Anti-viral action against type 1 diabetes autoimmunity: The GPPAD-AVAnT1A study protocol
-, -; Hummel, Sandra; Käßl, Alexandra; Arnolds, Stefanie; Achenbach, Peter; Berner, Reinhard; Casteels, Kristina; Hyöty, Heikki; Kordonouri, Olga; Larsson, Helena Elding; Lundgren, Markus; Marcovecchio, M. Loredana; Owen, Catherine; Pfirrmann, Markus; Robson, Steve; Szadkowska, Agnieszka; Szypowska, Agnieszka; Tree, Timothy; Weiss, Andreas; Ziegler, Anette Gabriele; Bonifacio, Ezio (2025-04)
-, -
Hummel, Sandra
Käßl, Alexandra
Arnolds, Stefanie
Achenbach, Peter
Berner, Reinhard
Casteels, Kristina
Hyöty, Heikki
Kordonouri, Olga
Larsson, Helena Elding
Lundgren, Markus
Marcovecchio, M. Loredana
Owen, Catherine
Pfirrmann, Markus
Robson, Steve
Szadkowska, Agnieszka
Szypowska, Agnieszka
Tree, Timothy
Weiss, Andreas
Ziegler, Anette Gabriele
Bonifacio, Ezio
04 / 2025
Contemporary clinical trials communications
101434
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202505024582
https://urn.fi/URN:NBN:fi:tuni-202505024582
Kuvaus
Peer reviewed
Tiivistelmä
Viral infections in the first year of life are associated with islet autoimmunity and type 1 diabetes risk. The Anti-Viral Action against Type 1 Diabetes Autoimmunity (AVAnT1A)- study is a clinical phase IV investigator initiated, randomised, controlled, multicentre, primary prevention trial conducted to determine whether vaccination against COVID-19 from 6 months of age reduces the cumulative incidence of islet autoantibodies or type 1 diabetes in children with elevated genetic risk. Additionally, it investigates the role of viral infections in the etiology of islet autoimmunity by intense surveillance within the first two years of life. Infants aged 3.00–4.00 months from Germany, Belgium, UK and Sweden are eligible if they have a >10 % expected risk to develop islet autoantibodies by age 6 years as determined by HLA DR/DQ genotype, polygenic risk score and family history of type 1 diabetes. A total of 2252 eligible children are randomized 1:1 to COVID-19 vaccine (Comirnaty® 3 μg Omicron XBB.1.5 or future new variants) or placebo (0.9 % Sodium Chloride) administered three times. Children are followed until the minimum age of 2.5 years and maximum age of 6 years. The intervention is accompanied by analyses of immune and metabolic parameters to determine changes induced by viral infections and to investigate mechanisms by which viral infection may lead to islet autoimmunity. The Sponsor is the Klinikum rechts der Isar, Technical University Munich. The study was approved by Clinical Trials Information System (CTIS, EU Trial number: 2023-507348-35-00) and by Integrated Research Application System (IRAS, IRAS-ID: 1009668).
Kokoelmat
- TUNICRIS-julkaisut [20263]