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GSK2374697, a novel albumin-binding domain antibody (AlbudAb), extends systemic exposure of exendin-4: first study in humans--PK/PD and safety.

Clin Pharmacol Ther · 2014

Last updated 2026-05-28

In a first human study, GSK2374697—a long-acting GLP-1 drug—showed a half-life of 6 to 10 days, meaning it stays in the body much longer than standard GLP-1 drugs. The drug reduced blood sugar spikes after meals, slowed stomach emptying, and was generally safe, with nausea improving over time as doses were slowly increased.

AI summary of the abstract below.

JournalClin Pharmacol Ther, 2014
Citations42
Relative citation ratio1.47
NIH percentile64
Molecules
Conditions studied Type 2 Diabetes, Obesity

Abstract

GSK2374697 is a genetically engineered fusion protein of a human domain antibody to exendin-4. This molecule binds with a high affinity to human serum albumin, creating a long-duration glucagon-like peptide-1 (GLP-1) receptor agonist. This study is the first evaluation of the albumin-binding domain antibody (AlbudAb) drug delivery platform in humans. The aim of this randomized clinical study was to determine the pharmacokinetics, pharmacodynamics, safety, and tolerability of GSK2374697. The pharmacokinetic profile was prolonged, with estimated half-lives ranging from 6 to 10 days. Postprandial glucose and insulin were reduced, and gastric emptying was delayed in healthy subjects, confirming anticipated GLP-1 receptor agonist pharmacology. The safety and tolerability were as expected for a potent GLP-1 agonist. Gradual titration of doses greatly improved tolerability. Rapid tolerance to nausea was observed. Study results support further investigation in type 2 diabetes and for weight loss.

Verbatim abstract via PubMed 25238251 ↗