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More info
You can access this
clinical trial
if you have
Rheumatoid Arthritis
and you are
over 18
years old
3
This is a trial in the final phase before the treatment is released on the market.
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The purpose

This open-label, single arm study will evaluate the safety and efficacy of RoActemra/Actemra (tocilizumab) in patients with active, moderate to severe rheumatoid arthritis who have an inadequate response to disease-modifying antirheumatic drugs (DMARDs) or anti-TNF. Patients will receive RoActemra/Actemra at a dose of 8 mg/kg (max 800 mg) intravenously every 4 weeks for a total of 6 infusions. Non-biologic DMARD therapy may be continued throughout the study. Anticipated time on study treatment is 24 weeks.

Provided treatments

  • Drug: tocilizumab [RoActemra/Actemra]

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01326962. The sponsor of the trial is Hoffmann-La Roche and it is looking for 28 volunteers for the current phase.
Official trial title:
Tocilizumab Efficacy and Safety in RA Patients After Inadequate Response to DMARDs or Anti-TNF