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Efficacy and Safety Study of PG201 Tablet in Patients With Osteoarthritis

Osteoarthritis of the Knee Clinical Trial

Official title:
For an 8-week, Single Center, Randomized, Double Blind, Placebo Controlled Exploratory Clinical Study to Assess the Efficacy, Dose Response and Safety of PG201 Tablet in Patients With Osteoarthritis

Clinical Trial Summary

The objective of this study was to explore the efficacy, dose-response and safety of PG201 tablet in Korean patients with osteoarthritis.

Clinical Trial Description

In this study, the PG201 extract, the study drug, was administered twice daily after a meal to two investigational groups, the lower-dose group and the higher-dose group. The efficacy of each of dose group was compared to that of the control group to determine if there was a statistically significant difference between the investigational groups and the placebo group. In addition, the efficacy between the lower dose group and the high dose group was also compared to determine if there was a statistically significant difference. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01122485
Study type Interventional
Source Helixmith Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date December 2006
Completion date September 2009
View Details
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