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ABSTRACT: Background
There are increasing reports of outbreaks of measles in countries that achieved measles elimination using two doses of measles-mumps-rubella (MMR) vaccine, particularly in health care settings. While responses to a third dose of MMR in two-dose recipients have been examined, these studies have all administered MMR by the standard (intramuscular or subcutaneous) route, and data on the duration of antibody are limited. We have developed a protocol for an open-label parallel-arm randomized-controlled trial to compare measles antibody responses and safety after intradermal and aerosol administration of MMR with intramuscular, the usual mode of administration in Aotearoa (New Zealand).Methods
Eligible participants are aged ≥ 18 years who have previously received two d
SUBMITTER: Saha S
PROVIDER: S-EPMC11927902 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature