Product Description
Mechanisms of Action: Vitamin K Antagonist
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: France | Luxembourg
Approved Indications: None
Known Adverse Events: None
Company: Daiichi Sankyo
Company Location: TOKYO M0 103-8426
Company CEO:
Additional Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 4: Atrial Fibrillation|Kidney Diseases|Venous Thrombosis|Pulmonary Embolism|Blood Coagulation Disorders|Calcinosis|Embolism and Thrombosis|Vascular Calcification|Hemostatic Disorders
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
PHRC-N/2020/BL-01 | P3 |
Unknown Status |
Unknown |
2026-11-30 |
|
AVKDIAL | P4 |
Terminated |
Atrial Fibrillation|Kidney Diseases |
2023-08-10 |
|
HEMA-HTP | N/A |
Completed |
Hypertension, Pulmonary |
2022-09-13 |
|
PRESAGE-ACO | N/A |
Completed |
Atrial Fibrillation |
2021-11-01 |