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临床试验/NCT00337636
NCT00337636已完成1 期

A Phase I Study of the Safety and Preliminary Effectiveness of Human CNS Stem Cells (HuCNS-SC) in Patients With Neuronal Ceroid Lipofuscinosis Caused by Palmitoyl Protein Thioesterase 1 (PPT1) or Tripeptidyl Peptidase 1 (TPP-I) Deficiency

StemCells, Inc.1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2006年5月最近更新:
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
6
试验地点
1
主要终点
Safety

研究概览

简要总结

Patients with infantile or late infantile NCL have either a reduced amount of, or are missing, the palmitoyl protein thioesterase 1 (PPT1) enzyme or the tripeptidyl peptidase 1 (TPP-I) enzyme. Human central nervous system stem cells (HuCNS-SC) are an investigational product derived from human brain cells. HuCNS-SC have been shown to survive and migrate within the brains of mice. When grown in the laboratory, HuCNS-SC have been shown to produce the PPT1 and TPP-I enzymes. In mice missing the PPT1 enzyme, HuCNS-SC have been shown to increase the amount of this enzyme in the brain, to reduce the amount of abnormal storage material in the brain, and to prevent the death of some neurons (a type of cell) in the brain.

Participation in this study will involve screening assessments, surgery to implant HuCNS-SC, medication to suppress the immune system, and a series of follow-up assessments. The length of time from the start of screening through to the last follow-up visit will be approximately 13 months, with frequent visits to the study center during this time. After completion of this study, patients will be monitored for an additional 4 years under a separate long term follow-up protocol.

研究设计

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

入排标准

年龄范围
18 Months 至 12 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Patients MAY be eligible to participate in this research study if they:
  • •Are age 18 months to 12 years old
  • •Have a clinical diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) or late infantile neuronal ceroid lipofuscinosis (LINCL)
  • •Have a mutation of the CLN1 or CLN2 gene
  • •Have severe cognitive, communication, behavior and language impairment

排除标准

  • •Patients may not be eligible to participate in this research study if they:
  • •Have cognitive, communication, behavior and language function less than that of a 1 year old
  • •Have previously received an organ, tissue or bone marrow transplantation
  • •Have previously participated in any gene or cell therapy study
  • •Have infection with hepatitis virus, Cytomegalovirus, Epstein Barr Virus, or Human Immunodeficiency Virus (HIV)
  • •Have a current or prior cancer
  • •Have a bleeding disorder
  • •Are unable to have an MRI scan

研究组 & 干预措施

HuCNS-SC

Experimental

human central nervous system stem cells

干预措施: Surgery to implant human CNS stem cells (HuCNS-SC) (Procedure)

HuCNS-SC

Experimental

human central nervous system stem cells

干预措施: Medication to suppress the immune system (Drug)

结局指标

主要结局

Safety

时间窗: one year post transpant

次要结局

  • Preliminary efficacy(one year post transplant)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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