ML28641 - Subcutaneous tocilizumab in rheumatoid arthritis
Research type
Research Study
Full title
Open-label, Phase IIIb study to evaluate the efficacy and safety of subcutaneous (SC) Tocilizumab monotherapy or combination therapy with methotrexate (MTX) or other non-biologic disease modifying anti-rheumatic drugs (DMARDs) in patients with severe Rheumatoid Arthritis (RA) who are being treated with an anti-tumour necrosis factor (anti-TNF) agent and that have not achieved an adequate response to treatment.
IRAS ID
133239
Contact name
John Isaacs
Contact email
Sponsor organisation
Roche Products Ltd
Eudract number
2013-000054-22
ISRCTN Number
n/a
REC name
Yorkshire & The Humber - Leeds East Research Ethics Committee
REC reference
13/YH/0282
Date of REC Opinion
9 Sep 2013
REC opinion
Favourable Opinion