- Trials with a EudraCT protocol (264)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
264 result(s) found for: Clinical dementia rating.
Displaying page 1 of 14.
EudraCT Number: 2017-004065-27 | Sponsor Protocol Number: TTP488-303 | Start Date*: 2018-03-19 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:vTv THERAPEUTICS LLC | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Open Label Extension Study For Continued Safety And Efficacy Evaluation Of Azeliragon In Patients With Mild Alzheimer's Disease | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: MILD ALZHEIMER'S DISEASE | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005438-24 | Sponsor Protocol Number: 1346.23 | Start Date*: 2016-06-30 | ||||||||||||||||
Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | ||||||||||||||||||
Full Title: A multi-centre, double-blind, parallel-group, randomised controlled study to investigate efficacy and safety of orally administered BI 425809 during a 12-week treatment period compared to placebo i... | ||||||||||||||||||
Medical condition: Cognitive impairment due to Alzheimer's Disease Patients with diagnosis of mild-to moderate Alzheimer's dementia according to the recommendations from the National Institute on Aging- Alzheimer'... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) HU (Completed) NO (Completed) FI (Completed) GR (Completed) GB (Completed) ES (Completed) FR (Completed) IT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000001-23 | Sponsor Protocol Number: 14861B | Start Date*: 2014-02-27 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: An open-label extension study to evaluate the long-term safety and tolerability of Lu AE58054 as adjunctive treatment to donepezil in patients with mild-moderate Alzheimer's disease | |||||||||||||
Medical condition: Alzheimer´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) EE (Completed) IT (Completed) BE (Completed) LT (Completed) ES (Completed) DK (Completed) BG (Completed) PT (Completed) GB (Completed) HU (Completed) FI (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000604-15 | Sponsor Protocol Number: PTC-19-602325 | Start Date*: 2020-10-29 | |||||||||||
Sponsor Name:UNIVERSITÀ DEGLI STUDI "G. D'ANNUNZIO" CHIETI-PESCARA | |||||||||||||
Full Title: Multicentre, randomized, double-blind, placebo-controlled, parallel-group Phase II study aimed at evaluating the efficacy and safety of “Zinco Solfato” in Mild Cognitive Impairment due to Alzheimer... | |||||||||||||
Medical condition: Prodromic Alzheimer's disease with evidence of cerebral amyloidosis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005829-88 | Sponsor Protocol Number: AH0003 | Start Date*: 2021-09-28 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Patient- and Investigator-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Bepranemab (UCB0107) in Study Participants With Prodromal to Mild Alzheimer’s Disea... | |||||||||||||
Medical condition: Alzheimer’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006490-24 | Sponsor Protocol Number: CL-758019 | Start Date*: 2007-04-19 | |||||||||||
Sponsor Name:Neurochem Inc | |||||||||||||
Full Title: An Open-Label Extension of the Phase III Study CL-758010 with Alzhemed™ in Patients with Alzheimer’s Disease. | |||||||||||||
Medical condition: Alzheimer's Disease (AD) is an irreversible, progressive neurodegenerative disorder, characterized by gradual cognitive decline, abnormal behaviour, and personality changes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Ongoing) SE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2012-004765-40 | Sponsor Protocol Number: 14863A | Start Date*: 2014-03-31 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Randomised, double-blind, parallel-group, placebo-controlled study of Lu AE58054 in patients with mild-moderate Alzheimer’s disease treated with an acetylcholinesterase inhibitor; Study 3 | |||||||||||||
Medical condition: Alzheimer´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) DE (Completed) SK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005625-39 | Sponsor Protocol Number: I8D-MC-AZET | Start Date*: 2016-09-16 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled and Delayed-Start Study of LY3314814 in Mild Alzheimer’s Disease Dementia (The DAYBREAK Study) | |||||||||||||
Medical condition: Alzheimer’s Disease with Dementia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PT (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) CZ (Prematurely Ended) DK (Completed) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005280-27 | Sponsor Protocol Number: AFF006A | Start Date*: 2013-06-11 | |||||||||||
Sponsor Name:AFFiRiS AG | |||||||||||||
Full Title: A randomized, controlled, parallel group, double-blind, multi-centre, phase IIb study to assess safety and clinical activity of continued AFFITOPE® AD02 vaccinations of patients who participated in... | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) SK (Completed) HR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005862-40 | Sponsor Protocol Number: CL2-38093-012 | Start Date*: 2012-09-06 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Efficacy and safety of 3 doses of S 38093 (2, 5 and 20 mg/day) versus placebo, in co-administration with donepezil (10 mg/day) in patients with moderate Alzheimer’s Disease. A 24-week international... | |||||||||||||
Medical condition: moderate Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FI (Completed) ES (Completed) GB (Completed) SE (Completed) PT (Completed) SK (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000870-20 | Sponsor Protocol Number: IMU-AD-001 | Start Date*: 2015-05-27 | |||||||||||
Sponsor Name:Immungenetics AG | |||||||||||||
Full Title: An open-label, multicenter, controlled pharmaco-dynamic clinical trial to explore the Amyloid beta draining effect of Thiethylperazine (TEP) in subjects with early-to-mild dementia due to Alzheimer... | |||||||||||||
Medical condition: Newly diagnosed early-to-mild dementia due to Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000108-27 | Sponsor Protocol Number: H8A-MC-LZBE | Start Date*: 2016-08-25 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A 24-Month, Phase 3, Multicenter, Placebo-Controlled Study of Efficacy and Safety of Solanezumab versus Placebo in Prodromal Alzheimer’s Disease | |||||||||||||
Medical condition: Prodromal Alzheimer’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) PL (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003475-20 | Sponsor Protocol Number: S1543016 | Start Date*: 2006-05-25 | |||||||||||
Sponsor Name:Solvay Pharmaceuticals, Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Efficacy, Safety and Tolerability Study of Bifeprunox in the Treatment of Elderly Subjects with Psychosis and Behavioural Disturbances Associated wit... | |||||||||||||
Medical condition: Dementia of the Alzheimer's type (DSM-IV TR) code 294.11 | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004352-30 | Sponsor Protocol Number: AB1601 | Start Date*: 2017-05-22 | |||||||||||
Sponsor Name:Araclon Biotech, S.L. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, 24 months Study in Patients with amnestic Mild Cognitive Impairment or Very Mild Alzheimer’s Disease to Investigate the Safety, Tolerabi... | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) SE (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002005-19 | Sponsor Protocol Number: TTP488-301 | Start Date*: 2016-08-19 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:vTv THERAPEUTICS LLC | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, MULTI-CENTER REGISTRATION TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF TTP488 IN PATIENTS WITH MILD ALZHEIMER'S DISEASE RECEIVING ACETYLCHOLINESTERASE ... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: MILD ALZHEIMER'S DISEASE RECEIVING ACETYLCHOLINESTERASE INHIBITORS AND/OR MEMANTINE | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003384-24 | Sponsor Protocol Number: NN6535-7519 | Start Date*: 2023-03-08 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A randomised double-blind placebo-controlled clinical study investigating the effects of semaglutide s.c. once-weekly versus placebo on central and peripheral inflammation in participants with Alzh... | |||||||||||||
Medical condition: Mild cognitive impairment (MCI) or mild dementia, both of the Alzheimer’s type | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005217-37 | Sponsor Protocol Number: I4O-MC-BACC(b) | Start Date*: 2012-08-22 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Assessment of Safety, Tolerability, and Pharmacodynamic Effects of LY2886721 in Patients with Mild Cognitive Impairment Due to Alzheimer’s Disease or Mild Alzheimer's Disease | |||||||||||||
Medical condition: Mild Cognitive Impairment Due to Alzheimer’s Disease or Mild Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004809-40 | Sponsor Protocol Number: GV1001-AD-CL2-007 | Start Date*: 2022-10-10 | |||||||||||
Sponsor Name:GemVax &KAEL Co., Ltd. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Prospective, 52-Week, Phase 2 Clinical Study to Evaluate the Safety and Efficacy of GV1001 Administered Subcutaneously ... | |||||||||||||
Medical condition: Mild to Moderate (stage 4 and 5) Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Temporarily Halted) FR (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) FI (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004325-80 | Sponsor Protocol Number: ANAVEX2-73-AD-EP-004 | Start Date*: 2022-01-10 | |||||||||||
Sponsor Name:Anavex Germany GmbH | |||||||||||||
Full Title: Open Label Extension Study for Patients with Early Alzheimer’s Disease (AD) Enrolled in Study ANAVEX2-73-AD-004 | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
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