- Trials with a EudraCT protocol (359)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
359 result(s) found for: Alzheimer Disease AND Dementia.
Displaying page 15 of 18.
| EudraCT Number: 2020-002511-22 | Sponsor Protocol Number: 20-05 | Start Date*: 2023-06-08 |
| Sponsor Name:Amsterdam UMC VUmc | ||
| Full Title: Synaptic density and tau pathology in Alzheimer's disease | ||
| Medical condition: Amyloid-beta positive individuals across the Alzheimer's disease continuum | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002606-37 | Sponsor Protocol Number: FBB-01-02-15 | Start Date*: 2015-09-24 |
| Sponsor Name:Piramal Imaging Ltd | ||
| Full Title: Multicenter study to explore the impact of florbetaben (FBB) in change of diagnosis in patients who are evaluated for AD at the CMRR, and are eligible for analysis of CSF according to HAS recommend... | ||
| Medical condition: Alzheimer Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-001184-25 | Sponsor Protocol Number: WN42444 | Start Date*: 2022-01-31 | |||||||||||
| Sponsor Name:Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, PARALLEL-GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF GANTENERUMAB IN PARTICIPANTS AT RISK FOR OR AT THE EARLIEST STAGE... | |||||||||||||
| Medical condition: Alzheimer's Disease (AD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) SE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004656-22 | Sponsor Protocol Number: IIBSP-THK-2015-77 | Start Date*: 2017-10-10 |
| Sponsor Name:Institut de Recerca HSCSP | ||
| Full Title: Pilot study of the [18F]THK-5351 positron emission tomography (PET) tracer in different tauopathies. | ||
| Medical condition: Taupatías | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-004454-42 | Sponsor Protocol Number: DIABMIND | Start Date*: 2018-04-27 | |||||||||||||||||||||
| Sponsor Name:Vall d'Hebron Research Institute | |||||||||||||||||||||||
| Full Title: English A pilot interventional study to arrest the progression of cognitive decline in diabetic patients at high risk of developing Alzheimer's disease by reducing hypoglycemic events. | |||||||||||||||||||||||
| Medical condition: Cognitive decline in patients affected with mild cognitive impairment | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-004244-28 | Sponsor Protocol Number: BAN2401-G000-303 | Start Date*: 2023-04-17 | |||||||||||
| Sponsor Name:Eisai Ltd. | |||||||||||||
| Full Title: AHEAD 3-45 Study: A Placebo-Controlled, Double-Blind, Parallel Treatment Arm, 216 Week Study with an Extension Phase to Evaluate Efficacy and Safety of Treatment With BAN2401 in Subjects With Prec... | |||||||||||||
| Medical condition: Preclinical Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000445-39 | Sponsor Protocol Number: ACI-24-1801 | Start Date*: 2018-06-19 | |||||||||||
| Sponsor Name:AC Immune SA | |||||||||||||
| Full Title: A Phase II Double-Blind, Randomized, Placebo-Controlled, Adaptive Design Study to Assess the Safety, Tolerability, Immunogenicity and Target Engagement of ACI-24 Formulations in Patients with Mild ... | |||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001339-38 | Sponsor Protocol Number: 17-AVP-786-305 | Start Date*: 2018-01-22 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 3, multicenter, randomized, double-blind, placebo-controlled, parallel-design study to assess the efficacy, safety, and tolerability of AVP-786 (deudextromethorphan hydrobromide [d6-DM]/qui... | |||||||||||||
| Medical condition: Agitation Associated with Dementia of the Alzheimer's Type | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Ongoing) FR (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) BG (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000148-28 | Sponsor Protocol Number: PIB | Start Date*: 2009-08-13 |
| Sponsor Name:Department of Neurology, Medical University of Vienna | ||
| Full Title: Amyloid Imaging in Alzheimer´s disease | ||
| Medical condition: Imaging amyloid plaques in patients with probable Alzheimer´s disease using [11C]PIB and [18F]FDDNP PET | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000630-30 | Sponsor Protocol Number: AC-AD-003 | Start Date*: 2015-11-26 |
| Sponsor Name:AXON NEUROSCIENCE SE | ||
| Full Title: “ADAMANT” A 24-months randomised, placebo-controlled, parallel group, double blinded, multi centre, phase 2 study to assess safety and efficacy of AADvac1 applied to patients with mild Alzheimer’s ... | ||
| Medical condition: Alzheimer’s disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) CZ (Completed) SE (Completed) DE (Completed) SK (Completed) SI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003891-11 | Sponsor Protocol Number: LMT-01-02-18 | Start Date*: 2019-07-16 | |||||||||||
| Sponsor Name:Life Molecular Imaging SA | |||||||||||||
| Full Title: An Open Label, Single Center Study, to evaluate the Safety and Imaging Characteristics of [18F]PI-2620 as PET Radioligand for Imaging Tau deposition in the brains of subjects with amnestic mild cog... | |||||||||||||
| Medical condition: Alzheimer's Disease Amnestic Mild Cognitive Impairment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000105-38 | Sponsor Protocol Number: 04/11/02 | Start Date*: 2006-08-04 |
| Sponsor Name:King's College London (IOP) | ||
| Full Title: A definitive multi-centre pragmatic randomised controlled double-blind trial of the clinical and cost effectiveness of mirtazapine and sertraline versus placebo for the treatment of depression in d... | ||
| Medical condition: Depression in dementia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (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: 2012-005542-38 | Sponsor Protocol Number: MK-8931-019 | Start Date*: 2014-03-17 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., | |||||||||||||
| Full Title: A Phase III, Randomized, Placebo-Controlled, Parallel-Group, Double-Blind Clinical Trial to Study the Efficacy and Safety of MK-8931 (SCH 900931) in Subjects with Amnestic Mild Cognitive Impairment... | |||||||||||||
| Medical condition: prodromal Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) IT (Prematurely Ended) DE (Completed) GB (Prematurely Ended) FI (Completed) NL (Prematurely Ended) BE (Completed) HU (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000342-19 | Sponsor Protocol Number: IIT-2017/02 | Start Date*: 2018-10-18 |
| Sponsor Name:Otto-von-Guericke-Universität Magdeburg, Medizinische Fakultät | ||
| Full Title: Prospective, randomized, double-blind clinical trial phase II for the anti-inflammatory effects of Curazink (zinc histidine) for 8 weeks in elderly patients with mild cognitive impairment in Alzhei... | ||
| Medical condition: Included are patients with the presence of a moderate or pronounced zinc deficienc and the diagnosis of a mild cognitive disorder, which may be due to an additional investigation (amyloid PET and /... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000381-39 | Sponsor Protocol Number: KCL/DS/MEM/1 | Start Date*: 2005-08-24 |
| Sponsor Name:King's College London | ||
| Full Title: Efficacy and Safety of Memantine Hydrochloride, a low affinity antagonist to N-Methyl-D-Aspartate (NMDA) type receptors, in the prevention of cognitive decline and disease progression in older peop... | ||
| Medical condition: Cognitive decline and dementia in Down's syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003306-40 | Sponsor Protocol Number: E2006-G000-202 | Start Date*: 2018-02-27 |
| Sponsor Name:Eisai Ltd. | ||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study with Open-Label Extension Phase of the Efficacy and Safety of Lemborexant in Subjects with Irregular Sleep-Wake Rhy... | ||
| Medical condition: Irregular Sleep-Wake Rhythm Disorder in Subjects with Mild to Moderate Alzheimer’s Disease Dementia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000148-24 | Sponsor Protocol Number: 1 | Start Date*: 2018-06-14 |
| Sponsor Name:Norwegian University of Science and Technology | ||
| Full Title: Safety and efficacy of plasma transfusion from exercise-trained donors in patients with early Alzheimer’s disease: the ExPlas Study | ||
| Medical condition: Early Alzheimer's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004125-32 | Sponsor Protocol Number: APOCT-004 | Start Date*: 2018-03-28 | |||||||||||
| Sponsor Name:Apodemus Aktiebolag | |||||||||||||
| Full Title: A randomised, double blind, placebo controlled trial to evaluate the safety, efficacy and pharmakokinetics of Pleconaril as an add on to AchEI/memantine for treatment of patients with Alzheimer’s d... | |||||||||||||
| Medical condition: Alzheimer's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021474-11 | Sponsor Protocol Number: GE-001-013 | Start Date*: Information not available in EudraCT |
| Sponsor Name:GE Healthcare Ltd. and its Affiliates | ||
| Full Title: A Multicentre, Randomised, Open-label, Comparative Phase IV Trial To Assess Changes in Dementia Diagnostic Category and Diagnostic Confidence After DaTSCAN Imaging in Subjects with an Uncertain Dia... | ||
| Medical condition: Subjects with possible Dementia with Lewy Bodies (DLB) who may or may not also fulfil the criteria for Alzheimers Disease (AD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
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