<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Frey SE</submitter><funding>HHS</funding><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><pagination>126702</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12096342</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>47</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>While it remains impossible to predict the timing of the next influenza pandemic, novel avian influenza A viruses continue to be considered a significant threat.&lt;h4>Methods&lt;/h4>A Phase II study was conducted in healthy adults aged 18-64 years to assess the safety and immunogenicity of two intramuscular doses of pre-pandemic 2017 influenza A(H7N9) inactivated vaccine administered 21 days apart. Participants were randomized (n = 105 in each of Arms 1-3) to receive 3.75 μg, 7.5 μg or 15 μg of hemagglutinin (HA) with MF59® adjuvant, or 15 μg of HA unadjuvanted vaccine (n = 57, Arm 4).&lt;h4>Results&lt;/h4>The three MF59 adjuvanted vaccines and the 15 μg unadjuvanted vaccine were safe and well-tolerated. Little antibody activity was detected against the A(H7N9) vaccine antigen af</pubmed_abstract><journal>Vaccine</journal><pubmed_title>Safety and immunogenicity of ascending doses of influenza A(H7N9) inactivated vaccine with or without MF59®.</pubmed_title><pmcid>PMC12096342</pmcid><funding_grant_id>UL1 TR002243</funding_grant_id><funding_grant_id>HHSN272201300019C</funding_grant_id><funding_grant_id>UM1 AI148685</funding_grant_id><funding_grant_id>HHSN27220139921I</funding_grant_id><funding_grant_id>HHSN272201300023I</funding_grant_id><funding_grant_id>HHSN27200015</funding_grant_id><funding_grant_id>HHSN272201300021I</funding_grant_id><funding_grant_id>75N93021C00012</funding_grant_id><funding_grant_id>HHSN272201300016C</funding_grant_id><funding_grant_id>HHSN272201300015C</funding_grant_id><funding_grant_id>HHSN272201300019I</funding_grant_id><funding_grant_id>HHSN272201300023C</funding_grant_id><funding_grant_id>HHSN272201300016I</funding_grant_id><funding_grant_id>HHSN272201300015I</funding_grant_id><pubmed_authors>Atmar RL</pubmed_authors><pubmed_authors>Abate G</pubmed_authors><pubmed_authors>Paulsen G</pubmed_authors><pubmed_authors>Rupp R</pubmed_authors><pubmed_authors>Goepfert P</pubmed_authors><pubmed_authors>Creech CB</pubmed_authors><pubmed_authors>Weiss J</pubmed_authors><pubmed_authors>Frey SE</pubmed_authors><pubmed_authors>Brady R</pubmed_authors><pubmed_authors>Wegel A</pubmed_authors><pubmed_authors>Roberts PC</pubmed_authors><pubmed_authors>El Sahly HM</pubmed_authors><pubmed_authors>Jackson L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and immunogenicity of ascending doses of influenza A(H7N9) inactivated vaccine with or without MF59®.</name><description>&lt;h4>Introduction&lt;/h4>While it remains impossible to predict the timing of the next influenza pandemic, novel avian influenza A viruses continue to be considered a significant threat.&lt;h4>Methods&lt;/h4>A Phase II study was conducted in healthy adults aged 18-64 years to assess the safety and immunogenicity of two intramuscular doses of pre-pandemic 2017 influenza A(H7N9) inactivated vaccine administered 21 days apart. Participants were randomized (n = 105 in each of Arms 1-3) to receive 3.75 μg, 7.5 μg or 15 μg of hemagglutinin (HA) with MF59® adjuvant, or 15 μg of HA unadjuvanted vaccine (n = 57, Arm 4).&lt;h4>Results&lt;/h4>The three MF59 adjuvanted vaccines and the 15 μg unadjuvanted vaccine were safe and well-tolerated. Little antibody activity was detected against the A(H7N9) vaccine antigen af</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-07-15T21:33:19.045Z</modification><creation>2026-07-09T10:14:46.613Z</creation></dates><accession>S-EPMC12096342</accession><cross_references><pubmed>39798434</pubmed><doi>10.1016/j.vaccine.2024.126702</doi></cross_references></HashMap>