Clinical Trials Directory

Trials / Completed

CompletedNCT00340327

Study Evaluating IMA-638 in Healthy Japanese

An Ascending Single Dose Study of the Safety and Pharmacokinetics of IMA-638 Administered to Healthy Japanese Subjects

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

Summary

The purpose of this study is to evaluate the safety and drug levels for single, ascending doses of IMA-638 in healthy Japanese subjects.

Conditions

Interventions

TypeNameDescription
DRUGIMA-638

Timeline

Start date
2006-06-01
Completion
2007-07-01
First posted
2006-06-21
Last updated
2007-12-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00340327. Inclusion in this directory is not an endorsement.