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Antidiabetic Effect of Abextide, a Long-Acting Exendin-4 Analogue in Cynomolgus Monkeys.

Adv Healthc Mater · 2019

Last updated 2026-05-28

In a study of elderly diabetic monkeys, Abextide—a modified version of the GLP-1 drug exendin-4—lowered blood sugar levels for up to 3 days after a single dose, unlike a placebo or another GLP-1 drug (Albiglutide). Monkeys given two doses of Abextide showed a rapid drop in blood sugar after each dose, with levels stabilizing by day 3. No severe side effects like low blood sugar or injection-site swelling were reported, though some monkeys temporarily lost their appetite after receiving Abextide.

AI summary of the abstract below.

JournalAdv Healthc Mater, 2019
Citations3
Relative citation ratio0.18
NIH percentile12
Molecules
Conditions studied Type 2 Diabetes

Abstract

Abextide, synthesized by conjugating an albumin-binding moiety-truncated Evans blue-to glucagon-like peptide 1 receptor (GLP-1R) agonist exendin-4, shows extended drug release and enhanced hypoglycemic effect in diabetic mice. The aim of this study is to evaluate the pharmacodynamics of Abextide in nonhuman primates. Two batches of elderly cynomolgus monkeys with naturally occurring diabetes are used for this study. During the whole experiment period, no abnormalities such as swelling at the injection site, lethargy, or hypoglycemia are observed in all animals. The monkeys in the Abextide group lose appetite after drug administration and then recover over time. In the single dose treatment, at day 1 and day 3 after treatment, decreased plasma glucose level is observed in the Abextide-treated group but not in placebo or Albiglutide-treated group. For monkeys that receive two doses of drug, the blood glucose level in all subjects in Abextide group decreases rapidly upon drug administration and return to a plateau by day 3. A similar pattern of response is seen after the second dose administration. The delayed drug release and hypoglycemic effect of Abextide make it potentially useful as an antidiabetic drug for weekly subcutaneous administration.

Verbatim abstract via PubMed 30300471 ↗