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Clinical Trials/NL-OMON36726
NL-OMON36726
Completed
N/A

A One-Way Drug-Drug Interaction Study to Assess the Effect of Ritonavir-boosted Atazanavir on the Pharmacokinetics, Safety and Tolerability of BMS-790052 in Healthy Subjects - BMS-790052/ritonavir-boosted atazanavir drug-drug interaction study

Bristol-Myers Squibb0 sites14 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hepatitis C
Sponsor
Bristol-Myers Squibb
Enrollment
14
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age: 18\-49 years, inclusive
  • BMI: 18\.0 \- 32\.0 kg/m2, inclusive
  • Women of child bearing potential should use adequate contraception (e.g., double barrier method) until at least 4 weeks after last dose of study medication

Exclusion Criteria

  • \- Any significant acute or chronic medical illness.
  • \- Current or recent (within 3 months of study drug administration) gastrointestinal disease indicated as clinically relevant by the Medical Investigator.
  • \- Any major surgery within 4 weeks of study drug administration.
  • \- Any gastrointestinal surgery that could impact upon the absorption of study drug.
  • \- Donation of blood or plasma to a blood bank or in a clinical study (except a screening visit) within 90 days of study drug administration.
  • \- Blood transfusion within 90 days of study drug administration.
  • \- Inability to tolerate oral medication.
  • \- Inability to swallow oral medication in the form of tablets or capsules.
  • \- Inability to be venipunctured and/or tolerate venous access.
  • \- Smoking more than 5 cigarettes per day.

Outcomes

Primary Outcomes

Not specified

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