drugset / Trial / NCT07252791

Safety and Immunogenicity of PCV20 in Pediatric Patients With Autoimmune Rheumatic Diseases

NCT07252791

Non-randomizedParallel-groupOpen-labelPrevention

Summary

This clinical trial evaluates the immunogenicity (humoral and cellular) and safety of the 20-valent pneumococcal conjugate vaccine (PCV20) in children, adolescents, and young adults aged 2-25 years with autoimmune rheumatic diseases (ARDs). All participants will receive PCV20 according to prior vaccine history. Antibody titers, opsonophagocytic activity, cellular immune responses, and adverse events will be measured up to 6 months post-vaccination. Effects of immunosuppressive therapy and physical activity levels related vaccine response will also be assessed.

Timeline

Start
2026-01-16
Primary completion
2026-12-30
Completion
2027-12-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject PCV20 Vaccine 0.5 ml Intramuscular

Indications