Phase 3 Open Label Randomised Multicentre Controlled Trial of Rituxmab and Mycophenolate Mofetil Without Oral Steroids for the Treatment of Lupus Nephritis
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 24
- 试验地点
- 11
- 主要终点
- Complete renal response (CR) at week 52 without the need to prescribe oral steroids within 1 year
研究概览
简要总结
The treatment of the multisystem autoimmune disease systemic lupus erythematosus (SLE) remains a challenge, particularly when there is renal involvement (lupus nephritis). For the last 60 years corticosteroids have been the backbone of the treatment of lupus nephritis but they are associated with significant toxicity.
Although randomized placebo controlled trials of Rituximab in non-renal lupus and lupus nephritis did not meet their primary end-points, there is accumulating data that suggests that B cell depletion with Rituximab may be efficacious in lupus disease refractory to conventional therapy. Furthermore, our pilot data suggests that the addition of Rituximab to mycophenolate mofetil (MMF) without oral steroids is at least as effective at inducing a renal response as the standard of care therapy comprising MMF and high dose oral corticosteroids.
RITUXILUP is a proof of concept, open labeled, randomized, controlled, multicentre trial that aims to demonstrate whether the addition of Rituximab to MMF therapy is useful in treating a new flare of lupus nephritis and whether it has a long lasting steroid-sparing, beneficial effect with equal efficacy and greater safety than a conventional regimen of MMF and oral prednisolone. If successful, this trial has the potential to dramatically change the management of lupus nephritis.
详细描述
TRIAL SUMMARY
TITLE RITUXILUP - An open label randomised multicentre controlled trial of RITUXImab and mycophenolate mofetil (MMF) without oral steroids for the treatment of LUPus nephritis
OBJECTIVES
- Is the combination of Rituximab, Methyl prednisolone and MMF as effective in treating lupus nephritis as Methyl prednisolone, oral steroids and MMF?
- Does the omission of oral steroids increase the safety of the treatment regimen?
DESIGN This is a 1:1 randomised, international open label, controlled phase III multicentre trial
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 12 Years 至 75 Years(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Rituximab
Rituximab, methyl prednisolone and mycophenolate mofetil
干预措施: Rituximab (Drug)
Rituximab
Rituximab, methyl prednisolone and mycophenolate mofetil
干预措施: Mycophenolate mofetil (Drug)
Rituximab
Rituximab, methyl prednisolone and mycophenolate mofetil
干预措施: Methyl prednisolone (Drug)
Oral prednisolone
Oral prednisolone, methyl prednisolone and mycophenolate mofetil
干预措施: Oral prednisolone (Drug)
Oral prednisolone
Oral prednisolone, methyl prednisolone and mycophenolate mofetil
干预措施: Mycophenolate mofetil (Drug)
Oral prednisolone
Oral prednisolone, methyl prednisolone and mycophenolate mofetil
干预措施: Methyl prednisolone (Drug)
结局指标
主要结局
Complete renal response (CR) at week 52 without the need to prescribe oral steroids within 1 year
时间窗: 1 year
The proportion of participants who achieve a complete renal response at week 52 without the need to prescribe oral steroids within 1 year, except for one course of maximum 30mg for a maximum of 14 days OR one intramuscular or intra-articular injection of steroids
次要结局
- Mean time to stable CR and mean time to PR(2 years)
- Metabolic abnormalities related to steroid exposure(2 years)
- Mean time to renal flare in patients achieving CR and PR(2 years)
- Proportion of patients with renal flare(2 years)
- Proportion of patients achieving CR at 6, 18 and 24 months(2 years)
- Introduction of oral steroids in the B cell depleted patients(2 years)
- Proportion of patients with only 1 or fewer BILAG 2004 Bs in any non-renal organ system at 1 year(2 years)
- Serious Infectious Episodes, Serious Adverse Events and Adverse events(2 years)
- Cumulative steroid exposure over 1 and 2 years(2 years)
- Patients requiring >10mg oral prednisolone at 1 year and 2 year(2 years)
- Proportion of patients achieving PR at 6,12,8 and 24 months(2 years)
- Proportion of patients achieving normal serum C3,C4 and anti-dsDNA antibodies at week 52(2 years)
- Proportion of patients in PR who achieve histological remission as judged by absence of proliferative lesions and no new subendothelial or subepithelial deposits(2 years)
