Clinical trial demonstrates safety and immune response of RSV vaccine in younger high-risk adults, suggesting its potential for broader use.
Adjuvanted RSVPreF3 was immunologically noninferior in 18-49-year-olds with underlying conditions compared with ≥60-year-olds in whom efficacy was previously demonstrated, supporting efficacy inference in this younger population. Up to 6 months postvaccination, the vaccine elicited robust immune responses, and the safety profile was acceptable. Clinical Trial Registration: NCT06389487.
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Snyman et al. (2026) studied this question.
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