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Last Updated: May 16, 2021

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CLINICAL TRIALS PROFILE FOR KETOPROFEN

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505(b)(2) Clinical Trials for Ketoprofen

This table shows clinical trials for potential 505(b)(2) applications. See the next table for all clinical trials
Trial Type Trial ID Title Status Sponsor Phase Start Date Summary
New Formulation NCT04678076 Bioequivalence of Ketoprofen Oral Gel vs Ketoprofen Lysine Salt as Granules for Oral Solution Completed Cross Research S.A. Phase 1 2018-07-23 This is a single dose, open-label, randomised, two period, two-way cross-over, two stage bioequivalenve study with the aim to investigate the bioequivalence between a new formulation of ketoprofen 25 mg versus OKI 80 mg granules for oral solution (half sachet), after single dose administration in two consecutive periods to healthy voluteers under fed conditions.
New Formulation NCT04678076 Bioequivalence of Ketoprofen Oral Gel vs Ketoprofen Lysine Salt as Granules for Oral Solution Completed Aziende Chimiche Riunite Angelini Francesco S.p.A Phase 1 2018-07-23 This is a single dose, open-label, randomised, two period, two-way cross-over, two stage bioequivalenve study with the aim to investigate the bioequivalence between a new formulation of ketoprofen 25 mg versus OKI 80 mg granules for oral solution (half sachet), after single dose administration in two consecutive periods to healthy voluteers under fed conditions.
>Trial Type >Trial ID >Title >Status >Phase >Start Date >Summary

All Clinical Trials for Ketoprofen

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00108810 Transdermal Ketoprofen to Treat Mild to Moderate Osteoarthritis (OA) Pain of the Knee Completed ZARS Pharma Inc. Phase 2 2005-04-01 The purpose of the study is to evaluate the safety and effectiveness of the investigational ketoprofen patch with a controlled heating patch, compared to placebo (inactive substance) for the treatment of pain caused by osteoarthritis.
NCT00188071 Postoperative Pain After Medical Abortion Under Local Anesthesia : Comparison of Several Analgesic Regimen Completed University Hospital, Angers N/A 2002-09-01 - To compare postoperative analgesia by paracetamol 1gr or ketoprofen 100 mg or the combination of these two analgesics - each treatment beeing allocated by randomization
NCT00265304 A Long-Term Safety Study of IDEA-033 in Comparison to Oral Naproxen for the Treatment of Osteoarthritis of the Knee Completed IDEA AG Phase 2 2005-07-01 The purpose of this study is to evaluate the long-term safety of IDEA-033 (an anti-inflammatory pain-relieving drug applied to the skin) in comparison to naproxen (an anti-inflammatory pain-relieving drug taken by mouth) for the treatment of osteoarthritis of both knees.
NCT00317733 Ketoprofen in Transfersome Compared to Oral Celecoxib and Placebo for Pain Associated With Osteoarthritis of the Knee Completed IDEA AG Phase 2 1969-12-31 The purpose of this study is to determine the safety and effectiveness of 110 mg ketoprofen in Transfersome applied to the skin twice daily as compared to placebo and oral celecoxib 200 mg per day for the relief of signs and symptoms of osteoarthritis of the knee for a period of six weeks.
NCT00351104 Efficacy and Safety of Ketoprofen Topical Patch 20% in the Treatment of Pain Associated With Ankle Sprain or Strain Completed Endo Pharmaceuticals Phase 3 2006-06-01 The purpose of this study is to evaluate the effect of a ketoprofen topical patch on the pain associated with ankle sprain or strain.
NCT00352625 Ketoprofen Topical Patch 20% in the Treatment of Pain Associated With Shoulder, Elbow or Knee Tendonitis or Bursitis Completed Endo Pharmaceuticals Phase 3 2006-06-01 The purpose of this study is to evaluate the effect of a ketoprofen topical patch on the pain associated with tendonitis or bursitis of the shoulder, elbow or knee.
NCT00365586 Ketoprofen Topical Patch, 20% in the Treatment of Pain Associated With Osteoarthritis Flare of the Knee Completed Endo Pharmaceuticals Phase 3 2006-08-01 The purpose of this study is to evaluate the effect of a ketoprofen topical patch on the pain associated with Osteoarthritis Flare of the Knee.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Ketoprofen

Condition Name

Condition Name for Ketoprofen
Intervention Trials
Pain, Postoperative 8
Postoperative Pain 6
Pain 6
Migraine 5
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Condition MeSH

Condition MeSH for Ketoprofen
Intervention Trials
Pain, Postoperative 18
Osteoarthritis 13
Osteoarthritis, Knee 11
Migraine Disorders 5
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Clinical Trial Locations for Ketoprofen

Trials by Country

Trials by Country for Ketoprofen
Location Trials
United States 137
Brazil 15
Italy 15
France 13
Mexico 5
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Trials by US State

Trials by US State for Ketoprofen
Location Trials
Texas 11
North Carolina 7
Florida 7
California 7
New York 6
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Clinical Trial Progress for Ketoprofen

Clinical Trial Phase

Clinical Trial Phase for Ketoprofen
Clinical Trial Phase Trials
Phase 4 30
Phase 3 34
Phase 2/Phase 3 3
[disabled in preview] 15
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Clinical Trial Status

Clinical Trial Status for Ketoprofen
Clinical Trial Phase Trials
Completed 47
Not yet recruiting 19
Recruiting 13
[disabled in preview] 12
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Clinical Trial Sponsors for Ketoprofen

Sponsor Name

Sponsor Name for Ketoprofen
Sponsor Trials
IDEA AG 5
Sanofi 4
University Hospital, Clermont-Ferrand 4
[disabled in preview] 15
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Sponsor Type

Sponsor Type for Ketoprofen
Sponsor Trials
Other 82
Industry 38
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Serving leading biopharmaceutical companies globally:

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