drugset / Trial / NCT02733094

Single-arm Study to Assess a Potential Effect of Anti-IL-17 (Secukinumab) in the Treatment of Pyoderma Gangrenosum

NCT02733094

Phase 1/2 Completed 8 enrolled Technical University of Munich Novartis · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to explore the efficacy and safety of anti-Interleukin-(IL)17 therapy (secukinumab, administered weekly for 4 weeks followed by four-weekly administration until week 16) for the treatment of pyoderma gangrenosum.

Timeline

Start
2016-04
Primary completion
2019-09-10
Completion
2019-09-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody 300 mg

Indications