Product Description
Mechanisms of Action: C5 Inhibitor
Novel Mechanism: No
Modality: Antibody
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Procter and Gamble
Company Location: CINCINNATI OH 45202
Company CEO: Jon R. Moeller
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Myocardial Infarction|Inflammation|Heart Failure|Myocardial Ischemia|Coronary Artery Disease|Heart Block|Pulmonary Infarction|Chest Pain|Myocardial Reperfusion Injury
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
APEX-AMI | P3 |
Completed |
Myocardial Infarction |
2007-05-01 |
54% |
APEX-AMI | P3 |
Terminated |
Myocardial Ischemia|Myocardial Reperfusion Injury|Myocardial Infarction |
2006-08-08 |
|
PRIMO-CABG II | P3 |
Completed |
Myocardial Infarction|Pulmonary Infarction |
2006-02-01 |
|
PRIMO-CABG II | P3 |
Completed |
Coronary Artery Disease |
2005-10-01 |
40% |