Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07633951

Multicenter Epidemiological Study for the Evaluation of the Seroprevalence of Total and Neutralizing Antibodies Against Adenoassociated Virus Serotypes Used in Gene Therapy in Patients With Neuromuscular Diseases of Genetic Origin.

This study aims to assess the overall seroprevalence of neutralizing antibodies against different AAVs potentially used in gene therapy in patients with genetic neuromuscular diseases.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

6 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

GENETHON

Évry, Île-de-France Region, 9100, France

Location contact

Céline LABETOULE, Master of Sciences

CONTACT

[email protected]

Philippe VERON, Master of Sciences

CONTACT

[email protected]

About this study

This research aims to determine the seroprevalence and immunological profiles of recent and/or emerging AAV capsids that could be used in future gene therapy programs. It will thus make it possible to: 1/ improve knowledge of the prevalence of anti-AAV antibodies (total and neutralizing) in these specific populations; 2/ identify the clinical, demographic or biological factors likely to influence this seroprevalence (age, sex, type of pathology, immunosuppressive treatment followed); 3/ to characterize the phenomena of cross-reactivity between different serotypes or variants of capsids, a major challenge for the design of new generations of vectors.

The data generated will contribute to a better estimation of the populations potentially eligible for gene therapies, by making it possible to anticipate exclusion rates related to pre-existing immunity. They may also guide the rational selection of alternative capsids that are less immunogenic or evade cross-immunity, as well as the development of immunomodulation or re-assay strategies.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Pediatric patient 6 years of age or older or adult under 60 years of age with genetic neuromuscular disease
  • Informed patient who signed informed consent
  • No opposition from the holders of parental authority or guardian, for minor patients.
  • Affiliated/beneficiary of a national health insurance scheme

Exclusion criteria

  • Gene or cell therapy treatment prior to blood collection

Treatment and study plan

Dosage of AAV neutralizing antibodies

Diagnostic Test

In each clinical site, the principal investigator will propose to his patients with neuromuscular disease of genetic origin to take a blood sample (4 mL of blood) to determine their level of immunity to certain AAVs used in gene therapy. The collected samples will be prepared and aliquoted on site and then sent frozen to the GENETHON laboratory for analysis.

Only one sample per patient will be analyzed. All samples will be analyzed in batches.

Primary outcomes

  1. Percentage of patients with anti-AAV neutralizing antibodies

    Time frame: Day 1

    The primary endpoint is the percentage of patients who tested positive for neutralizing antibodies against multiple AAVs that can be used in gene therapy.

Secondary outcomes

  1. To estimate seroprevalence in subgroups of patients (age; type of neuromuscular disease; gender; immunosuppressive therapy)

    Time frame: Day 1

    Estimation of seroprevalence (positive or negative) of anti-AAV neutralizing antibodies in different subgroups (age, sex, type of neuromuscular disease, immunosuppressive therapy)

  2. To analyze the co-prevalence between several AAV serotypes

    Time frame: Day 1

    Quantification of neutralizing antibody titers against various capsids using cellular tests

  3. Analyze the potential correlation between the presence of neutralizing antibodies and total antibody titer using cellular tests and ELISA method

    Time frame: Day 1

    Prevalence of cross-reactions between multiple capsids

Sponsors and collaborators

Lead sponsor

Genethon

Other

Registry information

Acronym: SeroDysMyo

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jun 8, 2026
Registry last updated
Jun 8, 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.

Published trials that share one or more normalized conditions with this study.