drugset / Trial / NCT01729754

A Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222) in Participants With Moderate-to-Severe Chronic Plaque Psoriasis Followed by a Long-term Extension Study (MK-3222-011)

NCT01729754 ↗

Phase 3 Completed 1090 enrolled Sun Pharmaceutical Industries, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is being conducted to evaluate the efficacy and safety/tolerability of tildrakizumab (SCH 900222/MK-3222) in a population of participants with moderate-to-severe plaque psoriasis. The primary hypotheses of the study are that tildrakizumab is superior to placebo in the treatment of moderate-to-severe chronic plaque psoriasis as measured by the proportion of participants achieving \>= Psoriasis Area Sensitivity Index of 75% (PASI-75) response and the proportion of participants with a Physician's Global Assessment (PGA) score of "clear" or "minimal" with at least a 2 grade reduction from baseline at Week 12.

Timeline

Start
2013-02-05
Primary completion
2015-09-28
Completion
2021-10-26

Outcome

Met primary endpoint

registry analysis (superiority test); Tildrakizumab 200 mg vs Placebo; p <0.001; Difference in percentages 59.8 (95% CI 52.9 to 65.9) NCT01729754 ↗

registry analysis (superiority test); Tildrakizumab 100 mg vs Placebo; p <0.001; Difference in percentages 55.5 (95% CI 48.3 to 61.8) NCT01729754 ↗

registry analysis (superiority test); Tildrakizumab 200 mg vs Placebo; p <0.001; Difference in percentages 54.7 (95% CI 47.9 to 60.8) NCT01729754 ↗

registry analysis (superiority test); Tildrakizumab 100 mg vs Placebo; p <0.001; Difference in percentages 50.2 (95% CI 43.2 to 56.5) NCT01729754 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Etanercept Protein / enzyme biologic 50 mg Subcutaneous
Subject Tildrakizumab Monoclonal antibody 100 mg Subcutaneous
Subject Tildrakizumab Monoclonal antibody 200 mg Subcutaneous

Indications