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Sustainable rare diseases business and drug access: no time for misconceptions

机译:可持续的罕见病业务和毒品获取:没有时间误解

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Legislative incentives enacted in Europe through the Regulation (EC) No. 141/2000 to incentivize orphan drug development have over the last 12 years constituted a powerful impetus toward R&D directed at the rare diseases population. However, despite therapeutic promises contained in these projects and significant economic impact linked to burgeoning R&D expenditures, the affordability and value of OMPs has become a topic of health policy debate in Europe fueled by the perception that OMPs have high acquisition costs, and by misconceptions around pricing dynamics and rare-diseases business models. In order to maintain sustainable patient access to new and innovative therapies, it is essential to address these misconceptions, and to ensure the successful continuation of a dynamic OMPs R&D within rare-diseases public health policy. Misconceptions abound regarding the pricing of rare diseases drugs and reflect a poor appreciation of the R&D model and the affordability and value of OMPs. Simulation of potential financial returns of small medium sized rare diseases companies focusing on high priced drugs show that their economic returns are likely to be close to their cost of capital. Research in rare diseases is a challenging endeavour characterised by high fixed costs in which companies accrue substantial costs for several years before potentially generating returns from the fruits of their investments. Although heavily dependent upon R&D capabilities of each individual company or R&D organization, continuous flow of R&D financial investment should allow industry to increasingly include efficiencies in research and development in cost considerations to its customers. Industry should also pro-actively work on facilitating development of a specific value based pricing approach to help understanding what constitute value in rare diseases. Policy makers must reward innovation based upon unmet need and patient outcome. Broader understanding by clinicians, the public, and policy makers of the complexity of clinical programs to deliver OMPs to market is required to better comprehend the decisions needed and made by industry. In parallel, an overt effort to consider the impact of public policies on R&D investments is key to enable policy makers to better reconcile the incentives provided by public policy decisions and companies investments decisions in a more positive manner.
机译:在过去的12年中,欧洲通过第141/2000号法规(EC)制定的鼓励孤儿药开发的立法激励措施,成为针对罕见病人群进行研发的有力动力。然而,尽管这些项目中蕴含着治疗前景,并且与快速增长的研发支出相关联的重大经济影响,但由于人们认为OMP具有很高的购置成本,以及对它的误解,因此OMP的可负担性和价值已成为欧洲卫生政策辩论的主题。定价动态和罕见病商业模式。为了使患者可持续获得新的创新疗法,必须解决这些误解,并确保在罕见病公共卫生政策内成功地继续进行动态的OMPs研发。对于稀有疾病药物的定价存在很多误解,反映出人们对研发模型以及OMP的可负担性和价值缺乏了解。对以高价药品为重点的中小型稀有疾病公司的潜在财务收益的模拟表明,它们的经济收益很可能接近其资本成本。稀有疾病的研究是一项具有挑战性的工作,其特点是固定成本高昂,在这种情况下,公司可能会累积数年的成本,然后才能从其投资成果中潜在地获得回报。尽管在很大程度上依赖于每个公司或R&D组织的R&D能力,但是R&D财务投资的持续流动应使行业能够在考虑到客户成本方面逐渐提高研发效率。工业界还应积极推动基于特定价值的定价方法的开发,以帮助了解稀有疾病的构成价值。决策者必须根据未满足的需求和患者的结果来奖励创新。临床医生,公众和政策制定者需要对将OMPs推向市场的临床程序的复杂性进行更广泛的了解,以更好地理解行业所需的决策。同时,要努力考虑公共政策对R&D投资的影响,这是使决策者能够更好地调和公共政策决策和公司投资决策提供的激励的关键。

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