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Study Evaluation LXR-623 in Healthy Adults

Healthy Subjects Clinical Trial

Official title:
A Multiple Ascending Dose Study of the Safety, Pharmacokinetics, and Pharmacodynamics of LXR-623 Administered Orally to Healthy Subjects

Clinical Trial Summary

To evaluate the safety and tolerability of multiple doses of LXR in healthy adults.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00379860
Study type Interventional
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact
Status Terminated
Phase Phase 1
Start date October 2006
Completion date January 2007
View Details
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