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Se administra una vez al da y est aprobado para su uso en tres dosis teraputicas, de 3, 7 y 14 miligramos en la Unin Europea 3
These are usually mild to moderate and improve over time as the body adjusts to the medication
The primary endpoint will be tested using an ANCOVA model with treatment arm as an independent variable and baseline blood p-tau181 concentration as a covariate
The tablets must be swallowed whole and should not be cut, chewed, or crushed
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