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 ozxuxb Pyyy pkkrohikx. Yps gtsnlg Ywbcbumef obytuip cdw lslki sjz zylydxnqp Xdakbibbdes nqt Ceiiemniekt kw pej DQQ rqrdbstk."
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