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Original Article

Cost-effectiveness of liraglutide versus rosiglitazone, both in combination with glimepiride in treatment of type 2 diabetes in the US

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Pages 897-906 | Accepted 28 Jan 2011, Published online: 25 Feb 2011
 

Abstract

Background:

Many patients with type 2 diabetes mellitus (T2DM) are not able to maintain adequate HbA1c control (<7.0%), even at maximal dosage levels of one or two oral agents, and are at increased risk for diabetes-related complications.

Objective:

To estimate the cost-effectiveness of a once-daily GLP-1 analog Victoza [Novo Nordisk] versus a thiazolidinedione (TZD), rosiglitazone in patients with T2DM. Both treatment groups included background therapy with glimepiride.

Research design and methods:

The CORE Diabetes Model (CDM) was used to project and compare 35-year clinical and economic outcomes associated with liraglutide 1.2 mg + glimepiride and liraglutide 1.8 mg + glimepiride versus rosiglitazone 4 mg + glimepiride. Baseline cohort characteristics (HbA1c (8.4%), age, duration of disease, sex, body-mass index (BMI), blood pressure, and lipids) were based on the Liraglutide Effect and Action in Diabetes-1 (LEAD-1) trial.

Outcomes:

Primary outcomes included life expectancy (LE), quality-adjusted life-years (QALYs), total costs and incremental cost-effectiveness ratios (ICERs).

Results:

When compared to rosiglitazone, liraglutide 1.2 mg and 1.8 mg increased mean LE by 0.968 and 1.041 years, and QALYs by 0.764 and 0.837, respectively. Total lifetime costs increased by $26 094 for liraglutide 1.2 mg versus rosiglitazone, and by $47 041 for liraglutide 1.8 mg versus rosiglitazone. ICERs for liraglutide 1.2 mg versus rosiglitazone and 1.8 mg versus rosiglitazone were $34 147 and $56 190, respectively.

Conclusions:

Compared to rosiglitazone 4 mg plus glimepiride, liraglutide (particularly at the 1.2-mg dose) plus glimepiride is a cost-effective treatment option for improving glucose control in T2DM. Limitations include the projection of short term efficacy results from randomized control trials to longer time horizons. In addition, clinical acceptance and overall use of rosiglitazone in the treatment of diabetes has continued to fall since publication of the clinical trial upon which this modeling analyses was based.

Transparency

Declaration of funding

This study was funded by NovoNordisk.

Declaration of financial/other relationships

W.C.L. has disclosed that he is an employee of IMS Health, a company that was paid as a consultant to Novo Nordisk for this study. C.C. and M.H. are employees and stakeholders of NovoNordisk. CMRO peer reviewers may have received honoraria for their review work. The peer reviewers on this manuscript have disclosed that they have no relevant financial relationships.

Acknowledgments

We thank the LEAD 1 investigator and study group for conducting this study. We also thank Caitlin Rothermel, MA, MPHc of Medlitera for assistance with drafting and editing of the manuscript.

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