<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Geiger RM</submitter><funding>Intramural FDA HHS</funding><pagination>1679626</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12690487</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5</volume><pubmed_abstract>&lt;h4>Background and purpose&lt;/h4>Nonclinical human cardiac new approach methodologies (NAMs), including human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) combined with multielectrode array (MEA) represent a highly predictive &lt;i>in vitro&lt;/i> model for identifying drug-induced cardiac liabilities of individual drugs. Here, we extend the use of an &lt;i>in vitro&lt;/i> cardiac NAM to evaluate the safety of a drug combination including moxifloxacin, an antibiotic, and QT prolonging drug, and cobicistat a pharmacokinetic booster shown to shorten repolarization &lt;i>in vitro&lt;/i>.&lt;h4>Methods&lt;/h4>To generate the &lt;i>in vitro&lt;/i> cardiac NAM, MEA coupled with hiPSC-CMs were cultured for 7-8 days. Cells were treated with moxifloxacin and cobicistat individually or in combination and change</pubmed_abstract><journal>Frontiers in drug discovery</journal><pubmed_title>Towards human cardiac new approach methodologies (NAMs) to evaluate the combination of repolarization prolonging and shortening drugs: a pilot study.</pubmed_title><pmcid>PMC12690487</pmcid><funding_grant_id>FD999999</funding_grant_id><pubmed_authors>Geiger RM</pubmed_authors><pubmed_authors>Bhardwaj B</pubmed_authors><pubmed_authors>Blinova K</pubmed_authors><pubmed_authors>Serna C</pubmed_authors><pubmed_authors>Feaster TK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Towards human cardiac new approach methodologies (NAMs) to evaluate the combination of repolarization prolonging and shortening drugs: a pilot study.</name><description>&lt;h4>Background and purpose&lt;/h4>Nonclinical human cardiac new approach methodologies (NAMs), including human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) combined with multielectrode array (MEA) represent a highly predictive &lt;i>in vitro&lt;/i> model for identifying drug-induced cardiac liabilities of individual drugs. Here, we extend the use of an &lt;i>in vitro&lt;/i> cardiac NAM to evaluate the safety of a drug combination including moxifloxacin, an antibiotic, and QT prolonging drug, and cobicistat a pharmacokinetic booster shown to shorten repolarization &lt;i>in vitro&lt;/i>.&lt;h4>Methods&lt;/h4>To generate the &lt;i>in vitro&lt;/i> cardiac NAM, MEA coupled with hiPSC-CMs were cultured for 7-8 days. Cells were treated with moxifloxacin and cobicistat individually or in combination and change</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-06T13:56:23.865Z</modification><creation>2026-05-31T03:09:58.944Z</creation></dates><accession>S-EPMC12690487</accession><cross_references><pubmed>41383657</pubmed><doi>10.3389/fddsv.2025.1679626</doi></cross_references></HashMap>