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Artikel im American Journal of Cardiology zeigt gute Gefäßheilung nach MiStent-SES-Implantation
Date:11/21/2013

Pressemitteilung enthält vorausschauende Aussagen. Diese sind daran zu erkennen, dass sie sich nicht streng auf historische oder aktuelle Fakten beziehen. Vorausschauende Aussagen können Wörter (einschließlich ihrer abgewandelten Formen) wie „erwarten", „schätzen", „vorhersehen", „können", „planen", „glauben" und Wörter und Ausdrücke ähnlicher Substanz in Zusammenhang mit der Leistung des MiStent SES® bei der Steuerung der Arzneimittelfreisetzung und der Begrenzung der Polymer-Expositionsdauer und seiner Leistung bei der Verringerung von Sicherheitsrisiken gegenüber herkömmlichen Arzneimittel-eluierenden Dauer-Polymer-Stents enthalten. Der Leser sollte sich nicht vorbehaltlos auf die vorausschauenden Aussagen in dieser Pressemitteilung verlassen, da es sich hierbei um Prognosen anhand unserer derzeitigen Analyse von und Erwartungen hinsichtlich zukünftiger Ereignisse handelt, die nur die Sicht zum entsprechenden Zeitpunkt widerspiegeln. Diese vorausschauenden Aussagen sind keine Garantien für die zukünftige Leistung und unterliegen Risiken und Unsicherheiten, unter anderem: den Ergebnissen zukünftiger klinischer Studien, einschließlich des Langzeit-Followup der Patienten, die an der klinischen DESSOLVE-I- und II-Studie teilgenommen haben; unserem Vermögen, die regulatorische Zulassung des MiStent SES in anderen Rechtsgebieten zu erhalten; der erfolgreichen Entwicklung und Kommerzialisierung des MiStent SES in Europa und anderen Märkten; dem Vermögen des MiStent SES, sich effektiv und erfolgreich gegenüber derzeit an europäischen und anderen Märkten erhältlichen Arzneimittel-eluierenden Stent-Technologien zu behaupten; sowie unserem Vermögen, unsere proprietäre Stent-Beschichtungstechnologie zu bewahren und zu schützen. Tatsächliche Ergebnisse, die tats&
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SOURCE Micell Technologies, Inc.
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