Pharmacokinetics and tolerability of semaglutide in people with hepatic impairment.
Diabetes Obes Metab · 2018
Last updated 2026-05-28A study tested how a single 0.5 mg dose of semaglutide is processed in people with normal liver function compared to those with mild, moderate, or severe liver impairment. The results showed that semaglutide levels in the blood were similar across all groups, suggesting that liver function does not significantly affect how the drug is absorbed or processed. No serious side effects were reported, and the drug was generally well tolerated.
AI summary of the abstract below.
| Journal | Diabetes Obes Metab, 2018 |
|---|---|
| Citations | 53 |
| Relative citation ratio | 2.22 |
| NIH percentile | 77 |
| Molecules | semaglutide |
| Conditions studied | Mash, Chronic Kidney Disease |
Abstract
AIMS: To investigate whether the pharmacokinetic characteristics of semaglutide were altered in people with hepatic impairment, assessed using Child-Pugh criteria, vs those with normal hepatic function.
METHODS: In this multicentre, open-label, parallel-group trial (sponsor Novo Nordisk, ClinicalTrials.gov ID NCT02210871), four groups of participants with normal hepatic function (n = 19) or mild (n = 8), moderate (n = 10) or severe (n = 7) hepatic impairment received a single, subcutaneous dose of 0.5 mg semaglutide. Semaglutide plasma concentrations were assessed frequently for 35 days after dosing. The primary endpoint was area under the semaglutide plasma concentration-time curve from time zero to infinity (AUC ). No effect of hepatic impairment was declared if the 90% confidence interval (CI) for the between-group ratio (hepatic impairment/normal function) was within the interval 0.70 to 1.43.
RESULTS: Semaglutide exposure was similar across all groups, with AUC treatment ratios for mild impairment/normal function of 0.95 (90% CI 0.77, 1.16), moderate impairment/normal function 1.02 (90% CI 0.93, 1.12), and severe impairment/normal function 0.97 (90% CI 0.84, 1.12). The maximum plasma semaglutide concentration (C ) did not appear to be influenced by hepatic function, with mild impairment/normal function treatment ratios of 0.99 (90% CI 0.80, 1.23), moderate impairment/normal function 1.02 (90% CI 0.88, 1.18) and severe impairment/normal function 1.15 (90% CI 0.89, 1.48; sensitivity analysis excluding one extreme semaglutide concentration: 1.05 [90% CI 0.88, 1.25]). In all, 10 participants reported 12 mild or moderate non-serious adverse events. No unexpected safety or tolerability issues were observed.
CONCLUSIONS: Semaglutide exposure did not appear to be affected by hepatic impairment, suggesting that dose adjustment may not be necessary in patients with hepatic impairment. Semaglutide was well tolerated and there were no unexpected safety issues.
Verbatim abstract via PubMed 29205786 ↗
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