drugset / Trial / NCT06130540

Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Intravenous Secukinumab in Patients With GCA or PMR

NCT06130540

Phase 1 Completed 65 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will examine how intravenous (i.v.) Secukinumab will be processed in the body (pharmacokinetics \[PK\]) and whether it will be safe and tolerable after multiple doses of i.v. Secukinumab infusion in adult patients with giant cell arteritis (GCA) or polymyalgia rheumatica (PMR).

Timeline

Start
2024-03-27
Primary completion
2025-03-12
Completion
2025-04-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody Intravenous