<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(Suppl 1)</volume><submitter>Fitz-Patrick D</submitter><pubmed_abstract>Abstract &lt;h4>Background&lt;/h4> Because of the number and variability of serotypes causing pneumococcal disease among different geographic regions, age groups, and environmental backgrounds, expanding serotype coverage with pneumococcal conjugate vaccines (PCVs) is a continued unmet need. &lt;h4>Methods&lt;/h4> This phase 1, randomized, double-blind study included healthy Japanese adults aged 18–49 years residing in the United States. Subjects were randomized 1:1:1 to receive a single dose of a 20-valent PCV (containing 13-valent PCV [PCV13] serotypes plus 8, 10A, 11A, 12F, 15B, 22F, 33F), a novel pneumococcal polysaccharide conjugate vaccine with extended coverage, or PCV13 (control). Safety was the primary endpoint and included reactogenicity events occurring ≤ 14 days after vaccination, adverse </pubmed_abstract><journal>Open forum infectious diseases</journal><pagination>S30-S31</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7776113</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>16. A Randomized Phase 1 Study of a Novel Pneumococcal Conjugate Vaccine in Healthy Japanese Adults in the United States</pubmed_title><pmcid>PMC7776113</pmcid><pubmed_authors>Peng Y</pubmed_authors><pubmed_authors>Watson W</pubmed_authors><pubmed_authors>Scott D</pubmed_authors><pubmed_authors>Baugher G</pubmed_authors><pubmed_authors>Gruber W</pubmed_authors><pubmed_authors>Scully I</pubmed_authors><pubmed_authors>Fitz-Patrick D</pubmed_authors><pubmed_authors>Jansen K</pubmed_authors><pubmed_authors>Young Jr. M</pubmed_authors></additional><is_claimable>false</is_claimable><name>16. A Randomized Phase 1 Study of a Novel Pneumococcal Conjugate Vaccine in Healthy Japanese Adults in the United States</name><description>Abstract &lt;h4>Background&lt;/h4> Because of the number and variability of serotypes causing pneumococcal disease among different geographic regions, age groups, and environmental backgrounds, expanding serotype coverage with pneumococcal conjugate vaccines (PCVs) is a continued unmet need. &lt;h4>Methods&lt;/h4> This phase 1, randomized, double-blind study included healthy Japanese adults aged 18–49 years residing in the United States. Subjects were randomized 1:1:1 to receive a single dose of a 20-valent PCV (containing 13-valent PCV [PCV13] serotypes plus 8, 10A, 11A, 12F, 15B, 22F, 33F), a novel pneumococcal polysaccharide conjugate vaccine with extended coverage, or PCV13 (control). Safety was the primary endpoint and included reactogenicity events occurring ≤ 14 days after vaccination, adverse </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-04-19T01:19:24.077Z</modification><creation>2021-02-20T21:00:48Z</creation></dates><accession>S-EPMC7776113</accession><cross_references/></HashMap>