FIELD: pharmaceutics; medicine.
SUBSTANCE: object 1 is a method for the treatment of Alzheimer’s disease, including administration to a subject who needs it of a combination of therapeutically effective amount of an antibody against Aβ protofibrils and therapeutically effective amount of N-[3-((4aS,5R,7aS)-2-amino-5-methyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazine-7a-yl)-4-fluorphenyl]-5-difluormethylpyrazine-2-carboxamide and/or its pharmaceutically acceptable salt. Object 2 is a combination for use in the treatment of Alzheimer’s disease, containing an antibody against Aβ protofibrils and N-[3-((4aS,5R,7aS)-2-amino-5-methyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazine-7a-yl)-4-fluorphenyl]-5-difluormethylpyrazine-2-carboxamide and/or its pharmaceutically acceptable salt.
EFFECT: reduction in a level of Aβ42 in the brain and increase in power of electroencephalograms in ranges α1 (11-13 Hz) and β1 (13-22 Hz) with administration of a combination.
7 cl, 2 dwg, 2 tbl, 4 ex
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Authors
Dates
2022-12-21—Published
2017-10-26—Filed