drugset / Trial / NCT06751238

Study to Evaluate the Pharmacokinetics (PK), Safety and Tolerability up to 6 Years of Intravenous (i.v.) Secukinumab in Pediatric Participants With Juvenile Psoriatic Arthritis (JPsA).

NCT06751238

Phase 1 Recruiting 20 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the PK, safety and tolerability of multiple doses of intravenous (i.v.) secukinumab in pediatric participants with JPsA

Timeline

Start
2025-09-24
Primary completion
2032-11-30
Completion
2032-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody Intravenous