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. 2017 Nov 4;17(4):631–643. doi: 10.1007/s40268-017-0214-8
In the fed state, pharmacokinetic parameters for TAK-063 were comparable at equivalent doses between healthy Japanese subjects and subjects with stable schizophrenia.
TAK-063 was safe and generally well tolerated when administered once daily over a 7-day period to healthy Japanese subjects (up to 20 mg) and subjects with stable schizophrenia (up to 100 mg).
Pharmacokinetic/adverse event modeling suggests that single daily doses up to 30 mg TAK-063 may be suitable for further development in schizophrenia.