2015年3月26日讯 /生物谷BIOON/ --日本制药巨头武田(Takeda)近日宣布,糖尿病新药Zafatek(trelagliptin succinate,曲格列汀琥珀酸盐)获日本卫生劳动福利部(MHLW)批准,用于2型糖尿病的治疗。此次批准,标志着Zafatek成为全球上市的首个每周口服一次的降糖药,同时也代表着武田在糖尿病市场投下的一枚重磅炸弹!
Zafatek由武田和Furiex研发,该药是一种超长效二肽基肽酶IV(DPP-4)抑制剂,每周口服一次,而市场上同类DPP-4抑制剂需要每天口服一次,Zafatek的用药优势无疑将为糖尿病患者提供了更为方便的治疗选择,有望大幅改善患者的便利性和依从性。
目前,美国制药巨头默沙东(Merck)也正在开发一款超长效DPP-4抑制剂omarigliptin,该公司于去年底向日本提交了全球首个监管申请。在临床试验中,omarigliptin疗效媲美自身年销40亿美元的每日一次DPP-4抑制剂Januvia(捷诺维,sitagliptin,西他列汀)。业界认为,omarigliptin将成为默沙东捍卫其口服降糖药市场霸主地位的重要筹码。
据了解,DPP-4抑制剂是首类可通过提高机体自身能力控制血糖水平的新型2型糖尿病药物,可用作单药,也可与其它口服降糖药联用,其作用机制独特,具有不产生低血糖、不引起体重增加,以及副作用小等独特优势,同时引起胃肠道不良反应的发生率亦很低。(生物谷Bioon.com)
英文原文:New Drug Application Approval of Zafatek?Tablets for the treatment of Type 2 Diabetes in Japan
Osaka, Japan, March 26, 2015 – Takeda Pharmaceutical Company Limited (“Takeda”) announced today that the Japanese Ministry of Health, Labour and Welfare has approved the New Drug Application of Zafatek?generic name: trelagliptin succinate), a drug for treating type 2 diabetes.
Zafatek is a once-weekly DPP-4 (dipeptidyl peptidase-IV) inhibitor. It controls blood glucose levels by selectively and continually inhibiting DPP-4, an enzyme that causes the inactivation of glucagon-like peptide-1 and glucagon-dependent insulinotropic polypeptide, incretin hormones* that play an
The approval granted is based on the safety and efficacy results of multiple clinical phase III studies in patients with type 2 diabetes in Japan. The efficacy of once-weekly trelagliptin succinate was confirmed in all studies, in addition to a good safety and tolerability profile.
Takeda expects that it can provide a new treatment option with Zafatek, the world's first once-weekly DPP-4 inhibitor, and contribute to improvement in drug adherence and continued treatment of patients. The approval granted is a very
* An insulinotropic gastrointestinal hormone