- Trials with a EudraCT protocol (94)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
94 result(s) found for: Donepezil 10 mg.
Displaying page 1 of 5.
EudraCT Number: 2005-003789-40 | Sponsor Protocol Number: DON DF 1 | Start Date*: 2005-11-11 |
Sponsor Name:Pharmapnea AB | ||
Full Title: A randomized, four-way cross-over, double-blind, controlled study of oral donepezil (2, 5, 10 mg) in patients with moderate to severe obstructive sleep apnea. | ||
Medical condition: Moderate to severe obstructive sleep apnea. Males and females; aged 25 to 65 years, previously diagnosed OSA defined as an oxygen desaturation (4%) index of 15 or more per hour of sleep obtained fr... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005442-20 | Sponsor Protocol Number: E2020-G000-334 | Start Date*: 2008-09-04 |
Sponsor Name:Eisai Limited | ||
Full Title: Randomized, Double-Blind, Placebo-Controlled Study of Efficacy and Safety of Donepezil Hydrochloride in Preadolescent and Adolescent Children with Attention Impairment Following Cancer Treatment | ||
Medical condition: Attention impairment after cancer treatment | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) ES (Completed) FR (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005435-28 | Sponsor Protocol Number: E2020-G000-333 | Start Date*: 2008-09-03 |
Sponsor Name:Eisai Limited | ||
Full Title: Randomized, Double-Blind, Placebo-Controlled Study of Efficacy and Safety of Donepezil Hydrochloride in Preadolescent and Adolescent Children with Attention Impairment Following Cancer Treatment | ||
Medical condition: Attention impairment after cancer treatment | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) NL (Completed) FR (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005472-27 | Sponsor Protocol Number: 70639 | Start Date*: 2009-03-30 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Die antidementive Therapie mit Acetylcholinesteraseinhibitoren: Untersuchung von Plasmakonzentrationen, Arzneimittelinteraktionen und Therapieeffekt in Abhängigkeit von genetischen Polymorphismen | ||
Medical condition: Anhand der vorliegenden Studie soll untersucht werden, ob genetische Polymorphismen im CYP2D6-, im MDR1- oder im ACHE Gen mit sub- bzw. supratherapeutischen Wirkstoffspiegeln im Plasma, mit relevan... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002007-33 | Sponsor Protocol Number: A2581078 | Start Date*: 2004-11-25 |
Sponsor Name:Pfizer Inc. | ||
Full Title: An 80-week, randomized, multi center, parallel group, double-blind study of the efficacy and safety of atorvastatin 80 mg plus an acetylcholinesterase inhibitor versus an acetylcholinesterase inhib... | ||
Medical condition: Alzheimer Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001172-36 | Sponsor Protocol Number: 2006/123 | Start Date*: 2007-08-16 | |||||||||||
Sponsor Name:King's College London | |||||||||||||
Full Title: Donepezil and Memantine in moderate to severe Alzheimer's Disease | |||||||||||||
Medical condition: Moderate to severe alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004888-54 | Sponsor Protocol Number: E2020-G000-326 | Start Date*: 2007-12-07 | |||||||||||
Sponsor Name:Eisai Ltd | |||||||||||||
Full Title: Double-Blind, Parallel-Group Comparison of 23 mg Donepezil Sustained Release to 10 mg Donepezil Immediate Release in Patients with Moderate to Severe Alzheimer’s Disease | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) LT (Completed) ES (Completed) AT (Completed) DK (Completed) SE (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015170-35 | Sponsor Protocol Number: 5137 | Start Date*: 2012-01-27 |
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: Multicentre UK Study of the Acetylcholinesterase Inhibitor Donepezil in Early Dementia Associated with Parkinson's Disease (MUSTARDD-PD) | ||
Medical condition: Parkinson's disease with mild dementia (PDD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-004946-27 | Sponsor Protocol Number: E2020-A001-219 | Start Date*: 2017-05-18 |
Sponsor Name:Eisai Inc. | ||
Full Title: A 10-Week, Double-Blind, Placebo-Controlled Study To Evaluate The Efficacy And Safety Of Donepezil Hydrochloride (Aricept) In The Treatment Of The Cognitive Dysfunction Exhibited By Children With D... | ||
Medical condition: Down Syndrome, Cognitive Dysfunction | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2004-001100-12 | Sponsor Protocol Number: 1198.022 | Start Date*: 2004-08-09 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma Ges mbH | |||||||||||||
Full Title: A multi-centre, double-blind, parallel-group, randomised, placebo-controlled study to investigate the safety and tolerability of 0.25, 0.5 and 1.0 mg NS 2330 orally and once daily during a 14-week ... | |||||||||||||
Medical condition: Mild to moderate dementia of the Alzheimer's type | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017317-30 | Sponsor Protocol Number: SC09-02 | Start Date*: 2010-02-02 | |||||||||||
Sponsor Name:FONDAZIONE SANTA LUCIA | |||||||||||||
Full Title: Investigating the neuroprotective effect of Donepezil in patients affected by Alzheimer disease: a 12 month longitudinal analysis of the peripheral levels of neurotrophins and inflammatory factors ... | |||||||||||||
Medical condition: Alzheimer`s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005161-18 | Sponsor Protocol Number: DEB-ZTSR-201 | Start Date*: 2007-01-17 | |||||||||||
Sponsor Name:Debiopharm | |||||||||||||
Full Title: A randomised, double-blind, double-dummy, oral donepezil controlled study on the safety and efficacy of repeated monthly subcutaneaous injections of a sustained-release implant of ZT-1 in patients ... | |||||||||||||
Medical condition: moderate Alzheimer disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001751-17 | Sponsor Protocol Number: IIBSP-DON-2022-43 | Start Date*: 2023-07-27 |
Sponsor Name:Institut de Recerca Hospital de la Santa Creu i Sant Pau - IIB Sant Pau | ||
Full Title: Multicenter, randomized, double-blind, placebo-controlled clinical trial evaluating the efficacy and safety of donepezil versus placebo in mild cognitive impairment associated with Parkinson's disease | ||
Medical condition: Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012035-15 | Sponsor Protocol Number: CL2-38093-009 | Start Date*: 2009-10-07 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Safety and efficacy of S 38093 and donepezil, during 4 weeks, in patients with mild to moderate Alzheimer's Disease. An international, multi-centre, randomised, double-blind, placebo controlled, ph... | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003410-15 | Sponsor Protocol Number: 6251 7976 | Start Date*: 2005-11-21 |
Sponsor Name:Neurology Unit | ||
Full Title: A twelve-month double-blind placebo-controlled cross-over study of the effect ofAricept treatment on cognitive dysfunction in multiple sclerosis. | ||
Medical condition: Multiple sclerosis is a devastating inflammation in the central nervous system and it can often give cognitive dysfunction, affecting memory, mental concentration. Lately it has been shown that the... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002957-37 | Sponsor Protocol Number: RVT-101-3001 | Start Date*: 2016-04-22 | |||||||||||
Sponsor Name:Axovant Sciences Ltd. | |||||||||||||
Full Title: A Phase 3, double-blind, randomized study of RVT-101 versus placebo when added to existing stable donepezil treatment in subjects with mild to moderate Alzheimer’s disease | |||||||||||||
Medical condition: Alzheimer’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) CZ (Completed) SK (Completed) ES (Completed) BG (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002707-10 | Sponsor Protocol Number: SJ-596 | Start Date*: 2018-04-10 | ||||||||||||||||||||||||||
Sponsor Name:Regional Dementia Research Centre, Dept of Neurology | ||||||||||||||||||||||||||||
Full Title: Serum-monitoring of anti-dementia drugs, and the relevance to side-effects, clinical efficacy and compliance | ||||||||||||||||||||||||||||
Medical condition: Dementia in Alzheimers Disease, Parkinsons Disease and Dementia with Lewy Bodies | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000826-37 | Sponsor Protocol Number: AZ3110865 | Start Date*: 2008-07-14 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study AZ3110865, a study comparing SB-742457 or donepezil versus placebo in subjects with mild-to-moderate Alzheimer’s disease | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) EE (Completed) BG (Completed) DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004764-22 | Sponsor Protocol Number: 14862A | Start Date*: 2014-09-10 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Randomised, double-blind, parallel-group, placebo-controlled, fixed-dose study of Lu AE58054 in patients with mild-moderate Alzheimer’s disease treated with donepezil; Study 2 | |||||||||||||
Medical condition: Alzheimer´s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) EE (Completed) IT (Completed) LT (Completed) PT (Completed) FI (Completed) IE (Completed) HU (Completed) HR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011582-88 | Sponsor Protocol Number: 41470956 | Start Date*: 2009-05-28 | |||||||||||
Sponsor Name:St James Hospital | |||||||||||||
Full Title: The differential effects of donepezil and placebo on EEG/ ERP measures and fMRI in mild cognitive impairment and elderly controls | |||||||||||||
Medical condition: Amnestic Mild cognitive Impairment (aMCI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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