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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

rodotti medicinali per uso umano) nel luglio 2013. L'uso di Alogliptin è approvato anche in Cina, Messico e Corea del Sud, sebbene la terapia non sia ancora disponibile in quei mercati.

L'efficacia di alogliptin è stata studiata quale complemento alla dieta e all' esercizio fisico e come terapia aggiuntiva a molte altri classi di farmaci antidiabetici, comprendenti metformina, pioglitazone, insulina e sulfonilurea. In questi studi, le compresse di alogliptin da 25 mg assunte una volta al giorno hanno dimostrato di produrre diminuzioni clinicamente e statisticamente significative dell'HbA1c, con un buon profilo di tollerabilità totale e una bassa incidenza di ipoglicemia in confronto a controllo attivo o placebo. I risultati dello studio hanno evidenziato che alogliptin somministrato insieme a metformina o pioglitazone ha determinato miglioramenti significativi del controllo della glicemia se confrontato con le rispettive monoterapie .

Informazioni su Takeda Pharmaceutical Company Limited
Con sede a Osaka, Giappone, Takeda è una società globale basata sulla ricerca con focus principale nel settore farmaceutico. Quale maggiore società farmaceutica in Giappone e una delle società primarie a livello mondiale settore industriale, Takeda è impegnata con tutte le sue forze a migliorare la salute delle persone nel mondo attraverso innovazioni d'avanguardia in medicina. Maggiori informazioni su Takeda sono disponibili nel sito web aziendale, www.takeda.com.

Il presente comunicato stampa contiene dichiarazioni previsionali. Le dichiarazioni previsionali comprendono dichiarazioni relative a piani, previsioni, strategie, risultati di Takeda per il futuro e altre dichiarazioni che non rappresentano descrizioni di verità storiche. Le dichiarazioni previsionali possono essere identificate
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SOURCE Takeda Pharmaceutical Company Limited
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