<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Cercato C</submitter><funding>Eurofarma Laboratórios S.A</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Evogliptin (EVO) is a potent and selective dipeptidyl peptidase-4 inhibitor (DPP4i) developed for the treatment of type 2 diabetes mellitus (T2DM). DPP4is are known to exhibit a better glucose-lowering effect in Asians compared to other ethnic groups. Once EVO's clinical development program was conducted in Asian patients, this bridging study was designed to validate for the Brazilian population the efficacy and safety of the approved dose regimen (once-daily 5.0 mg).&lt;h4>Methods&lt;/h4>In this randomized, double-blind, double-dummy, parallel trial, 146 patients with T2DM with inadequate glycemic control on diet and exercise (7.5% ≤ HbA1c ≤ 10.5%) were randomly assigned to a 12-week once-daily treatment with EVO 2.5 mg (N = 35), EVO 5 mg (N = 36), EVO 10 mg (N = 36), or sita</pubmed_abstract><journal>Diabetology &amp; metabolic syndrome</journal><pagination>107</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6923891</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Efficacy and safety of evogliptin in the treatment of type 2 diabetes mellitus in a Brazilian population: a randomized bridging study.</pubmed_title><pmcid>PMC6923891</pmcid><pubmed_authors>Felicio JS</pubmed_authors><pubmed_authors>Russo LAT</pubmed_authors><pubmed_authors>Borges JLC</pubmed_authors><pubmed_authors>Muskat P</pubmed_authors><pubmed_authors>Forti AC</pubmed_authors><pubmed_authors>Bonansea T</pubmed_authors><pubmed_authors>Eliaschewitz FG</pubmed_authors><pubmed_authors>Chacra AR</pubmed_authors><pubmed_authors>Salles J</pubmed_authors><pubmed_authors>Cercato C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and safety of evogliptin in the treatment of type 2 diabetes mellitus in a Brazilian population: a randomized bridging study.</name><description>&lt;h4>Background&lt;/h4>Evogliptin (EVO) is a potent and selective dipeptidyl peptidase-4 inhibitor (DPP4i) developed for the treatment of type 2 diabetes mellitus (T2DM). DPP4is are known to exhibit a better glucose-lowering effect in Asians compared to other ethnic groups. Once EVO's clinical development program was conducted in Asian patients, this bridging study was designed to validate for the Brazilian population the efficacy and safety of the approved dose regimen (once-daily 5.0 mg).&lt;h4>Methods&lt;/h4>In this randomized, double-blind, double-dummy, parallel trial, 146 patients with T2DM with inadequate glycemic control on diet and exercise (7.5% ≤ HbA1c ≤ 10.5%) were randomly assigned to a 12-week once-daily treatment with EVO 2.5 mg (N = 35), EVO 5 mg (N = 36), EVO 10 mg (N = 36), or sita</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2025-04-04T08:48:29.313Z</modification><creation>2020-05-22T01:29:48Z</creation></dates><accession>S-EPMC6923891</accession><cross_references><pubmed>31890041</pubmed><doi>10.1186/s13098-019-0505-z</doi></cross_references></HashMap>