The primary purpose of this proof-of-activity, phase 2 trial is to evaluate the safety and activity of orticumab in subjects with moderate to severe psoriasis and cardiometabolic risk factors.
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Mean percent change from Baseline in Psoriasis Area Severity Index (PASI)
Timeframe: 106 days (Week 15)
Percentage of participants achieving treatment success by the 5-point static Investigator's Global Assessment modified 2011 version (sIGA) Score
Timeframe: 106 days (Week 15)
Incidence of Treatment Emergent Adverse Events (TEAEs)
Timeframe: 106 days (Week 15)
Incidence of serious adverse events (SAEs)
Timeframe: 106 days (Week 15)
Incidence of abnormal hemodynamic parameters
Timeframe: Weeks 3, 7, 11 and 15
Incidence of abnormal laboratory tests results
Timeframe: Weeks 3 and 15
Incidence of abnormal physical examination findings
Timeframe: Weeks 3, 7, 11, 15