Status:

COMPLETED

Bioavailability Study Comparing Modified Release To Immediate Release Apixaban Tablets In Healthy Volunteers

Lead Sponsor:

Pfizer

Collaborating Sponsors:

Bristol-Myers Squibb

Conditions:

Thrombosis

Eligibility:

All Genders

18-45 years

Phase:

PHASE1

Brief Summary

To estimate the pharmacokinetics of apixaban when administered as three different modified release formulation tablets relative to that when apixaban is administered as an immediate release tablet

Eligibility Criteria

Inclusion

  • Healthy male or female patients
  • Body Mass Index (BMI) of 17.5 to 30.5 kg/m2

Exclusion

  • Any condition possibly affecting drug absorption
  • History or evidence of abnormal bleeding or clotting disorder

Key Trial Info

Start Date :

June 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 1 2009

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT00914641

Start Date

June 1 2009

End Date

August 1 2009

Last Update

August 25 2009

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Pfizer Investigational Site

New Haven, Connecticut, United States, 06511