drugset / Trial / NCT04638647

Secukinumab Open Label Roll-over Extension Protocol

NCT04638647

Phase 4 Recruiting 1000 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess long term safety in participants who have completed a Novartis trial with secukinumab, have been judged by the investigator to benefit from continued treatment with secukinumab, and are unable to obtain the marketed secukinumab formulation.

Timeline

Start
2020-12-22
Primary completion
2030-01-29
Completion
2030-04-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody 75 mg Subcutaneous
Subject Secukinumab Monoclonal antibody 150 mg Subcutaneous
Subject Secukinumab Monoclonal antibody 300 mg Subcutaneous