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Study breakdown

Once-Weekly Semaglutide Delivers More Diabetes Control per Pound Spent Than Other GLP-1 Drugs in the UK

Cost Effectiveness AnalysisModerate evidence
The takeaway

Despite similar UK drug costs, semaglutide got 21–51% more patients to diabetes treatment goals than exenatide ER, liraglutide, and dulaglutide.

21–51% advantage

semaglutide gets significantly more patients to diabetes treatment goals than three competitor GLP-1 drugs at similar UK cost

What the researchers found

Annual per-patient costs were similar across all four GLP-1 receptor agonists in the UK market. However, once-weekly semaglutide consistently outperformed the others in getting patients to treatment goals.

For the composite endpoint of HbA1c below 7.0% without weight gain or low blood sugar episodes, the competing drugs fell short: exenatide ER was 50.0% less effective, liraglutide was 51.3% less effective, and dulaglutide was 21.6% less effective than semaglutide.

Semaglutide also led in single endpoints including HbA1c targets (below 7.0% and below 7.5%) and meaningful weight loss (5% or more body weight reduction).

Why it matters

When multiple drugs in the same class cost about the same, the one that helps the most patients reach their goals offers the best value. This analysis showed semaglutide delivered more clinical benefit per pound spent across every measured outcome.

For healthcare systems making formulary decisions, this type of analysis helps justify choosing one drug over another when prices are similar.

The numbers in context

Exenatide ER 50.0% less effective; liraglutide 51.3% less effective; dulaglutide 21.6% less effective vs semaglutide at composite endpoint

How the study worked

This was a cost-of-control analysis using clinical data from the SUSTAIN trial program. Researchers compared the proportion of patients reaching various treatment targets across the four drugs and divided annual UK drug costs by efficacy rates to calculate cost per responder.

Who was studied

Type 2 diabetes patients from SUSTAIN clinical trial program

What this study cannot tell us

This analysis used data from the SUSTAIN clinical trials, which may not perfectly reflect real-world outcomes. Different patient populations, adherence rates, and healthcare settings could change the results.

Prices were based on July 2019 UK wholesale costs, which may have changed since then.

How to read the evidence

Moderate evidence from cost-of-control analysis based on SUSTAIN clinical trial data. Real-world results may differ.

When this study was published

Published in 2020. Drug costs and clinical evidence have evolved since this analysis.

The bigger picture

When drugs cost the same, the one that works best for more patients delivers the most value. This analysis provides ammunition for formulary inclusion of semaglutide and for patients and clinicians choosing among GLP-1 options.

Questions still open

  • Do real-world adherence differences change the cost-effectiveness picture?
  • How do these compare when weight loss and cardiovascular outcomes are included?
  • Will semaglutide biosimilars change the competitive landscape?

Common questions

If GLP-1 drugs cost the same, which should I choose?
This analysis suggests semaglutide gets more patients to their diabetes goals at the same cost. However, individual responses vary, and factors like injection frequency and side effects also matter.
Why compare cost-of-control instead of just drug price?
Two drugs can cost the same per year, but if one gets twice as many patients to target, it is twice as cost-effective. Cost-of-control captures this by dividing cost by efficacy.

Read the original research

A Relative Cost of Control Analysis of Once-Weekly Semaglutide Versus Exenatide Extended-Release, Dulaglutide and Liraglutide in the UK.

Advances in therapy, 37(3), 1248-1259

Citation

Johansen, Pierre; Sandberg, Anna; Capehorn, Matthew. (2020). A Relative Cost of Control Analysis of Once-Weekly Semaglutide Versus Exenatide Extended-Release, Dulaglutide and Liraglutide in the UK.. Advances in therapy, 37(3), 1248-1259. https://doi.org/10.1007/s12325-020-01242-z