Clinical Trials Directory

Trials / Completed

CompletedNCT00505973

Study Evaluating the Safety and Tolerability of SCA-136 in Healthy Japanese Male Subjects

An Ascending Multiple Dose Study of the Safety, Pharmacokinetics, and Pharmacodynamics of SCA-136 Administered 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

This study is being conducted to assess the safety and tolerability of ascending multiple oral doses of SCA-136 administered to healthy Japanese male subjects.

Conditions

Interventions

TypeNameDescription
DRUGSCA-136

Timeline

Start date
2007-07-01
Completion
2007-10-01
First posted
2007-07-25
Last updated
2007-12-05

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT00505973. Inclusion in this directory is not an endorsement.