<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>44(11)</volume><submitter>Sunnaker M</submitter><funding>AstraZeneca</funding><pubmed_abstract>&lt;h4>Background and objective&lt;/h4>Mitiperstat (AZD4831) is a novel irreversible oral myeloperoxidase inhibitor in clinical development for heart failure with preserved ejection fraction, metabolic dysfunction-associated steatohepatitis and chronic obstructive pulmonary disease. This study evaluated the pharmacokinetics, safety and tolerability of multiple ascending doses of mitiperstat in healthy male Japanese and Chinese volunteers.&lt;h4>Methods&lt;/h4>Three cohorts of eight Japanese participants were randomized to receive once-daily oral doses of mitiperstat 2.5, 5 or 10 mg or matching placebo for 10 days (six receiving mitiperstat and two receiving placebo, per cohort). One cohort of eight Chinese participants was randomized to receive mitiperstat 5 mg or matching placebo for 10 days (six rec</pubmed_abstract><journal>Clinical drug investigation</journal><pagination>863-874</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11564280</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pharmacokinetics and Tolerability of the Novel Myeloperoxidase Inhibitor Mitiperstat in Healthy Japanese and Chinese Volunteers.</pubmed_title><pmcid>PMC11564280</pmcid><pubmed_authors>Ericsson H</pubmed_authors><pubmed_authors>Trebski M</pubmed_authors><pubmed_authors>Heijer M</pubmed_authors><pubmed_authors>Holden J</pubmed_authors><pubmed_authors>Bhattacharya C</pubmed_authors><pubmed_authors>Sunnaker M</pubmed_authors><pubmed_authors>Collen A</pubmed_authors><pubmed_authors>Nelander K</pubmed_authors><pubmed_authors>Aurell M</pubmed_authors><pubmed_authors>Garkaviy P</pubmed_authors><pubmed_authors>Han D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacokinetics and Tolerability of the Novel Myeloperoxidase Inhibitor Mitiperstat in Healthy Japanese and Chinese Volunteers.</name><description>&lt;h4>Background and objective&lt;/h4>Mitiperstat (AZD4831) is a novel irreversible oral myeloperoxidase inhibitor in clinical development for heart failure with preserved ejection fraction, metabolic dysfunction-associated steatohepatitis and chronic obstructive pulmonary disease. This study evaluated the pharmacokinetics, safety and tolerability of multiple ascending doses of mitiperstat in healthy male Japanese and Chinese volunteers.&lt;h4>Methods&lt;/h4>Three cohorts of eight Japanese participants were randomized to receive once-daily oral doses of mitiperstat 2.5, 5 or 10 mg or matching placebo for 10 days (six receiving mitiperstat and two receiving placebo, per cohort). One cohort of eight Chinese participants was randomized to receive mitiperstat 5 mg or matching placebo for 10 days (six rec</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-05-29T11:55:53.786Z</modification><creation>2025-04-07T04:33:01.435Z</creation></dates><accession>S-EPMC11564280</accession><cross_references><pubmed>39495467</pubmed><doi>10.1007/s40261-024-01402-x</doi></cross_references></HashMap>