CLINICAL TRIALS PROFILE FOR KETOPROFEN
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505(b)(2) Clinical Trials for Ketoprofen
Trial Type | Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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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 | >Sponsor | >Phase | >Start Date | >Summary |
All Clinical Trials for Ketoprofen
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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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 | APR Applied Pharma Research s.a. | 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. |
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. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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