4.5 Review

Free fatty acid receptor agonists for the treatment of type 2 diabetes: drugs in preclinical to phase II clinical development

Journal

EXPERT OPINION ON INVESTIGATIONAL DRUGS
Volume 25, Issue 8, Pages 871-890

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/13543784.2016.1189530

Keywords

Free fatty acid; FFA1; GPR40; GPR120; GLP-1; type 2 diabetes

Funding

  1. National Natural Science Foundation of China [81172932, 81273376]
  2. Natural Science Foundation of Jiangsu Province [BK2012356]
  3. Fundamental Research Funds for the Central Universities, China Pharmaceutical University [JKZD2013001]

Ask authors/readers for more resources

Introduction: The alarming prevalence of type 2 diabetes mellitus (T2DM) stimulated the exploitation of new antidiabetic drugs with extended durability and enhanced safety. In this regard, the free fatty acid receptor 1 (FFA1) and FFA4 have emerged as attractive targets in the last decade. FFA1 has prominent advantages in promoting insulin and incretin secretion while FFA4 shows great potential in incretin secretion, insulin sensitization and anti-inflammatory effects.Area covered: Herein, the authors focus specifically on FFA1 and FFA4 agonists in clinical trials and preclinical development. LY2922470, P11187 and SHR0534 are currently active in clinical trials while the CNX-011-67, SAR1, DS-1558 and BMS-986118 are in preclinical phase. The information for this review is retrieved from Integrity, Scifinder, Espacenet and clinicaltrials.gov databases.Expert opinion: Current proof-of-concept in clinical trials suggests that FFA1 agonists have a significant improvement for T2DM without the risk of hypoglycemia. However, there are still several challenging problems including the mechanism of the receptor and the efficacy and safety of the ligands.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available