drugset / Trial / NCT03202368

An Extension Study to Evaluate Long-Term Safety of Subcutaneous (SC) Tocilizumab in Participants With Giant Cell Arteritis (GCA)

NCT03202368 ↗

Phase 3 Completed 3 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, interventional, open-label, long-term extension study of Study WA28119 (NCT01791153) to evaluate the long-term safety of SC tocilizumab in participants with GCA who subsequently have flare or persisting disease activity. A maximum of 11 participants from six centers in France that participated in the WA28119 study will be enrolled. The entire study duration is anticipated to be approximately 160 weeks.

Timeline

Start
2017-10-25
Primary completion
2019-08-21
Completion
2019-08-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Tocilizumab Monoclonal antibody 162 mg Subcutaneous

Indications