Study Evaluating LXR-623 in Healthy Japanese Adults
This study has been completed.
Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Information provided by:
Wyeth is now a wholly owned subsidiary of Pfizer
ClinicalTrials.gov Identifier:
NCT00385489
First received: October 5, 2006
Last updated: August 6, 2009
Last verified: August 2009
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Purpose
The purpose of this study is to evaluate the safety of LXR-623 in healthy Japanese subjects.
| Condition | Intervention | Phase |
|---|---|---|
|
Healthy |
Drug: LXR-623 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Single Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of LXR-623 Administered Orally to Healthy Japanese Male Subjects. |
Further study details as provided by Wyeth is now a wholly owned subsidiary of Pfizer:
Eligibility| Ages Eligible for Study: | 20 Years to 45 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Healthy, Japanese Males aged 20-45 years
Exclusion Criteria:
- A history or active presence of clinically important medical disease
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00385489 History of Changes |
| Other Study ID Numbers: | 3201A1-102 |
| Study First Received: | October 5, 2006 |
| Last Updated: | August 6, 2009 |
| Health Authority: | Japan: Pharmaceuticals and Medical Devices Agency |
ClinicalTrials.gov processed this record on June 18, 2013