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临床试验/NCT00137176
NCT00137176已完成不适用

EARLY IFNb-1a (Rebif) and Atorvastatin (Lipitor) Combination Therapy of Isolated Clinical Syndrome Suggestive of Multiple Sclerosis

University of North Carolina, Chapel Hill1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2004年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
To identify markers of therapeutic response and to predict patients' clinical response based on their in vitro response to this combination therapy measured by the gene expression levels in activated PBMCs

研究概览

简要总结

The primary purpose is to determine the changes in gene expression induced by IFNb-1a (Rebif) and atorvastatin (Lipitor) combination therapy in patients with an isolated clinical syndrome suggestive of multiple sclerosis (MS), to identify markers of therapeutic response, and to predict patients' clinical response based on their in vitro response to this combination therapy measured by the gene expression levels in activated peripheral blood mononuclear cells (PBMCs).

详细描述

Multiple Sclerosis (MS) is a chronic neurologic disease, characterized pathologically by focal areas of inflammation, demyelination, axonal injury and degeneration in the central nervous system. MS follows several different disease courses. Approximately, 90% of patients have a relapsing form of the disease. We propose that atorvastatin (Lipitor) may enhance the immunomodulatory effects of INFb-1a (Rebif) in patients with clinically isolated neurological syndrome suggestive of MS. This combination may be more effective in preventing development of definitive relapsing-remitting MS if administered early in the course of the disease. The study will identify markers of disease activity that are selectively affected by this combination therapy. Identified markers may be used in future clinical trials to predict patient's clinical response and to monitor the response to treatment as a secondary outcome measure.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with isolated clinical syndrome suggestive of MS
  • At least three out of four magnetic resonance imaging (MRI) findings on the initial scan:
  • One Gd-enhancing lesion or nine T2 hyperintense lesions;
  • At least one infratentorial lesion;
  • At least one juxtacortical lesion; and
  • At least three periventricular lesions.
  • Expanded Disability Status Scale (EDSS) 0-5.5
  • 18 to 60 years of age
  • At least one relapse in previous 12 months

排除标准

  • Patients with a diagnosis of clinically definitive relapsing-remitting (RR) MS, secondary progressive, or primary progressive MS.
  • Patients who have ever been treated with mitoxantrone, cytoxan, cyclophosphamide, or total lymphoid irradiation (TLI).
  • Patients treated with IFNb-1a, IFNb-1b, glatiramer acetate, intravenous immunoglobulins (IVIg), plasma exchange, methotrexate, or azathioprine in the previous 3 months.
  • Patients treated with intravenous or oral steroids within 30 days prior to baseline MRI.
  • Patients who have been treated with statins in the previous 3 months.
  • Pregnant or breast-feeding women.
  • Patients with a history of severe cardiac, hepatic, pulmonary, gastrointestinal, or renal disease.
  • Abnormal baseline blood tests including alanine transaminase (ALT) or aspartate transaminase (AST) greater than twice the upper limit of normal

研究组 & 干预措施

Rebif + Lipitor

Experimental

干预措施: Rebif (Drug)

结局指标

主要结局

To identify markers of therapeutic response and to predict patients' clinical response based on their in vitro response to this combination therapy measured by the gene expression levels in activated PBMCs

时间窗: 2 years

To determine the effects of IFNb-1a plus atorvastatin versus IFNb-1a plus placebo on the gene expression in peripheral blood mononuclear cells (PBMCs) derived from patients with isolated clinical syndrome suggestive of MS

时间窗: 2 years

次要结局

  • evaluate safety and efficacy of combination therapy with Rebif and Lipitor in patients with clinicayy isolated syndrome suggestive of MS.(2 years)

研究者

申办方类型
Other

研究点 (1)

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