A 64-Week, Phase 3, Randomized, Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222), Followed by an Optional Long-Term Safety Extension Study, in Subjects With Moderate-to-Severe Chronic Plaque Psoriasis (Protocol No. MK-3222-010)
Principal Investigator
Vincent C. HoOverview
Study Start/End
Oct 7, 2013 to Dec 29, 2017Locations
Vancouver Community, Vancouver General Hospital
Name/Title
Sze Wai Ho, Clinical Trial CoordinatorPhone
604-875-5296Email Address
szewai.ho@ubc.caPurpose of Study
This study is being conducted to evaluate the efficacy and safety/tolerability of subcutaneous MK-3222, followed by an optional long-term safety extension study, in participants with moderate-to-severe chronic plaque psoriasis.
Eligibility
Visit ClinicalTrials.gov for more information.
Disclaimer
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