<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(11)</volume><submitter>Wang X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>A phase 3 trial was conducted to evaluate the efficacy and safety of ongericimab, a monoclonal antibody that inhibits proprotein convertase subtilisin/kexin type 9, as an add-on treatment to optimized lipid-lowering therapy in Chinese patients with primary hypercholesterolemia and mixed dyslipidemia.&lt;h4>Methods and results&lt;/h4>A total of 806 patients who were receiving stable and optimized lipid-lowering therapy but did not achieve their low-density lipoprotein cholesterol (LDL-C) targets were enrolled and randomly assigned in a 2:1:2:1 ratio to receive either ongericimab 150 mg or matching placebo every 2 weeks, or ongericimab 300 mg or matching placebo every 4 weeks for 52 weeks. Efficacy and safety were evaluated in 802 patients who received at least 1 dose of ongeric</pubmed_abstract><journal>Journal of the American Heart Association</journal><pagination>e033669</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11255649</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Efficacy and Safety of Ongericimab in Chinese Patients With Primary Hypercholesterolemia and Mixed Dyslipidemia.</pubmed_title><pmcid>PMC11255649</pmcid><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Zhu H</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Han Y</pubmed_authors><pubmed_authors>Qiu M</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Bai X</pubmed_authors><pubmed_authors>Su G</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Cheng Z</pubmed_authors><pubmed_authors>Shao C</pubmed_authors><pubmed_authors>Yao Z</pubmed_authors><pubmed_authors>Ji X</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Huang Z</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and Safety of Ongericimab in Chinese Patients With Primary Hypercholesterolemia and Mixed Dyslipidemia.</name><description>&lt;h4>Background&lt;/h4>A phase 3 trial was conducted to evaluate the efficacy and safety of ongericimab, a monoclonal antibody that inhibits proprotein convertase subtilisin/kexin type 9, as an add-on treatment to optimized lipid-lowering therapy in Chinese patients with primary hypercholesterolemia and mixed dyslipidemia.&lt;h4>Methods and results&lt;/h4>A total of 806 patients who were receiving stable and optimized lipid-lowering therapy but did not achieve their low-density lipoprotein cholesterol (LDL-C) targets were enrolled and randomly assigned in a 2:1:2:1 ratio to receive either ongericimab 150 mg or matching placebo every 2 weeks, or ongericimab 300 mg or matching placebo every 4 weeks for 52 weeks. Efficacy and safety were evaluated in 802 patients who received at least 1 dose of ongeric</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-06-01T07:38:49.567Z</modification><creation>2025-04-06T17:11:46.519Z</creation></dates><accession>S-EPMC11255649</accession><cross_references><pubmed>38818934</pubmed><doi>10.1161/JAHA.123.033669</doi></cross_references></HashMap>