跳至主要内容
临床试验/NCT06342544
NCT06342544招募中3 期

Immediate Corticosteroid Therapy and Rituximab to Prevent Generalization in Ocular Myasthenia: a PROBE Multicenter Open-label Randomized Controlled Trial.

Fondation Ophtalmologique Adolphe de Rothschild1 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2025年4月29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
招募中
入组人数
128
试验地点
1
主要终点
proportion of patients who progressed to generalized myasthenia within 2 years of follow-up

研究概览

简要总结

Myasthenia is an autoimmune disease causing dysfunction of the neuromuscular junction, resulting in fluctuating and variable muscle weakness.

In the initial phase of the disease, 70% of patients present with ocular onset myasthenia (OMG), i.e. weakness limited to the oculomotor muscles. Generalization to skeletal, bulbar and axial muscles occurs in 20-40% of cases, with a higher frequency in the first and second years, respectively 46% and 60% of generalizations. This reflects the maturation of the autoimmune response in the early years of the disease, and represents a therapeutic window of opportunity to modify the course of the disease.

Generalization is a critical event, putting the patient at risk of admission to an intensive care unit and necessitating the use of long-term immunosuppressants.

There is currently no validated strategy for preventing generalization. On the one hand, a preventive role for corticosteroid therapy in ocular-onset myasthenia has been observed in some studies, but not confirmed by others. These contradictory results may be explained by the bias of retrospective observational studies and the use of different corticosteroid administration regimens.

On the other hand, recent data on the use of low-dose Rituximab in the early phase of the disease shows greater efficacy than later use, enabling prolonged remission of the disease with a very good tolerability profile.

We propose to compare in a randomized controlled trial the usual practice with a proactive strategy with a standardized corticosteroid regimen immediate at diagnosis.

Patients with ocular myasthenia are usually treated symptomatically with acetylcholinesterase inhibitors. The introduction of corticosteroids is delayed and limited to patients with persistent disabling diplopia or ptosis with occlusion. When corticosteroids are tapered off, ocular symptoms may recur. This level of corticosteroid dependence observed in patients treated for ocular myasthenia has not been specifically studied. In order to reduce the levels of corticosteroids administered and avoid recurrence of ocular symptoms and their delayed generalization, it is usually proposed to introduce another immunosuppressant.

The aim of this study is to evaluate the efficacy of a standardized proactive prevention strategy on the generalization of ocular onset myasthenias during the first 2 years. It will combine immediate treatment with corticosteroids at the time of diagnosis, with the addition of rituximab in the event of recurrence of ocular symptoms as corticosteroids are tapered off.

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
Single (Outcomes Assessor)

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 over 18 years of age
  • Diagnosis of ocular myasthenia within the last 6 months, defined :
  • either by a typical clinical examination objectified by an expert clinician: ptosis and/or binocular diplopia, with a variable and fluctuating character (either spontaneous or provoked by effort or rest)
  • or by positive anti-AChR antibodies or the presence of decrement on repetitive nerve stimulation or a positive edrophonium test
  • Ocular symptoms lasting at least one month and limited to extra-ocular muscles (weakness in one or both orbicularis oculi)
  • No non-ocular symptoms on MMS, MGC and MG-ADL.
  • Naïve to immunosuppressive therapy for ocular myasthenia gravis.

排除标准

  • Pupillary anomaly other than that resulting from previous local disease or surgery.
  • Signs of restrictive abduction or supraduction myopathy due to dysthyroid ophthalmopathy.
  • Graves' ophthalmopathy
  • Onset of ocular symptoms more than one year before screening date
  • Hypersensitivity to rituximab, murine proteins, prednisone, methylprednisone, aziathioprine or 6-mercaptopurine, paracetamol, dexchlorpheniramine.
  • Any infectious condition
  • Patients with severe immune deficiency
  • Severe heart failure (New York Heart Association (NYHA) Class IV) or severe uncontrolled heart disease
  • Severe hepatic insufficiency
  • Psychotic states not yet controlled by treatment
  • Hyperuricemia on xanthine oxidase inhibitors (allopurinol and febuxostat)
  • Risk of angle-closure glaucoma
  • Risk of urinary retention due to urethro-prostatic disorders
  • Vaccination with live attenuated vaccine required during study and up to 6 months after rituximab discontinuation
  • Women of childbearing age who do not wish to use effective contraception during their participation and at least 12 months after
  • Pregnant or breast-feeding women

研究组 & 干预措施

immediate treatment with corticosteroids addition of rituximab if recurrence

Experimental

干预措施: immediate treatment with corticosteroids (Drug)

immediate treatment with corticosteroids addition of rituximab if recurrence

Experimental

干预措施: addition of rituximab if recurrence (Drug)

结局指标

主要结局

proportion of patients who progressed to generalized myasthenia within 2 years of follow-up

时间窗: Day0 to month24

Generalization is defined by a loss of 5 points or more on any Myasthenic Muscle Score (MMS) item, excluding "eyelid occlusion" and "extrinsic ocular musculature". Progress towards generalization will be assessed by an expert physician, blinded to the intervention arm.

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

研究点 (1)

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