Comirnaty Injectable Product
DrugVaccination
Other names: Comirnaty 3µg/dose for children for 6 month - 4 years
NCT Number: NCT06452654
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.
Interested in participating?
Request Info3 month–4 month
All sexes
Interventional
Phase 4
Medical University of Vienna, Dept. of Pediatric and Adolescent Medicine, Waehringer Gürtel 18-20, 1090 Vienna, Austria, Vienna, Austria
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Vaccination
Other names: Comirnaty 3µg/dose for children for 6 month - 4 years
Vaccination
Other names: Solution for Injection
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.
Time frame: Through study completion, up to 6 years
Elapsed time from first vaccination to persistent confirmed multiple islet autoantibodies;
Time frame: Through study completion, up to 6 years
Elapsed time from first vaccination to type 1 diabetes.
Time frame: Through study completion, up to 6 years
Elapsed time from first vaccination to the development of persistent confirmed transglutaminase autoantibodies.
Contact information is provided by the study sponsor or research team.
Anette-G. Ziegler, Prof. Dr.
CONTACT
+49-89-3187 ext. 2896
Peter Achenbach, Prof. Dr.
CONTACT
+49-89-3187 ext. 2896
Technical University of Munich
Other
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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