- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
4 result(s) found for: Sulindac.
Displaying page 1 of 1.
| EudraCT Number: 2019-001496-36 | Sponsor Protocol Number: DDD19CRCSUL | Start Date*: 2019-07-15 |
| Sponsor Name:KU Leuven | ||
| Full Title: The intestinal disposition of sulindac in healthy volunteers | ||
| Medical condition: Healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000427-41 | Sponsor Protocol Number: CPPFAP-310 | Start Date*: 2014-05-15 |
| Sponsor Name:Cancer Prevention Pharmaceuticals, Inc. | ||
| Full Title: A Double-Blind, Randomized, Phase III Trial of the Safety and Efficacy of CPP-1X/Sulindac Compared With CPP-1X, Sulindac as Single Agents in Patients with Familial Adenomatous Polyposis (FAP) | ||
| Medical condition: Familial Adenomatous Polyposis (FAP) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) NL (Completed) ES (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-006051-12 | Sponsor Protocol Number: ICORG 06-03 | Start Date*: 2007-04-04 | |||||||||||
| Sponsor Name:ICORG | |||||||||||||
| Full Title: PHASE II TRIAL OF THE MULTI-DRUG RESISTANCE PROTEIN MODULATING AGENT SULINDAC IN COMBINATION WITH EPIRUBICIN IN PATIENTS WITH ADVANCED MELANOMA | |||||||||||||
| Medical condition: Metastatic malignant melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003721-22 | Sponsor Protocol Number: A4091058 | Start Date*: 2016-01-14 | ||||||||||||||||
| Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
| Full Title: A PHASE 3 RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED, MULTICENTER STUDY OF THE LONG-TERM SAFETY AND EFFICACY OF SUBCUTANEOUS ADMINISTRATION OF TANEZUMAB IN SUBJECTS WITH OSTEOARTHRITIS OF THE HIP ... | ||||||||||||||||||
| Medical condition: Osteoarthritis of the hip or knee | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BG (Completed) SK (Completed) LT (Completed) HR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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