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NCT Number: NCT06452654

Anti-viral Action Against Type 1 Diabetes Autoimmunity

The study GPPAD-05 AVAnT1A is a phase 4 clinical trial intending to enroll 2252 children, who will be randomly assigned to receive COVID-19 vaccination (Comirnaty® 3 μg Omicron XBB.1.5 or new variant Comirnaty vaccines ) or placebo from age 6 months.

The study is an investigator initiated, randomized, controlled, multicentre, multinational, primary prevention trial for children at increased risk of type 1 diabetes.

The primary objective is to determine whether vaccination of children with elevated genetic risk for type 1 diabetes against COVID-19 from 6 months of age reduces the cumulative incidence of islet autoantibodies or type 1 diabetes in childhood.

Secondary objectives are:

1. to determine whether vaccination against COVID-19 similarly reduces the cumulative incidence of multiple islet autoantibodies in childhood. 2. to determine whether vaccination against COVID-19 similarly reduces the cumulative incidence of type 1 diabetes in childhood and 3. to determine whether vaccination against COVID-19 similarly reduces the cumulative incidence of celiac disease-associated transglutaminase autoantibodies in childhood.

Further exploratory objectives are described in the study protocol.

Study participants will be identified through an ongoing study screening for genetic risk of type 1 diabetes using a polygenic risk score (NCT03316261).

Eligible participants will be enrolled at age 3.00 to 4.00 months (baseline visit).

Randomization to vaccine or placebo will occur at age 6.00 to 7.00 months at visit 2. Consent will be obtained by the custodial parents prior to enrollment.

Recruiting

Interested in participating?

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Key information

Age range

3 month–4 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Medical University of Vienna, Dept. of Pediatric and Adolescent Medicine, Waehringer Gürtel 18-20, 1090 Vienna, Austria, Vienna, Austria

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Ages between 3.00 and 4.00 months at the time of enrollment.
  • A high genetic risk (>10%) to develop islet autoantibodies by age 6 years as determined by a HLA DR/DQ genotype, polygenic risk score and first-degree family history of type 1 diabetes status.
  • Written informed consent signed by the custodial parent(s).

Exclusion criteria

  • Previous hypersensitivity to the excipients of the vaccine.
  • Any medical condition, concomitant disease or treatment that may interfere with the assessments or may jeopardize the participant's safe participation in the study. These include immune deficiencies, and conditions or treatments that lead to immune suppression.
  • Likely poor compliance due to expected change in residency.
  • Diagnosis of diabetes prior to recruitment or randomisation
  • Current use of any other investigational drug

Treatment and study plan

Comirnaty Injectable Product

Drug

Vaccination

Other names: Comirnaty 3µg/dose for children for 6 month - 4 years

Sodium Chloride 0.9% Inj

Drug

Vaccination

Other names: Solution for Injection

Primary outcomes

  1. Persistent confirmed islet autoantibodies or type 1 diabetes

    Time frame: Through study completion, up to 6 years

    The primary outcome is the elapsed time from first vaccination to the development of persistent confirmed islet autoantibodies or type 1 diabetes.

Secondary outcomes

  1. Persistent confirmed multiple islet autoantibodies

    Time frame: Through study completion, up to 6 years

    Elapsed time from first vaccination to persistent confirmed multiple islet autoantibodies;

  2. Type 1 diabetes

    Time frame: Through study completion, up to 6 years

    Elapsed time from first vaccination to type 1 diabetes.

  3. Persistent confirmed transglutaminase autoantibodies

    Time frame: Through study completion, up to 6 years

    Elapsed time from first vaccination to the development of persistent confirmed transglutaminase autoantibodies.

Study contacts

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

Anette-G. Ziegler, Prof. Dr.

CONTACT

[email protected]

+49-89-3187 ext. 2896

Peter Achenbach, Prof. Dr.

CONTACT

[email protected]

+49-89-3187 ext. 2896

Sponsors and collaborators

Lead sponsor

Technical University of Munich

Other

Collaborators

  • Birmingham Women's and Children's NHS Foundation Trust
  • Cambridge University Hospitals NHS Foundation Trust
  • Helmholtz Zentrum München
  • Kinderkrankenhaus auf der Bult
  • Newcastle-upon-Tyne Hospitals NHS Trust
  • Skane University Hospital
  • Universitaire Ziekenhuizen KU Leuven
  • University Hospital Carl Gustav Carus

Registry information

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Jun 11, 2024
Registry last updated
Sep 23, 2025

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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