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.authorRosenstock, Julio (7006091173)
dc.contributor.authorEmral, Rifat (6603414622)
dc.contributor.authorSauque-Reyna, Leobardo (6505644318)
dc.contributor.authorMohan, Viswanathan (57216603627)
dc.contributor.authorTrescolı, Carlos (7801372356)
dc.contributor.authorAl Sifri, Saud (56085622300)
dc.contributor.authorLalic, Nebojsa (13702597500)
dc.contributor.authorAlvarez, Agustina (57223047397)
dc.contributor.authorPicard, Pascaline (57209307089)
dc.contributor.authorBonnemaire, Mireille (6507073079)
dc.contributor.authorDemil, Nacima (26325264700)
dc.contributor.authorMcCrimmon, Rory J. (6701669267)
dc.date.accessioned2025-07-02T12:03:47Z
dc.date.available2025-07-02T12:03:47Z
dc.date.issued2021
dc.description.abstractOBJECTIVE: 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.urihttps://doi.org/10.2337/dc21-0393
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85114762701&doi=10.2337%2fdc21-0393&partnerID=40&md5=c8a866c642b2a1d3345c77c45238c537
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/12350
dc.titleAdvancing 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.typePublication

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