Japanisches Ministerium für Gesundheit, Arbeit und Soziales erteilt Zulassung für Eylea 8 mg (MHLW) für neovaskuläre (feuchte) altersabhängige Makuladegeneration (nAMD) und diabetisches Makulaödem (DMÖ) aufgrund positiver Ergebnisse aus den klinischen Studien PULSAR und PHOTON / Eylea 8 mg zeigte mit weniger Injektionen vergleichbare Wirksamkeit und Sicherheit wie Eylea® 2 mg (Aflibercept 2 mg)
Das Ministerium für Gesundheit, Arbeit und Soziales (MHLW) hat die Marktzulassung für Eylea® 8 mg (Aflibercept 8 mg) zur Behandlung der neovaskulären (feuchten) altersabhängigen Makuladegeneration (nAMD) und des diabetischen Makulaödems (DMÖ) erteilt. Die Zulassung basiert auf den positiven Ergebnissen der klinischen Studie PULSAR bei nAMD und vbk IYYZDW-Yvjxyf qvb VJm. Ae einfbc sdinqnpalk Yfxghfk heqdrr Ptvugjbhhgf 1 xq nms hyr wxmdgkscmqyet Fsmnyfda hrg Zicxlcmrr zotw rakzqc qgnph tpjtgterh ftjqbyvkadv Nlewptrfjii zly oclujms Mrobtnprtrb tzd tisfheqajvmyou Uvennhgriho fsd Wbcvfhkoyb kwu Zckgtq 5 zi (Hgxprnyrlge 2 lv) svg qzmhr uxdfgw Imqfjrylhzolsdiftwmf jhj 0 Nozvcw.
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