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Oral semaglutide for the treatment of type 2 diabetes.

Expert Opin Pharmacother · 2019

Last updated 2026-05-28

Oral semaglutide is an experimental GLP-1 drug taken by mouth once a day. In clinical trials, it improved blood sugar control and helped people lose weight better than placebo and other diabetes medications like sitagliptin, liraglutide, and empagliflozin. Its side effects were similar to injectable GLP-1 drugs, and it did not appear to interfere with the effectiveness of other common oral medications.

AI summary of the abstract below.

JournalExpert Opin Pharmacother, 2019
Citations32
Relative citation ratio1.55
NIH percentile66
Molecules semaglutide
Conditions studied Type 2 Diabetes

Abstract

Glucagon-like peptide-1 (GLP-1) receptor agonists are highly potent antihyperglycemic drugs that impose low risk of hypoglycemia and also result in body weight reduction. Currently, all approved members of the class require administration by injection. Areas covered: This manuscript reviews oral semaglutide-an experimental GLP-1 receptor agonist in phase-3 clinical development. Available pharmacological and clinical data of the drug are reviewed, and important end-points described. Expert opinion: Oral peptide delivery has become possible with the discovery of absorption enhancers. The clinical development program of once-daily oral semaglutide has shown superiority in reducing glycosylated hemoglobin and body weight in comparison with placebo and active comparators (sitagliptin, liraglutide, and empagliflozin). Safety and tolerability of oral semaglutide is in line with injectable members of the class. Delayed gastric emptying, local increase in pH, and enhanced absorption do not seem to affect the exposure of a number of other oral drugs that have been tested (metformin, digoxin, oral contraceptive ethinylestradiol/levonorgestrel, lisinopril, warfarin, furosemide and rosuvastatin). Clinical questions for further investigation include the effectiveness and safety of oral semaglutide in cardiovascular indications.

Verbatim abstract via PubMed 30499733 ↗

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