治疗罕见病的先进再生药物:产业赞助商投资动机综述

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Ubaka Ogbogu, Anja Nel
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引用次数: 0

摘要

尽管监管法规的变化旨在刺激对罕见病疗法的投资,但许多罕见病仍缺乏政府批准的治疗方法。先进的再生医学是旨在治疗或替代受损或有缺陷的人体细胞、组织和器官的疗法和临床干预措施,为治疗许多罕见病带来了巨大希望。治疗罕见病的先进再生医学面临的一大挑战是如何获得资金支持,以帮助将疗法推向市场。本文介绍了全球制药业赞助开发罕见病先进再生药物的因素。本文研究了符合后一种标准的 53 家赞助商的动机。各赞助商的投资动机大致相同,并与先进治疗产品的临床开发和上市授权的监管要求密切相关,包括监管审批存在加速或减弱途径、用于未满足医疗需求较高的适应症,和/或与现有疗法相比具有优势,以及临床前数据强劲。其他因素还包括是否有投资激励措施,以及在批准后阶段的标示外使用机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advanced Regenerative Medicines for Rare Diseases: A Review of Industry Sponsors Investment Motivations

Despite regulatory changes designed to stimulate investment in therapies for rare diseases, many of these conditions lack government-approved treatments. Advanced regenerative medicines, which are therapies and clinical interventions aimed at healing or replacing damaged or defective human cells, tissues, and organs, offer great promise for addressing many rare diseases. A major challenge facing advanced regenerative medicines for rare diseases is securing financial support to assist in bringing a therapy to market. This paper describes the factors cited by pharmaceutical industry players globally for sponsoring the development of advanced regenerative medicines for rare diseases. The paper examines the motivations of 53 sponsors that meet the latter criteria. The motivations behind investments were broadly similar amongst sponsors and map closely onto regulatory requirements for clinical development and marketing authorization of advanced therapeutic products, including the presence of accelerated or attenuated pathways for regulatory approval, use for indications with high unmet medical needs, and/or that have advantages over existing therapies, and robust preclinical data. Other factors include availability of investment incentives and opportunities for off-label use in the post-approval stages.

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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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