphoid 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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