drugset / Trial / NCT03162796

A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis Including Those Previously Treated With Biologic Anti -Tumor Necrosis Factor (TNF) Alpha Agent(s)

NCT03162796 ↗

Phase 3 Completed 383 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy of guselkumab treatment in participants with active Psoriatic Arthritis (PsA) by assessing the reduction in signs and symptoms of PsA.

Timeline

Start
2017-08-24
Primary completion
2019-03-14
Completion
2019-11-18

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Guselkumab 100 mg q8w; p < 0.001; Difference in percentage 29.8 (95% CI 18.6 to 41.1); Cochran-Mantel-Haenszel NCT03162796 ↗

registry analysis (superiority test); Placebo vs Guselkumab 100 mg q4w; p < 0.001; Difference in percentage 37.1 (95% CI 26.1 to 48.2); Cochran-Mantel-Haenszel NCT03162796 ↗

release “DISCOVER-1 and DISCOVER-2, which showed TREMFYA reached each study’s primary endpoint of ACR 20 response at 24 weeks.” jnj.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Guselkumab Monoclonal antibody 100 mg —

Indications