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临床试验/2024-513545-37-00
2024-513545-37-00招募中4 期

REDUCE PMR: Rituximab Effect on Decreasing glUcoCorticoid Exposition in relapsing PolyMyalgia Rheumatica

Sint Maartenskliniek Stichting9 个研究点 分布在 1 个国家目标入组 174 人开始时间: 2024年11月21日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
174
试验地点
9
主要终点
The proportion of patients in GC free remission one year after RTX treatment compared to placebo

研究概览

简要总结

The main objective is to study the efficacy of treatment with rituximab in patients with relapsing polymyalgia rheumatica compared to placebo

入排标准

年龄范围
18 years 至 65+ years(65+ Years, 18-64 Years)
接受健康志愿者

入选标准

  • A clinical diagnoses of PMR according to the 2012 EULAR/ACR classification criteria
  • Re-emerging PMR symptoms and elevated ESR or CRP levels
  • Unable to reduce glucocorticoid dose below 5mg/day prednisolone or equivalent.

排除标准

  • Treatment with systemic immunosuppressants (other than GC, MTX, leflunomide and azathioprine) 3 months prior to inclusion
  • (clinical) suspect concomitant giant cell arteritis or other rheumatic inflammatory disease
  • Concomitant conditions that might significantly interfere with evaluation of PMR pain or movement as judged by the investigator
  • Previous hypersensitivity for RTX or contra-indications to RTX
  • Not being able to speak, read or write Dutch

结局指标

主要结局

The proportion of patients in GC free remission one year after RTX treatment compared to placebo

The proportion of patients in GC free remission one year after RTX treatment compared to placebo

次要结局

  • Proportion of patients in GC free remission at week 21
  • Proportion of patients with low dose GC (≤5mg/day) remission at week 21, week 52, 1.5 year and 2 years.
  • PMR-AS at each visit
  • The number of disease relapses/recurrences up to week 52
  • The proportion of patients with a disease relapse/recurrence at week 52
  • The time from baseline to GC free remission and to relapse
  • GC cumulative dose at 52 weeks, 1.5 and 2 years.
  • Proportion of patients with RTX/PCB retreatment
  • Proportion of patients who start methotrexate, leflunomide, tocilizumab or sarilumab or possible other bDMARD being registered for PMR
  • Sex differences in frequencies of GC-remission and adverse events
  • Changes in patient reported outcomes, concerning pain, fatigue, stiffness and physical function (as recommended by the OMERACT)
  • Medical consumption and productivity loss
  • (Changes in) modified glucocorticoid toxicity index (which excludes bone mineral density scan to improve feasibility)
  • Frequency, types, proportion of patients with, and total numbers of ( especially GC- and RTX-related) AE during the 52 week study
  • Proportion of patients in GC free remission 1.5 years after RTX/PCB infusion
  • Proportion of patients in GC free remission 2 years after RTX/PCB infusion
  • The number of disease relapses/recurrences up to 2 years.
  • The proportion of patients with a disease relapse/recurrence at 2 years.
  • The proportion of patients lost-to follow-up and the reason for loss to follow-up at 1.5 and 2 years
  • The proportion of patients that had a (different) DMARD started (and reason for starting the DMARD) at 1.5 and 2 years
  • The proportion (and number) of patients in which a (concomitant) rheumatic (inflammatory) disease was diagnosed at 1.5 and 2 years

研究者

发起方
Sint Maartenskliniek Stichting
申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Aatke van der Maas

Scientific

Sint Maartenskliniek Stichting

研究点 (9)

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