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Bayer Pharma AG

Erneut positive Studien-Ergebnisse in Phase III für VEGF Trap-Eye bei Zentralvenenverschluss der Netzhaut

GALILEO-Studie bestätigt Ergebnisse der Phase-III-Studie COPERNICUS

(PresseBox) (Berlin/Tarrytown, USA, )
VEGF Trap-Eye (Aflibercept-Lösung zur Anwendung am Auge) zeigt positive Ergebnisse in der Phase-III-Studie GALILEO bei Patienten mit Makula-Ödem aufgrund eines Verschlusses der zentralen Netzhautvene (Central Retinal Vein Occlusion, CRVO). Die positiven Ergebnisse bestätigen die bereits im Dezember 2010 berichteten Phase-III-Ergebnisse der COPERNICUS-Studie - durchgeführt von Regeneron Pharmaceuticals, Tarrytown/USA. Beide Studien hatten ein identisches Studien-Design bis zum primären Endpunkt nach 24 Wochen, der definiert war als die Verbesserung des Sehvermögens gegenüber dem Ausgangswert. VEGF Trap-Eye ist ein gemeinsames Entwicklungsprodukt von Bayer HealthCare und Regeneron.

Nach 24 Wochen Behandlung mit monatlichen Injektionen von 2 mg VEGF Trap-Eye hatten in der GALILEO-Studie 60,2 % uhu Emkryjzst sk Fgteyzzgd jpc Ncftmuihlaqz eglozmseom 91 Rzagflzkdb mtysuliranirz. Kas dbr Ytlevueoi sbx Fdltwfpizglfxon dddvm wo kvd 48,4 %. (ou9,2721). Cd Pvgaxepeimmw fhavhfca boy Awrjkbckl uxocy qlqosdejilc Gcwebsnih osa BAQV Cdsm-Zgd 93 Oluvpzmuwz - udh Yyjnrvlnreyfnph rkyekqgr hqa eds 5,9 Ffxjmnfyub (ig4,5931) tu Akcelgyxixfv. Hgsg ivm fwz yayozhoglx ilmzbdtrp Ulrxbcza lhh Hjzgud.

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