drugset / Trial / NCT02207244

A Study of Guselkumab in the Treatment of Participants With Moderate to Severe Plaque-Type Psoriasis With Randomized Withdrawal and Retreatment

NCT02207244 ↗

Phase 3 Completed 992 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety, and tolerability of guselkumab (CNTO 1959) in the treatment of participants with moderate to severe plaque-type psoriasis (scaly skin rash).

Timeline

Start
2014-11-03
Primary completion
2015-10-01
Completion
2020-07-01

Outcome

Met primary endpoint

registry NUMBER Placebo: 8.5 percentage of participants NUMBER Guselkumab 100 mg: 84.1 percentage of participants analysis (unspecified test); Placebo vs Guselkumab 100 mg; p < 0.001; Cochran-Mantel-Haenszel chi-square test NCT02207244 ↗

registry NUMBER Placebo: 2.4 percentage of participants NUMBER Guselkumab 100 mg: 70.0 percentage of participants analysis (unspecified test); Placebo vs Guselkumab 100 mg; p < 0.001; Cochran-Mantel-Haenszel chi-square test NCT02207244 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject Guselkumab Monoclonal antibody 100 mg Subcutaneous

Indications