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Sponsored by: |
Wyeth |
Information provided by: | Wyeth |
ClinicalTrials.gov Identifier: | NCT00427687 |
This study will evaluate the effect of AGG-523 administration on biomarkers related to osteoarthritis. Safety and tolerability of AGG-523 will also be assessed.
Condition | Intervention | Phase |
Osteoarthritis |
Drug: AGG-523 |
Phase I |
MedlinePlus related topics: | Osteoarthritis |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment |
Official Title: | A Randomized, Double-Blind, Placebo-Controlled, Multiple-Dose, Parallel-Group Study of the Pharmacodynamics, Safety, Tolerability, and Pharmacokinetics of AGG-523 Administered Orally to Subjects With Mild to Moderate Osteoarthritis |
Ages Eligible for Study: | 40 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion:
United States, California | |||||
Anaheim, California, United States, 92801 | |||||
United States, Florida | |||||
Miami, Florida, United States, 33143 | |||||
United States, Pennsylvania | |||||
Altoona, Pennsylvania, United States, 16635 |
Wyeth |
Study Director: | Medical Monitor | Wyeth |
Study ID Numbers: | 3189A1-104 |
First Received: | January 25, 2007 |
Last Updated: | August 1, 2008 |
ClinicalTrials.gov Identifier: | NCT00427687 |
Health Authority: | United States: Food and Drug Administration |
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