PMID- 28281218 OWN - NLM STAT- MEDLINE DCOM- 20170911 LR - 20221207 IS - 1865-8652 (Electronic) IS - 0741-238X (Print) IS - 0741-238X (Linking) VI - 34 IP - 4 DP - 2017 Apr TI - Evaluation of the Short-Term Cost-Effectiveness of IDegLira Versus Continued Up-Titration of Insulin Glargine U100 in Patients with Type 2 Diabetes in the USA. PG - 954-965 LID - 10.1007/s12325-017-0502-2 [doi] AB - INTRODUCTION: Effective glycemic control can reduce the risk of complications and their related costs in type 2 diabetes mellitus (T2DM). However, many patients fail to reach glycemic targets, often because of adverse effects of treatment (including hypoglycemia or weight gain). The present analysis evaluated the short-term cost-effectiveness of IDegLira versus continued up-titration of insulin glargine U100 in patients with T2DM failing to achieve glycemic control on basal insulin in the US setting. METHODS: The cost per patient achieving treatment target (cost of control) was assessed for various single and composite endpoints for the entire trial population and in patients with baseline glycated hemoglobin (HbA1c) >8.0% and HbA1c >9.0%. The proportions of patients achieving treatment targets were analyzed using data obtained in the DUAL V study. Costs were accounted based on published wholesale acquisition costs. RESULTS: When assessing the full trial population, IDegLira was associated with lower annual cost of control than continued up-titration of insulin glargine U100 for patients achieving HbA1c 8.0% and HbA1c >9.0%, IDegLira was associated with a lower cost of control for all treatment targets. CONCLUSION: The significantly greater clinical efficacy in terms of bringing patients to treatment targets identified in the DUAL V study results in lower cost of control values for IDegLira versus continued up-titration of insulin glargine U100 in the USA. This suggests IDegLira is a cost-effective treatment option in the USA. FUNDING: Novo Nordisk A/S and Novo Nordisk Inc. FAU - Hunt, Barnaby AU - Hunt B AUID- ORCID: 0000-0001-5420-279X AD - Ossian Health Economics and Communications, Basel, Switzerland. hunt@ossianconsulting.com. FAU - Mocarski, Michelle AU - Mocarski M AD - Novo Nordisk Inc., Plainsboro, NJ, USA. FAU - Valentine, William J AU - Valentine WJ AD - Ossian Health Economics and Communications, Basel, Switzerland. FAU - Langer, Jakob AU - Langer J AD - Novo Nordisk A/S, Soborg, Denmark. LA - eng PT - Journal Article PT - Randomized Controlled Trial DEP - 20170309 PL - United States TA - Adv Ther JT - Advances in therapy JID - 8611864 RN - 0 (Blood Glucose) RN - 0 (Drug Combinations) RN - 0 (Glycated Hemoglobin A) RN - 0 (Hypoglycemic Agents) RN - 0 (IDegLira) RN - 0 (Insulin, Long-Acting) RN - 2ZM8CX04RZ (Insulin Glargine) RN - 839I73S42A (Liraglutide) EIN - Adv Ther. 2017 Jun;34(6):1500-1501. PMID: 28523624 MH - Blood Glucose/drug effects MH - Cost-Benefit Analysis MH - Diabetes Mellitus, Type 2/*drug therapy MH - Dose-Response Relationship, Drug MH - Drug Combinations MH - Glycated Hemoglobin/analysis MH - Humans MH - Hypoglycemia/chemically induced MH - Hypoglycemic Agents/*economics/therapeutic use MH - Insulin Glargine/*economics/therapeutic use MH - Insulin, Long-Acting/*economics/therapeutic use MH - Liraglutide/*economics/therapeutic use MH - Weight Gain PMC - PMC5435780 OTO - NOTNLM OT - Cost OT - Cost-effectiveness OT - Endocrinology OT - IDegLira OT - Type 2 diabetes mellitus OT - USA EDAT- 2017/03/11 06:00 MHDA- 2017/09/12 06:00 PMCR- 2017/03/09 CRDT- 2017/03/11 06:00 PHST- 2017/01/23 00:00 [received] PHST- 2017/03/11 06:00 [pubmed] PHST- 2017/09/12 06:00 [medline] PHST- 2017/03/11 06:00 [entrez] PHST- 2017/03/09 00:00 [pmc-release] AID - 10.1007/s12325-017-0502-2 [pii] AID - 502 [pii] AID - 10.1007/s12325-017-0502-2 [doi] PST - ppublish SO - Adv Ther. 2017 Apr;34(4):954-965. doi: 10.1007/s12325-017-0502-2. Epub 2017 Mar 9.