drugset / Trial / NCT03090100

A Study to Evaluate the Comparative Efficacy of CNTO 1959 (Guselkumab) and Secukinumab for the Treatment of Moderate to Severe Plaque-type Psoriasis

NCT03090100 ↗

Phase 3 Completed 1048 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy of guselkumab compared with secukinumab for the treatment of participants with moderate to severe plaque-type psoriasis.

Timeline

Start
2017-04-27
Primary completion
2018-08-02
Completion
2018-09-20

Outcome

Met primary endpoint

paper The proportion of patients with a PASI 90 response at week 48 was greater in the guselkumab group (451 [84%]) than in the secukinumab group (360 [70%]; p<0·0001). PMID 31402114 ↗

release “announced results from the ECLIPSE study demonstrating that TREMFYA® (guselkumab) was superior to Cosentyx® (secukinumab)*” jnj.com ↗

release “84.5 percent of patients receiving TREMFYA achieved the primary endpoint of a PASI 90 response at week 48” jnj.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Guselkumab Monoclonal antibody 100 mg Subcutaneous
Comparator Secukinumab Monoclonal antibody 300 mg Subcutaneous

Indications