Study of the Response and Cardiorespiratory Endurance in Early RA Patients Treated With Tocilizumab or Methotrexate (TOMERA)
Comparative Study of the Clinical Response and Cardiorespiratory Endurance in Early Rheumatoid Arthritis Patients Treated With Tocilizumab or Methotrexate Addendum Protocol : Global Gene Expression Profiles in Synovial Biopsies
To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.
The secondary endpoints : analyze the clinical efficacy of Tocilizumab in this population and correlate the CRE response with other marker (CRP, Hb, DAS, HAQ) and evaluate the safety profile of Tocilizumab.
研究概览
详细说明
Rheumatoid arthritis (RA) is the most prevalent (about 1%) inflammatory rheumatic disorder.
Interleukin-6 (IL-6) has emerged as a potential therapeutic target in RA. This is based on the greater understanding of the role this cytokine can play in various aspects of the pathogenesis of RA. It has been shown that IL-6 is responsible for various clinical symptoms, including,fatigue, anemia, anorexia, fever, as well as the production of autoantibodies and increase in the erythrocyte sedimentation rate, all of which develop in patients with RA. Tocilizumab, as monotherapy and in combination with methotrexate, has been shown to be effective for RA patients with insufficient response to methotrexate or other disease-modifying antirheumatic drugs. These observations about the effects of tocilizumab were extended to patients refractory to tumor necrosis factor inhibitors. Tocilizumab also slows down the progression of structural joint damage. Furthermore, a 5-year long-term safety and efficacy has been shown. The place of Tocilizumab therapy in early RA is still unknown.
Cardiorespiratory endurance (CRE), the most fundamental component of physical fitness can be severely impaired in patients with rheumatoid arthritis (RA). It has been shown that intensive and early treatment of RA can induce sustained clinical remission, improve general health and physical fitness and might therefore have an impact on the quality of life of RA patient. This study was planned to measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Bruxelles、比利时、1200
- Université Catholique de Louvain
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Diagnosis of RA (according to American College of Rheumatology ACR criteria)
- Disease duration < 2 years.
- Age between 18 and 70 years old.
- Active RA defined by a disease activity score 28 DAS28-CRP score > 3.2 with a swollen joint count ≥ 4
- MTX naive
- Stable therapy with corticosteroids or nonsteroidal anti-inflammatory drug NSAIDs
- Presence of knee arthralgia or synovitis (addendum protocol with synovial biopsy).
Exclusion Criteria:
Previous MTX treatment. Exclusion for severe physical handicap to perform CRE. Exclusion for general safety (history of severe allergic reaction, sepsis, malignancy within 5 years, pregnancy, severe heart failure) Concurrent treatment with other DMARDs than MTX or any anti-TNF and biological therapies.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Tocilizumab
Tocilizumab (8 mg/kg monthly from week 0 to 20)
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Tocilizumab (8 mg/kg monthly from week 0 to 20)
其他名称:
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有源比较器:Methotrexate
MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8
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MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.
大体时间:2 years
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not necessary
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2 years
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
To analyze the clinical efficacy of Tocilizumab in this population.
大体时间:2 years
|
no necessary
|
2 years
|
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To correlate the CRE response with other marker (CRP, Hb, Disease activity score DAS, HAQ).
大体时间:2 years
|
no necessary
|
2 years
|
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To evaluate the safety profile of Tocilizumab.
大体时间:2 years
|
no necessary
|
2 years
|
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To assess the effect of Tocilizumab on synovial histopathology of early RA
大体时间:2 years
|
not necessary
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2 years
|
合作者和调查者
调查人员
- 首席研究员:Patrick Durez, MD、Université Catholique de Louvain
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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