Status:

COMPLETED

To Evaluate the Effect of Ritonavir or Omeprazole on the Pharmacokinetics of Samatasvir (IDX719) in Healthy Participants (MK-1894-006)

Lead Sponsor:

Merck Sharp & Dohme LLC

Conditions:

Chronic Hepatitis C Infection

Eligibility:

All Genders

19-65 years

Phase:

PHASE1

Brief Summary

This study is designed to evaluate the potential for an effect of Ritonavir (Norvir®) or omeprazole (Prilosec®) on the pharmacokinetics of samatasvir and to assess the safety and tolerability of the s...

Eligibility Criteria

Inclusion

  • Read and signed the written informed consent form (ICF) after the nature of the study has been fully explained.
  • All participants of childbearing potential must agree to use a double method of birth control (one of which must be a barrier) from Screening through at least 90 days after the last dose of the study drug.

Exclusion

  • Pregnant or breastfeeding.

Key Trial Info

Start Date :

February 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2013

Estimated Enrollment :

24 Patients enrolled

Trial Details

Trial ID

NCT01813552

Start Date

February 1 2013

End Date

March 1 2013

Last Update

January 22 2016

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To Evaluate the Effect of Ritonavir or Omeprazole on the Pharmacokinetics of Samatasvir (IDX719) in Healthy Participants (MK-1894-006) | DecenTrialz