跳至主要内容
临床试验/NCT03296501
NCT03296501Unknown1 期

Safety and Efficacy of Intraspinal Transplantation of Autologous ADRC in ALS Patients

Mossakowski Medical Research Centre Polish Academy of Sciences2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年10月13日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
30
试验地点
2
主要终点
Functional progression rate

研究概览

简要总结

The goal of our nonrandomized, open label study is to investigate the safety and efficacy of autologous adipose derived mesenchymal regenerative cells (ADRC) transplantation into the individuals with diagnosed amyotrophic lateral sclerosis (ALS). All enrolled patients will have a documented at least 3-months clinical and electrophisiological observation of ALS disease course prior to study enrollment. Each patient will recive 3 injections of ADRC every 3 months: an intraspinal injection followed by 2 subsequent intrathecal infusions. Safety, adverse events and efficacy will be confirmed by clinical, elecrophisiological ( EMG, MUNIX), neuroimmaging and spirometry together with functional (ALSFRS-R) and objective motor assesment (MRC and dynamometer).

详细描述

Amyotrophic Lateral Sclerosis (ALS) is an incurable disease of unknown etiology that in a short time leads to significant impairment of motor functions and death. The frequency of ALS is 4-8/100 000. Mostly it affects people between 40 and 70 years old, but it can occur at a younger age. Since the symptom onset is most frequently in the fifth or sixth decade, ALS is a huge economic burden for the society. There are many studies conducted to treat the disease and prevent it, but currently the medicine offers only one drug that can slow the appearance of disease symptoms but could not stop the progression. Yet, improvements in medical management, including nutrition and breathing, regularly increase patient survival - 50% of affected patients live at least 3 or more years after diagnosis; 20% live 5 years or more; and up to 10% will survive more than 10 years. The stem-cell-based therapies could be therefore a new waited strategy for ALS clinical treatment.

Since the clinical course of ALS may vary substantially between patients, we are planning to qualify them with a primarily established clinical course based on a detailed anamnesis and clinical assessment. The goal of our nonrandomized, open label study is to investigate the safety and efficacy of autologous adipose derived mesenchymal regenerative cells (ADRC) transplantation into the individuals with diagnosed amyotrophic lateral sclerosis. In order to select a group of 30 ALS patients for the ADRC treatment, approximately 50 ALS patients will be examined. All patients enrolled will have a documented at least 3-months clinical and electrophisiological observation of ALS disease course prior to study enrollment. Each patient will recive 3 injections of ADRC every 3 months: an intraspinal injection followed by 2 subsequent intrathecal infusions. Safety, adverse events and efficacy will be confirmed by clinical, elecrophisiological ( EMG, MUNIX), neuroimmaging and spirometry together with functional (ALSFRS-R) and objective motor assesment (MRC and dynamometer).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • clinically definite or probable ALS according to El Escorial criteria
  • life expectancy of more than 1 year
  • INR ≤2 before liposuction
  • lack of treatment with immune-suppressants and/or corticosteroids within min. 20 days prior to recruitment
  • constant riluzole treatment (50 mg/bid) throughout the study period
  • compliance with treatment regimen e.g. will and possibility to attend check-up visits
  • Polish citizens

排除标准

  • primary haematological disease, including hypercoagulable states
  • Presence of comorbidity that would stand in the way of neurosurgical treatment-
  • previous history of a spinal-cord surgery at the clinically affected level
  • previous/current history of neoplasm or comorbidity that could impact upon patient's survival
  • pregnancy /lactation
  • noninvasive/invasive mechanical ventilation at time of recruitment
  • alcohol abuse, cocaine amphetamine, etc.

结局指标

主要结局

Functional progression rate

时间窗: 3 months

Delta ALS Functional Rating Scale (ALSFRS-R)/month

次要结局

  • Electrophisiological progression rate(3 months)

研究者

发起方
Mossakowski Medical Research Centre Polish Academy of Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anna Sarnowska

M.D., Ph.D.

Mossakowski Medical Research Centre Polish Academy of Sciences

研究点 (2)

Loading locations...

相似试验