Adis RD Insight, Springer Healthcare, Auckland, New Zealand.
Drugs. 2012 Nov 12;72(16):2167-75. doi: 10.2165/11470590-000000000-00000.
Linaclotide is a once-daily, orally administered, first-in-class agonist of guanylate cyclase-C that is minimally absorbed. It is being developed to treat gastrointestinal disorders by Ironwood Pharmaceuticals and its partners, Forest Laboratories (North America), Almirall (Europe) and Astellas Pharma (Asia-Pacific). Linaclotide has received its first global approval in the US for the treatment of constipation-predominant irritable bowel syndrome (IBS-C) and chronic idiopathic constipation (CIC), and a marketing submission has been filed in the EU for IBS-C. This article summarizes the milestones in the development of linaclotide leading to this first approval for IBS-C and CIC. This profile has been extracted and modified from the Adis R&D Insight drug pipeline database. Adis R&D Insight tracks drug development worldwide through the entire development process, from discovery, through pre-clinical and clinical studies to market launch.
利那洛肽是一种每日一次、口服、鸟苷酸环化酶-C 的首创新类激动剂,几乎不被吸收。它由 Ironwood 制药及其合作伙伴 Forest Laboratories(北美)、Almirall(欧洲)和安斯泰来制药(亚太)开发,用于治疗胃肠道疾病。利那洛肽已在美国首次获得全球批准,用于治疗便秘为主的肠易激综合征(IBS-C)和慢性特发性便秘(CIC),并已在欧盟提交 IBS-C 的上市申请。本文总结了利那洛肽开发过程中的重要里程碑,最终使其获得 IBS-C 和 CIC 的首次批准。本概要已从 Adis R&D Insight 药物管道数据库中提取并修改。Adis R&D Insight 通过整个开发过程,从发现、临床前和临床研究到市场推出,在全球范围内跟踪药物开发。