SCO-267, a GPR40 Full Agonist, Stimulates Islet and Gut Hormone Secretion and Improves Glycemic Control in Humans

Diabetes. 2021 Oct;70(10):2364-2376. doi: 10.2337/db21-0451. Epub 2021 Jul 28.

Abstract

SCO-267 is a full agonist of the free fatty acid receptor 1 (GPR40), which regulates the secretion of islet and gut hormones. In this phase 1 study, we aimed to evaluate the clinical profile of single and multiple once-daily oral administration of SCO-267 in healthy adults and patients with diabetes. Plasma SCO-267 concentration was seen to increase in a dose-dependent manner after administration, and its plasma exposure was maintained for 24 h. Repeated dose did not alter the pharmacokinetic profile of SCO-267 in healthy adults. SCO-267 was generally safe and well tolerated at all evaluated single and multiple doses. Single and repeated doses of SCO-267 stimulated the secretion of insulin, glucagon, glucagon-like peptide 1, glucose-dependent insulinotropic polypeptide, and peptide YY in healthy adults. Furthermore, a single dose of SCO-267 stimulated the secretion of these hormones, decreased fasting hyperglycemia, and improved glycemic control during an oral glucose tolerance test in patients with diabetes, without inducing hypoglycemia. This study is the first to demonstrate the clinical effects of a GPR40 full agonist. SCO-267 is safe and well tolerated and exhibits once-daily oral dosing potential. Its robust therapeutic effects on hormonal secretion and glycemic control make SCO-267 an attractive drug candidate for the treatment of diabetes.

Publication types

  • Clinical Trial, Phase I
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Blood Glucose / drug effects*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / drug therapy
  • Double-Blind Method
  • Gastrointestinal Hormones / metabolism*
  • Glucose Intolerance / drug therapy
  • Glucose Intolerance / metabolism
  • Glucose Tolerance Test
  • Glycemic Control / methods
  • Humans
  • Insulin Secretion / drug effects
  • Islets of Langerhans / drug effects*
  • Islets of Langerhans / metabolism
  • Japan
  • Male
  • Middle Aged
  • Piperidines / administration & dosage
  • Piperidines / pharmacology*
  • Pyridines / administration & dosage
  • Pyridines / pharmacology*
  • Receptors, G-Protein-Coupled / agonists
  • Young Adult

Substances

  • Blood Glucose
  • FFAR1 protein, human
  • Gastrointestinal Hormones
  • Piperidines
  • Pyridines
  • Receptors, G-Protein-Coupled
  • SCO-267

Associated data

  • figshare/10.2337/figshare.15036009
  • JapicCTI/JapicCTI-195057