跳至主要内容
临床试验/NCT07177677
NCT07177677尚未招募1 期

Intravenous Injection of Human Bone Marrow Mesenchymal Stem Cell (hBMMSC) in the Treatment of Autism Spectrum Disorder (ASD): An Exploratory Study on the Safety and Preliminary Efficacy

Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd.0 个研究点目标入组 42 人开始时间: 2025年9月30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
尚未招募
发起方
入组人数
42
主要终点
Safety Evaluation of hBMMSC Injection in ASD Patients

研究概览

简要总结

This clinical trial aims to evaluate the safety and preliminary efficacy of intravenous administration of human bone marrow-derived mesenchymal stem cells (hBMMSCs) in patients with autism spectrum disorder (ASD).

详细描述

Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder characterized primarily by impaired social communication, restricted interests, and repetitive, stereotyped behaviors. Currently, there are no effective therapeutic drugs, and main interventions consist of educational rehabilitation and behavioral management.The purpose of this study is to evaluate the safety and preliminary efficacy of hBMMSC intravenous treatment in patients with ASD. The clinical trial intends to involve 42 participants. The trial is expected to last approximately 2 years.

研究设计

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

入排标准

年龄范围
6 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Male or female ≥6 years old
  • •Body weight ≥ 17 kg
  • •Meets the diagnostic criteria for Autism Spectrum Disorder (ASD) as defined by the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), and confirmed by the Autism Diagnostic Interview-Revised (ADI-R) and the Autism Diagnostic Observation Schedule-2 (ADOS-2)
  • •Has either not received any psychotropic medication in the three months prior to enrollment or has been on a stable regimen of psychotropic medication for at least three months
  • •The subject and/or their legal guardian(s) agree to participate in the trial and provide signed informed consent.

排除标准

  • •Inability of the subject or their guardian to sufficiently understand instructions in Chinese
  • •Active infection (viral, bacterial, fungal, or mycobacterial)
  • •A confirmed diagnosis of Rett syndrome, childhood disintegrative disorder, fragile X syndrome, or other genetic/metabolic diseases that may impact cognitive development
  • •History of epileptic seizures within 6 months prior to enrollment
  • •History of suicide attempts/self-harm, presentation of suicidal ideation, or being judged as the risk of suicidal by the investigator
  • •Severe hematologic diseases or active malignancy
  • •Severe hepatic or renal disease
  • •Participation in a drug clinical trial within 3 months prior to enrollment (unless beyond the protocol-defined wash-out period) or participation in any other stem cell study within the past year
  • •A positive skin test result
  • •Any other condition which, in the opinion of the investigator, would make the subject unsuitable for participation in this study

研究组 & 干预措施

hBMMSC 0.5×10^6 cells/kg

Experimental

human Bone Marrow Mesenchymal Stem Cell (hBMMSC) 0.5×10^6 cells/kg、 1.0×10^6 cells/kg、 2.0×10^6 cells/kg

干预措施: hBMMSC (Biological)

结局指标

主要结局

Safety Evaluation of hBMMSC Injection in ASD Patients

时间窗: 48 weeks

Adverse events and serious adverse events.

次要结局

  • Preliminary Efficacy Evaluation of hBMMSC Injection for Patients with ASD(48 weeks)

研究者

发起方
Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd.
申办方类型
Other
责任方
Sponsor

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