Clinical Potential of GIP in Type 2 Diabetes and Obesity.

Incretin-based pharmacology has revolutionized the medical treatment of type 2 diabetes and obesity. The most effective drug to date is tirzepatide, a dual incretin receptor agonist that engages both the glucagon-like peptide-1 receptor (GLP-1R) and the glucose-dependent insulinotropic polypeptide receptor (GIPR). While the relative contributions of GIPR and GLP-1R actions to the clinical effects of tirzepatide have not been established, the potency of this agent has reignited interest in the clinical potential of GIPR agonism. Here, we discuss incretin biology as it relates to metabolic pharmacology and contextualize the mechanisms by which GIPR activity could contribute to the development of new and effective drugs. We explore current and future applications of GIPR agonists and antagonists, to underscore the potential that this signaling system could add to treatment of type 2 diabetes and obesity.

Authors

Publication Details

Journal
Apollo (University of Cambridge)
Published
2026-04-13
DOI
https://doi.org/10.17863/cam.129561
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
0.00

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article

Clinical Potential of GIP in Type 2 Diabetes and Obesity.

Frank Reimann, Fiona Gribble, Michael Nauck, David A D'Alessio et al.
Apollo (University of Cambridge)
Diabetes Treatment and Management
article

Clinical Potential of GIP in Type 2 Diabetes and Obesity.

Frank Reimann, Fiona Gribble, Michael Nauck, David A D'Alessio, Jonathan E Campbell
article en

Abstract

Incretin-based pharmacology has revolutionized the medical treatment of type 2 diabetes and obesity. The most effective drug to date is tirzepatide, a dual incretin receptor agonist that engages both the glucagon-like peptide-1 receptor (GLP-1R) and the glucose-dependent insulinotropic polypeptide receptor (GIPR). While the relative contributions of GIPR and GLP-1R actions to the clinical effects of tirzepatide have not been established, the potency of this agent has reignited interest in the clinical potential of GIPR agonism. Here, we discuss incretin biology as it relates to metabolic pharmacology and contextualize the mechanisms by which GIPR activity could contribute to the development of new and effective drugs. We explore current and future applications of GIPR agonists and antagonists, to underscore the potential that this signaling system could add to treatment of type 2 diabetes and obesity.

Apollo (University of Cambridge)
National Institutes of Health, Medical Research Council, National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 6%
Diabetes Treatment and Management
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Clinical Potential of GIP in Type 2 Diabetes and Obesity. — Frank Reimann, Fiona Gribble, et al. · Apollo (University of Cambridge) (2026) | TGRS Research Map | TGRS