Product Description
Mechanisms of Action: ETa Antagonist
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Gilead Sciences
Company Location: FOSTER CITY CA 94404
Company CEO: Daniel P. O’Day
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Hypertension|Resistant Hypertension
Phase 2: Myocardial Ischemia|Coronary Artery Disease|Hypertension
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
Darusentan | P2 |
Completed |
Coronary Artery Disease|Myocardial Ischemia |
2011-08-01 |
|
DORADO-AC-EX | P3 |
Terminated |
Resistant Hypertension |
2010-02-24 |
|
Darusentan | P3 |
Terminated |
Hypertension |
2010-02-01 |
|
Darusentan | P3 |
Terminated |
Hypertension |
2010-02-01 |