drugset / Trial / NCT01995201

A Study of Subcutaneous RoActemra/Actemra (Tocilizumab) as Monotherapy or in Combination With Methotrexate or Other Non-Biologic DMARDs in Patients With Active Rheumatoid Arthritis

NCT01995201 ↗

Phase 3 Completed 401 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This multicenter, open-label study will evaluate the efficacy and safety of subcutaneously administered RoActemra/Actemra (tocilizumab) as monotherapy or in combination with methotrexate or other non-biologic DMARDs in patients with active rheumatoid arthritis and an inadequate response to non-biologic DMARDs or to one anti-TNF. In Phase 1, all patients will receive RoActemra/Actemra 162 mg subcutaneously (sc) weekly for Weeks 1 to 24, with or without methotrexate or other non-biologic DMARDs. For Part 2, patients who achieve sustained clinical DAS28-ESR remission at Weeks 20 and 24 will be randomized to receive RoActemra/Actemra 162 mg sc either weekly or every 2 weeks for Weeks 24 to 48, with or without methotrexate or other non-biologic DMARDs. Patients who do not achieve sustained clinical remission but achieve low disease activity (DAS-ESR \</= 3.2) will continue the initial treatment of RoActemra/Actemra 162 mg sc weekly for Weeks 24 to 48, with or without methotrexate or other non-biologic DMARDs.

Timeline

Start
2013-09
Primary completion
2015-07
Completion
2016-03

Outcome

Missed primary endpoint

registry analysis (other test); Phase 1: Tocilizumab Monotherapy vs Phase 1: Combination Therapy; p = 0.5231; Chi-squared NCT01995201 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tocilizumab Monoclonal antibody 162 mg Subcutaneous
Background Methotrexate Small molecule — —

Indications