Sam Amir H, Salem Victoria, Ghatei Mohammad A
Section of Investigative Medicine, Division of Diabetes, Endocrinology and Metabolism, Hammersmith Hospital, Imperial College London, Du Cane Road, London W12 0NN, UK.
J Obes. 2011;2011:432607. doi: 10.1155/2011/432607. Epub 2011 Jul 6.
Endocannabinoid antagonism as a treatment for obesity and the metabolic syndrome became a hugely anticipated area of pharmacology at the start of the century. The CB1 receptor antagonist Rimonabant entered the European mass market on the back of several trials showing weight loss benefits alongside improvements in numerous other elements of the metabolic syndrome. However, the drug was quickly withdrawn due to the emergence of significant side effects-notably severe mood disorders. This paper provides a brief overview of the Rimonabant story and places the recent spate of FDA rejections of other centrally acting weight loss drugs entering Phase 3 trials in this context.
在本世纪初,内源性大麻素拮抗作用作为肥胖症和代谢综合征的一种治疗方法,成为药理学中一个备受期待的领域。CB1受体拮抗剂利莫那班在多项试验表明其具有减肥益处以及能改善代谢综合征的许多其他方面之后,进入了欧洲大众市场。然而,由于出现了严重的副作用——尤其是严重的情绪障碍,该药物很快就被撤市了。本文简要概述了利莫那班的情况,并在此背景下探讨了美国食品药品监督管理局(FDA)最近接连拒绝其他进入3期试验的中枢性减肥药物的情况。