A Phase II Study of hCT-MSC, an Umbilical Cord-Derived Mesenchymal Stromal Cell Product, in Children With Autism Spectrum Disorder
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 137
- 试验地点
- 2
- 主要终点
- Change on the Socialization and Communication Subscale Standard Scores on the Vineland Behavior Scales
研究概览
简要总结
The purpose of this Phase II study is to determine the efficacy of human umbilical cord tissue-derived mesenchymal stromal cells (hCT-MSC) for improving social communication abilities in children with autism spectrum disorder (ASD).
详细描述
The purpose of this double blinded Phase II study is to determine the efficacy of human umbilical cord tissue-derived mesenchymal stromal cells (hCT-MSC), administered in two different dosing strategies, in children with autism spectrum disorder (ASD).
This study will be enrolling children with ASD, aging 4-11 years of age. Qualifying subjects will undergo neuropsychological evaluation, EEG testing, eye tracking, CVA assessments, and infusion of study product. Subjects will be randomized to one of two study arms; 1) a single infusion of 6.0x106 cells/Kg at baseline, followed by a blinded placebo infusion at six months or, 2) Placebo infusion at baseline, followed by an intravenous dose of 6x106 cells/Kg at six months. The second infusion was included primarily as an incentive to ensure that all participants ultimately receive an infusion of MSC, to reduce the risk of unblinding, and to encourage study completion. Efficacy outcome measures were only evaluated 6 months before the second infusion. Safety outcomes were assessed during the entire 12 months of the study.
The primary endpoint of this study is the change in social communication skill from baseline to six months. The potential risks associated with infusion of MSCs include a reaction to the product (rash, shortness of breath, wheezing, difficulty breathing, hypotension, swelling around the mouth, throat or eyes, tachycardia, diaphoresis), transmission of infection, and HLA sensitization.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
Blinded infusion
入排标准
- 年龄范围
- 4 Years 至 11 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 4 years to < 12 years (11 years, 364 days) at the time of consent
- •Confirmed clinical DSM-5 diagnosis of Autism Spectrum Disorder using the DSM-5 Checklist as informed by the Brief Observation of Symptoms of Autism (BOSA) and the Autism Diagnostic Interview-Revised (ADI-R)
- •Fragile X testing performed and negative; CMA and/or whole exome sequencing performed and results not linked to autism diagnosis
- •Stable on current psychiatric medication regimen (dose and dosing schedule) for at least 2 months prior to infusion of study product
- •Normal absolute lymphocyte count (≥1200/uL for African American participants and ≥1500/uL for all other participants)
- •GAI ≥ 65 via cognitive testing by study personnel
- •Participant and parent/guardian are English speaking
- •Able to travel to Duke University two times (baseline, six months), and parent/guardian is able to participate in interim surveys and interviews
- •Parental/guardian consent from at least one parent/guardian
排除标准
- •Review of medical records and/or screening assessments indicates ASD diagnosis and/or GAI > 65 not confident
- •Known diagnosis of any of the following coexisting psychiatric conditions: depression, bipolar disorder, schizophrenia, obsessive compulsive disorder associated with bipolar disorder, Tourette syndrome
- •Screening data suggests that participant would not be able to comply with the requirements of the study procedures as assessed by the study team
- •Family is unwilling or unable to commit to participation in all study-related assessments, including protocol follow up
- •Sibling is enrolled in this (Duke IMPACT) study
- •Records indicate that child has a known genetic syndrome such as (but not limited to) Fragile X syndrome, neurofibromatosis, Rett syndrome, tuberous sclerosis, PTEN mutation, cystic fibrosis, muscular dystrophy or a genetic defect definitively known to be associated with ASD
- •Known pathogenic mutation or copy number variation (CNV) associated with ASD (e.g., 16p11.2, 15q13.2, 2q13.3)
- •Infectious:
- •Known active CNS infection
- •Evidence of uncontrolled infection based on records or clinical assessment
- •Known HIV positivity
- •Exposure to COVID-19 in the preceding 14 days or positive COVID-19 test in the previous 28 days. Subjects with a past history of infection with COVID-19 must be symptom-free for 14 days prior to the initial visit.
- •Known metabolic disorder
- •Known mitochondrial dysfunction
- •History of unstable epilepsy or uncontrolled seizure disorder, infantile spasms, Lennox Gastaut syndrome, Dravet syndrome, or other similar chronic seizure disorder
- •Active malignancy or prior malignancy that was treated with chemotherapy
- •History of a primary immunodeficiency disorder
- •History of autoimmune cytopenias (i.e., ITP, AIHA)
- •Coexisting medical condition that would place the child at increased risk for complications of study procedures
- •Concurrent genetic or acquired disease or comorbidity(ies) that could require a future stem cell transplant
- •Significant sensory (e.g., blindness, deafness, uncorrected hearing impairment) or motor (e.g., cerebral palsy) impairment
- •Impaired renal or liver function as determined by serum creatinine >1.5mg/dL or total bilirubin >1.3mg/dL, except in patients with known Gilbert's disease
- •Significant hematologic abnormalities defined as: Hemoglobin <10.0 g/dL, Platelets <150 x 10e9/uL, WBC <3,000 cells/mL, ALC <1200/uL for African Americans or <1500/uL for all other participants.
- •Evidence of clinically relevant physical dysmorphology indicative of a genetic syndrome as assessed by the PIs or other investigators, including a medical geneticist and psychiatrists trained in identifying dysmorphic features associated with neurodevelopmental conditions.
- •Current/Prior Therapy:
- •a. Availability of a banked, qualified autologous cord blood unit or parents deferred use of qualified, autologous cord blood unit b. History of prior cell therapy c. Current or prior use of IVIG or other anti-inflammatory medications with the exception of NSAIDs d. Current or prior immunosuppressive therapy i. No systemic steroid therapy that has lasted >2 weeks, and no systemic steroids within 3 months prior to enrollment. Topical and inhaled steroids are permitted.
研究组 & 干预措施
MSC
One dose of 6x10e6 cells/kg administered intravenously.
干预措施: Cord Tissue Mesenchymal Stromal Cells (Biological)
Placebo Infusion
Placebo infusion
干预措施: Placebo Infusion (Other)
结局指标
主要结局
Change on the Socialization and Communication Subscale Standard Scores on the Vineland Behavior Scales
时间窗: Baseline, 6 months
The primary outcome measure is the mean of the change on the Socialization and Communication Subscale Standard Scores on the Vineland Adaptive Behavior Scales (VABS-3). The primary endpoint is the change on this outcome measure from baseline to six months.
次要结局
- Change in CGI-Severity score(Baseline, 6 months)
- Change in VABS-3 Socialization Standard Score(Baseline, 6 months)
- Change in the Pediatric Quality of Life Scale(Baseline, 6 months)
- CGI-Intervention score(Baseline, 6 months)
- Change in VABS-3 Communication Standard Score(Baseline, 6 months)
研究者
Joanne Kurtzberg, MD
Professor of pediatrics
Duke University