Mycophenolate Mofetil Versus Azathioprine for Maintenance Therapy in ANCA Associated Systemic Vasculitis
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 160
- 试验地点
- 4
- 主要终点
- or the end of the protocol (at 48 months)
研究概览
简要总结
The aim of IMPROVE is to define the optimal maintenance therapy for ANCA-associated vasculitides (AASV) by comparing the AZA (standard regimen) with MMF in terms of efficacy, i.e. in preventing relapses.
HYPOTHESIS :
MMF might be more effective than azathioprine as maintenance drug in AASV patients, reducing by 50% relapse rate, with a same frequency of adverse effects
详细描述
AASV, including Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA) and renal limited vasculitis (RLV), are progressive, multisystem, autoimmune diseases which require the prescription of immunosuppressive therapy. Treatment using corticosteroids and cytotoxic drugs has been standardised (ECSYSVASTRIAL project), but relapse rate remains high and treatment-related toxicity is non negligible. The IMPROVE trial aims to reduce this relapse rate by using mycophenolate mofetil (MMF) for maintenance therapy. The potential benefit of MMF has been suggested in a published open and uncontrolled study. Patients with newly diagnosed systemic AASV will be randomly assigned to receive either MMF or reference treatment with azathioprine (AZA), once remission has been obtained with cyclophosphamide and prednisone. MMF and AZA will be continued for a total of 42 months of therapy with concomitant prednisone dose tapering. The study will last 48 months. Hence, within the last 6 months of the study duration, the patients will not receive any immunosuppressive drugs.
The primary end-point will the disease-free period, taken as the period of time from remission until relapse or study end; secondary end-points will be adverse events, cumulative damage (assessed using damage score VDI) and immunosuppressive drug cumulative dose.
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
- 否
入选标准
- •Newly diagnosed patients with WG, MPA or renal-limited vasculitis.
- •ANCA positivity. ANCA positivity requires PR3-ANCA or a typical cANCA pattern by indirect immunofluorescence (IIF), preferably confirmed by anti-PR3 ELISA. MPO-ANCA determined by ELISA requires demonstration of pANCA, and pANCA by IIF requires confirmation by anti-MPO ELISA. Optionally, central review of ANCA serology can be performed.
- •Age 18 to 75 years
排除标准
- •Any cytotoxic drug within previous year, unless started within one months of entry and according to the protocol design
- •Co-existence of another systemic autoimmune disease, e.g. SLE
- •Hepatitis B or Hepatitis C infection
- •HIV positivity
- •Failure to achieve remission after 6 months of CYC therapy
- •Failure to control progressive disease with induction protocol
- •Malignancy (usually exclude unless agreed with trial co-ordinator)
- •Pregnancy or inadequate contraception
- •Age below 18 and above 75 years*
- •Endstage renal failure unless active extrarenal disease requires treatment (temporal dependency of hemodialysis is not an exclusion criterion)
- •Inability for informed consent
- •After discussion with the trial administrator, patients less than 18 years may be incorporated on separate application according to the appropriate local ethic committee.
结局指标
主要结局
or the end of the protocol (at 48 months)
of the maintenance therapy (AZA or MMF) and the first relapse (minor or major)
the disease-free period, defined as the time between the beginning
次要结局
- relapse rate
- rate of side-effects and intolerance
- cumulative doses (AZA, CS, MMF)
- AUC for BVAS, SF-36 or VDI
- Evolution of titers of ANCA and CRP