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NCT Number: NCT07243561

Prospective Clinical Study on Human Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes for the Treatment of Childhood Autism

This clinical study aims to evaluate whether a nasal spray containing exosomes derived from human umbilical cord mesenchymal stem cells (hUC-MSC-EXOs) can safely and effectively improve core symptoms in children aged 3-7 years with autism spectrum disorder (ASD). It is a 24-week, non-randomized, controlled, open-label trial. Sixty pediatric patients with ASD will be non-randomly assigned at a 1:2 ratio to two groups: a no-intervention control group and an active exosome nasal spray treatment group. The treatment group will receive the nasal spray on Mondays, Wednesdays, and Fridays, totaling 10 administrations throughout the study. The no-intervention control group will receive no experimental treatment but will undergo the same assessments and safety checks with the treatment group. This design aims to monitor the safety and efficacy of the hUC-MSC-EXOs nasal spray.

Recruiting

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Key information

Age range

3 year–7 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis meets the ICD-11 ASD criteria or DSM-5 ASD clinical diagnostic standards.
  • No significant improvement in core symptoms was observed after ≥3 months of standardized behavioral intervention.
  • Score ≥30 on the CARS2, indicating mild-to-moderate or more severe autism.
  • Aged 3 (inclusive) to 7 (inclusive) years, regardless of gender
  • Voluntary participation in this clinical study, with written informed consent provided by the patient's legal guardian, and willingness to undergo examinations, treatment, and cooperate with follow-up visits.
  • In the investigator's judgment, the patient is capable of understanding and complying with study requirements.

Exclusion criteria

  • History of severe allergic reactions.
  • Any severe mental disorder or other types of autism spectrum disorders.
  • History of epileptic seizures within the past six months.
  • Autism secondary to epilepsy, cerebrovascular disease, or traumatic brain injury.
  • Disease severity rated as normal, borderline mental disorder, or mild mental disorder on the Clinical Global Impression scale.
  • Moderate or severe extrapyramidal symptoms or tardive dyskinesia.
  • Severe self-injurious behavior.
  • Active systemic or severe localized infections, including human immunodeficiency virus, syphilis, and hepatitis.
  • Autoimmune diseases.
  • Major organ impairment.
  • Severe pulmonary or hematological diseases, malignancies, or immunodeficiency.
  • Concurrent treatments that may interfere with the safety and efficacy evaluation of stem cell therapy.
  • Participation in other clinical trials within the past three months.
  • Other clinical conditions deemed by investigators as unsuitable for study inclusion.

Treatment and study plan

hUC-MSC-Exos Nasal Spray

Biological

The total therapeutic dosage is set at 400 billion hUC-MSC-EXOs particles. Each nasal administration delivers 40 billion particles, with a total of 10 administrations completing the full course. The treatment is administered on an alternate-day schedule.

Primary outcomes

  1. Number of Participants with Treatment-Related Adverse Events

    Time frame: Week 2, Week 6, Week 24

    The incidence of treatment-related adverse events will be assessed and graded according to the Common Terminology Criteria for Adverse Events version 5.0. The number of participants experiencing any treatment-related adverse event will be recorded and reported.

  2. Childhood Autism Rating Scale, Second Edition (CARS-2) Score

    Time frame: Week 6, Week 24

    Scale Description: The CARS-2 is a 15-item behavior rating scale used to diagnose and assess the severity of ASD.

    Range of Scores: 15 to 60. Interpretation: A higher score indicates a worse outcome.

Secondary outcomes

  1. Autism Behavior Checklist (ABC)

    Time frame: Week 6, Week 24

    Scale Description: The ABC is a 57-item checklist used to screen for and assess behaviors associated with ASD.

    Range of Scores: 0 to 158. Interpretation: A higher score indicates a worse outcome.

  2. Serum Level of Tumor Necrosis Factor-Alpha (TNF-α)

    Time frame: Week 6, Week 24

    Serum concentration of the inflammatory cytokine TNF-α. The unit of measure is pg/mL.

Study contacts

Contact information is provided by the study sponsor or research team.

Zhongmin Liu

CONTACT

[email protected]

+86-0898-38932608

Sponsors and collaborators

Lead sponsor

Dongfang People's Hospital

Other

Collaborators

  • Shanghai Tongjin Stem Cell Technology Co., Ltd.

Registry information

Acronym: EXO-ASD

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 24, 2025
Registry last updated
Jul 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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