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生长调节素-1结合蛋白-3:胰岛素样生长因子-1结合蛋白-3,胰岛素样生长因子-1载体蛋白。

Somatomedin-1 binding protein-3: insulin-like growth factor-1 binding protein-3, insulin-like growth factor-1 carrier protein.

出版信息

BioDrugs. 2003;17(5):375-9. doi: 10.2165/00063030-200317050-00008.

Abstract

Somatomedin-1 binding protein-3 [insulin-like growth factor-1 binding protein-3, SomatoKine] is a recombinant complex of insulin-like growth factor-1 (rhIGF-1) and binding protein-3 (IGFBP-3), which is the major circulating somatomedin (insulin-like growth factor) binding protein; binding protein-3 regulates the delivery of somatomedin-1 to target tissues. Somatomedin-1 binding protein-3 has potential as replacement therapy for somatomedin-1 which may become depleted in indications such as major surgery, organ damage/failure and traumatic injury, resulting in catabolism. It also has potential for the treatment of osteoporosis; diseases associated with protein wasting including chronic renal failure, cachexia and severe trauma; and to attenuate cardiac dysfunction in a variety of disease states, including after severe burn trauma. Combined therapy with somatomedin-1 and somatomedin-1 binding protein-3 would prolong the duration of action of somatomedin-1 and would reduce or eliminate some of the undesirable effects associated with somatomedin-1 monotherapy. Somatomedin-1 is usually linked to binding protein-3 in the normal state of the body, and particular proteases clip them apart in response to stresses and release somatomedin-1 as needed. Therefore, somatomedin-1 binding protein-3 is a self-dosing system and SomatoKine would augment the natural supply of these linked compounds. Somatomedin-1 binding protein-3 was developed by Celtrix using its proprietary recombinant protein production technology. Subsequently, Celtrix was acquired by Insmed Pharmaceuticals on June 1 2000. Insmed and Avecia, UK, have signed an agreement for the manufacturing of SomatoKine and its components, IGF-1 and binding protein-3. CGMP clinical production of SomatoKine and its components will be done in Avecia's Advanced Biologics Centre, Billingham, UK, which manufactures recombinant-based medicines and vaccines with a capacity of up to 1000 litres. In 2003, manufacturing of SomatoKine is planned to move to Avecia's larger facility with a capacity of 10 000 litres. Somatomedin-1 binding protein-3 was originally licenced to Welfide for Japan. On October 1 2001, Welfide Corporation merged with Mitsubishi-Tokyo Pharmaceuticals to form Mitsubishi Pharma Corporation. The new company is a subsidiary of Mitsubishi Chemical. In April 2003 Insmed initiated a named patient programme in Europe, that will make available somatomedin-1 binding protein-3 for the treatment of growth hormone insensitivity syndrome (GHIS)--Laron syndrome. The treatment of patients was initiated in Scandinavia, with authorisation pending in several other European countries. Somatomedin-1 binding protein-3 will be made available to those GHIS patients who, in the opinion of their doctor, may benefit from IGF-1 therapy. At precommercial scale quantities, the drug will be available on a limited basis. Safety data generated from the named patient programme will be used to support marketing applications in 2004. A phase II dose-ranging study in children with GHIS was completed at Saint Bartholomew's and the Royal London School of Medicine, London, UK. A single dose of somatomedin-1 binding protein-3 delivered the same amount of IGF-1 as two daily injections of unbound IGF-1. There were no adverse events reported. GHIS is a genetic condition in which patients do not produce adequate quantities of IGF because of a failure to respond to the growth hormone signal. This results in a slower growth rate and short stature. Insmed has acquired an exclusive licence to Pharmacia's regulatory filings concerning yeast-derived IGF-1. These filings were used by Pharmacia to receive marketing approvals in several European countries and also in the investigational New Drug Application with the US FDA. This licence will facilitate the development of SomatoKine for the treatment of children with GHIS. In January 2003, Insmed announced positive results from a double-blind, placebo-controlled, dose-ranging study of SomatoKine in adolescent patients with type 1 diabetes mellitus redolescent patients with type 1 diabetes mellitus receiving insulin therapy. The study was conducted at the University of Cambridge, Cambridge, UK, under the supervision of Professor D. Dunger. It has also been granted orphan drug status for the treatment of GHIS--Laron syndrome in the US and in Europe. Celtrix has been granted 11 US patents for its recombinant protein production technology, which it used for developing somatomedin-1 binding protein-3. Subsequently, Celtrix was acquired by Insmed Pharmaceuticals on June 1 2000. Following the acquisition, Insmed announced that it intends to maintain the US rights to Celtrix's products portfolio. These US patents will expire between 2010 through 2017. Insmed is holding a US patent (expires in 2019) for the use of SomatoKine in the treatment of both type 1 and type 2 diabetes mellitus.

摘要

生长调节素-1结合蛋白-3[胰岛素样生长因子-1结合蛋白-3,生长激素结合蛋白]是胰岛素样生长因子-1(重组人胰岛素样生长因子-1)与结合蛋白-3(IGFBP-3)的重组复合物,IGFBP-3是循环中主要的生长调节素(胰岛素样生长因子)结合蛋白;结合蛋白-3调节生长调节素-1向靶组织的递送。生长调节素-1结合蛋白-3有潜力作为生长调节素-1的替代疗法,在诸如大手术、器官损伤/衰竭和创伤性损伤等情况下,生长调节素-1可能会耗尽,从而导致分解代谢。它还具有治疗骨质疏松症的潜力;治疗与蛋白质消耗相关的疾病,包括慢性肾衰竭、恶病质和严重创伤;以及减轻多种疾病状态下的心脏功能障碍,包括严重烧伤创伤后。生长调节素-1与生长调节素-1结合蛋白-3联合治疗将延长生长调节素-1的作用持续时间,并减少或消除与生长调节素-1单一疗法相关的一些不良影响。在身体的正常状态下,生长调节素-1通常与结合蛋白-3相连,特定的蛋白酶会在应激反应时将它们分开,并根据需要释放出生长调节素-1。因此,生长调节素-1结合蛋白-3是一种自我给药系统,生长激素结合蛋白将增加这些相连化合物的天然供应。生长调节素-1结合蛋白-3由Celtrix公司利用其专有的重组蛋白生产技术开发。随后,Celtrix于2000年6月1日被Insmed制药公司收购。Insmed与英国的Avecia公司签署了一项关于生产生长激素结合蛋白及其成分IGF-1和结合蛋白-3的协议。生长激素结合蛋白及其成分的CGMP临床生产将在英国比林厄姆的Avecia先进生物制品中心进行,该中心生产基于重组的药品和疫苗,生产能力高达1000升。2003年,计划将生长激素结合蛋白的生产转移到Avecia更大的、生产能力为10000升的工厂。生长调节素-1结合蛋白-3最初授权给日本的卫材公司。2001年10月1日,卫材公司与三菱东京制药公司合并,成立了三菱制药公司。新公司是三菱化学的子公司。2003年4月,Insmed在欧洲启动了一项指定患者计划,该计划将提供生长调节素-1结合蛋白-3用于治疗生长激素不敏感综合征(GHIS)——拉伦综合征。患者治疗在斯堪的纳维亚开始,其他几个欧洲国家的授权正在等待中。生长调节素-1结合蛋白-3将提供给那些经医生判断可能从IGF-1治疗中受益的GHIS患者。在商业化前规模的数量下,该药物将限量供应。指定患者计划产生的安全数据将用于支持2004年的上市申请。在英国伦敦圣巴塞洛缪医院和皇家伦敦医学院完成了一项针对GHIS儿童的II期剂量范围研究。单次注射生长调节素-1结合蛋白-3所递送的IGF-1量与每日两次注射未结合的IGF-1相同。没有不良事件报告。GHIS是一种遗传性疾病,由于患者对生长激素信号无反应,导致不能产生足够量的IGF。这导致生长速度减慢和身材矮小。Insmed已获得辉瑞公司关于酵母衍生IGF-1的监管申报文件的独家许可。这些申报文件被辉瑞公司用于在几个欧洲国家获得上市批准,以及在美国食品药品监督管理局的研究性新药申请中使用。该许可将促进生长激素结合蛋白用于治疗GHIS儿童的开发。2003年1月,Insmed宣布了一项针对接受胰岛素治疗的1型糖尿病青少年患者的生长激素结合蛋白双盲、安慰剂对照、剂量范围研究的阳性结果。该研究在英国剑桥大学由D.邓杰教授监督进行。它还在美国和欧洲被授予用于治疗GHIS——拉伦综合征的孤儿药地位。Celtrix公司因其用于开发生长调节素-1结合蛋白-3的重组蛋白生产技术已获得11项美国专利。随后,Celtrix于2000年6月1日被Insmed制药公司收购。收购后,Insmed宣布打算保留Celtrix产品组合在美国的权利。这些美国专利将于2010年至2017年到期。Insmed持有一项关于生长激素结合蛋白用于治疗1型和2型糖尿病的美国专利(2019年到期)。

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