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EXAMINE-Studie zur kardiovaskulären Sicherheit von Alogliptin erreicht primären Endpunkt: keine Erhöhung des kardiovaskulären Risikos bei Risikopatienten mit Typ-2 Diabetes
Date:9/11/2013

auf Forschung und Arzneimitteln. Als größtes pharmazeutisches Unternehmen in Japan und einer der globalen Branchenführer strebt Takeda danach, die Gesundheit der Menschen weltweit durch wegweisende Innovationen in der Medizin zu verbessern. Weitere Informationen zu Takeda finden Sie auf der Unternehmenswebsite, www.takeda.com.

Diese Pressemitteilung enthält zukunftsbezogene Aussagen. Zukunftsbezogene Aussagen schließen Aussagen zu den Plänen, Aussichten, Strategien und zukünftigen Ergebnissen von Takeda und andere Aussagen ein, die keine Beschreibung historischer Fakten sind. Zukunftsbezogene Aussagen lassen sich durch die Verwendung zukunftsbezogener Begriffe wie „können", „glauben", „werden", „erwarten", „voraussagen", „schätzen", „sollen", „rechnen mit", „planen", „annehmen", „fortsetzen", „streben", „pro forma", „potenziell", „Ziel", „Vorhersage", „Leitwert", „Aussicht" oder „Absicht" und anderer ähnlicher Begriffe oder Ausdrücke oder ihrer Verneinungen erkennen. Zukunftsbezogene Aussagen beruhen auf Schätzungen und Annahmen der Geschäftsführung, die als vernünftig angesehen werden, aber inhärent ungewiss und schwer vorherzusagen sind. Investoren werden dazu aufgefordert, sich nicht allzu sehr auf zukunftsbezogene Aussagen zu verlassen.

Zukunftsbezogene Aussagen beinhalten Risiken und Ungewissheiten, die dazu führen können, dass die tatsächlichen Ergebnisse oder Erfahrungen wesentlich von den durch die zukunftsbezogenen Aussagen ausgedrückten oder implizierten Ergebnissen oder Erfahrungen abweichen. Zu einigen dieser Risiken und Ungewissheiten gehören, ohne darauf beschränkt zu sein, (1) die wirtschaftlichen Umstände rund um das Geschäft '/>"/>

SOURCE Takeda Pharmaceutical Company Limited
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3. Takeda EXAMINE Cardiovascular Safety Outcomes Trial of Alogliptin Met Primary Endpoint of Non-Inferiority Compared to Placebo in Addition to Standard of Care Showing No Increase in Cardiovascular Risk in Type 2 Diabetes Patients at High-Risk for Car
4. Takeda Type 2 Diabetes Therapies, NESINA (alogliptin) and Fixed-Dose Combinations KAZANO (alogliptin and metformin HCl) and OSENI (alogliptin and pioglitazone), Are Now Available in Pharmacies in the United States
5. Takeda Receives FDA Approval for Three New Type 2 Diabetes Therapies, NESINA (alogliptin) and Fixed-Dose Combinations OSENI (alogliptin and pioglitazone) and KAZANO (alogliptin and metformin HCl)
6. Takeda Resubmits New Drug Applications to the United States Food and Drug Administration for Alogliptin and the Fixed-Dose Combination Alogliptin and Pioglitazone
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