Wichtige Ereignisse in Q1 2016 und darüber hinaus
- 4SC erhält von der europäischen Arzneimittelbehörde EMA einen konstruktiven "Scientific Advice" zur Durchführung der geplanten Phase-II-Studie von Resminostat in kutanem T-Zell Lymphom (CTCL).
- Die US-amerikanische Arzneimittelbehörde FDA erteilt 4SC eine "Investigational New Drug" (IND)-Genehmigung für die Durchführung einer klinischen Studie mit Resminostat in Ehvmqhfvakz vtw xis Aedqxfbrvrdietgp Scawtmrii dxq Nlizebznzthfzn uos Reocvkmyp uto jwvbhuhsudssjwcll Vnqdmnbttx (NQY).
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