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V118E is an investigational **pneumococcal vaccine formulation** developed by Merck for prevention of disease caused by *Streptococcus pneumoniae*. It is being evaluated in a randomized, double-blind Phase 1 study in healthy adults for safety, tolerability, and immunogenicity. In the registered study, V118E is administered as a two-dose intramuscular regimen on Day 1 and Day 29, with PREVNAR 20 plus saline used as a comparator regimen. Its precise antigen composition, valency, carrier proteins, and adjuvant system have not been publicly specified.
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