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临床试验/NCT02495766
NCT02495766已完成1 期

Treatment of Autologous Mesenchymal Stem Cells Derived From Bone Marrow as a Potential Therapeutic Strategy for the Treatment of Multiple Sclerosis

Banc de Sang i Teixits1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2015年5月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
8
试验地点
1
主要终点
Adverse events

研究概览

简要总结

This study evaluates the effect of cryopreserved autologous adult bone-marrow mesenchymal stromal cells (BM-MSC) in patients with active multiple sclerosis, compared to placebo.

Patients will be allocated to one of the 2 treatment arms (BM-MSC or placebo)and at month 6, the treatment will be crossed to receive the other product. The objective is to assess the safety of a single infusion BM-MSC, and to explore its efficacy in these patients.

Patients will be evaluated at month 12 and will be followed-up for a total of 3 years.

详细描述

To date, there is no effective therapy to cure multiple sclerosis (MS). Immunomodulatory therapies are useful in reducing the frequency of inflammatory processes (relapses) but don't delay significantly the progression of the disease, prevent long term disability or induce the repair of damaged tissue. This proposal contemplates the use of adult autologous bone marrow mesenchymal stromal cells (BM-MSC) as an alternative therapeutic strategy to treat patients with active MS. This is a randomized, double blind, crossover clinical trial in which 8 patients with active forms of MS and moderate disability will enter the trial with the primary objective of assessing the safety and tolerability of a single intravenous infusion of BM-MSC. Secondary objectives are to assess the efficacy by gadolinium enhancing lesions though magnetic resonance imaging, neurophysiological effects and immunological effects. Once randomized, patients will undergo BM extraction and once confirmed the availability of the needed dose, they will be randomized to one of the 2 treatment arms (BM-MSC named XCEL-MC-ALPHA, or placebo). XCEL-MC-ALPHA will be cryopreserved for all patients regardless the allocated arm. At month 6, the treatment will be crossed. Patients will be evaluated at month 12 and will be followed-up for a total of 3 years.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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 between 18 and 60 years of age
  • Patients with MS
  • Relapsing-remitting or secondary progressive MS
  • Patients to whom are not indicated or are not in a position to initiate treatment with disease-modifying drugs
  • Expanded Disability Status Scale (EDDS) score <6.5
  • Nine T2 lesions at least
  • Active multiple sclerosis as defined either by 1 outbreak in the last year or at least one Gadolinium-enhancing lesion in the last 6 months
  • Signed informed consent form

排除标准

  • Interferon beta or glatiramer acetate 3 months prior the screening
  • Natalizumab or fingolimod in the 6 months prior the screening
  • Mitoxantrone, cyclophosphamide or other immunosuppressive therapy at any time
  • Has received an experimental treatment within 3 months prior the screening
  • MS outbreak within the 4 weeks prior the randomization
  • Serum creatinine> 2.0 mg/dl
  • Infectious disease active or uncontrolled
  • Fertile patients who are not using a suitable method of contraception
  • Pregnant or lactating woman
  • Immunodeficiency
  • Positive serology to HIV, Hepatitis B, Hepatitis C or syphilis

研究组 & 干预措施

Treatment A: XCEL-MC-ALPHA/Placebo

Experimental

Single infusion of cryopreserved bone-marrow adult mesenchymal stromal cells followed by placebo infusion at month 6.

干预措施: XCEL-MC-ALPHA (Drug)

Treatment A: XCEL-MC-ALPHA/Placebo

Experimental

Single infusion of cryopreserved bone-marrow adult mesenchymal stromal cells followed by placebo infusion at month 6.

干预措施: Placebo (Drug)

Treatment B: Placebo/XCEL-MC-ALPHA

Experimental

Single infusion of placebo followed by cryopreserved bone-marrow adult mesenchymal stromal cells infusion at month 6.

干预措施: XCEL-MC-ALPHA (Drug)

Treatment B: Placebo/XCEL-MC-ALPHA

Experimental

Single infusion of placebo followed by cryopreserved bone-marrow adult mesenchymal stromal cells infusion at month 6.

干预措施: Placebo (Drug)

结局指标

主要结局

Adverse events

时间窗: 12 months

Safety profile

次要结局

  • Expanded Disability Status Scale (EDDS) score(12 months)
  • Cumulative number of lesions visualized on T2 sequence(12 months)
  • Cumulative number of MRI Gd-enhancing lesions(12 months)
  • Multiple Sclerosis Outbreaks(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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