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Study of ABT-333 in Both Healthy Volunteers and Hepatitis C Virus (HCV) + Genotype 1 Infected Subjects
The purpose of this study is to assess the safety, tolerability, pharmacokinetics of ABT-333 in healthy volunteers and the antiviral activity in HCV infected subjects.
Details
| Lead sponsor | AbbVie |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 133 |
| Start date | 2008-06 |
Conditions
- HCV Infection
Interventions
- ABT-333
- Placebo
Primary outcomes
- Analysis of pharmacokinetic variables and mean change in HCV RNA level from baseline. — approximately 1 week or less
- Analysis of safety measures, including but not limited to tabulation of adverse events, physical exam, clinical lab results (include chemistry, hematology and urine) and vital signs. — approximately 1 week