Study Evaluating IMA-638 in Healthy Japanese

This study has been completed.
Sponsor:
Information provided by:
Wyeth is now a wholly owned subsidiary of Pfizer
ClinicalTrials.gov Identifier:
NCT00340327
First received: June 16, 2006
Last updated: December 3, 2007
Last verified: December 2007

June 16, 2006
December 3, 2007
June 2006
Not Provided
Safety will be measured by evaluating physical examinations, vital signs, electrocardiograms (ECGs), and clinical laboratory test results.
Safety will be measured by evaluating physical examinations, vital signs, ECGs, and clinical laboratory test results.
Complete list of historical versions of study NCT00340327 on ClinicalTrials.gov Archive Site
Drug levels and associated biomarkers will be evaluated.
Same as current
Not Provided
Not Provided
 
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

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

Not Provided
Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Double-Blind
Primary Purpose: Diagnostic
Healthy
Drug: IMA-638
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
Not Provided
July 2007
Not Provided

Inclusion Criteria:

  • First generation healthy Japanese men and women of non-childbearing potential.
Both
20 Years to 45 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00340327
3174K1-101
Not Provided
Not Provided
Wyeth is now a wholly owned subsidiary of Pfizer
Not Provided
Study Director: Medical Monitor Wyeth is now a wholly owned subsidiary of Pfizer
Wyeth is now a wholly owned subsidiary of Pfizer
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP