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临床试验/NCT03096275
NCT03096275已完成3 期

Comparison of the Efficacy of Mycophenolate Mofetil Combined With Methotrexate and Cyclophosphamide for the Treatment of Takayasu's Arteritis

Chinese SLE Treatment And Research Group7 个研究点 分布在 1 个国家目标入组 138 人开始时间: 2017年3月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
138
试验地点
7
主要终点
Proportion of patients with complete remission

研究概览

简要总结

Takayasu's arteritis(TAK) is a rare systemic vasculitis which can cause ischemia or inflammation of the involved organs and increase the overall mortality rate.The traditional treatment of TAK is primarily empirical. The most commonly used drugs for treating active TAK are glucocorticosteroids(GC) and immunosuppressants. However, the genital toxicity of CYC has limited its long term use. In a pilot study carried out by the principal investigator of this study has shown that mycophenolate mofetil(MMF) combined with MTX is effective and with few adverse effects. The purpose of this prospective open-label study is to compare the efficacy and safety of GC+MMF+MTX with GC+CYC followed by GC+AZA for the treatment of active TAK. 150 patients with active TAK will be recruited and randomized in a 2:1 ratio to GC+MMF+MTX group and C+CYC and AZA group. Patients were followed for 52 weeks for efficacy and safety assessment.

详细描述

Takayasu's arteritis(TAK) is a rare systemic vasculitis which mainly involves aorta and its major branches. However,it is more prevalent in countries and areas along the silk road.Young women at child-bearing age is the most prevalent population.It can cause ischemia or inflammation of the involved organs and increase the overall mortality rate.Although it may be lethal in some patients,it is not well studied due to the rareness of the disease.The traditional treatment of TAK is primarily empirical. The most commonly used drugs for treating active TAK are glucocorticosteroids(GC) and immunosuppressants including cyclophosphamide(CYC), methotrexate(MTX) and azathioprine(AZA) etc. However,no of these drugs have been well studied. In addition, the genital toxicity of CYC, the first line medication for active TAK, has become the major limitation for its long term use for a chronic disease like TAK. Therefore, new immunosuppressants with less toxicity,especially with much less genital toxicity and low malignancy risk is essentially necessary. In a pilot study carried out by the principal investigator of this study has shown that mycophenolate mofetil(MMF) combined with MTX is effective and with few adverse effects. The purpose of this prospective open-label study is to compare the efficacy and safety of GC+MMF+MTX with GC+CYC followed by GC+AZA for the treatment of active TAK. 150 patients with active TAK will be recruited and randomized in a 2:1 ratio to GC+MMF+MTX group and C+CYC and AZA group. Patients were followed for 52 weeks to assess the efficacy and safety.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients older than 18 years-old either sex
  • Patients with signed informed consent
  • Fulfill the 1990 ACR Classification Criteria for TAK
  • Patients with active disease according to GACTA criteria

排除标准

  • Prior adverse events when treated with MTX that resulted in dose reduction or discontinuation;
  • Prior treatment with MMF but failed response to MMF;
  • Prior treatment with CYC but failed response to CYC;
  • Renal dysfunction, defined as the estimated GFR <80% or serum creatinine level higher than 1.5 times of upper normal limit;
  • Severe liver function damage defined by serum ALT or AST higher than 2 times of the upper normal limits;
  • Uncontrolled diabetes melitus;
  • Uncontrolled heart failure at baseline;
  • Active infection including tuberculosis , hepatitis B virus, hepatitis C virus, HIV or bacterial or fungal infection;
  • Active upper GI bleeding in the past 3 months.

研究组 & 干预措施

MMF+MTX+Glucocorticoids

Experimental

Patients were treated with Glucocorticoids combined with mycphenolate mofetil(MMF) as well as methotrexate(MTX) treatment for 52 weeks and were followed for 52 weeks.

干预措施: MMF (Drug)

MMF+MTX+Glucocorticoids

Experimental

Patients were treated with Glucocorticoids combined with mycphenolate mofetil(MMF) as well as methotrexate(MTX) treatment for 52 weeks and were followed for 52 weeks.

干预措施: Glucocorticoids (Drug)

CYC/AZA+Glucocoticoids

Active Comparator

Patients were treated with Glucocorticoids combined with cyclophosphamide(CYC)/azathioprine(AZA) for 52 weeks and were followed for 52 weeks

干预措施: Glucocorticoids (Drug)

MMF+MTX+Glucocorticoids

Experimental

Patients were treated with Glucocorticoids combined with mycphenolate mofetil(MMF) as well as methotrexate(MTX) treatment for 52 weeks and were followed for 52 weeks.

干预措施: MTX (Drug)

CYC/AZA+Glucocoticoids

Active Comparator

Patients were treated with Glucocorticoids combined with cyclophosphamide(CYC)/azathioprine(AZA) for 52 weeks and were followed for 52 weeks

干预措施: CYC (Drug)

CYC/AZA+Glucocoticoids

Active Comparator

Patients were treated with Glucocorticoids combined with cyclophosphamide(CYC)/azathioprine(AZA) for 52 weeks and were followed for 52 weeks

干预措施: AZA (Drug)

结局指标

主要结局

Proportion of patients with complete remission

时间窗: 52 weeks

The proportion of patients who reached the pre-defined criteria of complete remission in both groups

次要结局

  • Safety profile of MMF combined with MTX(52 weeks)
  • Proportion of patients with partial remission(52 weeks)
  • Rate of complications(52 weeks)

研究者

发起方
Chinese SLE Treatment And Research Group
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xinping Tian

Professor of Medicine

Peking Union Medical College Hospital

研究点 (7)

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