drugset / Trial / NCT02165345

Extension Study Evaluating the Safety and Efficacy of Subcutaneous Tocilizumab (RoActemra/Actemra) Administration in Systemic and Polyarticular-Course Juvenile Idiopathic Arthritis

NCT02165345

Phase 1 Completed 82 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

This open-label extension of the JIGSAW studies (WA28117 \[NCT01904279\] and WA28118 \[NCT01904292\]) is designed to evaluate the long-term safety and efficacy of subcutaneous (SC) tocilizumab treatment in participants with polyarticular-course and systemic juvenile idiopathic arthritis (pJIA and sJIA). Participants from the 2 JIGSAW studies will continue to receive 162 milligrams (mg) of SC tocilizumab with treatment schedule according to arthritis subtype and body weight. Participants will receive the treatment until commercial availability of the drug or for a maximum of 5 years, whichever is earlier.

Timeline

Start
2014-07-16
Primary completion
2021-11-24
Completion
2021-11-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Tocilizumab Monoclonal antibody 162 mg Subcutaneous