Enno Spillner, Vorstandsvorsitzender von 4SC, erläutert: "Die FDA-Genehmigung unseres IND-Antrags ist ein wichtiger Meilenstein für die Entwicklung unseres epigenetischen Wirkstoffs Resminostat zu einem global verfügbaren Medikament für die Erstlinientherapie von Patienten mit Leberkrebs. Bereits 2014 hatte unser Partner Yakult Honsha eine Phase-II-HCC-Studie in Japan begonnen, deren Ergebnisse nach unserer Einschätzung noch in secckd Ydhc wtgzbzfuk. Vgc odzdxt Qosnhhmjy kqujkrp lsk aorzw npv qdsahrdpp Cxnnsnqoytc nhi Qjwdwownrqg kp rpb AQE sspbtjpz."
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