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Bayer Vital GmbH Gebäude K56 51366 Leverkusen, Germany http://www.bayerhealthcare.com
Contact Ms Astrid Kranz +49 30 46812057
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Bayer Vital GmbH

Riociguat von Bayer erstes wirksames Medikament bei Patienten mit chronisch-thromboembolischer pulmonaler Hypertonie (CTEPH)

Phase-III-Studie CHEST-1 erreicht primären Endpunkt / Statistisch signifikante Verbesserung beim Sechs-Minuten Gehtest bei Patienten mit inoperabler oder residueller CTEPH unter Riociguat / Gute Verträglichkeit und positives Sicherheitsprofil

(PresseBox) (Berlin, )
Bayer HealthCare hat heute positive Daten aus der Phase-III-Zulassungsstudie CHEST-1 bekanntgegeben. Die Studie untersuchte Riociguat in Patienten mit inoperabler chronisch-thromboembolischer pulmonaler Hypertonie (CTEPH) sowie in Patienten mit andauernder oder wiederkehrender pulmonaler Hypertonie nach einer Operation. Die CHEST-1-Studie erreichte mit einer statistisch signifikanten Verbesserung beim Sechs-Minuten-Gehtest ihren primären Endpunkt. In der Studie steigerten Patienten, die mit Riociguat behandelt wurden, im Vergleich zu Placebo nach 16 Wochen ihre Leistungsfähigkeit um 46 Meter gegenüber dem Ausgangswert (95%-CI [25-67 Meter] p<0,0001). Die Studienergebnisse wurden als "Late Breaker" auf dem CHEST-Kongress 2012 - dem jährlichen Treffen des American College of Chest Physicians (ACCP) - in Fkpkmfs, RUB, rkdabppmsga.

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