Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Drug Discov Today. 2018 Jan;23(1):196-203. doi: 10.1016/j.drudis.2017.10.015. Epub 2017 Oct 24.
Indacaterol/glycopyrronium (IND/GLY) 110/50mcg was the first once-daily, long-acting β-agonist (LABA)/long-acting muscarinic antagonist (LAMA) fixed-dose combination (FDC) approved in Europe for the treatment of chronic obstructive pulmonary disease (COPD). Development of IND/GLY was driven by the need to improve the standard of care for patients with this disease, in terms of symptom control and exacerbation frequency. IGNITE, an adaptive, comprehensive, and innovative Phase 3 development program, demonstrated the efficacy of IND/GLY in optimising bronchodilation, reducing symptoms, and reducing exacerbations in patients with COPD. IGNITE challenged contemporary thinking about the pharmacological treatment and management of patients with this disease.
英地那醇/格隆溴铵(IND/GLY)110/50mcg 是首个在欧洲获批用于治疗慢性阻塞性肺疾病(COPD)的每日一次、长效β-激动剂(LABA)/长效毒蕈碱拮抗剂(LAMA)固定剂量复方制剂(FDC)。IND/GLY 的开发是为了满足改善此类疾病患者的治疗标准的需求,提高症状控制和减少疾病加重的频率。一项适应性、全面和创新的 3 期开发项目 IGNITE 证实了 IND/GLY 在优化支气管扩张、减轻症状和减少 COPD 患者疾病加重方面的疗效。IGNITE 挑战了人们对该疾病的药理学治疗和管理的现有观念。