drugset / Trial / NCT01780987

AStudy To Evaluate Safety And Eficacy Of Apixaban In Japanese Acute Deep Vein Thrombosis (DVT) And Pulmonary Embolism (PE) Patients

NCT01780987

Phase 3 Completed 80 enrolled Pfizer Bristol-Myers Squibb · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to investigate safety of apixaban in Japanese acute DVT/PE subjects when symptomatic DVT/PE subjects are treated with 10 mg BID apixaban for 7 days as initial therapy followed by 5 mg BID apixaban for 23 weeks as long-term therapy (total treatment period is 24 weeks)

Timeline

Start
2013-01
Primary completion
2014-09
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Apixaban Small molecule 5 mg
Comparator Heparin Other / unclassified
Comparator Warfarin Small molecule