The purpose of this study is to evaluate the long-term efficacy and safety of combined formulation of xanomeline tartrate/trospium chloride in an immediate release (IR) capsule (KarXT) and xanomeline enteric capsules (KarX-EC) in participants with agitation associated with Alzheimer's Disease who completed the parent studies CN012-0023 or CN012-0024.
Specified dose on specified days
Specified dose on specified days
Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
Site 2005
La Plata, Buenos Aires, Argentina
Site 1001
Mar del Plata, Buenos Aires, Argentina
Site 1002
Buenos Aires, Buenos Aires F.D., Argentina
Site 2006
Rosario, Santa Fe Province, Argentina
Site 1006
Buenos Aires, Argentina
Site 2004
Buenos Aires, Argentina
Site 1003
Córdoba, Argentina
Site 1004
Córdoba, Argentina
Site 2000
Córdoba, Argentina
Site 2002
Córdoba, Argentina
Site 1005
Córdoba, Argentina
Site 1000
Córdoba, Argentina
Site 2003
Mendoza, Argentina
Site 2001
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