Cited by 35Diabetes Treatment and ManagementDiabetes Management and ResearchPharmacology and Obesity Treatment

A randomized non-inferiority study comparing the addition of exenatide twice daily to sitagliptin or switching from sitagliptin to exenatide twice daily in patients with type 2 diabetes experiencing inadequate glycaemic control on metformin and sitagliptin

Violante, R., Oliveira, J. H. A., Yoon, K.‐H., Reed, V. A., Yu, M. B., Bachmann, O. P., Lüdemann, J., Chan, J. Y. C.·2012·Diabetic Medicine

Abstract

Aims To test the hypothesis that glycaemic control achieved when switching sitagliptin to exenatide twice daily plus metformin is non-inferior to adding exenatide twice daily to sitagliptin and metformin. Methods Patients with Type 2 diabetes inadequately controlled with sitagliptin plus metformin were randomly assigned to 20 weeks of treatment with twice-daily exenatide plus placebo and metformin (SWITCH, n = 127) or twice-daily exenatide plus sitagliptin and metformin (ADD, n = 128). Results Non-inferiority (0.4% margin) of SWITCH to ADD treatment, measured by change in HbA(1c) from baseline to week 20, was not shown {between-treatment difference in least-squares mean [95% CI 3 mmol/mol (0.30%)] [0.8-5.8 (0.07-0.53)]}. A greater reduction (P = 0.012) in HbA(1c) [least-squares mean (se)] was experienced by patients in the ADD group {-7 mmol/mol [-0.68%] [0.9 (0.08)]}, compared with those in the SWITCH group {-4 mmol/mol [-0.38%] [1.0 (0.09)]} and a greater proportion (P = 0.027) of patients in the ADD group (41.7%) reached Conclusions Non-inferiority of SWITCH to ADD treatment was not supported by the results of this study. In patients with Type 2 diabetes inadequately controlled with sitagliptin plus metformin, adding exenatide provided better glycaemic control than switching to exenatide. These results are consistent with the clinical approach that adding is better than switching to another oral anti-hyperglycaemic medication.

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Crossref · 10.1111/j.1464-5491.2012.03624.x

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  • There is no added glucose-lowering benefit of using GLP-1 RAs (or dual GIP and GLP-1 RA) together with a DPP-4 inhibitor beyond that of the GLP-1 RA alone.

    “We do not recommend using GLP-1 RAs (or the dual GIP and GLP-1 RA) together with a DPP-4 inhibitor as there is no added glucose-lowering benefit beyond that of the GLP-1 RA alone (119-121).”

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Authors
Violante, R., Oliveira, J. H. A., Yoon, K. ‐., Reed, V. A., Yu, M. B., Bachmann, O. P., Lüdemann, J., & Chan, J. Y. C.
Affiliations
  • Mexican Social Security Institute (MX)
  • Eli Lilly (United States) (US)
  • The Catholic University of Korea Seoul St. Mary's Hospital (KR)
  • Eli Lilly (Australia) (AU)
  • Eli Lilly (Canada) (CA)
  • Eli Lilly (Germany) (DE)
Corresponding author
Chan, J. Y. C.
Venue
Diabetic Medicine
Publisher
Wiley
Published
2012-10-08
Volume
29
Issue
11
Pages
e417-24
ISSN
  • 0742-3071 (ISSN-L)
  • 1464-5491
OpenAlex
W1615542701
Cited by
35
References
2
Citations by year
2025: 4 · 2024: 1 · 2020: 4 · 2019: 4 · 2018: 1 · 2017: 1 · 2016: 5 · 2015: 4 · 2014: 5 · 2013: 5 · 2012: 1
FWCI
3.85
Type
journal article
Language
en
Open access
closed
Locations
  • Diabetic Medicine (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Eli Lilly and Company
  • World Health Organization
  • Novo Nordisk
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
Keywords
exenatide twice daily, sitagliptin, type 2 diabetes, inadequate glycaemic control, metformin, non-inferiority, HbA1c, glycemic control, drug switching, GLP-1 receptor agonists, DPP-4 inhibitors, nausea and vomiting, fasting serum glucose, postprandial blood glucose
MeSH terms
Sitagliptin Phosphate, Exenatide, Adolescent, Adult, Aged, Argentina, Australia, Blood Glucose, Diabetes Mellitus, Type 2, Double-Blind Method, Drug Administration Schedule, Female, Germany, Greece, Glycated Hemoglobin, Humans, Hypoglycemia, Hypoglycemic Agents, India, Male, Metformin, Mexico, Middle Aged, Peptides, Pyrazines, Triazoles, Venoms, Treatment Outcome, Dipeptidyl-Peptidase IV Inhibitors, Republic of Korea

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