药品定价:对改善处方药可及性和可负担性建议的审查。

Annals of health law Pub Date : 2010-01-01
Paula Tironi
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引用次数: 0

摘要

这篇文章讨论了制药创新如何在人类健康方面取得了显著的进步,但美国人口的很大一部分负担不起处方药。作者考察了专利保护、仿制药、供应链复杂性以及创新和推广成本对获取和负担能力的影响。然后,作者着眼于营销策略和行业趋势的影响,如新药的专利悬崖和管道,生物技术和基因组学的创新,比较有效性分析,以及付款人和雇主策略对药品价格的影响。对行业趋势背景下改革建议的分析表明,通过教育促进仿制药的使用和可得性,禁止授权仿制药,限制开发后续药物和在专利到期后停止使用原始配方的做法,可以最迅速和最显著地改善获取和负担能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmaceutical pricing: a review of proposals to improve access and affordability of prescription drugs.

This article discusses how pharmaceutical innovation achieves remarkable improvements in human health but a significant portion of the U.S. population cannot afford prescription drugs. The author examines ways that patent protection, generics, supply chain complexity, and the cost of innovation and promotion affect access and affordability. The author then looks at the influences of marketing strategies and industry trends such as the patent cliff and pipeline for new drugs, innovations in biotechnology and genomics, comparative effectiveness analysis, and payor and employer strategies on drug prices. An analysis of reform proposals in the context of industry trends suggests that promoting generic drug use and availability through education, prohibiting authorized generics, and restricting the practice of developing follow-on drugs and discontinuing the original formulations upon patent expiration could improve access and affordability most quickly and significantly.

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