drugset / Trial / NCT00395772
Once-daily Oral Direct Factor Xa Inhibitor BAY59-7939 in Patients With Acute Symptomatic Deep-vein Thrombosis
Phase 2
Completed
543 enrolled
Bayer
Johnson & Johnson Pharmaceutical Research & Development, L.L.C. · collab
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to determine the optimal dose of BAY 59-7939 and to compare the safety and effectiveness of this new drug with the standard way of treatment of deep vein thrombosis (heparin infusion plus one of the vitamin K antagonists), taking into account new events of thrombosis and pulmonary embolism and bleeding risk.
Timeline
- Start
- 2004-12
- Primary completion
- —
- Completion
- 2005-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Rivaroxaban | Other / unclassified | 20 mg | Oral |
| Subject | Rivaroxaban | Other / unclassified | 30 mg | Oral |
| Subject | Rivaroxaban | Other / unclassified | 40 mg | Oral |