<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>96(8)</volume><submitter>Rosner A</submitter><pubmed_abstract>BriLife&lt;sup>®&lt;/sup>, a vector-based vaccine that utilizes the recombinant vesicular stomatitis virus (VSV) platform to express and present the spike antigen of SARS-CoV-2, is undergoing testing in a phase 2 clinical trial in Israel. A nonclinical repeated-dose (GLP) toxicity study in New Zealand white rabbits was performed to evaluate the potential toxicity, local tolerance, immunogenicity and biodistribution of the vaccine. rVSV-ΔG-SARS-CoV-2-S (or vehicle) was administered intramuscularly to two groups of animals (10&lt;sup>6&lt;/sup>, 10&lt;sup>7&lt;/sup> PFU/animal, n = 10/sex/group) on three occasions, at 2-week intervals, followed by a 3-week recovery period. Systemic clinical signs, local reactions, body weight, body temperature, food consumption, ophthalmology, urinalysis, clinical pathology, </pubmed_abstract><journal>Archives of toxicology</journal><pagination>2329-2339</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9110212</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>rVSV-ΔG-SARS-CoV-2-S vaccine: repeated intramuscular (IM) toxicity, local tolerance, immunogenicity and biodistribution study in NZW rabbits.</pubmed_title><pmcid>PMC9110212</pmcid><pubmed_authors>Yahalom-Ronen Y</pubmed_authors><pubmed_authors>Marcus H</pubmed_authors><pubmed_authors>Politi B</pubmed_authors><pubmed_authors>Madar-Balakirski N</pubmed_authors><pubmed_authors>Madar-Shapiro L</pubmed_authors><pubmed_authors>Achdout H</pubmed_authors><pubmed_authors>Tamir H</pubmed_authors><pubmed_authors>Stein D</pubmed_authors><pubmed_authors>Kronfeld N</pubmed_authors><pubmed_authors>Weiss S</pubmed_authors><pubmed_authors>Yitzhaki S</pubmed_authors><pubmed_authors>Vitner E</pubmed_authors><pubmed_authors>Avraham R</pubmed_authors><pubmed_authors>Mechaly A</pubmed_authors><pubmed_authors>Rosner A</pubmed_authors><pubmed_authors>Cherry L</pubmed_authors><pubmed_authors>Fatelevich E</pubmed_authors><pubmed_authors>Beth-Din A</pubmed_authors><pubmed_authors>Melamed S</pubmed_authors><pubmed_authors>Paran N</pubmed_authors><pubmed_authors>Levy H</pubmed_authors><pubmed_authors>Israely T</pubmed_authors><pubmed_authors>Fisher M</pubmed_authors><pubmed_authors>Nyska A</pubmed_authors><pubmed_authors>Steiner M</pubmed_authors></additional><is_claimable>false</is_claimable><name>rVSV-ΔG-SARS-CoV-2-S vaccine: repeated intramuscular (IM) toxicity, local tolerance, immunogenicity and biodistribution study in NZW rabbits.</name><description>BriLife&lt;sup>®&lt;/sup>, a vector-based vaccine that utilizes the recombinant vesicular stomatitis virus (VSV) platform to express and present the spike antigen of SARS-CoV-2, is undergoing testing in a phase 2 clinical trial in Israel. A nonclinical repeated-dose (GLP) toxicity study in New Zealand white rabbits was performed to evaluate the potential toxicity, local tolerance, immunogenicity and biodistribution of the vaccine. rVSV-ΔG-SARS-CoV-2-S (or vehicle) was administered intramuscularly to two groups of animals (10&lt;sup>6&lt;/sup>, 10&lt;sup>7&lt;/sup> PFU/animal, n = 10/sex/group) on three occasions, at 2-week intervals, followed by a 3-week recovery period. Systemic clinical signs, local reactions, body weight, body temperature, food consumption, ophthalmology, urinalysis, clinical pathology, </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-05-31T07:10:18.492Z</modification><creation>2025-02-19T05:04:53.496Z</creation></dates><accession>S-EPMC9110212</accession><cross_references><pubmed>35577986</pubmed><doi>10.1007/s00204-022-03302-5</doi></cross_references></HashMap>