<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(6)</volume><submitter>Girndt M</submitter><funding>Dynavax Technologies Corporation</funding><pubmed_abstract>This study compared the immunogenicity and safety of a booster dose of HepB-CpG (HEPLISAV-B® vaccine) with HepB-Eng (Engerix-B®) and HepB-AS04 (Fendrix®) in patients receiving chronic hemodialysis. This was a multicenter, randomized, open-label, phase 3 study of adults receiving hemodialysis with antibodies to HBsAg (anti-HBs) &lt;10 mIU/mL at study entry. The objective was to compare the seroprotection rate (SPR) induced by HepB-CpG with HepB-Eng or HepB-AS04. The SPR was defined as the percentage of patients with anti-HBs ≥10 mIU/mL post-vaccination. At 20 sites in Germany, 155 participants were randomized: HepB-CpG = 54; HepB-Eng = 50; and HepB-AS04 = 51. Of the 149 participants in the modified intention-to-treat population, 76.5% had not previously responded to at least one series of hepa</pubmed_abstract><journal>Human vaccines &amp; immunotherapeutics</journal><pagination>2136912</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9746491</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunogenicity and safety of a booster dose of the hepatitis B vaccine HepB-CpG (HEPLISAV-B®) compared with HepB-Eng (Engerix-B®) and HepB-AS04 (Fendrix®) in adults receiving hemodialysis who previously received hepatitis B vaccination and are not seroprotected: Results of a randomized, multicenter phase 3 study.</pubmed_title><pmcid>PMC9746491</pmcid><pubmed_authors>Wehweck HJ</pubmed_authors><pubmed_authors>Beige J</pubmed_authors><pubmed_authors>Hafezi Rachti S</pubmed_authors><pubmed_authors>Faust J</pubmed_authors><pubmed_authors>Pluer M</pubmed_authors><pubmed_authors>Toussaint K</pubmed_authors><pubmed_authors>Dellanna F</pubmed_authors><pubmed_authors>Michelsen AK</pubmed_authors><pubmed_authors>Koch M</pubmed_authors><pubmed_authors>Witzke O</pubmed_authors><pubmed_authors>HBV-18 Study Investigators</pubmed_authors><pubmed_authors>Janssen RS</pubmed_authors><pubmed_authors>Bosselmann HP</pubmed_authors><pubmed_authors>Girndt M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunogenicity and safety of a booster dose of the hepatitis B vaccine HepB-CpG (HEPLISAV-B®) compared with HepB-Eng (Engerix-B®) and HepB-AS04 (Fendrix®) in adults receiving hemodialysis who previously received hepatitis B vaccination and are not seroprotected: Results of a randomized, multicenter phase 3 study.</name><description>This study compared the immunogenicity and safety of a booster dose of HepB-CpG (HEPLISAV-B® vaccine) with HepB-Eng (Engerix-B®) and HepB-AS04 (Fendrix®) in patients receiving chronic hemodialysis. This was a multicenter, randomized, open-label, phase 3 study of adults receiving hemodialysis with antibodies to HBsAg (anti-HBs) &lt;10 mIU/mL at study entry. The objective was to compare the seroprotection rate (SPR) induced by HepB-CpG with HepB-Eng or HepB-AS04. The SPR was defined as the percentage of patients with anti-HBs ≥10 mIU/mL post-vaccination. At 20 sites in Germany, 155 participants were randomized: HepB-CpG = 54; HepB-Eng = 50; and HepB-AS04 = 51. Of the 149 participants in the modified intention-to-treat population, 76.5% had not previously responded to at least one series of hepa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-27T04:01:25.266Z</modification><creation>2024-11-13T10:38:40.929Z</creation></dates><accession>S-EPMC9746491</accession><cross_references><pubmed>36269938</pubmed><doi>10.1080/21645515.2022.2136912</doi></cross_references></HashMap>