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Novel investigational biologics for the treatment of cancer cachexia

机译:用于治疗恶病质的新型研究生物制剂

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摘要

Introduction: Cancer cachexia is a complex multifactorial syndrome characterized by ongoing, irreversible skeletal muscle loss, leading to progressive functional impairment. Several investigational biologics targeting key inflammatory pathways and/or the myostatin/activin type II receptor pathway are in development.Areas covered: Novel therapies include ALD518, MABp1, IP-1510, OHR/AVR118, bimagrumab and REGN1033 and are discussed. For each investigational therapy, the mechanism of action, preclinical data, cachexia definition, indication and clinical data are discussed.Expert opinion: A critical look of the study protocols and two key challenges limiting the successful evaluation of these agents include: i) lack of a clinically meaningful cachexia definition; and ii) identification and treatment of cachexia in late stage. We describe our observations and clinical experience in an effort to redirect and promote successful strategies to evaluate these novel investigational biologics.
机译:简介:恶病质是一种复杂的多因素综合症,其特征是持续的不可逆的骨骼肌丢失,导致进行性功能障碍。一些针对关键炎症途径和/或肌生长抑制素/激活素II型受体途径的研究性生物制剂正在开发中。涉及的领域:新型疗法包括ALD518,MABp1,IP-1510,OHR / AVR118,bimagrumab和REGN1033,并进行了讨论。对于每种研究疗法,都讨论了作用机理,临床前数据,恶病质定义,适应症和临床数据。专家意见:对研究方案的批判性看法以及限制对这些药物成功评估的两个关键挑战包括:具有临床意义的恶病质定义; ii)晚期恶病质的鉴定和治疗。我们描述我们的观察和临床经验,以努力重定向和促进成功的策略来评估这些新颖的研究生物制剂。

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