<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nguyen MH</submitter><funding>Cystic Fibrosis Foundation</funding><funding>Bundesamt für Gesundheit</funding><pagination>106103</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12804157</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>123</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Current treatment regimens for nontuberculous mycobacteria (NTM) infections, especially Mycobacterium abscessus, have suboptimal clinical outcomes, demanding novel therapeutic options. The aminoglycoside apramycin (APR) has been suggested as a therapeutic alternative to amikacin (AMK). Here, we report experimental data as part of an ongoing preclinical assessment of APR.&lt;h4>Methods&lt;/h4>Antimicrobial activity against 828 isolates comprising the clinically most relevant NTM species were determined by broth microdilution. Bactericidal activity and killing kinetics of APR were determined across a variety of assay conditions against rough and smooth M. abscessus isolates in vitro and in vivo.&lt;h4>Findings&lt;/h4>Both the MIC&lt;sub>90&lt;/sub> and tentative epidemiological cutoff (TECO</pubmed_abstract><journal>EBioMedicine</journal><pubmed_title>Multicentre preclinical profiling of apramycin for the treatment of nontuberculous mycobacteria.</pubmed_title><pmcid>PMC12804157</pmcid><funding_grant_id>JUVABIS22W0</funding_grant_id><funding_grant_id>HOBBIE19I0</funding_grant_id><pubmed_authors>Krishnamurthy RV</pubmed_authors><pubmed_authors>Haldimann K</pubmed_authors><pubmed_authors>Plattner M</pubmed_authors><pubmed_authors>Becker K</pubmed_authors><pubmed_authors>Narayanan S</pubmed_authors><pubmed_authors>Xie M</pubmed_authors><pubmed_authors>Kaur P</pubmed_authors><pubmed_authors>Bulman ZP</pubmed_authors><pubmed_authors>Hobbie SN</pubmed_authors><pubmed_authors>Shandil RK</pubmed_authors><pubmed_authors>Calado Nogueira de Moura V</pubmed_authors><pubmed_authors>Verma D</pubmed_authors><pubmed_authors>Schulthess B</pubmed_authors><pubmed_authors>Singh M</pubmed_authors><pubmed_authors>Daley CL</pubmed_authors><pubmed_authors>Mitarai S</pubmed_authors><pubmed_authors>Lang R</pubmed_authors><pubmed_authors>Nguyen MH</pubmed_authors><pubmed_authors>Dick T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multicentre preclinical profiling of apramycin for the treatment of nontuberculous mycobacteria.</name><description>&lt;h4>Background&lt;/h4>Current treatment regimens for nontuberculous mycobacteria (NTM) infections, especially Mycobacterium abscessus, have suboptimal clinical outcomes, demanding novel therapeutic options. The aminoglycoside apramycin (APR) has been suggested as a therapeutic alternative to amikacin (AMK). Here, we report experimental data as part of an ongoing preclinical assessment of APR.&lt;h4>Methods&lt;/h4>Antimicrobial activity against 828 isolates comprising the clinically most relevant NTM species were determined by broth microdilution. Bactericidal activity and killing kinetics of APR were determined across a variety of assay conditions against rough and smooth M. abscessus isolates in vitro and in vivo.&lt;h4>Findings&lt;/h4>Both the MIC&lt;sub>90&lt;/sub> and tentative epidemiological cutoff (TECO</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T16:07:51.392Z</modification><creation>2026-06-02T03:11:14.511Z</creation></dates><accession>S-EPMC12804157</accession><cross_references><pubmed>41478260</pubmed><doi>10.1016/j.ebiom.2025.106103</doi></cross_references></HashMap>