Status:

COMPLETED

Evaluate the Pharmacokinetics of BMS-986177 From Two Formulations in Healthy Participants

Lead Sponsor:

Bristol-Myers Squibb

Conditions:

Thrombosis

Eligibility:

All Genders

18-55 years

Phase:

PHASE1

Brief Summary

Assess the pharmacokinetics (fasting and fed), safety, and tolerability of BMS-986177 following oral dosing of Form A and Form B

Eligibility Criteria

Inclusion

  • Body mass index 18.0 to 32.0 kg/m2, inclusive
  • Women must not be of childbearing potential (cannot become pregnant)

Exclusion

  • Any significant acute or chronic medical illness
  • Head injury in the last 2 years
  • History of bleeding disorder including rectal bleeding (ie, hemorrhoids), spontaneous nosebleeds, etc.
  • Other protocol defined inclusion / exclusion criteria could apply

Key Trial Info

Start Date :

November 15 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 28 2017

Estimated Enrollment :

12 Patients enrolled

Trial Details

Trial ID

NCT03362437

Start Date

November 15 2017

End Date

December 28 2017

Last Update

March 14 2018

Active Locations (1)

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1

Quotient Clinical

Ruddington, Nottingham, United Kingdom, NG11 6JS