Publication: Advancing therapy in suboptimally controlled basal insulin–treated type 2 diabetes: Clinical outcomes with iglarlixi versus premix biasp 30 in the solimix randomized controlled trial
dc.contributor.author | Rosenstock, Julio (7006091173) | |
dc.contributor.author | Emral, Rifat (6603414622) | |
dc.contributor.author | Sauque-Reyna, Leobardo (6505644318) | |
dc.contributor.author | Mohan, Viswanathan (57216603627) | |
dc.contributor.author | Trescolı, Carlos (7801372356) | |
dc.contributor.author | Al Sifri, Saud (56085622300) | |
dc.contributor.author | Lalic, Nebojsa (13702597500) | |
dc.contributor.author | Alvarez, Agustina (57223047397) | |
dc.contributor.author | Picard, Pascaline (57209307089) | |
dc.contributor.author | Bonnemaire, Mireille (6507073079) | |
dc.contributor.author | Demil, Nacima (26325264700) | |
dc.contributor.author | McCrimmon, Rory J. (6701669267) | |
dc.date.accessioned | 2025-07-02T12:03:47Z | |
dc.date.available | 2025-07-02T12:03:47Z | |
dc.date.issued | 2021 | |
dc.description.abstract | OBJECTIVE: To directly compare the efficacy and safety of a fixed-ratio combination, of insulin glargine 100 units/mL and the glucagon-like peptide 1 receptor agonist lixisenatide (iGlar- Lixi), with those of a premix insulin analog, biphasic aspart insulin 30 (30% insulin aspart and 70% insulin aspart protamine) (BIAsp 30) as treatment advancement in type 2 diabetes suboptimally controlled on basal insulin plus oral antihyperglycemic drugs (OADs). RESEARCH DESIGN AND METHODS: In SoliMix, a 26-week, open-label, multicenter study, adults with suboptimally controlled basal insulin–treated type 2 diabetes (HbA1c ‡7.5% and ©10%) were randomized to once-daily iGlarLixi or twice-daily BIAsp 30. Primary efficacy end points were noninferiority in HbA1c reduction (margin 0.3%) or superiority in body weight change for iGlarLixi versus BIAsp 30. RESULTS: Both primary efficacy end points were met: After 26 weeks, baseline HbA1c (8.6%) was reduced by 1.3% with iGlarLixi and 1.1% with BIAsp 30, meeting noninferiority (least squares [LS] mean difference -0.2% [97.5% CI -0.4, -0.1]; P < 0.001). iGlarLixi was also superior to BIAsp 30 for body weight change (LS mean difference -1.9 kg [95% CI -2.3, -1.4]) and percentage of participants achieving HbA1c <7% without weight gain and HbA1c <7% without weight gain and without hypoglycemia (all P < 0.001). iGlarLixi was also superior versus BIAsp 30 for HbA1c reduction (P < 0.001). Incidence and rates of American Diabetes Association level 1 and 2 hypoglycemia were lower with iGlarLixi versus BIAsp 30. CONCLUSIONS: Once-daily iGlarLixi provided better glycemic control with weight benefit and less hypoglycemia than twice-daily premix BIAsp 30. iGlarLixi is a more efficacious, simpler, and well-tolerated alternative to premix BIAsp 30 in suboptimally controlled type 2 diabetes requiring treatment beyond basal insulin plus OAD therapy. © 2021 by the American Diabetes Association. | |
dc.identifier.uri | https://doi.org/10.2337/dc21-0393 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85114762701&doi=10.2337%2fdc21-0393&partnerID=40&md5=c8a866c642b2a1d3345c77c45238c537 | |
dc.identifier.uri | https://remedy.med.bg.ac.rs/handle/123456789/12350 | |
dc.title | Advancing therapy in suboptimally controlled basal insulin–treated type 2 diabetes: Clinical outcomes with iglarlixi versus premix biasp 30 in the solimix randomized controlled trial | |
dspace.entity.type | Publication |