High-dose semaglutide starts raise early discontinuation risk 25% in US claims study
Among 48,658 commercially insured adults, 14.5% began injectable semaglutide at 1.0 mg/week or above, against label titration guidance.
MH
By Maren Holt · Senior Reporter, GLP-1
Oct 18 20:00 ETSource: Diabetes, obesity & metabolism
The wire
- 01MarketScan data from 2018-2021 showed off-label high-dose initiation cut 1-year persistence (p=0.01) and raised early discontinuation risk (HR 1.25, 95% CI 1.17-1.34), independent of age, obesity status, comorbidity and cost.
- 02Prescribers and telehealth operators have a modifiable lever: titration practice itself, not just cost or side-effect tolerance, predicts who stays on therapy at a year.
- 03Odds of high-dose starts were higher in the West and South, among endocrinologists, and for male, younger patients; the retrospective claims design cannot establish causation.
From the source
Read at pubmed.ncbi.nlm.nih.govReal-World Semaglutide Initiation Behaviours in the United States: Impact on Early Treatment Discontinuation and on 1-Year Persistence
Diabetes, obesity & metabolism · 2026 Oct 19 · Belalcazar LM, Gao D, Modi S et al.
Source URL https://pubmed.ncbi.nlm.nih.gov/42897121/
