- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07494331
Exploring the Physiological Mechanisms of Austism Through Organoids (EXPECT HYPE)
March 20, 2026 updated by: Assistance Publique - Hôpitaux de Paris
Exploring the Physiologicla Mechainisms of Austism Through Organoids Derived Differentiated Cells of Individuals With Autism
Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder affecting approximately 1% of the population, characterized by difficulties with social interaction and communication.
Studies have identified more than 200 genes linked to ASD, particularly those involved in chromatin remodeling and synaptic neuronal connectivity (CHD8, SCN2A, NLGN3-4X, SHANK1-3).
The goal of the project is to decipher the biological mechanisms underlying ASD in order to develop therapeutic strategies, using innovative preclinical models such as organoids.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
Each participant's involvement in this study is limited to one visit.
This study requires only a blood draw (5 to 30 minutes), which will be performed at the CIC at Robert-Debré, and the completion of questionnaires for parents (SRS) and unaffected siblings (SRS, ADHD-RS, SDQ).
Additional tests or questionnaires may be offered at a later stage if clinically necessary.
Study Type
Observational
Enrollment (Estimated)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Richard DELORME, Prof
- Phone Number: 0033(0)140034130
- Email: richard.delorme@aphp.fr
Study Locations
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Paris, France, 75019
- Robert Debré Hospital
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Contact:
- Richard DELORME, Prof
- Phone Number: 0033(0)140034130
- Email: richard.delorme@aphp.fr
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
A child with an autism spectrum disorder, a sibling over the age of 2 who does not have an autism spectrum disorder, and biological parents
Description
Inclusion Criteria:
A child diagnosed with an autism spectrum disorder in accordance with clinical practice guidelines
- A sibling without an autism spectrum disorder (SRS < 65)
- Biological parents
- Children and parents must be enrolled in a social security program, Universal Health Coverage (CMU), or an equivalent program.
Exclusion Criteria:
- Refusal to undergo a blood test
- Uncontrolled (unstabilized) medical condition (including psychiatric conditions) that precludes participation in the study
- Sibling with an SRS score > 65 at screening or under 2 years old
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Cohort of patients
Blood sample and quetsionnaire if required by the investigator
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Production of organoïds
Time Frame: 2 years
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To study the cellular mechanisms affected by the presence of the abnormalities identified in the participant with ASD
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2 years
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2026
Primary Completion (Estimated)
May 1, 2028
Study Completion (Estimated)
May 1, 2028
Study Registration Dates
First Submitted
March 20, 2026
First Submitted That Met QC Criteria
March 20, 2026
First Posted (Actual)
March 27, 2026
Study Record Updates
Last Update Posted (Actual)
March 27, 2026
Last Update Submitted That Met QC Criteria
March 20, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- APHP250983
- 2025-A01511-48 (Other Identifier: ANSM)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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