- Trials with a EudraCT protocol (243)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
243 result(s) found for: Alzheimer Disease AND Alzheimers Disease AND Alzheimer's Disease.
Displaying page 4 of 13.
| EudraCT Number: 2016-000429-38 | Sponsor Protocol Number: PLX108-15 | Start Date*: 2016-08-31 | ||||||||||||||||
| Sponsor Name:Plexxikon Inc. | ||||||||||||||||||
| Full Title: A Phase 2a Study of the Safety, Tolerability, and Pharmacodynamic Effects of Pexidartinib 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: DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-005031-24 | Sponsor Protocol Number: 1289.5 | Start Date*: 2014-12-04 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A multi-centre, double-blind, parallel-group, randomised controlled study to investigate efficacy, safety and tolerability of orally administered BI 409306 during a 12-week treatment period compare... | |||||||||||||
| Medical condition: Patients with diagnosis of AD according to the following criteria: • Symptoms noticed by the patients and/or informant • Cognitive testing confirming symptoms • Biomarker evidence of AD patholog... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) PT (Completed) ES (Completed) BE (Completed) AT (Completed) NL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004012-13 | Sponsor Protocol Number: WN22018 | Start Date*: 2009-03-04 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: Estudio multicéntrico de búsqueda de dosis, randomizado, doble ciego, controlado con placebo, con grupos de tratamiento paralelos, de RO5313534 administrado como tratamiento adyuvante a donepezilo ... | |||||||||||||
| Medical condition: Enfermedad de Alzheimer leve a moderada Mild to moderate Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) SK (Completed) IT (Completed) DE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001403-11 | Sponsor Protocol Number: AVA102672 | Start Date*: 2006-09-27 | |||||||||||
| Sponsor Name:GlaxoSmithKline R&D Limited | |||||||||||||
| Full Title: A 54-week, double-blind, randomized, placebo-controlled, parallel-group study to investigate the effects of rosiglitazone (extended release tablets) as adjunctive therapy to donepezil on cognition ... | |||||||||||||
| Medical condition: Alzheimers Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) PT (Completed) ES (Completed) HU (Completed) AT (Completed) CZ (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012748-17 | Sponsor Protocol Number: ELN115727-301 | Start Date*: 2010-03-11 | |||||||||||
| Sponsor Name:Janssen Alzheimer Immunotherapy | |||||||||||||
| Full Title: A phase 3, multicenter, randomised, double-blind, placebo-controlled, parallel group, efficacy and safety trial of bapineuzumab (AAB-001, ELN115727) in subjects with mild to moderate Alzheimer's di... | |||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001273-23 | Sponsor Protocol Number: 2021NanoLi-CT01 | Start Date*: 2021-09-20 | ||||||||||||||||
| Sponsor Name:MEDESIS PHARMA SA | ||||||||||||||||||
| Full Title: A prospective, multicenter, with a first part randomized, placebo-controlled, parallel-group, double-blind period followed by an open-label trial period trial to evaluate the clinical safety and ef... | ||||||||||||||||||
| Medical condition: Sufficient clinical and paraclinical information for the diagnosis of Alzheimer’s Disease (AD) according to the international diagnosis criteria from McKhann G. M. et al. 2011 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-003966-38 | Sponsor Protocol Number: CADPT06A12201 | Start Date*: 2021-06-30 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: EXploratory PLatform trial on Anti-INflammatory agents in Alzheimer’s Disease (EXPLAIN-AD): A randomized, placebo controlled, multicenter platform study to evaluate the efficacy, safety, tolerabili... | |||||||||||||
| Medical condition: Mild cognitive impairment due to Alzheimer’s disease and mild Alzheimer’s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) IS (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002133-20 | Sponsor Protocol Number: ELN115727-351 | Start Date*: 2011-09-16 | |||||||||||
| Sponsor Name:Janssen Alzheimer Immunotherapy | |||||||||||||
| Full Title: A Phase 3 Extension, Multicenter, Double-Blind, Long Term Safety and Tolerability Treatment Trial of Bapineuzumab (AAB-001, ELN115727) in Subjects with Alzheimer's Disease Who Participated in Study... | |||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002598-36 | Sponsor Protocol Number: 16IC3372 | Start Date*: 2017-03-03 | |||||||||||||||||||||
| Sponsor Name:Imperial College London | |||||||||||||||||||||||
| Full Title: Randomised Clinical Trial of Noradrenergic Add-on Therapy with Extended-Release Guanfacine in Alzheimer's Disease | |||||||||||||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Temporarily Halted) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-006336-94 | Sponsor Protocol Number: MK-1942-008 | Start Date*: 2022-10-24 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
| Full Title: A Phase 2a/2b Randomized, Placebo-Controlled Clinical Study to Evaluate the Safety and Efficacy of MK-1942 as Adjunctive Therapy in Participants with Mild to Moderate Alzheimer’s Disease Dementia. | |||||||||||||
| Medical condition: Alzheimer’s Disease dementia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021218-50 | Sponsor Protocol Number: AB09004 | Start Date*: 2011-05-25 | |||||||||||
| Sponsor Name:AB Science | |||||||||||||
| Full Title: A multicenter, double-blind, placebo-controlled, randomised, parallel-group phase 3 study to evaluate the safety and efficacy of masitinib in patients with mild to moderate Alzheimer’s disease | |||||||||||||
| Medical condition: mild to moderate Alzheimer’s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prohibited by CA) ES (Completed) SK (Prohibited by CA) PL (Completed) GR (Completed) GB (GB - no longer in EU/EEA) BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023322-21 | Sponsor Protocol Number: NP031112-10B04 | Start Date*: 2011-04-13 | |||||||||||
| Sponsor Name:Noscira S.A | |||||||||||||
| Full Title: A multicenter, Randomized, Double-blind, Placebo-controlled, 4-arm, 26 week Parallel-Group Study to evaluate the Efficacy, Safety and Tolerability of Two Oral Doses and Two Regimes of Tideglusib vs... | |||||||||||||
| Medical condition: Alzheimer's Disease (mild to moderate) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) FI (Completed) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000503-17 | Sponsor Protocol Number: 331-12-284 | Start Date*: 2015-01-29 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 3, 12-week, Multicenter, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of Flexible Dosing of Brexpiprazole (OPC-34712) in the Treatme... | |||||||||||||
| Medical condition: Agitation Associated with Dementia of the Alzheimer’s Type | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) FI (Prematurely Ended) SI (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002102-31 | Sponsor Protocol Number: 221AD205 | Start Date*: 2019-03-20 | |||||||||||
| Sponsor Name:Biogen Idec Research Limited | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Parallel-Group, Double-Blind, Controlled Study of Aducanumab (BIIB037) in Subjects With Mild Cognitive Impairment due to Alzheimer’s Disease or With Mild Alzheim... | |||||||||||||
| Medical condition: Mild Cognitive Impairment due to Alzheimer's Disease and Mild Alzheimer's Dementia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) FR (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005260-14 | Sponsor Protocol Number: ACI-91-0801 | Start Date*: 2008-11-26 | |||||||||||
| Sponsor Name:AC Immune SA | |||||||||||||
| Full Title: A double-blind placebo-controlled study of the safety, tolerability and efficacy of 12 months’ treatment with ACI-91 in patients with mild to moderate Alzheimer’s Disease | |||||||||||||
| Medical condition: Mild to moderate Alzheimer’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004117-33 | Sponsor Protocol Number: H3B109689 | Start Date*: 2007-12-17 | |||||||||||
| Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
| Full Title: A single blind, placebo-controlled, randomised study in mild to moderate Alzheimer's disease patients to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK239512, a selec... | |||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005292-17 | Sponsor Protocol Number: TRx-237-008 | Start Date*: 2012-10-02 | |||||||||||
| Sponsor Name:TauRx Therapeutics Ltd | |||||||||||||
| Full Title: A Double-Blind, Placebo-Controlled, Randomised, 4-Week Safety and Tolerability Study of LMTM in Subjects with Mild to Moderate Alzheimer’s Disease on Pre-Existing Stable Acetylcholinesterase Inhibi... | |||||||||||||
| Medical condition: Alzheimer’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002004-32 | Sponsor Protocol Number: M10-985 | Start Date*: 2012-02-14 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo- and Active-Controlled Phase 2 Dose-Ranging Study to Evaluate the Efficacy and Safety of ABT-126 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: GB (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001478-28 | Sponsor Protocol Number: 3098B1-204-EU | Start Date*: 2007-02-28 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc., Clinical Research and Development | |||||||||||||
| Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, LONG-TERM EXTENSION STUDY TO DETERMINE THE SAFETY, TOLERABILITY, AND PRELIMINARY LONG TERM EFFICACY OF LECOZOTAN (SRA-333) SR IN PATIENTS WITH MILD TO MODER... | |||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) ES (Completed) GB (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004897-26 | Sponsor Protocol Number: Lu-11829A | Start Date*: 2008-05-23 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Memantine for the Long Term Management of Neuropsychiatric Symptoms in Alzheimer's disease - MAIN-AD | |||||||||||||
| Medical condition: Alzheimer's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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