A Comprehensive Review on the Pharmacokinetics and Drug−Drug Interactions of Approved GLP-1 Receptor Agonists and a Dual GLP-1/GIP Receptor Agonist
Catholic University of Korea · University at Buffalo, State University of New York · +3 more institutions
Abstract
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are peptide-derived analogs that were initially investigated to treat type 2 diabetes. Recently, a drug targeting the receptors of both GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) (tirzepatide) has been introduced to the market, and its indications have expanded to include treating obesity. Here, we review the pharmacokinetics, pharmacokinetic drug-drug interactions (DDIs), and pharmacokinetic modeling approaches of four currently available GLP-1 RAs (exenatide, liraglutide, dulaglutide, and semaglutide) and tirzepatide. To address the extremely short half-life (2 min) of native human GLP-1, structural modifications have been applied to…
Citation impact
- FWCI
- 42.26
- Percentile
- 100%
- References
- 199
Authors
7Topics & keywords
- Pharmacokinetics
- Drug
- Pharmacology
- Agonist
- Medicine
- Glucagon-like peptide 1 receptor
- Receptor
- Internal medicine