<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>39(1)</volume><submitter>Kamrul-Hasan ABM</submitter><pubmed_abstract>&lt;h4>Backgruound&lt;/h4>No recent meta-analysis has holistically analyzed and summarized the efficacy and safety of omarigliptin in type 2 diabetes mellitus (T2DM). We conducted a meta-analysis to address this knowledge gap.&lt;h4>Methods&lt;/h4>Electronic databases were searched to identify randomized controlled trials (RCTs) that included patients with T2DM who received omarigliptin in the intervention arm. The control arm consisted of either a placebo (passive control group [PCG]) or an active comparator (active control group [ACG]). The primary outcome assessed was changes in hemoglobin A1c (HbA1c), while secondary outcomes included variations in glucose levels, achievement of glycemic targets, adverse events (AEs), and hypoglycemic events.&lt;h4>Results&lt;/h4>From 332 initially screened articles, data from 16 RCTs involving 8,804 subjects were analyzed. Omarigliptin demonstrated superiority over placebo in reducing HbA1c levels (mean difference, -0.58%; 95% confidence interval, -0.75 to -0.40; P&lt;0.00001; I2=91%). Additionally, omarigliptin outperformed placebo in lowering fasting plasma glucose, 2-hour postprandial glucose, and in the percentage of participants achieving HbA1c levels below 7.0% and 6.5%. The glycemic efficacy of omarigliptin was similar to that of the ACG across all measures. Although the omarigliptin group experienced a higher incidence of hypoglycemic events compared to the PCG, the overall AEs, serious AEs, hypoglycemia, and severe hypoglycemia were comparable between the omarigliptin and control groups (PCG and ACG).&lt;h4>Conclusion&lt;/h4>Omarigliptin has a favorable glycemic efficacy and safety profile for managing T2DM.</pubmed_abstract><journal>Endocrinology and metabolism (Seoul, Korea)</journal><pagination>109-126</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10901664</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Efficacy and Safety of Omarigliptin, a Novel Once-Weekly Dipeptidyl Peptidase-4 Inhibitor, in Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis.</pubmed_title><pmcid>PMC10901664</pmcid><pubmed_authors>Selim S</pubmed_authors><pubmed_authors>Dutta D</pubmed_authors><pubmed_authors>Kamrul-Hasan ABM</pubmed_authors><pubmed_authors>Talukder SK</pubmed_authors><pubmed_authors>Alam MS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and Safety of Omarigliptin, a Novel Once-Weekly Dipeptidyl Peptidase-4 Inhibitor, in Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis.</name><description>&lt;h4>Backgruound&lt;/h4>No recent meta-analysis has holistically analyzed and summarized the efficacy and safety of omarigliptin in type 2 diabetes mellitus (T2DM). We conducted a meta-analysis to address this knowledge gap.&lt;h4>Methods&lt;/h4>Electronic databases were searched to identify randomized controlled trials (RCTs) that included patients with T2DM who received omarigliptin in the intervention arm. The control arm consisted of either a placebo (passive control group [PCG]) or an active comparator (active control group [ACG]). The primary outcome assessed was changes in hemoglobin A1c (HbA1c), while secondary outcomes included variations in glucose levels, achievement of glycemic targets, adverse events (AEs), and hypoglycemic events.&lt;h4>Results&lt;/h4>From 332 initially screened articles, data from 16 RCTs involving 8,804 subjects were analyzed. Omarigliptin demonstrated superiority over placebo in reducing HbA1c levels (mean difference, -0.58%; 95% confidence interval, -0.75 to -0.40; P&lt;0.00001; I2=91%). Additionally, omarigliptin outperformed placebo in lowering fasting plasma glucose, 2-hour postprandial glucose, and in the percentage of participants achieving HbA1c levels below 7.0% and 6.5%. The glycemic efficacy of omarigliptin was similar to that of the ACG across all measures. Although the omarigliptin group experienced a higher incidence of hypoglycemic events compared to the PCG, the overall AEs, serious AEs, hypoglycemia, and severe hypoglycemia were comparable between the omarigliptin and control groups (PCG and ACG).&lt;h4>Conclusion&lt;/h4>Omarigliptin has a favorable glycemic efficacy and safety profile for managing T2DM.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-04T20:39:48.551Z</modification><creation>2025-02-19T03:10:05.541Z</creation></dates><accession>S-EPMC10901664</accession><cross_references><pubmed>38417828</pubmed><doi>10.3803/EnM.2023.1839</doi></cross_references></HashMap>