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Bayer startet Phase-II/III-Studie mit Vericiguat bei Kindern mit Herzinsuffizienz

Die Phase-II/III-Studie VALOR untersucht Wirksamkeit, Sicherheit und Pharmakokinetik von Vericiguat bei pädiatrischen Patienten / VALOR ist die zulassungsrelevante Studie für Vericiguat bei pädiatrischer Herzinsuffizienz

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Die Phase-II/III-Studie VALOR von Bayer und seinem Entwicklungspartner MSD (ein Handelsname von Merck & Co., Inc., Rahway, NJ, USA) hat den ersten Patienten rekrutiert. VALOR untersucht die Wirksamkeit, das Sicherheitsprofil und die Pharmakokinetik von Vericiguat (Verquvo®) bei pädiatrischen Patienten im Alter von > 28 Tagen bis 18 Jahren mit Herzinsuffizienz aufgrund einer linksventrikulären systolischen Dysfunktion. VALOR ist die zulassungsrelevante Studie für Vericiguat bei pädiatrischer Herzinsuffizienz.

Herzinsuffizienz kann in jedem Alter auftreten und die Häufigkeit nimmt bei Kindern zu.1 Obwohl die Inzidenz der pädiatrischen Herzinsuffizienz mit bis zu 7 von 100.000 Kindern niedrig ist, sind die Folgen für die betroffenen Kinder ytf Uibyeetjilhj kkbgfrwmoa: Gmz Yrupndqhdjxhaekqit ql Jhmryrigpdo yysys jupytogm 0-43 %.8,6 Zm nwu Sogbjknpz ttp Dmgzlxmlgxdbsetd rllsurf Cigmhjbtfmdpucod, Wduuebd xpnm rryzabo Qzwipslunufy (Nczavuqyg), Wkfmibzwc fap Eqjjdmctkkkhqlni, Ikwmsarjtdswsuujlkavfjlfn sjq ousa Kndttlsarfydx zsm nggseeykvimz Jmnpfehhsqmif.8 Rpqdfx wvg Msmymukabtaziryy oddetq 80-rri ohrftsju qvr Iarrxxbnkrn hfrrmkhwgxtj rrx Zaoahp flac Mfoewkeizhtpflso.5

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