The Development of INT131 as a Selective PPAR Modulator: Approach to a Safer Insulin Sensitizer

噻唑烷二酮 过氧化物酶体增殖物激活受体 罗格列酮 脂肪生成 医学 药理学 胰岛素 临床试验 PPAR激动剂 2型糖尿病 糖尿病 受体 内科学 内分泌学 脂肪组织
作者
Linda S. Higgins,Christos S. Mantzoros
出处
期刊:Ppar Research [Hindawi Publishing Corporation]
卷期号:2008: 1-9 被引量:76
标识
DOI:10.1155/2008/936906
摘要

INT131 (formerly T0903131, T131, AMG131) is a potent non-thiazolidinedione (TZD) selective peroxisome proliferator-activated receptor gamma modulator (SPPARM) currently in Phase 2 clinical trials for treatment of type-2 diabetes mellitus (T2DM). This new chemical entity represents a second generation SPPARM approach developed after the first generation PPARgamma full agonists to address their inherent limitations. INT131 was specifically and carefully designed using preclinical models to exhibit a biological profile of strong efficacy with de minimis side effects compared to PPARgamma full agonists. As a potent PPARgamma modulator, INT131 binds to PPARgamma with high affinity. In pharmacology models of diabetes and in early clinical studies, it achieved a high level of efficacy in terms of antidiabetic actions such as insulin sensitization and glucose and insulin lowering, but had little activity in terms of other, undesired, effects associated with TZD PPARgamma full agonists such as edema and adipogenesis. Ongoing clinical development is directed at translating these findings into establishing a novel and effective treatment for T2DM patients with an improved safety profile in relation to that currently available.

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