This is a Phase 3 global, multicenter, 52-week, open-label extension (OLE) rollover study for subjects completing study CN012-0026, CN012-0027 or CN012-0056. Subjects (randomized or non-randomized) who complete the 38-week CN012-0026 study, 14-week CN012-0027 study or 14-week CN012-0056 study will be eligible to enroll in CN012-0028. The primary objective of the study is to assess the long-term safety and tolerability of KarXT in subjects with psychosis associated with Alzheimer's Disease.
KarXT 20/2 mg TID (total daily dose \[TDD\] 60/6 mg) KarXT 30/3 mg TID (TDD 90/9 mg) KarXT 40/4 mg TID (TDD 120/12 mg) KarXT 50/5 mg TID (TDD 150/15 mg) KarXT 66.7/6.67 mg TID (TDD 200/20 mg)
Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Site 5004
Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Site 5009
Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Site 5005
Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Site 5001
Rosario, Santa Fe Province, Argentina
Site 5008
Buenos Aires, Argentina
Site 5002
Buenos Aires, Argentina
Site 5006
Córdoba, Argentina
Site 5003
San Rafael, Argentina
Site 5007
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