- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02477800
221AD301 Phase 3 Study of Aducanumab (BIIB037) in Early Alzheimer's Disease (ENGAGE)
August 9, 2021 updated by: Biogen
A Phase 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Aducanumab (BIIB037) in Subjects With Early Alzheimer's Disease
The primary objective of the study is to evaluate the efficacy of monthly doses of aducanumab in slowing cognitive and functional impairment as measured by changes in the Clinical Dementia Rating-Sum of Boxes (CDR-SB) score as compared with placebo in participants with early AD.
Secondary objectives are to assess the effect of monthly doses of aducanumab as compared with placebo on clinical progression as measured by Mini-Mental State Examination (MMSE), AD Assessment Scale-Cognitive Subscale (13 items) [ADAS-Cog 13], and AD Cooperative Study-Activities of Daily Living Inventory (Mild Cognitive Impairment version) [ADCS-ADL-MCI].
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
1653
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New South Wales
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Darlinghurst, New South Wales, Australia, 2010
- St Vincent's Hospital Sydney
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East Gosford, New South Wales, Australia, 2250
- Central Coast Neurosciences Research, Gosford
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Erina, New South Wales, Australia, 2250
- Central Coast Neurosciences Research
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North Ryde, New South Wales, Australia, 2113
- KARA Institute for Neurological Diseases
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Waratah, New South Wales, Australia, 2298
- Calvary Mater Newcastle
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Queensland
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Chermside, Queensland, Australia, 4032
- The Prince Charles Hospital
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Herston, Queensland, Australia, 4006
- Royal Brisbane and Women's Hospital
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Toowoomba, Queensland, Australia, 4350
- Toowoomba Base Hospital
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Victoria
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Box Hill, Victoria, Australia, 3128
- Box Hill Hospital
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Heidelberg, Victoria, Australia, 3084
- Austin Hospital
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Parkville, Victoria, Australia, 3050
- Royal Melbourne Hospital
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Western Australia
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West Perth, Western Australia, Australia, 6005
- Neurodegenerative Disorders Research
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Graz, Austria, 8036
- LKH - Universitaetsklinikum Graz
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Salzburg, Austria, 5020
- Christian-Doppler-Klinik - Universitätsklinikum Salzburg
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Quebec, Canada, G1J 1Z4
- CHU de Quebec - Hôpital de l' Enfant Jésus
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Alberta
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Calgary, Alberta, Canada, T2N 1N4
- Heritage Medical Research Clinic
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British Columbia
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Penticton, British Columbia, Canada, V2A 5C8
- The Medical Arts Health Research Group
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Vancouver, British Columbia, Canada, V6T 2B5
- UBC Hospital
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Ontario
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Toronto, Ontario, Canada, M4N 3M5
- Toronto Sunnybrook Hospital
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Toronto, Ontario, Canada, M3B 2S7
- Toronto Memory Program (Neurology Research Inc.)
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Quebec
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Montreal, Quebec, Canada, H3A 2B4
- The Montreal Neurological Institute
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Verdun, Quebec, Canada, H4H 1R3
- McGill Centre for Studies in Aging
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Ballerup, Denmark, 2750
- CCBR - Ballerup - DK
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København Ø, Denmark, 2100
- Rigshospitalet
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Vejle, Denmark, 7100
- CCBR - Vejle - DK
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Ålborg, Denmark, 9100
- CCBR - Ålborg - DK
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Paris, France, 75013
- Groupe Hospitalier Pitie-Salpetriere
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Paris, France, 75013
- Groupe hospitalier Broca - La Rochefoucauld - La Collégiale
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Bas Rhin
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Strasbourg, Bas Rhin, France, 67091
- Hopital Louis Pasteur Colmar
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Strasbourg Cedex, Bas Rhin, France, 67098
- CHU Strasbourg - Hôpital Hautepierre
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Gironde
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Bordeaux, Gironde, France, 33076
- Groupe Hospitalier Pellegrin - Hôpital Pellegrin
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Marne
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Reims, Marne, France, 51092
- CHU Reims - Hôpital Maison Blanche
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Rhone
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Bron Cedex, Rhone, France, 69677
- Hopital Neurologique Pierre Wertheimer
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Berlin, Germany, 14050
- Charite Universitaetsmedizin Berlin - Campus Benjamin Franklin
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Baden Wuerttemberg
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Boeblingen, Baden Wuerttemberg, Germany, 71034
- Praxis Dr. Scholz
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Ostfildern, Baden Wuerttemberg, Germany, 73760
- Aerztliche Gemeinschaftspraxis
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Stuttgart, Baden Wuerttemberg, Germany, 70182
- Neuro MVZ Stuttgart
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Bayern
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Frankfurt, Bayern, Germany, 97080
- Klinikum der Johann Wolfgang Goethe-Universitaet
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Neuburg, Bayern, Germany, 86633
- Praxis Dr. med. Bergmann
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Hessen
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Kassel, Hessen, Germany, 34121
- Neurologische Gemeinschaftspraxis Kassel
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Niedersachsen
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Hannover, Niedersachsen, Germany, 30159
- Klinische Forschung Hannover-Mitte GmbH
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Nordrhein Westfalen
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Aachen, Nordrhein Westfalen, Germany, 52074
- Universitaetsklinikum Aachen AOeR
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Bonn, Nordrhein Westfalen, Germany, 53127
- Universitaetsklinikum Bonn AoeR
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Cologne, Nordrhein Westfalen, Germany, 53105
- Universitaetsklinikum Koeln
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Bergamo, Italy, 24100
- Azienda Ospedaliera Ospedali Riuniti di Bergamo
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Brescia, Italy, 25100
- Azienda Ospedaliera Spedali Civili di Brescia
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Genova, Italy, 16132
- Azienda Ospedaliero Universitaria San Martino
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Milano, Italy, 20132
- Ospedale San Raffaele
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Milano, Italy, 20144
- Casa di Cura del Policlinico
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Napoli, Italy, 80131
- Azienda Ospedaliera Universitaria "Federico II"
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Napoli, Italy, 80138
- Seconda Università degli Studi di Napoli
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Pisa, Italy, 56126
- Azienda Ospedaliero Universitaria Pisana
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Roma, Italy, 00168
- Policlinico Universitario Agostino Gemelli
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Salerno, Italy, 84131
- Azienda Ospedaliera Universitaria OO. RR. S. Giovanni di Dio e Ruggi D'Aragona
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Siena, Italy, 53100
- A.O.U. Senese Policlinico Santa Maria alle Scotte
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Ancona
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Torrette Di Ancona, Ancona, Italy, 60126
- Azienda Ospedaliero Universitaria Ospedali Riuniti
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Palermo
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Cefalù, Palermo, Italy, 90015
- Fondazione Istituto G.Giglio di Cefalù
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Itabashi-ku, Japan, 173-8610
- Research Site
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Itabashi-ku, Japan, 173-0015
- Research Site
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Kiyose-shi, Japan
- Research Site
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Kodaira-shi, Japan, 187-8551
- Research Site
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Chiba-Ken
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Chiba-Shi, Chiba-Ken, Japan, 263-0043
- Research Site
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Inzai-shi, Chiba-Ken, Japan
- Research Site
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Fukuoka-ken
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Kurume-shi, Fukuoka-ken, Japan, 830-0011
- Research Site
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Fukushima-Ken
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Aizuwakamatsu-shi, Fukushima-Ken, Japan, 965-8585
- Research Site
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Hokkaido
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Asahikawa-shi, Hokkaido, Japan, 070-8644
- Research Site
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Sapporo-shi, Hokkaido, Japan, 006-8555
- Research Site
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Sapporo-shi, Hokkaido, Japan, 064-8570
- Research Site
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Kanagawa-Ken
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Atsugi-shi, Kanagawa-Ken, Japan, 243-8551
- Research Site
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Kamakura-shi, Kanagawa-Ken, Japan, 247-8533
- Research Site
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Kawasaki-Shi, Kanagawa-Ken, Japan, 211-8533
- Research Site
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Yokohama-shi, Kanagawa-Ken, Japan, 225-0013
- Research Site
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Yokohama-shi, Kanagawa-Ken, Japan, 225-0025
- Research Site
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Kanagawa-ken
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Yokohama-shi, Kanagawa-ken, Japan, 223-0059
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Kyoto-Fu
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Kyoto-shi, Kyoto-Fu, Japan, 616-8255
- Research Site
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Niigata-Ken
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Nagaoka-shi, Niigata-Ken, Japan, 940-2081
- Research Site
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Saitama-Ken
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Iruma-gun, Saitama-Ken, Japan, 350-0495
- Research Site
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Kasukabe-shi, Saitama-Ken, Japan, 344-0036
- Research Site
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Tokyo
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Ota-ku, Tokyo, Japan, 143-8541
- Research Site
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Tokyo-To
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Bunkyo-ku, Tokyo-To, Japan, 113-0034
- Research Site
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Shinjuku-ku, Tokyo-To, Japan, 162-8655
- Research Site
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Shinjuku-ku (I), Tokyo-To, Japan, 162-8655
- Research Site
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Yamagata-Ken
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Yamagata-shi, Yamagata-Ken, Japan, 990-0834
- Research Site
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Incheon, Korea, Republic of, 21565
- Gachon University Gil Medical Center
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Seoul, Korea, Republic of, 143-729
- Konkuk University Medical Center
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Seoul, Korea, Republic of, 05505
- Asan Medical Center
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Seoul, Korea, Republic of, 06351
- Samsung Medical Center
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Gyeonggi-do
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Incheon, Gyeonggi-do, Korea, Republic of, 22332
- Inha University Hospital
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Seongnam-si, Gyeonggi-do, Korea, Republic of, 13620
- Seoul National University Bundang Hospital
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Amadora, Portugal, 2720-276
- Hospital Professor Doutor Fernando Fonseca, E.P.E.
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Braga, Portugal, 4710-243
- Hospital de Braga
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Coimbra, Portugal, 3040-278
- Centro Hospitalar e Universitario de Coimbra E.P.E
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Lisboa, Portugal, 1600-618
- CUF Alvalade
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Loures, Portugal, 2674-514
- Hospital Beatriz Angelo
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Torres Vedras, Portugal, 2560-280
- Campus Neurologico Senior
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Barcelona, Spain, 08041
- Hospital de la Santa Creu i Sant Pau
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Barcelona, Spain, 08036
- Hospital Clinic i Provincial de Barcelona
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Barcelona, Spain, 08028
- Fundacio ACE
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Madrid, Spain, 28006
- Clinica Ruber
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Valencia, Spain, 46026
- Hospital Universitari i Politecnic La Fe
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Valencia, Spain, 46017
- Hospital Universitario Dr. Peset
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Guipuzcoa
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San Sebastian, Guipuzcoa, Spain, 20014
- Policlinica Guipuzcoa
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Vizcaya
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Barakaldo, Vizcaya, Spain, 48903
- Hospital De Cruces
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Changhua, Taiwan, 500
- Changhua Christian Hospital
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Kaohsiung, Taiwan, 807
- Kaohsiung Medical University Chung-Ho Memorial Hospital
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Kaohsiung, Taiwan, 83301
- Kaohsiung Chang Gung Memorial Hospital
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Tainan, Taiwan, 704
- National Cheng Kung University Hospital
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Taipei, Taiwan, 100
- National Taiwan University Hospital
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Taoyuan County, Taiwan, 333
- Chang Gung Memorial Hospital, Linkou
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Avon
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Bristol, Avon, United Kingdom, BS16 1LE
- Southmead Hospital
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Greater London
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London, Greater London, United Kingdom, W1G 9JF
- Re:Cognition Health Ltd
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London, Greater London, United Kingdom, W6 8RF
- Charing Cross Hospital
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London, Greater London, United Kingdom, WC1N 3BG
- The National Hospital for Neurology and Neurosurgery Centre
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Greater Manchester
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Salford, Greater Manchester, United Kingdom, M6 8HD
- Salford Royal
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Lothian Region
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Edinburgh, Lothian Region, United Kingdom, EH8 9YL
- The University of Edinburgh
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Merseyside
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Blackburn, Merseyside, United Kingdom, BB3 2HH
- Manchester Royal Infirmary
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Somerset
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Bath, Somerset, United Kingdom, BA1 3NG
- The RICE Centre
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Strathclyde
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Glasgow, Strathclyde, United Kingdom, G20 0XA
- Glasgow Memory Clinic Ltd
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Glasgow, Strathclyde, United Kingdom, G21 3UW
- Stobhill ACH Hospital
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Tayside Region
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Dundee, Tayside Region, United Kingdom, DD2 1GZ
- Ninewells Hospital
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Tyne & Wear
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Newcastle upon Tyne, Tyne & Wear, United Kingdom, NE4 5PL
- Newcastle University
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Wiltshire
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Chippenham, Wiltshire, United Kingdom, SN15 1GG
- Kingshill Research Centre
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Arizona
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Phoenix, Arizona, United States, 85013
- St. Joseph's Hospital and Medical Center
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Tucson, Arizona, United States, 85718
- Center for Neurosciences
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California
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Fullerton, California, United States, 92835
- Neurology Center of North Orange County
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Laguna Hills, California, United States, 92653
- Senior Clinical Trials, Inc.
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Lomita, California, United States, 90717
- Torrance Clinical Research Institute, Inc.
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Los Angeles, California, United States, 90095
- University of California - Los Angeles
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San Francisco, California, United States, 94158
- UCSF - Memory and Aging Center
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Sherman Oaks, California, United States, 91403
- California Neuroscience Research Medical Group Inc.
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Simi Valley, California, United States, 93065
- Southern California Research LLC
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Connecticut
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New Haven, Connecticut, United States, 06510
- Institute for Neurodegenerative Disorders
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District of Columbia
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Washington, District of Columbia, United States, 20057
- Georgetown University Hospital
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Florida
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Delray Beach, Florida, United States, 33445
- Brain Matters Research, Inc.
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Fort Myers, Florida, United States, 33912
- Neuropsychiatric Research Center of Southwest Florida
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Jacksonville, Florida, United States, 32216
- Jacksonville Center for Clinical Research
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Miami, Florida, United States, 33136
- University of Miami
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Miami, Florida, United States, 33137
- Miami Jewish Health Systems
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Orlando, Florida, United States, 32806
- Compass Research Main
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Palm Beach Gardens, Florida, United States, 33410
- Palm Beach Neurological Center
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Tampa, Florida, United States, 33613
- Stedman Clinical Trials, LLC
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Tampa, Florida, United States, 33634
- Meridien Research
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Tampa, Florida, United States, 33616
- USF Health Byrd Institute
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The Villages, Florida, United States, 32162
- Compass Research Main
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West Palm Beach, Florida, United States, 33407
- Premiere Research Institute
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Weston, Florida, United States, 33331
- Cleveland Clinic Florida - Weston
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Illinois
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Elk Grove Village, Illinois, United States, 60007
- Alexian Brothers Neurosciences Institute
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Park Ridge, Illinois, United States, 60068
- Advocate Lutheran General Hospital
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Indiana
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Fort Wayne, Indiana, United States, 46804
- Fort Wayne Neurological Center
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Indianapolis, Indiana, United States, 46202
- Indiana University School of Medicine
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Kansas
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Kansas City, Kansas, United States, 66160
- University of Kansas Medical Center Research Institute, Inc.
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Wichita, Kansas, United States, 67214
- Via Christi Research, a division of Via Christi Hospitals Wichita, Inc.
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Kentucky
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Lexington, Kentucky, United States, 40503
- Baptist Health Lexington
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Massachusetts
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Boston, Massachusetts, United States, 02215
- Beth Israel Deaconess Medical Center
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Boston, Massachusetts, United States, 02115
- Brigham & Women's Hosp End/Dbt
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Methuen, Massachusetts, United States, 01844
- ActivMed Practices & Research
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Plymouth, Massachusetts, United States, 02360
- Donald S. Marks, M.D., P.C.
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Minnesota
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Rochester, Minnesota, United States, 55905
- Mayo Clinic
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Missouri
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Saint Louis, Missouri, United States, 63131
- Washington University
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Nevada
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Las Vegas, Nevada, United States, 89113
- Las Vegas Medical Research
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New Jersey
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Toms River, New Jersey, United States, 08755
- Advanced Memory Research Institute of NJ, PC
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New York
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Albany, New York, United States, 12208
- Albany Medical College
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New York, New York, United States, 10016
- New York University Medical Center PRIME
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Rochester, New York, United States, 14620
- University of Rochester
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North Carolina
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Charlotte, North Carolina, United States, 28270
- ANI Neurology, PLLC d/b/a Alzheimer's Memory Center
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Raleigh, North Carolina, United States, 27607-6010
- Raleigh Neurology Associates, P.A.
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Ohio
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Cleveland, Ohio, United States, 44195
- Cleveland Clinic
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Oklahoma
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Oklahoma City, Oklahoma, United States, 73112
- Lynn Health Science Institute
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Pennsylvania
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Jenkintown, Pennsylvania, United States, 19046
- The Clinical Trial Center, LLC
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Pittsburgh, Pennsylvania, United States, 15213
- University of Pittsburgh
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Plains, Pennsylvania, United States, 18705
- Northeastern Pennsylvania Memory and Alzheimer's Center
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Rhode Island
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East Providence, Rhode Island, United States, 02915
- Rhode Island Mood & Memory Research Institute
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Providence, Rhode Island, United States, 02906
- Butler Hospital
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South Carolina
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Charleston, South Carolina, United States, 29425
- Medical University of South Carolina (MUSC)
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Tennessee
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Cordova, Tennessee, United States, 38108
- Neurology Clinic, PC
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Knoxville, Tennessee, United States, 37920
- University of Tennessee Medical Center. Knoxville
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Memphis, Tennessee, United States, 38119
- Clinical Neuroscience Solutions, Inc.
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Texas
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Dallas, Texas, United States, 75390
- Ut Southwestern Medical Center At Dallas
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Houston, Texas, United States, 77030
- Baylor College of Medicine
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Virginia
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Richmond, Virginia, United States, 23294
- National Clinical Research Inc.-Richmond
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Wisconsin
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Milwaukee, Wisconsin, United States, 53266
- Medical College of Wisconsin, Inc.
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Key Inclusion Criteria:
- Must meet all of the following clinical criteria for MCI due to AD or mild AD and must have:
- A Clinical Dementia Rating (CDR)-Global Score of 0.5.
- Objective evidence of cognitive impairment at screening
- An MMSE score between 24 and 30 (inclusive)
- Must have a positive amyloid Positron Emission Tomography (PET) scan
- Must consent to apolipoprotein E (ApoE) genotyping
- If using drugs to treat symptoms related to AD, doses must be stable for at least 8 weeks prior to screening visit 1
- Must have a reliable informant or caregiver
Key Exclusion Criteria:
- Any medical or neurological condition (other than Alzheimer's Disease) that might be a contributing cause of the subject's cognitive impairment
- Have had a stroke or Transient Ischemic Attack (TIA) or unexplained loss of consciousness in the past 1 year
- Clinically significant unstable psychiatric illness in past 6 months
- History of unstable angina, myocardial infarction, advanced chronic heart failure, or clinically significant conduction abnormalities within 1 year prior to Screening
- Indication of impaired renal or liver function
- Have human immunodeficiency virus (HIV) infection
- Have a significant systematic illness or infection in past 30 days
- Relevant brain hemorrhage, bleeding disorder and cerebrovascular abnormalities
- Any contraindications to brain magnetic resonance imaging (MRI) or PET scans
- Alcohol or substance abuse in past 1 year
- Taking blood thinners (except for aspirin at a prophylactic dose or less)
NOTE: Other protocol defined Inclusion/Exclusion criteria may apply
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Low Dose
Monthly intravenous (IV) infusion
|
Placebo
Low dose
High dose
|
Experimental: High Dose
Monthly intravenous (IV) infusion
|
Placebo
Low dose
High dose
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change From Baseline in Clinical Dementia Rating Sum of Boxes (CDR-SB) Score at Week 78
Time Frame: Baseline, Week 78
|
CDR-SB integrates assessments from 3 domains of cognition (memory, orientation, judgment/problem-solving) and 3 domains of function (community affairs, home/hobbies, personal care).
Following caregiver interview and systematic patient examination, the rater assigns a score describing the participant's current performance level in each of these domains of life functioning.
Prespecified severity anchors range from none = 0, questionable = 0.5, mild = 1, moderate = 2 to severe = 3 (the personal care domain omits the 0.5 score).
"Sum of boxes" scoring methodology sums the score for each of the 6 domains and provides a value ranging from 0 to 18 that can change in increments of 0.5 or greater.
Higher scores indicate greater disease severity.
Mixed model for repeated measures (MMRM) analysis was used to analyze change from baseline in CDR-SB.
A positive change from baseline indicates clinical decline.
|
Baseline, Week 78
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change From Baseline in Mini-Mental State Examination (MMSE) Score at Week 78
Time Frame: Baseline, Week 78
|
The MMSE is a widely used performance-based test of global cognitive status.
It consists of 11 tasks that assess orientation, word recall, attention and calculation, language abilities, and visuospatial functions.
The scores from the 11 tests are combined to obtain the total score, which ranges from 0 to 30, with lower scores over time indicating increasing cognitive impairment.
MMRM analysis was used to analyze change from baseline in MMSE.
A negative change from baseline indicates clinical decline.
|
Baseline, Week 78
|
Change From Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (13 Items) (ADAS-Cog 13) Score at Week 78
Time Frame: Baseline, Week 78
|
ADAS-Cog13 comprises both cognitive tasks and clinical ratings of cognitive performance.
The scale items capture word recall, ability to follow commands, the ability to correctly copy or draw an image, naming, the ability to interact with everyday objects, orientation, word recognition, memory, comprehension of spoken language, word-finding, and language ability, with a measure for delayed word recall and concentration/distractibility.
The total score ranges from 0 to 85.
An increase in score over time indicates increasing cognitive impairment.
MMRM analysis was used to analyze change from baseline in ADAS-Cog 13.
A positive change from baseline indicates clinical decline.
|
Baseline, Week 78
|
Change From Baseline in Alzheimer's Disease Cooperative Study-Activities of Daily Living Inventory (Mild Cognitive Impairment Version) (ADCS-ADL-MCI) Score at Week 78
Time Frame: Baseline, Week 78
|
The ADCS-ADL-MCI consists of 17 instrumental items (e.g., shopping, preparing meals, using household appliances) and 1 basic item (getting dressed).
Ratings reflect caregiver observations about the patient's actual functioning over the previous month and provide an assessment of change in the functional state of the participant over time.
The total score ranges from 0 to 53, with lower values over time reflecting functional deterioration.
MMRM analysis was used to analyze change from baseline in ADAS-ADL-MCI.
A negative change from baseline indicates clinical decline.
|
Baseline, Week 78
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 13, 2015
Primary Completion (Actual)
August 8, 2019
Study Completion (Actual)
August 8, 2019
Study Registration Dates
First Submitted
June 18, 2015
First Submitted That Met QC Criteria
June 18, 2015
First Posted (Estimate)
June 23, 2015
Study Record Updates
Last Update Posted (Actual)
September 2, 2021
Last Update Submitted That Met QC Criteria
August 9, 2021
Last Verified
August 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 221AD301
- 2015-000966-72 (EudraCT Number)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Novoic LimitedRecruitingAlzheimer Disease | Mild Cognitive Impairment | Prodromal Alzheimer's Disease | Alzheimer's Disease (Incl Subtypes) | Preclinical Alzheimer's DiseaseUnited Kingdom
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Novoic LimitedCompletedAlzheimer Disease | Mild Cognitive Impairment | Prodromal Alzheimer's Disease | Alzheimer's Disease (Incl Subtypes) | Preclinical Alzheimer's DiseaseUnited States
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Novoic LimitedCompletedAlzheimer Disease | Mild Cognitive Impairment | Prodromal Alzheimer's Disease | Alzheimer's Disease (Incl Subtypes) | Preclinical Alzheimer's DiseaseUnited Kingdom
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Novoic LimitedRecruitingAlzheimer Disease | Mild Cognitive Impairment | Prodromal Alzheimer's Disease | Alzheimer's Disease (Incl Subtypes) | Preclinical Alzheimer's DiseaseUnited Kingdom
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Novoic LimitedRecruitingAlzheimer Disease | Mild Cognitive Impairment | Prodromal Alzheimer's Disease | Alzheimer's Disease (Incl Subtypes) | Preclinical Alzheimer's Disease | Normal CognitionUnited States
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University Hospital, BordeauxMinistry for Health and Solidarity, FranceCompletedAlzheimer's Disease (AD) | Alzheimer's Disease (AD) Related DisordersFrance
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University of Colorado, DenverNational Institute on Aging (NIA)Active, not recruitingSuspected Typical Alzheimer's Disease (AD) | Suspected Atypical Alzheimer's Disease (AD)United States
Clinical Trials on Placebo
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SamA Pharmaceutical Co., LtdUnknownAcute Bronchitis | Acute Upper Respiratory Tract InfectionKorea, Republic of
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National Institute on Drug Abuse (NIDA)CompletedCannabis UseUnited States
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AstraZenecaParexel; Spandauer Damm 130; 14050; Berlin, GermanyCompletedMale Subjects With Type II Diabetes (T2DM)Germany
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Heptares Therapeutics LimitedCompletedPharmacokinetics | Safety IssuesUnited Kingdom
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GlaxoSmithKlineCompletedPulmonary Disease, Chronic ObstructiveUnited Kingdom, Netherlands
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Shijiazhuang Yiling Pharmaceutical Co. LtdXuanwu Hospital, BeijingCompleted
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ItalfarmacoCompletedBecker Muscular DystrophyNetherlands, Italy
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GlaxoSmithKlineCompletedInfections, BacterialUnited States
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West Penn Allegheny Health SystemCompletedAsthma | Allergic RhinitisUnited States