Clinical Trials Directory

Trials / Completed

CompletedNCT00448032

Study Evaluating Multiple Oral Doses of PPM-204 in Healthy Japanese Male Subjects

A Multiple Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of Ppm-204 Administered Orally to Healthy Male Japanese Subjects

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

Summary

A study evaluating the safety and pharmacokinetics of multiple oral doses of an investigational oral diabetic agent when given to healthy Japanese male volunteers.

Conditions

Interventions

TypeNameDescription
DRUGPPM-204

Timeline

Start date
2006-11-01
Completion
2007-03-01
First posted
2007-03-15
Last updated
2007-12-05

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT00448032. Inclusion in this directory is not an endorsement.