<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Happe M</submitter><funding>NCI NIH HHS</funding><funding>Division of Intramural Research, National Institute of Allergy and Infectious Diseases</funding><pagination>67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10980745</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>Ebola virus disease (EVD) is a filoviral infection caused by virus species of the Ebolavirus genus including Zaire ebolavirus (EBOV) and Sudan ebolavirus (SUDV). We investigated the safety and immunogenicity of a heterologous prime-boost regimen involving a chimpanzee adenovirus 3 vectored Ebola vaccine [either monovalent (cAd3-EBOZ) or bivalent (cAd3-EBO)] prime followed by a recombinant modified vaccinia virus Ankara EBOV vaccine (MVA-EbolaZ) boost in two phase 1/1b randomized open-label clinical trials in healthy adults in the United States (US) and Uganda (UG). Trial US (NCT02408913) enrolled 140 participants, including 26 EVD vaccine-naïve and 114 cAd3-Ebola-experienced participants (April-November 2015). Trial UG (NCT02354404) enrolled 90 participants, including 60 EVD vaccine-naïve </pubmed_abstract><journal>NPJ vaccines</journal><pubmed_title>Heterologous cAd3-Ebola and MVA-EbolaZ vaccines are safe and immunogenic in US and Uganda phase 1/1b trials.</pubmed_title><pmcid>PMC10980745</pmcid><funding_grant_id>75N91019D00024</funding_grant_id><pubmed_authors>Nesheim W</pubmed_authors><pubmed_authors>Dropulic LK</pubmed_authors><pubmed_authors>Kelley CF</pubmed_authors><pubmed_authors>Carr D</pubmed_authors><pubmed_authors>Courneya J</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Grimes V</pubmed_authors><pubmed_authors>Zephir KL</pubmed_authors><pubmed_authors>Strom L</pubmed_authors><pubmed_authors>Ploquin A</pubmed_authors><pubmed_authors>Costner PJM</pubmed_authors><pubmed_authors>Nakibuuka L</pubmed_authors><pubmed_authors>DeCederfelt H</pubmed_authors><pubmed_authors>Kimbugne G</pubmed_authors><pubmed_authors>Gordon IJ</pubmed_authors><pubmed_authors>Ananworanich J</pubmed_authors><pubmed_authors>Larkin B</pubmed_authors><pubmed_authors>Sullivan NJ</pubmed_authors><pubmed_authors>Chen GL</pubmed_authors><pubmed_authors>Chrisley L</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Beck A</pubmed_authors><pubmed_authors>Girmay T</pubmed_authors><pubmed_authors>Sanders J</pubmed_authors><pubmed_authors>Ledgerwood JE</pubmed_authors><pubmed_authors>Chen WH</pubmed_authors><pubmed_authors>Mulligan MJ</pubmed_authors><pubmed_authors>Nakabuye I</pubmed_authors><pubmed_authors>Novik L</pubmed_authors><pubmed_authors>Campbell JD</pubmed_authors><pubmed_authors>Lee M</pubmed_authors><pubmed_authors>Stanley DA</pubmed_authors><pubmed_authors>Stein J</pubmed_authors><pubmed_authors>Gaudinski MR</pubmed_authors><pubmed_authors>Koup RA</pubmed_authors><pubmed_authors>Berkowitz NM</pubmed_authors><pubmed_authors>Billington M</pubmed_authors><pubmed_authors>Whalen WR</pubmed_authors><pubmed_authors>Ashman C</pubmed_authors><pubmed_authors>Hofstetter AR</pubmed_authors><pubmed_authors>Bailer RT</pubmed_authors><pubmed_authors>Luzinda K</pubmed_authors><pubmed_authors>Cham F</pubmed_authors><pubmed_authors>Casazza JP</pubmed_authors><pubmed_authors>Greenberg N</pubmed_authors><pubmed_authors>Kamya MR</pubmed_authors><pubmed_authors>Kwon A</pubmed_authors><pubmed_authors>Mascola JR</pubmed_authors><pubmed_authors>Kajumba F</pubmed_authors><pubmed_authors>Happe M</pubmed_authors><pubmed_authors>Michael NL</pubmed_authors><pubmed_authors>Sitar S</pubmed_authors><pubmed_authors>Osinski E</pubmed_authors><pubmed_authors>Sadowski J</pubmed_authors><pubmed_authors>Kiweewa F</pubmed_authors><pubmed_authors>Murray T</pubmed_authors><pubmed_authors>Plummer SH</pubmed_authors><pubmed_authors>Straling J</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Coates EE</pubmed_authors><pubmed_authors>Kaltovich F</pubmed_authors><pubmed_authors>DeZure A</pubmed_authors><pubmed_authors>Rouphael N</pubmed_authors><pubmed_authors>Tsukerman S</pubmed_authors><pubmed_authors>Kibuuka H</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Mendoza F</pubmed_authors><pubmed_authors>Pittman IR</pubmed_authors><pubmed_authors>Wakabi S</pubmed_authors><pubmed_authors>Ogilvie M</pubmed_authors><pubmed_authors>Dorsey B</pubmed_authors><pubmed_authors>Lyke KE</pubmed_authors><pubmed_authors>Mwesigwa B</pubmed_authors><pubmed_authors>Enama ME</pubmed_authors><pubmed_authors>Hendel CS</pubmed_authors><pubmed_authors>Bailey CA</pubmed_authors><pubmed_authors>Houser KV</pubmed_authors><pubmed_authors>Becker J</pubmed_authors><pubmed_authors>VRC 208 and RV 422 study team</pubmed_authors><pubmed_authors>Bower M</pubmed_authors><pubmed_authors>Komninou P</pubmed_authors><pubmed_authors>Edupuganti S</pubmed_authors><pubmed_authors>Nguyen TA</pubmed_authors><pubmed_authors>Tindikahwa A</pubmed_authors><pubmed_authors>Vasilenko O</pubmed_authors><pubmed_authors>Matovu R</pubmed_authors><pubmed_authors>Kabbani S</pubmed_authors><pubmed_authors>Schwartz R</pubmed_authors><pubmed_authors>Ake JA</pubmed_authors><pubmed_authors>Mukyala MG</pubmed_authors><pubmed_authors>Holman LA</pubmed_authors><pubmed_authors>Millard M</pubmed_authors><pubmed_authors>Graham BS</pubmed_authors><pubmed_authors>Conan-Cibotti M</pubmed_authors><pubmed_authors>Kabahubya M</pubmed_authors><pubmed_authors>Robb ML</pubmed_authors><pubmed_authors>Yamshchikov GV</pubmed_authors><pubmed_authors>Lai L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterologous cAd3-Ebola and MVA-EbolaZ vaccines are safe and immunogenic in US and Uganda phase 1/1b trials.</name><description>Ebola virus disease (EVD) is a filoviral infection caused by virus species of the Ebolavirus genus including Zaire ebolavirus (EBOV) and Sudan ebolavirus (SUDV). We investigated the safety and immunogenicity of a heterologous prime-boost regimen involving a chimpanzee adenovirus 3 vectored Ebola vaccine [either monovalent (cAd3-EBOZ) or bivalent (cAd3-EBO)] prime followed by a recombinant modified vaccinia virus Ankara EBOV vaccine (MVA-EbolaZ) boost in two phase 1/1b randomized open-label clinical trials in healthy adults in the United States (US) and Uganda (UG). Trial US (NCT02408913) enrolled 140 participants, including 26 EVD vaccine-naïve and 114 cAd3-Ebola-experienced participants (April-November 2015). Trial UG (NCT02354404) enrolled 90 participants, including 60 EVD vaccine-naïve </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-01T21:47:49.977Z</modification><creation>2025-04-22T08:17:26.526Z</creation></dates><accession>S-EPMC10980745</accession><cross_references><pubmed>38553525</pubmed><doi>10.1038/s41541-024-00833-z</doi></cross_references></HashMap>