Product Description
Mechanisms of Action: N/A
Novel Mechanism: No
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: Regeneron
Company Location: TARRYTOWN NY 10591
Company CEO: Leonard S. Schleifer
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 2: Wet Macular Degeneration|Neovascular age-related macular degeneration
Phase 1: Wet Macular Degeneration
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
CAPELLA | P2 |
Terminated |
Wet Macular Degeneration|Neovascular age-related macular degeneration |
2016-08-17 |
|
R2176-3-AMD-1303 | P1 |
Completed |
Wet Macular Degeneration |
2014-12-01 |