A Follow-up Evaluation for Safety in Subjects Who Participated in a Phase 1 Study With BMS-986094 (INX-08189)
NCT01732848 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 113
Last updated 2014-08-15
Summary
The purpose of this study is to determine the rate of kidney or heart impairment, if any, in subjects who received BMS-986094 (INX-08189) in Phase 1 clinical trials
Conditions
- Healthy
- Hepatitis C
Interventions
- DRUG
-
BMS-986094/INX-08189
- DRUG
-
Placebo matching BMS-986094/INX-08189
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Bristol-Myers Squibb · Bristol-Myers Squibb
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-11-30
- Primary Completion
- 2014-06-30
- Completion
- 2014-06-30
Countries
- United States
- Puerto Rico
Study Locations
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