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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
2,252
Vaccination
Vaccination
Medical University of Vienna, Dept. of Pediatric and Adolescent Medicine, Waehringer Gürtel 18-20, 1090 Vienna, Austria
Vienna, Austria
NOT_YET_RECRUITINGUniversity Hospitals Leuven, Faculty of Medicine, Catholic University of Leuven
Leuven, Belgium
RECRUITINGKlinikum rechts der Isar of Technical University Munich and Institute for Diabetes Research, Helmholtz Munich
Munich, Bavaria, Germany
RECRUITINGAUF DER BULT, Kinder- und Jugendkrankenhaus
Hanover, Lower Saxony, Germany
RECRUITINGKlinik und Poliklinik f. Kinder und Jugendmedizin, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden
Dresden, Saxony, Germany
RECRUITINGLund University Dep. of Clinical Sciences Malmo, Skane University Hospital SUS
Malmo, Sweden
RECRUITINGBirmingham Women's and Children's NHS Foundation Trust
Birmingham, United Kingdom
NOT_YET_RECRUITINGCambridge University Hospitals NHS Foundation Trust
Cambridge, United Kingdom
NOT_YET_RECRUITINGThe Newcastle upon Tyne Hospitals NHS Foundation Trust
Newcastle, United Kingdom
RECRUITINGPersistent confirmed islet autoantibodies or type 1 diabetes
The primary outcome is the elapsed time from first vaccination to the development of persistent confirmed islet autoantibodies or type 1 diabetes.
Time frame: Through study completion, up to 6 years
Persistent confirmed multiple islet autoantibodies
Elapsed time from first vaccination to persistent confirmed multiple islet autoantibodies;
Time frame: Through study completion, up to 6 years
Type 1 diabetes
Elapsed time from first vaccination to type 1 diabetes.
Time frame: Through study completion, up to 6 years
Persistent confirmed transglutaminase autoantibodies
Elapsed time from first vaccination to the development of persistent confirmed transglutaminase autoantibodies.
Time frame: Through study completion, up to 6 years
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