<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ignatius EH</submitter><funding>HHS | National Institutes of Health</funding><funding>NIAID NIH HHS</funding><funding>Paratek Pharmaceuticals Inc</funding><pagination>e0038124</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11288010</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(7)</volume><pubmed_abstract>Treatment outcomes for &lt;i>Mycobacteroides abscessus&lt;/i> (&lt;i>Mab&lt;/i>, also known as &lt;i>Mycobacterium abscessus&lt;/i>) disease are still unsatisfactory, mainly due to issues with drug toxicity, tolerability, and efficacy. Treating &lt;i>Mab&lt;/i> disease is challenging due to its high baseline antibiotic resistance, initial requirement for intravenous therapy, and poor medication tolerance. Omadacycline, a new tetracycline, is active against &lt;i>Mab&lt;/i>. Since any new antibiotic effective against &lt;i>Mab&lt;/i> is expected to be used in combination with other antibiotics, we evaluated the efficacy of two triple-drug combinations comprising omadacycline, omadacycline + amikacin + imipenem, and omadacycline + clofazimine + linezolid against two contemporary &lt;i>Mab&lt;/i> clinical isolates in a mouse model of</pubmed_abstract><journal>mSphere</journal><pubmed_title>Efficacies of omadacycline + amikacin + imipenem and an all-oral regimen omadacycline + clofazimine + linezolid in a mouse model of &lt;i>M. abscessus&lt;/i> lung disease.</pubmed_title><pmcid>PMC11288010</pmcid><funding_grant_id>K23 AI159145</funding_grant_id><pubmed_authors>Belz DC</pubmed_authors><pubmed_authors>Lippincott CK</pubmed_authors><pubmed_authors>Lamichhane G</pubmed_authors><pubmed_authors>Serio AW</pubmed_authors><pubmed_authors>Rimal B</pubmed_authors><pubmed_authors>Panthi CM</pubmed_authors><pubmed_authors>Ignatius EH</pubmed_authors><pubmed_authors>Deck DH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacies of omadacycline + amikacin + imipenem and an all-oral regimen omadacycline + clofazimine + linezolid in a mouse model of &lt;i>M. abscessus&lt;/i> lung disease.</name><description>Treatment outcomes for &lt;i>Mycobacteroides abscessus&lt;/i> (&lt;i>Mab&lt;/i>, also known as &lt;i>Mycobacterium abscessus&lt;/i>) disease are still unsatisfactory, mainly due to issues with drug toxicity, tolerability, and efficacy. Treating &lt;i>Mab&lt;/i> disease is challenging due to its high baseline antibiotic resistance, initial requirement for intravenous therapy, and poor medication tolerance. Omadacycline, a new tetracycline, is active against &lt;i>Mab&lt;/i>. Since any new antibiotic effective against &lt;i>Mab&lt;/i> is expected to be used in combination with other antibiotics, we evaluated the efficacy of two triple-drug combinations comprising omadacycline, omadacycline + amikacin + imipenem, and omadacycline + clofazimine + linezolid against two contemporary &lt;i>Mab&lt;/i> clinical isolates in a mouse model of</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-02T09:19:24.096Z</modification><creation>2026-04-16T03:13:16.086Z</creation></dates><accession>S-EPMC11288010</accession><cross_references><pubmed>38980071</pubmed><doi>10.1128/msphere.00381-24</doi></cross_references></HashMap>