Diabetologie und Stoffwechsel 2025; 20(S 01): S44
DOI: 10.1055/s-0045-1807441
Abstracts | DDG 2025
Poster
Posterwalk 5: Diabeteskomplikationen I Niere I Fuß

Near-Normoglycemia and Insulin Regression Induced by Tirzepatide in Basal Insulin–Treated Type 2 Diabetes

Authors

  • J Rosenstock

    1   Velocity Clinical Research at Medical City, Senior Scientific Advisor, Dallas, Texas, United States
  • S Tofé

    2   Department of Endocrinology and Nutrition, University Hospital Son Espases, Palma, Spain
  • C Wysham

    3   Rockwood Clinic, Department of Diabetes and Endocrinology, Spokane, United States
  • V Thieu

    4   Eli Lilly and Company, Cardiometabolic Health-Incretins, Indianapolis, United States
  • J Kiljanski

    5   Eli Lilly and Company, Cardiometabolic Health, Indianapolis, United States
  • C Lee

    6   Eli Lilly and Company, Global Medical Affairs Obesity/NILEX, Indianapolis, United States
  • H Wang

    7   TechData Service Company LLC, TechData Service Company LLC, Philadelphia, United States
  • H Patel

    8   Eli Lilly and Company, Type 2 Diabetes Development, Indianapolis, United States
  • J Simon

    9   MVZ im Altstadt-Caree Fulda GmbH, Specialist in internal medicine, diabetology, sports medicine, preventive medicine, Fulda, Germany
 

In SURPASS-6, how efficacious and safe was tirzepatide (TZP) based on residual insulin use at Week 52?

Methods: In the SURPASS-6 trial, TZP was added to basal insulin glargine U100 in participants with inadequately controlled long-standing type 2 diabetes (T2D). “Insulin regressor” was defined as basal insulin discontinuation or<10 IU/day, and “insulin non-regressor” as≥10 IU/day, at 52 weeks. Included only participants receiving TZP at Week 52 (≥75% compliance) without rescue medication. Efficacy analyses used a mixed model for repeated measures.

Results: Overall, 145 and 496 TZP-treated participants were included in the insulin regressor vs. insulin non-regressor groups, respectively. At baseline, mean age was 58.4 vs. 58.2 years, and median basal insulin dose was 40.0 vs. 48.0 IU/day. From baseline to Week 52 in the insulin regressor and insulin non-regressor groups, respectively, mean HbA1c of 8.5% and 8.9% was reduced to 5.9% and 6.7%, while weight was substantially reduced by 16 kg and 8 kg. Clinically significant hypoglycemia was also less frequent in the insulin regressor group.

Conclusion: In basal insulin–treated T2D, participants who regressed on insulin use also achieved near-normoglycemia and substantial weight loss.



Publikationsverlauf

Artikel online veröffentlicht:
28. Mai 2025

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