hCT-MSC in Children With Autism Spectrum Disorder (IMPACT)

• ClinicalTrials.gov Identifier: NCT04089579
• Recruitment Status: Completed
• First Posted: September 13, 2019
• Last Update Posted: February 14, 2024
• Sponsor: Joanne Kurtzberg, MD
• Collaborators: The Marcus Foundation; Cryo-Cell International
• Information provided by (Responsible Party): Joanne Kurtzberg, MD, Duke University

Study Description

Brief Summary:

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).

Condition or disease	Intervention/treatment	Phase
Autism; Autism Spectrum Disorder	Biological: Cord Tissue Mesenchymal Stromal Cells; Other: Placebo Infusion	Phase 2

Detailed Description:

The purpose of this double blinded Phase II study is to determine the efficacy of human umbilical cord tissue-derived mesencymal 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 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.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 137 participants
• Allocation: Randomized
• Intervention Model: Crossover Assignment
• Intervention Model Description: This study is a phase II, prospective, randomized, blinded, cross over, clinical trial designed to assess the efficacy of intravenous dosing of hCT-MSC for improving social communication abilities in young children with ASD. All participants will ultimately be treated with hCT-MSC. Participants randomized to arm A will each receive a single intravenous dose of 6x106 hCT-MSC per kilogram at baseline, followed by a placebo infusion at six months. Participants randomized to arm B will each receive a placebo infusion at baseline, followed by an intravenous dose of 6x106 hCT-MSC per kilogram at six months.
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Masking Description: Blinded infusion
• Primary Purpose: Treatment
• Official Title: A Phase II Study of hCT-MSC, an Umbilical Cord-Derived Mesenchymal Stromal Cell Product, in Children With Autism Spectrum Disorder
• Actual Study Start Date: October 12, 2020
• Actual Primary Completion Date: May 2, 2023
• Actual Study Completion Date: February 1, 2024

Arms and Interventions

Arm	Intervention/treatment
Experimental: MSC; One dose of 6x10e6 cells/kg administered intravenously.	Biological: Cord Tissue Mesenchymal Stromal Cells; Human Umbilical Cord Tissue Derived Mesenchymal Stromal Cells (hCT-MSC), isolated and expanded from umbilical cord tissue from allogeneic unrelated donors. One dose of 6x10e6 cells/kg administered intravenously.
Placebo Comparator: Placebo Infusion; Placebo infusion	Other: Placebo Infusion; Placebo comparative infusion

Outcome Measures

Primary Outcome Measures :

1. Change on the Socialization and Communication Subscale Standard Scores on the Vineland Behavior Scales [ Time Frame: 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.

Secondary Outcome Measures :

1. Change in VABS-3 Socialization Standard Score [ Time Frame: Baseline, 6 months ]
   Change in VABS-3 (Vineland Adaptive Behavior Scales) Socialization Standard Score
2. Change in VABS-3 Communication Standard Score [ Time Frame: Baseline, 6 months ]
   Change in VABS-3 (Vineland Adaptive Behavior Scales) Communication Standard Score
3. Change in CGI-Severity score [ Time Frame: Baseline, 6 months ]
   Clinical Global Impression- Severity Scale
4. CGI-Intervention score [ Time Frame: Baseline, 6 months ]
   Clinical Global Impression- Impression
5. Change in the Pediatric Quality of Life Scale [ Time Frame: Baseline, 6 months ]
   Pediatric Quality of Life Scale, raw scale range of 0-2300 with higher scores indicating a higher quality of life (better outcome)

Other Outcome Measures:

1. Incidence and severity of infusion reactions [ Time Frame: Baseline, 6 months ]
   Assess for infusion reactions
2. Incidence and severity of product-related infections [ Time Frame: Baseline, 6 months ]
   Assess for infections directly related to the study product infusions
3. Evidence of formation of anti-HLA antibodies [ Time Frame: Baseline, 6 months, 12 months ]
   Assess for anti-HLA antibodies
4. Incidence and severity of graft versus host disease [ Time Frame: 6 months, 12 months ]
   Assess for signs and symptoms of graft versus host disease
5. Incidence and severity of unexpected adverse events related to the study product [ Time Frame: Baseline, 6 months, 12 months ]
   Assess for study related and unexpected adverse events

Eligibility Criteria

• Ages Eligible for Study: 4 Years to 11 Years (Child)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria

1. Age ≥ 4 years to < 12 years (11 years, 364 days) at the time of consent
2. 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)
3. Fragile X testing performed and negative; CMA and/or whole exome sequencing performed and results not linked to autism diagnosis
4. Stable on current psychiatric medication regimen (dose and dosing schedule) for at least 2 months prior to infusion of study product
5. Normal absolute lymphocyte count (≥1200/uL for African American participants and ≥1500/uL for all other participants)
6. GAI ≥ 65 via cognitive testing by study personnel
7. Participant and parent/guardian are English speaking
8. Able to travel to Duke University two times (baseline, six months), and parent/guardian is able to participate in interim surveys and interviews
9. Parental/guardian consent from at least one parent/guardian

Exclusion Criteria

1. General:

   1. Review of medical records and/or screening assessments indicates ASD diagnosis and/or GAI > 65 not confident
   2. Known diagnosis of any of the following coexisting psychiatric conditions: depression, bipolar disorder, schizophrenia, obsessive compulsive disorder associated with bipolar disorder, Tourette syndrome
   3. Screening data suggests that participant would not be able to comply with the requirements of the study procedures as assessed by the study team
   4. Family is unwilling or unable to commit to participation in all study-related assessments, including protocol follow up
   5. Sibling is enrolled in this (Duke IMPACT) study

2. Genetic:

   1. 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
   2. Known pathogenic mutation or copy number variation (CNV) associated with ASD (e.g., 16p11.2, 15q13.2, 2q13.3)

3. Infectious:

   1. Known active CNS infection
   2. Evidence of uncontrolled infection based on records or clinical assessment
   3. Known HIV positivity
   4. 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.

4. Medical:

   1. Known metabolic disorder
   2. Known mitochondrial dysfunction
   3. History of unstable epilepsy or uncontrolled seizure disorder, infantile spasms, Lennox Gastaut syndrome, Dravet syndrome, or other similar chronic seizure disorder
   4. Active malignancy or prior malignancy that was treated with chemotherapy
   5. History of a primary immunodeficiency disorder
   6. History of autoimmune cytopenias (i.e., ITP, AIHA)
   7. Coexisting medical condition that would place the child at increased risk for complications of study procedures
   8. Concurrent genetic or acquired disease or comorbidity(ies) that could require a future stem cell transplant
   9. Significant sensory (e.g., blindness, deafness, uncorrected hearing impairment) or motor (e.g., cerebral palsy) impairment
   10. 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
   11. 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.
   12. 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.

5. 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.

Contacts and Locations

Locations

United States, North Carolina

Duke University Medical Center

Durham, North Carolina, United States, 27705

Sponsors and Collaborators

Joanne Kurtzberg, MD

The Marcus Foundation

Cryo-Cell International

Investigators

• Principal Investigator: Beth Shaz, MD; Duke University
• Principal Investigator: Lauren Franz, MBChB; Duke University

More Information

• Responsible Party: Joanne Kurtzberg, MD, Professor of pediatrics, Duke University
• ClinicalTrials.gov Identifier: NCT04089579
• Other Study ID Numbers: Pro00113011; Pro00102894 ( Other Identifier: Duke IRB )
• First Posted: September 13, 2019
• Last Update Posted: February 14, 2024
• Last Verified: February 2024

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Joanne Kurtzberg, MD, Duke University:

Autism; Autism Spectrum Disorder; Stem cell; Mesenchymal Stromal Cells

Additional relevant MeSH terms:

Autistic Disorder; Autism Spectrum Disorder; Child Development Disorders, Pervasive; Neurodevelopmental Disorders; Mental Disorders