Articles

Results of this post-hoc analysis of the TARGET study demonstrated that patients with active, moderate-to-severe rheumatoid arthritis (RA) and inadequate response to tumor necrosis factor (TNF) inhibitors treated with sarilumab 150 mg or 200 mg every 2 weeks on a conventional synthetic disease-modifying antirheumatic drug (csDMARD) background achieved greater clinical responses compared with those treated with placebo, regardless of baseline disease activity. However, a greater sarilumab treatment effect was achieved by patients with higher baseline disease activity.

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In this analysis of the TARGET study, a sustained clinically significant response was achieved by more patients with active, moderate-to-severe rheumatoid arthritis (RA) and inadequate response to, or intolerance of, tumor necrosis factor (TNF) inhibitors treated with sarilumab plus conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) versus those treated with placebo plus csDMARDs.

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This post-hoc analysis showed that the efficacy of sarilumab was maintained or improved in patients with rheumatoid arthritis (RA) who switched or continued into the open-label EXTEND trial to receive sarilumab 200 mg every 2 weeks (q2w) after completion of the ASCERTAIN trial, with particularly increased efficacy occurring in those who initially received tocilizumab or sarilumab 150 mg q2w

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This post-hoc analysis showed that ongoing sarilumab treatment on the MOBILITY and TARGET studies resulted in achievement of remission or low disease activity increased through week 24 in patients with rheumatoid arthritis (RA) and inadequate response to methotrexate and inadequate response to, or intolerance of, tumor necrosis factor inhibitors. Read More ›

Highly sensitive cardiac troponin may provide prognostic information on long-term cardiovascular (CV) event risk assessment in patients with rheumatoid arthritis (RA) without prior diagnosis of CV disease. Read More ›

Post-hoc pooled analyses of the MOBILITY and TARGET trials showed that sarilumab plus disease-modifying antirheumatic drug (DMARD) treatment in diabetic patients with rheumatoid arthritis (RA) led to reductions in glycosylated hemoglobin (HbA1c) and lowered fasting glucose levels; reductions in HbA1c were also achieved by nondiabetic patients with RA. Read More ›

Results of the randomized, placebo-controlled, phase 3 SELECT-NEXT study showed that upadacitinib, a selective JAK-1 inhibitor, at 15 mg and 30 mg once daily, was efficacious in patients with rheumatoid arthritis (RA) who had inadequate response to conventional synthetic disease-modifying antirheumatic drugs (DMARDs), with a safety and tolerability profile that was consistent with that previously reported. Read More ›

In this long-term efficacy and safety analysis of the global phase 3 SIRROUND-D trial, improvements in signs and symptoms of rheumatoid arthritis (RA) and health-related physical and emotional well-being were maintained with sirukumab treatment in patients with active RA despite disease-modifying antirheumatic drugs (DMARDs). Read More ›

In this post-hoc analysis of the AMPLE trial, subcutaneous (SC) abatacept treatment was associated with lower cost per responder compared with SC adalimumab in patients with seropositive, erosive early rheumatoid arthritis (RA). Read More ›

This analysis showed that patients with active, moderate-to-severe rheumatoid arthritis (RA) treated with sarilumab plus methotrexate (MTX) achieved longer duration of response versus those treated with placebo plus MTX, regardless of the definition of response used. Read More ›

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