Product Description
Mechanisms of Action: BLyS Antagonist
Novel Mechanism: No
Modality: Antibody
Route of Administration: Subcutaneous,Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Eli Lilly
Company Location: INDIANAPOLIS IN 46285
Company CEO: David A. Ricks
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Arthritis, Rheumatoid|Lupus Erythematosus, Systemic
Phase 2: Arthritis, Rheumatoid|Multiple Myeloma|Multiple Sclerosis, Relapsing-Remitting|Kidney Failure, Chronic
Phase 1: Multiple Myeloma|Arthritis, Rheumatoid
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
Illuminate-X | P3 |
Terminated |
Lupus Erythematosus, Systemic |
2015-10-01 |
|
H9S-JE-JDCI | P1 |
Completed |
Multiple Myeloma |
2015-02-01 |
|
ILLUMINATE-2 | P3 |
Terminated |
Lupus Erythematosus, Systemic |
2014-12-10 |
|
ILLUMINATE-X | P3 |
Completed |
Lupus Erythematosus, Systemic |
2014-12-10 |