drugset / Trial / NCT03158285

A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis

NCT03158285 ↗

Phase 3 Completed 741 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
2017-07-12
Primary completion
2019-02-25
Completion
2020-11-10

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo to Guselkumab 100 mg q4w vs Guselkumab 100 mg q8w; p < 0.001 NCT03158285 ↗

paper Significantly greater proportions of patients in the guselkumab every 4 weeks group (156 [64%] of 245 [95% CI 57-70]) and every 8 weeks group PMID 32178766 ↗

release “In DISCOVER-2, the primary endpoint was also met; 64 percent of patients receiving TREMFYA q4w or q8w achieved an ACR20 response” jnj.com ↗

release “In DISCOVER-2, 64 percent of patients who received TREMFYA every 8 weeks achieved an ACR20 response, versus 33 percent treated with placebo (p<0.0001).” jnj.com ↗

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 Subcutaneous

Indications