<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(2)</volume><submitter>Yale JF</submitter><funding>Sanofi</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>For people with type 2 diabetes mellitus who do not achieve glycated hemoglobin A1C targets after treatment with basal insulin therapies, additional therapy with a glucagon-like peptide-1 receptor agonist (GLP-1 RA) may be required. One option is to use a once-daily fixed-ratio combination (FRC) of basal insulin and a GLP-1 RA such as iGlarLixi (which is composed of insulin glargine 100 U/ml and lixisenatide). However, the ease of transitioning from basal insulin to an FRC has not been studied.&lt;h4>Methods&lt;/h4>This sub-study of the LixiLan ONE CAN trial (NCT03767543) was conducted to assess the ease of transitioning from insulin glargine 100 U/ml to the FRC, iGlarLixi, using the iGlarLixi SoloStar&lt;sup>®&lt;/sup> pen. Patients completed a validated, ten-item questionnaire, </pubmed_abstract><journal>Diabetes therapy : research, treatment and education of diabetes and related disorders</journal><pagination>377-386</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9943797</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ease of Use of the iGlarLixi SoloStar Pen from the LixiLan ONE CAN Pen Sub-Study: Questionnaire Findings from People Living with Type 2 Diabetes and Their HealthCare Providers.</pubmed_title><pmcid>PMC9943797</pmcid><pubmed_authors>Stewart J</pubmed_authors><pubmed_authors>Hramiak I</pubmed_authors><pubmed_authors>Roborel de Climens A</pubmed_authors><pubmed_authors>Dex T</pubmed_authors><pubmed_authors>Harris S</pubmed_authors><pubmed_authors>Aggarwal N</pubmed_authors><pubmed_authors>Gerstein HC</pubmed_authors><pubmed_authors>Yale JF</pubmed_authors><pubmed_authors>Leiter LA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ease of Use of the iGlarLixi SoloStar Pen from the LixiLan ONE CAN Pen Sub-Study: Questionnaire Findings from People Living with Type 2 Diabetes and Their HealthCare Providers.</name><description>&lt;h4>Introduction&lt;/h4>For people with type 2 diabetes mellitus who do not achieve glycated hemoglobin A1C targets after treatment with basal insulin therapies, additional therapy with a glucagon-like peptide-1 receptor agonist (GLP-1 RA) may be required. One option is to use a once-daily fixed-ratio combination (FRC) of basal insulin and a GLP-1 RA such as iGlarLixi (which is composed of insulin glargine 100 U/ml and lixisenatide). However, the ease of transitioning from basal insulin to an FRC has not been studied.&lt;h4>Methods&lt;/h4>This sub-study of the LixiLan ONE CAN trial (NCT03767543) was conducted to assess the ease of transitioning from insulin glargine 100 U/ml to the FRC, iGlarLixi, using the iGlarLixi SoloStar&lt;sup>®&lt;/sup> pen. Patients completed a validated, ten-item questionnaire, </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-04T14:17:52.147Z</modification><creation>2025-02-19T02:24:05.997Z</creation></dates><accession>S-EPMC9943797</accession><cross_references><pubmed>36574199</pubmed><doi>10.1007/s13300-022-01353-6</doi></cross_references></HashMap>