drugset / Trial / NCT03504852

Efficacy and Safety of 2 Secukinumab Regimens in 90kg or More Weight Group With Moderate/Severe Chronic Plaque Psoriasis

NCT03504852 ↗

Phase 3 Completed 331 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindOther

Summary

The purpose of this study is to assess secukinumab high dose (every 2 weeks) vs standard dose (every 4 weeks) in heavy body weight subjects with moderate to severe plaque psoriasis.

Timeline

Start
2018-06-25
Primary completion
2019-09-13
Completion
2020-07-15

Outcome

Met primary endpoint

paper At week 16, Q2W dosing (n = 165) led to significantly higher PASI 90 responses vs. Q4W [n = 166; 73.2% vs. 55.5%, one-sided P-value = 0.0003, PMID 34981829 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody 300 mg Subcutaneous

Indications