HKT-500-US12 In Adult Patients With OA Knee Pain

• Status: Completed
• Trial end date: 2008-08-01
• Target enrollment: 0
• Participant gender: All

Summary

The objective of this study is to characterize the analgesic properties of single dose study of HKT-500 in subjects with pain caused by mild to moderate OA of the knee

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Hisamitsu Pharmaceutical Co., Inc.
• Treatments: Analgesics; Ketoprofen

Criteria

Inclusion Criteria:

• male or female 45 years of age or older

• with osteoarthritis of the knee

Exclusion Criteria:

• subject is a woman of childbearing potential

• who has a positive urine pregnancy test,

• is lactating, or who is not surgically sterile