Ketoprofen in a topical patch formulation has been demonstrated to be effective for treating mild to moderate pain caused by various musculoskeletal disorders.
The objective of this study is to demonstrate the short-term multiple dose efficacy and safety of HKT-500 in subjects with pain caused by mild to moderate osteoarthritis of the knee. The goal of the study is to gather additional information about the analgesic efficacy and safety of repeated, 24-hour applications of 2 HKT-500 patches per knee for a total of 28 days in subjects with pain caused by mild to moderate osteoarthritis of the knee.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
380
2 topical patches applied once daily for 28 days
2 topical placebo patches applied once daily for 28 days
Change from the baseline of the WOMAC pain subscale score at Visit 6 (Day 14 ± 2 days)
Time frame: 14 days ± 2 days
WOMAC: Change from the baseline of the pain subscale score at Visit 5 (Day 7 ±1 day), Visit 7 (Day 21 ±3 days) and Visit 8 (Day 28 ±3 days)
Time frame: 28 days (±3 days)
WOMAC: Change from the baseline of the subscale scores for stiffness and physical function at Visit 5, Visit 6, Visit 7 and Visit 8
Time frame: 28 days (±3 days)
WOMAC: Change from the baseline of the composite score at Visit 5, Visit 6, Visit 7 and Visit 8
Time frame: 28 days (±3 days)
Pain Intensity differences at rest, on motion and of overall assessment using a VAS scale at each follow-up assessments time point through Day 28.
Time frame: 28 days
Subject's Global Assessment at Visit 6 and Visit 8
Time frame: 28 days (±3 days)
Investigator's Global Assessment at Visit 6 and Visit 8
Time frame: 28 days (±3 days)
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