<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hamer MJ</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>Intramural NIH HHS</funding><funding>National Institutes of Health</funding><pagination>294-302</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10127441</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>401(10373)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>WHO has identified Marburg virus as an emerging virus requiring urgent vaccine research and development, particularly due to its recent emergence in Ghana. We report results from a first-in-human clinical trial evaluating a replication-deficient recombinant chimpanzee adenovirus type 3 (cAd3)-vectored vaccine encoding a wild-type Marburg virus Angola glycoprotein (cAd3-Marburg) in healthy adults.&lt;h4>Methods&lt;/h4>We did a first-in-human, phase 1, open-label, dose-escalation trial of the cAd3-Marburg vaccine at the Walter Reed Army Institute of Research Clinical Trials Center in the USA. Healthy adults aged 18-50 years were assigned to receive a single intramuscular dose of cAd3-Marburg vaccine at either 1 × 10&lt;sup>10&lt;/sup> or 1 × 10&lt;sup>11&lt;/sup> particle units (pu). Primar</pubmed_abstract><journal>Lancet (London, England)</journal><pubmed_title>Safety, tolerability, and immunogenicity of the chimpanzee adenovirus type 3-vectored Marburg virus (cAd3-Marburg) vaccine in healthy adults in the USA: a first-in-human, phase 1, open-label, dose-escalation trial.</pubmed_title><pmcid>PMC10127441</pmcid><funding_grant_id>Z99 AI999999</funding_grant_id><pubmed_authors>Hickman S</pubmed_authors><pubmed_authors>Murray T</pubmed_authors><pubmed_authors>Schech S</pubmed_authors><pubmed_authors>Trofymenko O</pubmed_authors><pubmed_authors>Wilson H</pubmed_authors><pubmed_authors>Scott PT</pubmed_authors><pubmed_authors>Strom L</pubmed_authors><pubmed_authors>Coates EE</pubmed_authors><pubmed_authors>Ploquin A</pubmed_authors><pubmed_authors>Costner P</pubmed_authors><pubmed_authors>Gordon IJ</pubmed_authors><pubmed_authors>Amare MF</pubmed_authors><pubmed_authors>Kioko V</pubmed_authors><pubmed_authors>Larkin B</pubmed_authors><pubmed_authors>O'Connell S</pubmed_authors><pubmed_authors>Gall JG</pubmed_authors><pubmed_authors>Sullivan NJ</pubmed_authors><pubmed_authors>Hamer MJ</pubmed_authors><pubmed_authors>McCauley MD</pubmed_authors><pubmed_authors>Widge AT</pubmed_authors><pubmed_authors>Lampley R</pubmed_authors><pubmed_authors>Dulan CNM</pubmed_authors><pubmed_authors>McDermott AB</pubmed_authors><pubmed_authors>Preston A</pubmed_authors><pubmed_authors>RV 507 Study Team</pubmed_authors><pubmed_authors>Ledgerwood JE</pubmed_authors><pubmed_authors>Houser KV</pubmed_authors><pubmed_authors>Basappa M</pubmed_authors><pubmed_authors>Waterman PE</pubmed_authors><pubmed_authors>Flach B</pubmed_authors><pubmed_authors>Stanley DA</pubmed_authors><pubmed_authors>Andrews C</pubmed_authors><pubmed_authors>Narpala SR</pubmed_authors><pubmed_authors>Read M</pubmed_authors><pubmed_authors>Padilla M</pubmed_authors><pubmed_authors>Gaudinski MR</pubmed_authors><pubmed_authors>Lee C</pubmed_authors><pubmed_authors>Augustine B</pubmed_authors><pubmed_authors>Koup RA</pubmed_authors><pubmed_authors>Cox JH</pubmed_authors><pubmed_authors>Swanson PA</pubmed_authors><pubmed_authors>Hofstetter AR</pubmed_authors><pubmed_authors>Vazquez S</pubmed_authors><pubmed_authors>Ake JA</pubmed_authors><pubmed_authors>Storme C</pubmed_authors><pubmed_authors>Holman LA</pubmed_authors><pubmed_authors>Modjarrad K</pubmed_authors><pubmed_authors>Mascola JR</pubmed_authors><pubmed_authors>Ortega-Villa AM</pubmed_authors><pubmed_authors>Hunegnaw R</pubmed_authors><pubmed_authors>Robb ML</pubmed_authors><pubmed_authors>Yamshchikov GV</pubmed_authors><pubmed_authors>Hutter JN</pubmed_authors><pubmed_authors>Thillainathan J</pubmed_authors><pubmed_authors>Morgan P</pubmed_authors><pubmed_authors>Happe M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety, tolerability, and immunogenicity of the chimpanzee adenovirus type 3-vectored Marburg virus (cAd3-Marburg) vaccine in healthy adults in the USA: a first-in-human, phase 1, open-label, dose-escalation trial.</name><description>&lt;h4>Background&lt;/h4>WHO has identified Marburg virus as an emerging virus requiring urgent vaccine research and development, particularly due to its recent emergence in Ghana. We report results from a first-in-human clinical trial evaluating a replication-deficient recombinant chimpanzee adenovirus type 3 (cAd3)-vectored vaccine encoding a wild-type Marburg virus Angola glycoprotein (cAd3-Marburg) in healthy adults.&lt;h4>Methods&lt;/h4>We did a first-in-human, phase 1, open-label, dose-escalation trial of the cAd3-Marburg vaccine at the Walter Reed Army Institute of Research Clinical Trials Center in the USA. Healthy adults aged 18-50 years were assigned to receive a single intramuscular dose of cAd3-Marburg vaccine at either 1 × 10&lt;sup>10&lt;/sup> or 1 × 10&lt;sup>11&lt;/sup> particle units (pu). Primar</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-06-02T06:12:41.119Z</modification><creation>2024-11-12T22:32:29.008Z</creation></dates><accession>S-EPMC10127441</accession><cross_references><pubmed>36709074</pubmed><doi>10.1016/S0140-6736(22)02400-X</doi><doi>10.1016/s0140-6736(22)02400-x</doi></cross_references></HashMap>