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

Author:

Rosenstock Julio1ORCID,Emral Rifat2,Sauque-Reyna Leobardo3,Mohan Viswanathan4,Trescolí Carlos5,Al Sifri Saud6,Lalic Nebojsa7,Alvarez Agustina8,Picard Pascaline9,Bonnemaire Mireille10,Demil Nacima11,McCrimmon Rory J.12

Affiliation:

1. Dallas Diabetes Research Center at Medical City, Dallas, TX

2. Department of Endocrinology and Metabolic Diseases, Ankara University Faculty of Medicine, Ankara, Turkey

3. Instituto de Diabetes Obesidad y Nutrición S.C., Cuernavaca, Morelos, Mexico

4. Dr. Mohan’s Diabetes Specialities Centre & Madras Diabetes Research Foundation, IDF Centre of Excellence in Diabetes Care & ICMR Centre for Advanced Research on Diabetes, Chennai, India

5. Hospital Universitario de La Ribera, Alzira, Spain

6. Al Hada Military Hospital, Taif, Saudi Arabia

7. Faculty of Medicine of the University of Belgrade, Clinic for Endocrinology, Diabetes and Metabolic Diseases, Clinical Center of Serbia, Belgrade, Serbia

8. Sanofi, Buenos Aires, Argentina

9. IviData LIFE SCIENCES, Levallois-Perret, France

10. Sanofi, Paris, France

11. Diabetes Medical Operation Department, Sanofi, Chilly-Mazarin, France

12. Division of Systems Medicine, School of Medicine, University of Dundee, Dundee, U.K.

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 (iGlarLixi), 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. Video 1

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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