For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com
Inclusion Criteria:
- Healthy subjects
- Body Mass Index (BMI) of 18 to 30 kg/m2
- Ages 18 to 45 years, including
- Women of childbearing potential (WOCBP) on acceptable contraception and with negative pregnancy test and not breastfeeding
Exclusion Criteria:
- History or evidence of coagulopathy
- History or evidence of thrombosis such as deep vein thrombosis or other thromboembolic disease or having a first degree relative under 50 years of age with a history of thromboembolic disease
- Any significant acute or chronic medical illness or relevant trauma
- Any major surgery within 4 weeks of dosing (prior to dosing) or planned within 2 weeks after completion of the study
- History of heavy menstrual bleeding that has produced anemia within the past 1 year
- Current symptomatic or recent gastrointestinal disease or surgery that could impact the absorption of study drug
- History of smoking within 1 month prior to dosing
- Recent history (within 6 months of dosing) of pregnancy
- Use of hormonal contraceptives
- Exposure to any investigational drug or placebo within 4 weeks of study drug administration
- Use of any agent, including but not limited to Aspirin, Nonsteroidal anti-inflammatory drugs (NSAIDs), Anticoagulants, Fish oil capsules, Gingko, etc, that are known to increase the potential for bleeding, within 2 weeks prior to dosing
- History of any severe drug allergy including allergy to Heparin or history of Heparin-induced thrombocytopenia, hypersensitivity to PCCs or Factor Xa inhibitors, or history of allergy to human blood plasma derived products; history of any adverse drug reaction to Anticoagulants or Antiplatelet agents that resulted in excessive bleeding requiring medical intervention