University of Rochester Medical Center | Emergency Medicine Research
Status and phase
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About
The purpose of the study is to evaluate the safety, reactogenicity, and immunogenicity of mRNA-1345 in children aged 2 to <5 years (Cohort 1 and Cohort 3) and in children at high risk of respiratory syncytial virus (RSV) disease 5 to <18 years of age (Cohort 2) to inform the dose level selection for the next phase of development (Phase 3).
Enrollment
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Inclusion and exclusion criteria
Key Inclusion Criteria:
Cohort 1 and Cohort 3:
Cohort 2:
Key Exclusion Criteria (All Cohorts):
Note: Other protocol-defined inclusion and exclusion criteria may apply.
Primary purpose
Allocation
Interventional model
Masking
400 participants in 3 patient groups
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Central trial contact
Moderna Clinical Trials Support Center
Data sourced from clinicaltrials.gov
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