Status:

COMPLETED

Study to Assess the Effect of BMS-791325 on the Pharmacokinetics of Midazolam in Healthy Subjects

Lead Sponsor:

Bristol-Myers Squibb

Conditions:

Hepatitis C

Eligibility:

All Genders

18-49 years

Phase:

PHASE1

Brief Summary

The purpose of this study is to assess the effect of BMS-791325 on the pharmacokinetics of the CYP3A4 Probe Midazolam.

Eligibility Criteria

Inclusion

  • Healthy male and female subjects aged 18 to 49 years, with BMI of 18-32 kg/m²
  • Women who are not of childbearing potential

Exclusion

  • Women of childbearing potential
  • Women who are pregnant, breastfeeding, or unwilling or unable to use an acceptable method of birth control.
  • Gastrointestinal disease that may impact the absorption of study drug
  • History of any chronic respiratory disease (asthma, COPD)

Key Trial Info

Start Date :

May 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2013

Estimated Enrollment :

48 Patients enrolled

Trial Details

Trial ID

NCT00996879

Start Date

May 1 2013

End Date

September 1 2013

Last Update

May 6 2014

Active Locations (1)

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1

Wcct Global, Llc

Cypress, California, United States, 90630