- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Alzheimer Disease AND Aggression.
Displaying page 1 of 2.
EudraCT Number: 2016-001127-32 | Sponsor Protocol Number: ACP-103-032 | Start Date*: 2016-09-19 | |||||||||||
Sponsor Name:ACADIA Pharmaceuticals Inc. | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled Study to Examine the Safety and Efficacy of Pimavanserin for the Treatment of Agitation and Aggression in Alzheimer’s Disease | |||||||||||||
Medical condition: Agitation and Aggression in Alzheimer’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001128-78 | Sponsor Protocol Number: ACP-103-033 | Start Date*: 2017-03-21 | |||||||||||
Sponsor Name:ACADIA Pharmaceuticals Inc. | |||||||||||||
Full Title: A 52-Week Open-Label Extension Study of Pimavanserin for the Treatment of Agitation and Aggression in Subjects with Alzheimer’s Disease | |||||||||||||
Medical condition: Agitation and Aggression in Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000217-30 | Sponsor Protocol Number: 3098012 | Start Date*: 2015-06-16 | |||||||||||
Sponsor Name:Orion Corporation | |||||||||||||
Full Title: EFFICACY OF ORM-12741 ON AGITATION/AGGRESSION SYMPTOMS IN PATIENTS WITH ALZHEIMER’S DISEASE: A RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTICENTRE STUDY OF 12 WEEKS | |||||||||||||
Medical condition: The agitation/aggression symptoms in patients with Alzheimer’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) FI (Completed) PL (Completed) BG (Completed) RO (Suspended by CA) HR (Completed) | |||||||||||||
Trial results: View results |
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: 2006-000860-10 | Sponsor Protocol Number: 10729 | Start Date*: 2006-06-30 |
Sponsor Name:H. Lundbeck A/S | ||
Full Title: An Open-Label Study Investigating the Specific Effects of Memantine in Institutionalised Patients with Alzheimer’s Disease | ||
Medical condition: Effects of memantine treatment in institutionalised patients with Alzheimer's Disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) BE (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000504-41 | Sponsor Protocol Number: 331-12-283 | Start Date*: 2013-12-10 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: Country-specific protocol amendment for Germany entitled: A Phase 3, 12-week, Multicenter, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of 2... | |||||||||||||
Medical condition: Agitation Associated with Dementia of the Alzheimer’s Type | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) HR (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 |
EudraCT Number: 2012-004299-20 | Sponsor Protocol Number: ELND005-AG201 | Start Date*: 2013-04-25 |
Sponsor Name:Transition Therapeutics Ireland Ltd | ||
Full Title: A Prospective, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Efficacy and Safety Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheime... | ||
Medical condition: Agitation and Aggression in Moderate to Severe Alzheimer’s Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005524-15 | Sponsor Protocol Number: ELND005-AG251 | Start Date*: 2013-09-03 |
Sponsor Name:Elan Pharma International Ltd | ||
Full Title: A 36-Week Safety Extension Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheimer's Disease. | ||
Medical condition: Agitation and Aggression in Moderate to severe Alzheimer's Disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-003405-22 | Sponsor Protocol Number: CTP3S1502HT6 | Start Date*: 2022-09-02 | |||||||||||
Sponsor Name:Suven Life Sciences Ltd. | |||||||||||||
Full Title: A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Masupirdine (SUVN-502) for the Tre... | |||||||||||||
Medical condition: Agitation with Dementia of the Alzheimer's Type | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) HR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003940-19 | Sponsor Protocol Number: 331-14-213 | Start Date*: 2018-08-06 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: A Phase 3, 12-Week, Multicenter, Randomized, Double-blind, Placebo controlled, 2 Arm, Fixed-dose Trial to Evaluate the Efficacy, Safety, and Tolerability 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: BG (Completed) ES (Ongoing) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005289-39 | Sponsor Protocol Number: GER001-02-02 | Start Date*: 2012-05-16 | |||||||||||||||||||||||||||||||
Sponsor Name:Radboud university medical center | |||||||||||||||||||||||||||||||||
Full Title: Efficacy and safety of delta-9-tetrahydrocannabinol (delta-THC) in behavioural disturbances and pain in dementia | |||||||||||||||||||||||||||||||||
Medical condition: Subjects with mild to severe Alzheimer's dementia and/or vascular dementia with behavioural disturbances, with at least agitation, aggression or aberrant motor disturbances. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002140-88 | Sponsor Protocol Number: CL04-ORY-2001 | Start Date*: 2018-09-06 | |||||||||||
Sponsor Name:Oryzon Genomics S.A. | |||||||||||||
Full Title: An unicenter, open-label, 1-arm, 8-week study to evaluate the efficacy, safety and tolerability of ORY-2001 in aggression in adult population with Alzheimer’s Disease (AD), Lewy Body Dementia (LBD)... | |||||||||||||
Medical condition: Agression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001436-54 | Sponsor Protocol Number: CL06-ORY-2001 | Start Date*: 2019-06-05 | |||||||||||
Sponsor Name:Oryzon Genomics S. A. | |||||||||||||
Full Title: A single-center, open-label, single-arm, 13-week study to evaluate the efficacy, safety and tolerability of ORY-2001 in aggression in Alzheimer’s Disease (AD) – REIMAGINE-AD | |||||||||||||
Medical condition: Aggression in Alzheimer’s Disease (AD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000243-33 | Sponsor Protocol Number: FARM68SY5C | Start Date*: 2008-09-24 | |||||||||||
Sponsor Name:ISTITUTO SUPERIORE DI SANITA' | |||||||||||||
Full Title: Alzheimer disease and antipsycotics: a long term multicenter randomized clinical trial | |||||||||||||
Medical condition: BPSD in Alzheimer disease | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020008-31 | Sponsor Protocol Number: ACP-103-019 | Start Date*: 2013-10-25 |
Sponsor Name:ACADIA Pharmaceuticals Inc | ||
Full Title: A Single center, Double-Blind, Placebo-Controlled Study to Examine the Safety and Efficacy of Pimavanserin for the Treatment of Psychosis in Alzheimer’s Disease | ||
Medical condition: Psychosis associated with Alzheimer's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001056-17 | Sponsor Protocol Number: 3606 | Start Date*: 2020-08-14 | ||||||||||||||||
Sponsor Name:Kings's College London [...] | ||||||||||||||||||
Full Title: A randomised feasibility trial investigating Sativex® for the treatment of the Agitation & Aggression (A/A) in Alzheimer’s Dementia. | ||||||||||||||||||
Medical condition: Clinically significant agitation in Alzheimer's Diseases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005087-93 | Sponsor Protocol Number: | Start Date*: 2006-11-17 |
Sponsor Name:East Kent Hospitals NHS Trust | ||
Full Title: A randomized double blind placebo controlled trial of Memantine in the treatment of Agitation in Alzheimers Dementia | ||
Medical condition: Alzheimers dementia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
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: (No results available) |
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 |
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