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Lo studio EXAMINE della Takeda sulla sicurezza cardiovascolare di alogliptin in aggiunta alla terapia standard ha soddisfatto l'endpoint primario di non inferiorità rispetto al placebo dimostrando che non si verifica nessun incremento del rischio ca
Date:9/17/2013

Nel caso in cui Takeda aggiornasse o rettificasse una o più delle presenti dichiarazioni, gli investitori e le altre parti non ne devono dedurre che Takeda farà ulteriori aggiornamenti o rettifiche.


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SOURCE Takeda Pharmaceutical Company Limited
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