A Study to Compare Subcutaneous Versus Intravenous Administration of RoActemra/Actemra (Tocilizumab) in Participants With Moderate to Severe Active Rheumatoid Arthritis

Completed · Phase 3 · Has a placebo group

Conditions studied: Rheumatoid Arthritis

In brief

This randomized, double-blind, parallel group study compares the efficacy and safety of subcutaneous (sc) versus intravenous (iv) administration of tocilizumab in participants with moderate to severe active rheumatoid arthritis. Participants were randomized to receive either tocilizumab 162 mg sc weekly plus iv placebo every 4 weeks, or tocilizumab 8 mg/kg iv every 4 weeks plus sc placebo weekly during the double-blind period from baseline to Week 24. The double-blind period was followed by a 72-week open-label treatment with some switching of sc and iv administration. No placebo was administered in the open-label phase. Participants continued on their stable dose of disease-modifying antirheumatic drugs (DMARDs) throughout the study. Anticipated time on study treatment was 2 years.

Key facts

Study ID

NCT01194414

Run by

Hoffmann-La Roche

People needed

1262

Starts

2010-09-01

Expected to finish

2013-08-01

Last updated by the study team

2016-06-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult participants, ≥ 18 years of age
• Rheumatoid arthritis of ≥ 6 months duration, according to American College of Rheumatology (ACR) criteria
• Swollen joint count (SJC) ≥ 4 (66 joint count), tender joint count (TJC) ≥ 4 (68 joint count) at screening and baseline
• Inadequate response to current DMARD therapy
• Permitted DMARDs must be at stable dose for ≥ 8 weeks prior to baseline
• Oral corticosteroids (≤ 10 mg/day prednisone or equivalent) and NSAIDs (up to maximum recommended dose) must be at stable dose for ≥ 4 weeks prior to baseline

You may not qualify if…

• Major surgery (including joint surgery) within 8 weeks prior to screening or planned major surgery within 6 months following randomization
• Rheumatic autoimmune disease other than RA
• Functional class IV (ACR classification)
• Diagnosis of juvenile idiopathic arthritis (JIA) or juvenile rheumatoid arthritis (JRA) and/or RA before the age of 16
• Prior history of or current inflammatory joint disease other than RA
• Intra-articular or parenteral corticosteroids within 4 weeks prior to baseline
• Previous treatment with tocilizumab
• Active current or history of recurrent infection

Where it is running

• Study site — Tuscaloosa, Alabama, United States
• Study site — Tucson, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Long Beach, California, United States
• Study site — Los Angeles, California, United States
• Study site — Upland, California, United States
• Study site — Van Nuys, California, United States
• Study site — Denver, Colorado, United States
• Study site — Bridgeport, Connecticut, United States
• Study site — Delray Beach, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Ocala, Florida, United States
• Study site — Orlando, Florida, United States
• Study site — Palm Harbor, Florida, United States
• Study site — Pinellas Park, Florida, United States
• Study site — South Miami, Florida, United States
• Study site — Tampa, Florida, United States
• Study site — Coeur d'Alene, Idaho, United States
• Study site — Morton Grove, Illinois, United States
• Study site — Wichita, Kansas, United States
• Study site — Monroe, Louisiana, United States
• Study site — Petoskey, Michigan, United States
• Study site — Saint Claire Shores, Michigan, United States
• Study site — Eagan, Minnesota, United States
• Study site — Huntsville, Alabama, United States

Full record on ClinicalTrials.gov

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