- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: Alzheimer Disease AND Control.
Displaying page 3 of 4.
| EudraCT Number: 2013-000307-17 | Sponsor Protocol Number: DIAN-TU-001 | Start Date*: 2014-01-08 |
| Sponsor Name:Washington University in St. Louis | ||
| Full Title: A Phase II/III randomized, double-blind, placebo-controlled, cognitive endpoint, multicenter study of potential disease modifying therapies in individuals at risk for and with dominantly inherited ... | ||
| Medical condition: Dominantly Inherited Alzheimer Disease (DIAD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Trial now transitioned) ES (Temporarily Halted) DE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004169-18 | Sponsor Protocol Number: Sat-CIEN-02 | Start Date*: 2017-02-22 | |||||||||||
| Sponsor Name:Centro de Investigación Biomédica en Red, Enfermedades Neurodegenerativas (CIBERNED) | |||||||||||||
| Full Title: A multicenter, randomized, double-blind, placebo-controlled, 4-arm, 26 week parallel-group study to evaluate the safety, tolerability and anti-inflammatory effect of three oromucosal doses of Sativ... | |||||||||||||
| Medical condition: Patients with mild cognitive impairment of Alzheimer type or early Alzheimer dementia. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004462-18 | Sponsor Protocol Number: CRCFL12 | Start Date*: 2013-04-23 |
| Sponsor Name:Service of Neurology CHU Liege | ||
| Full Title: An exploratory research on the influence of amyloid deposit (measured with (18F)flutemetamol) on disconnection in the “core episodic network” and between regions involved in anosognosia for memory ... | ||
| Medical condition: Alzheimer's disease (mild, moderate and moderately severe stage) and control population | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000914-21 | Sponsor Protocol Number: 161003 | Start Date*: 2012-02-13 | |||||||||||
| Sponsor Name:Baxter Innovations GmbH | |||||||||||||
| Full Title: A PHASE 3 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF THE SAFETY AND EFFECTIVENESS OF IMMUNE GLOBULIN INTRAVENOUS (HUMAN), 10% SOLUTION (IGIV, 10%) FOR THE TREATMENT OF MILD TO MODERATE A... | |||||||||||||
| Medical condition: Mild to moderate Alzheimer’s disease (AD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| 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: 2011-001756-12 | Sponsor Protocol Number: UCL-2010-412 | Start Date*: 2012-04-27 |
| Sponsor Name:Cliniques Universitaires Saint Luc - UCL | ||
| Full Title: Surrogate markers evaluation in pre-demented Alzheimer’s disease patients and healthy elderly controls | ||
| Medical condition: Healthy volunteers and Mild Cognitive Impaired patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002595-13 | Sponsor Protocol Number: 18F-AV-45-A18 | Start Date*: 2013-03-01 | |||||||||||
| Sponsor Name:AVID RADIOPHARMACEUTICALS, INC. | |||||||||||||
| Full Title: A randomized, multicenter, multicountry study to evaluate the effectiveness of Florbetapir (18F) PET imaging in changing patient management and to evaluate the relationship between Florbetapir (1... | |||||||||||||
| Medical condition: Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| 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: 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: 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: 2022-002171-11 | Sponsor Protocol Number: 010622 | Start Date*: 2024-07-02 |
| Sponsor Name:Medical University of Łódź | ||
| Full Title: Randomized, double-blind, placebo-controlled trial evaluating efficacy and safety of dimethyl fumarate in brain atrophy reduction, synaptic functional connectivity, cognitive functions, quality of ... | ||
| Medical condition: dementia and mild cognitice impairment due to Alzheimer's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001261-42 | Sponsor Protocol Number: 3002 | Start Date*: 2006-05-18 |
| Sponsor Name:Evotec NeuroSciences GmbH | ||
| Full Title: Assessment of Inhibition of Brain MAO-B by EVT 301 after Repeated Dosing to Steady-state in Patients with Alzheimer’s Disease and in Elderly Control Subjects | ||
| Medical condition: Subjects with probable Alzheimer's Disease and healthy voulunteers | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002159-24 | Sponsor Protocol Number: 54861911ALZ2002 | Start Date*: 2014-10-27 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Phase 2a Randomized, Double-blind, Placebo-Controlled, Parallel-Group, Multi-center Study Investigating the Safety and Tolerability of JNJ-54861911 in Subjects in the Early (Predementia) Alzheime... | |||||||||||||
| Medical condition: Early Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) SE (Completed) ES (Completed) NL (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000163-89 | Sponsor Protocol Number: COG0104 | Start Date*: 2018-04-23 | |||||||||||
| Sponsor Name:Cognition Therapeutics, Inc. | |||||||||||||
| Full Title: A Pilot Study to Evaluate the Effect of CT1812 Treatment on Aβ Oligomer Displacement into CSF in Subjects with Mild to Moderate Alzheimer's Disease Followed by a Six-Month Open Label Extension of a... | |||||||||||||
| Medical condition: Sponsor is developing an oral formulation of CT1812 fumarate to treat AD and mild cognitive impairment. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000016-10 | Sponsor Protocol Number: 3098A1-201-EU | Start Date*: 2004-10-12 |
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc., Clinical Research and Development | ||
| Full Title: A 3-MONTH, RANDOMIZED, DOUBLE-BLIND, PLACEBO- CONTROLLED, MULTICENTER, SAFETY, TOLERABILITY, AND EFFICACY STUDY OF 3 DOSES OF SRA-333 IN OUTPATIENTS WITH MILD TO MODERATE ALZHEIMER’S DISEASE WITH ... | ||
| Medical condition: Alzheimer's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004283-23 | Sponsor Protocol Number: Emboli Inhibition | Start Date*: 2006-05-05 |
| Sponsor Name:South Manchester University Hospital | ||
| Full Title: An evaluation of potential therapies to inhibit cerebral emboli in dementia | ||
| Medical condition: Alzheimer's Disease and Vascular Dementia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-002027-26 | Sponsor Protocol Number: 2405 | Start Date*: 2016-04-13 |
| Sponsor Name:University of Bristol | ||
| Full Title: TARGETING DOPAMINE TO TREAT IMPAIRED MEMORY CONSOLIDATION IN NEURODEGENERATIVE DISEASE: A DOUBLE-BLIND PLACEBO-CONTROLLED TRIAL | ||
| Medical condition: Mild Cognitive Impairment Mild Alzheimer's disease | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020724-21 | Sponsor Protocol Number: ADR16SUS2 | Start Date*: 2011-04-06 |
| Sponsor Name:Universitätsklinik für Neurologie, Medizinische Universität Wien | ||
| Full Title: Amyloid Imaging with [11C]PIB PET and MRI in MCI – a pilot study | ||
| Medical condition: Patients with Mild Cognitive Impairment (MCI) will be investigated with PIB PET to determin amyloid pathology | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002455-29 | Sponsor Protocol Number: 15-AVP-786-303 | Start Date*: 2018-07-31 | |||||||||||
| Sponsor Name:Avanir Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Long-term, Extension Study of the Safety and Efficacy of AVP-786 (deuterated [d6] dextromethorphan hydrobromide [d6-DM]/quinidine sulfate [Q]) for the Treatment of Agitation... | |||||||||||||
| 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) PL (Completed) BG (Completed) CZ (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000219-15 | Sponsor Protocol Number: 13-10 | Start Date*: 2014-11-27 |
| Sponsor Name:VU Medical Center | ||
| Full Title: Amyloid pathology in cognitively normal elderly subjects | ||
| Medical condition: Cognitively healthy elderly, aged 60-100 years old. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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