Drug intelligence / Profile preview

AZD1979

Development stage
Discontinued
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

AZD1979 is a potent, orally administered small molecule antagonist of the melanin-concentrating hormone receptor 1 (MCHR1). It was developed by AstraZeneca for the treatment of obesity. The drug acts by blocking MCHR1, a G protein-coupled receptor involved in regulating food intake and energy expenditure. Preclinical studies demonstrated that AZD1979 reduced body weight in diet-induced obese mice and dogs, primarily through decreased food intake and preserved energy expenditure. Its specificity for MCHR1 was confirmed using knockout models. Despite promising preclinical results, clinical development was discontinued after phase 1 trials assessing safety and pharmacokinetics in healthy male volunteers[2][3][7].

02

Targets

KCNH2 (Voltage-gated potassium channel subfamily H member 2)MCHR2 (MCH receptor 2 / MCHR2)MCHR1 (Melanin-concentrating hormone receptor 1)

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