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Phase 3 N=772 A Study to Evaluate the Efficacy and Safety of Subcutaneous MK-3222, Followed by an Optional Long-Term Safety Extension Study, in Participants With Moderate-to-Severe Chronic Plaque Psoriasis (MK-3222-010)

Plaque Psoriasis
Primary: Percentage of Participants With Psoriasis Area Sensitivity Index 75 (PASI-75) Response at Week 12 (Base Study) — 62.3; 63.8; 5.8 Percentage of Participants — p=<0.001
Sun Pharmaceutical Industries Limited Results Jun 2018 2.9% serious AE View details