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Effect of Monoclonal Anti-IL6 Antibody (Tocilizumab) on the Cardiovascular Risk in Patients With Rheumatoid Arthritis (TOCRIVAR)

2017年2月7日 更新者:Hospital Universitario de Canarias

The purpose of this study is to determine whether tocilizumab changes the cardiovascular risk factors on patients with arthritis rheumatoid.

Study hypothesis: the IL-6 contributes to increase the cardiovascular risk factors of patients with rheumatoid arthritis because it produces systemic effects as increasing weight and atherogenic body fat, changing energy homeostasis and inducing the adipokines production and the insulin resistence.

研究概览

地位

未知

研究类型

介入性

注册 (预期的)

28

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Santa Cruz de Tenerife
      • La Laguna、Santa Cruz de Tenerife、西班牙、38320
        • Hospital Universitario de Canarias

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 70年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥ 18 and <70 years.
  2. Diagnosis of active Rheumatoid Arthritis, moderate to severe (≥ 3.2 DAS28) of ≥ 6 months duration.
  3. Patients with an inadequate clinical response to a stable dose of non-biological DMARDs or anti-TNF treatment for a period ≥ 8 weeks before treatment.
  4. If patients are receiving oral corticosteroids, the dose should have been ≤ 10 mg predinosona and stable for at least one month before the start of treatment (day 1).
  5. Patients who are able and wish to sign the informed consent and comply with the requirements of the study protocol.

Exclusion Criteria:

  1. Major surgery (including joints surgery) within eight weeks prior to the screening visit or major surgery scheduled for six months after first infusion.
  2. Other Rheumatic autoimmune diseases, including systemic lupus erythematosus (SLE), mixed connective tissue disease (MCTD), scleroderma, polymyositis or systemic involvement secondary to AR (such as vasculitis, pulmonary fibrosis or Felty's syndrome). It's allowed the inclusion of patients with interstitial pulmonary fibrosis and be still able to tolerate treatment with MTX. Sjögren's syndrome with RA is not considered exclusion criterion.
  3. Rheumatoid arthritis with Functional Class IV as defined in the RA Classification of the ACR (complete or significant disability of patients, confined to bed or to the wheelchair and without possibilities to take care themselves).
  4. Prior or actual inflammatory joint disease different of RA (eg, gout, reactive arthritis, psoriatic arthritis, seronegative spondyloarthropathy, Lyme disease).

    Specific drug criteria

  5. Treatment with any investigational agent in the four weeks before the screening visit (or time equivalent to five half-lives of the investigational drug, whichever is longer).
  6. Immunization with a live vaccine / attenuated in the four weeks prior to the baseline visit.
  7. Pretreatment with TCZ Laboratory Tests (at the screening visit)
  8. Serum creatinine> 142 mmol / l (1.6 mg / dL) in women and> 168 mmol / l (1.9 mg / dl) in men and absence of active renal disease.
  9. ALT (SGPT) and AST (SGOT)> 1.5 ULN (if the initial sample of ALT [SGPT] or AST [SGOT] gives a value> 1.5 times ULN, you can take and analyze a second sample during the selection period).
  10. Platelet count <100 x 109 / l (100.000/mm3).
  11. Hemoglobin <85 g / dl (<8.5 g / l, 5.3 mmol / l).
  12. Leukocytes <1.0 x 109 / l (1000/mm3), ANC <0.5 x 109 / L (500/mm3).
  13. RAL <0.5 x 109 / L (500/mm3).
  14. Positivity for surface antigen of hepatitis B (HBsAg) and antibodies to hepatitis C.
  15. Total bilirubin> ULN (if the initial sample of bilirubin> ULN, you can take and analyze a second sample during the selection period).
  16. Triglycerides> 10 mmol / l (> 900 mg / dl) at the screening visit (non fasting).
  17. Pregnant or lactating women.
  18. not use of reliable means of contraception, such as a physical barrier (patient and partner), pill or contraceptive patch, spermicide and barrier or IUD.
  19. Background of serious allergic or anaphylactic reactions to human monoclonal antibodies, humanized or murine.
  20. RXT evidence of clinically significant abnormality.
  21. Evidence of uncontrolled concomitant serious illness, cardiovascular, nervous system, lung (including obstructive pulmonary disease), renal, hepatic, endocrine (including uncontrolled diabetes mellitus), or gastrointestinal.
  22. history of diverticulitis, diverticulosis in antibiotic treatment, the physician should consider the benefit-risk ratio.
  23. Background of lower GI ulcer disease as the Crohn's disease, ulcerative colitis or other symptomatic conditions predisposed to perforations lower GI
  24. Uncontrolled diseases such as asthma, psoriasis or inflammatory bowel disease,... treated normally with corticosteroids orally or parenterally.
  25. Ongoing liver disease as determined by the principal investigator. (Patients with a history of elevated ALT (SGPT) will not be excluded)
  26. Active infections or recurrent infections in the past by mycobacteria, fungus, virus or bacteria (for example: tuberculosis, atypical mycobacterial disease, clinically significant abnormalities in RXT, hepatitis B and C, herpes zoster), or any major episode infection that required hospitalization or IV antibiotic treatment in the 4 weeks preceding the screening visit or oral antibiotic in the 2 weeks prior to the screening visit.
  27. Primary or secondary immunodeficiency.
  28. Evidence of active malignancy diagnosed within 5 years before the inclusion(including solid tumors and hematological), or breast cancer diagnosed in the previous 5 years.
  29. Active tuberculosis (TB) requiring treatment within 3 years above. Patients with a positive skin test tuberculin purified protein derivative (PPD) at the screening visit. Patients treated for tuberculosis no recurrence in the last three years will not be excluded.
  30. HIV positive patients.
  31. History of alcoholism, drug addiction or drug abuse in the six months before the screening visit.
  32. Painful neuropathies or other conditions that may interfere with the pain assessment.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:tocilizumab

All the patients are treated with tocilizumab before inclusion. The doses, frequency and duration are in acordance with the Summary of Characteristics of the Product authorised by EMA.

Usually 8mg/kg (not minor than 480 mg), once each 4 weeks.

At the moment of the ecography, the clinician evaluates the endothelial responses via applying braquial ischemia and administering sublingual nitroglicerin spray to evaluate vasodilation.

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
Framingham Point Scores
大体时间:Baseline and 52 weeks
Proportion of changes in Framingham Point Scores
Baseline and 52 weeks

次要结果测量

结果测量
措施说明
大体时间
Liver enzymes
大体时间:Baseline, 12, 24 and 52 weeks
Number of patients with liver enzymes elevated.
Baseline, 12, 24 and 52 weeks
Lipoprotein levels
大体时间:Baseline, 12, 24 and 52 weeks
Number of patients with elevated lipoprotein levels
Baseline, 12, 24 and 52 weeks
DAS28 score
大体时间:Baseline and 52 week
Variation in DAS28 score after tocilizumab
Baseline and 52 week
Number of patients with Adverse Drug Reactions
大体时间:up to 52 weeks
Number of patients with Adverse Drug Reactions as a measure of safety
up to 52 weeks
Insulinemia
大体时间:Baseline and 52 week
Change in insulinemia 52 weeks later.
Baseline and 52 week

其他结果措施

结果测量
措施说明
大体时间
Proportion of brachial artery vasodilation
大体时间:Baseline, 24 and 52 weeks
To evaluate the endothelial responses to ischemia and vasodilatation by ecography
Baseline, 24 and 52 weeks
cytokines, adipokines and adhesion molecules levels
大体时间:Baseline and 52 week
To evaluate changes in cytokines, adipokines and adhesion molecules
Baseline and 52 week

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

调查人员

  • 首席研究员:Federico Díaz González, MD, PhD、Hospital Universitario de Canarias

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2011年12月1日

初级完成 (预期的)

2017年3月1日

研究完成 (预期的)

2017年3月1日

研究注册日期

首次提交

2012年12月3日

首先提交符合 QC 标准的

2012年12月18日

首次发布 (估计)

2012年12月19日

研究记录更新

最后更新发布 (估计)

2017年2月9日

上次提交的符合 QC 标准的更新

2017年2月7日

最后验证

2017年2月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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