Somapacitan: a long-acting growth hormone derivative for treatment of growth hormone deficiency.

IF 1.8 4区 医学 Q2 Medicine
David M Paton
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引用次数: 0

Abstract

Growth hormone deficiency (GHD) is characterized by inadequate HG production from the anterior pituitary gland. Adult patients with GHD have increased fat mass, an abnormal lipid profile, decreased lean body mass and bone mineral density, decreased muscle strength and exercise endurance, and a diminished quality of life. Adult GHD (AGHD) has been treated with GH replacement therapy by daily subcutaneous injections. However, the administration of daily injections can be burdensome for some patients and affect treatment adherence. Somapacitan is a new long-acting human GH (hGH) analogue that is administered once a week by subcutaneous injection. It was first approved by the U.S. Food and Drug Administration (FDA) as GH replacement therapy for adults with GHD, becoming the first hGH therapy for AGHD administered by once-weekly injection, compared with other approved hGH therapies for AGHD administered by daily injection. This article reviews the pharmacokinetic, clinical and safety data that led to the approval of somapacitan as the first long-acting GH therapy for adults with GHD.

Somapacitan:一种治疗生长激素缺乏症的长效生长激素衍生物。
生长激素缺乏症(GHD)的特征是垂体前叶产生的HG不足。成年GHD患者脂肪量增加,脂质异常,瘦体重和骨密度下降,肌肉力量和运动耐力下降,生活质量下降。成人GHD (AGHD)已通过每日皮下注射的生长激素替代疗法治疗。然而,对一些患者来说,每日注射可能是负担,并影响治疗依从性。Somapacitan是一种新的长效人生长激素(hGH)类似物,每周一次皮下注射。它首先被美国食品和药物管理局(FDA)批准为成人GHD的生长激素替代疗法,成为第一个每周一次注射的AGHD生长激素疗法,与其他批准的每日注射的AGHD生长激素疗法相比。这篇文章回顾了导致somapacitan被批准作为成人GHD的第一个长效生长激素治疗的药代动力学、临床和安全性数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drugs of today
Drugs of today 医学-药学
CiteScore
3.90
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: An international, peer-reviewed journal publishing monographs on new products entering the market and review articles. Since its inception in 1965, Drugs of Today has established a reputation for excellence in providing physicians and other key healthcare professionals with practical, up-to-date monographs on recently approved and launched drugs.
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