Resminostat met the primary endpoint in the RESMAIN study, demonstrating a statistically significant improvement in progression free survival in CTCL patients by ninety seven point six percent (97.6%) with a risk reduction of thirty eight percent (38%) compared to placebo
Resminostat is the first and only drug to show statistically proven PFS improvement in the maintenance setting in CTCL
Resminostat did not meet the key secondary endpoint – time to symptom (pruritus) worsening
4SC intends to approach the European Medicines Agency in order to evaluate the preparation of its Marketing Authorization Application
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