Clinical Trials Directory

Trials / Completed

CompletedNCT00385190

Study Evaluating the Pharmacokinetics of HCV-796 in Healthy Japanese Men

An Ascending Multiple Dose Study of the Safety, Tolerability, and Pharmacokinetics of Study Drug Administred Orally to Healthy Japanese Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (planned)
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer · Industry
Sex
Male
Age
20 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to assess the safety and tolerability of ascending multiple oral doses of HCV-796 in healthy Japanese male subjects.

Conditions

Interventions

TypeNameDescription
DRUGHCV-796

Timeline

Start date
2006-07-01
Primary completion
2006-11-01
Completion
2006-12-01
First posted
2006-10-06
Last updated
2009-08-18

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT00385190. Inclusion in this directory is not an endorsement.