<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(5)</volume><submitter>Bailey TS</submitter><funding>Eli Lilly and Company</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>To evaluate time in range metrics and HbA1c in people with type 2 diabetes (T2D) treated with ultra rapid lispro (URLi) using continuous glucose monitoring (CGM) for the first time in this population.&lt;h4>Methods&lt;/h4>This was a Phase 3b, 12-week, single-treatment study in adults with T2D on basal-bolus multiple daily injection (MDI) therapy using basal insulin glargine U-100 along with a rapid-acting insulin analog. Following a 4-week baseline period, 176 participants were newly treated with prandial URLi. Participants used unblinded CGM (Freestyle Libre). Primary endpoint was time in range (TIR) (70-180 mg/dl) during the daytime period at Week 12 compared to baseline with gated secondary endpoints of HbA1c change from baseline and 24-h TIR (70-180 mg/dl).&lt;h4>Results&lt;/h</pubmed_abstract><journal>Diabetes therapy : research, treatment and education of diabetes and related disorders</journal><pagination>883-897</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10081815</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Increased Time in Range with Ultra Rapid Lispro Treatment in Participants with Type 2 Diabetes: PRONTO-Time in Range.</pubmed_title><pmcid>PMC10081815</pmcid><pubmed_authors>Bode BW</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Knights AW</pubmed_authors><pubmed_authors>Chang AM</pubmed_authors><pubmed_authors>Bailey TS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Increased Time in Range with Ultra Rapid Lispro Treatment in Participants with Type 2 Diabetes: PRONTO-Time in Range.</name><description>&lt;h4>Introduction&lt;/h4>To evaluate time in range metrics and HbA1c in people with type 2 diabetes (T2D) treated with ultra rapid lispro (URLi) using continuous glucose monitoring (CGM) for the first time in this population.&lt;h4>Methods&lt;/h4>This was a Phase 3b, 12-week, single-treatment study in adults with T2D on basal-bolus multiple daily injection (MDI) therapy using basal insulin glargine U-100 along with a rapid-acting insulin analog. Following a 4-week baseline period, 176 participants were newly treated with prandial URLi. Participants used unblinded CGM (Freestyle Libre). Primary endpoint was time in range (TIR) (70-180 mg/dl) during the daytime period at Week 12 compared to baseline with gated secondary endpoints of HbA1c change from baseline and 24-h TIR (70-180 mg/dl).&lt;h4>Results&lt;/h</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2026-07-14T19:13:02.317Z</modification><creation>2025-04-04T14:29:54.34Z</creation></dates><accession>S-EPMC10081815</accession><cross_references><pubmed>37029268</pubmed><doi>10.1007/s13300-023-01400-w</doi></cross_references></HashMap>