Anti-viral Action Against Type 1 Diabetes Autoimmunity

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age3-4
SponsorTechnical University of Munich

About this trial

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.

Eligibility criteria

Qualifiers

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).

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Comirnaty Injectable Product
  • Sodium Chloride 0.9% Inj

Treatment groups

2,252 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Technical University of Munich

Lead sponsor

Helmholtz Zentrum München

Collaborator

University Hospital Carl Gustav Carus

Collaborator

Kinderkrankenhaus auf der Bult

Collaborator

Skane University Hospital

Collaborator

Universitaire Ziekenhuizen KU Leuven

Collaborator

Newcastle-upon-Tyne Hospitals NHS Trust

Collaborator

Cambridge University Hospitals NHS Foundation Trust

Collaborator

Birmingham Women's and Children's NHS Foundation Trust

Collaborator