Tocilizumab + methotrexate(MTX)
DrugTocilizumab:8 mg/kg every4weeks,IV infusion methotrexate:10-20 mg/week
NCT Number: NCT01258712
This is a Phase III study to evaluate efficacy and safety of Tocilizumab in patients with Rheumatoid Arthritis.
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Notify Me20 year–75 year
All sexes
Interventional
Phase 3
Buddhist Dalin Tzu Chi General Hospital, Chiayi City, Taiwan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tocilizumab:8 mg/kg every4weeks,IV infusion methotrexate:10-20 mg/week
Tocilizumab placebo:8 mg/kg every 4 weeks,IV infusion methotrexate:10-20 mg/week
Time frame: at baseline and week 24
Time frame: at baseline and week 24
Time frame: at baseline and week 24
Time frame: at baseline and week 24
Time frame: at baseline and week 24
Time frame: at week 24
Time frame: from baseline to week 24
Time frame: from baseline to week 24
Time frame: from baseline to week 24
Time frame: from baseline to week 24
Time frame: from baseline to week 24
Time frame: from baseline to week 24
Time frame: from baseline to week 24
Chugai Pharma Taiwan
Industry
Randomized, Placebo-controlled Study of Tocilizumab in Combination With Methotrexate for Treatment of Moderate to Severe Rheumatoid Arthritis Patients
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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