探索强制许可作为印度抗逆转录病毒药物的有效政策工具。

Dipika Jain, Jonathan J Darrow
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引用次数: 0

摘要

在巴西、南非和印度等许多发展中国家,获得治疗艾滋病毒/艾滋病和其他疾病的负担得起的药物越来越具有挑战性。这些挑战在一定程度上是1994年《与贸易有关的知识产权条约》(TRIPS)授权加强专利法的结果。然而,政府可以利用《与贸易有关的知识产权协定》中一些未得到充分利用的工具来限制专利保护的不利影响,从而确保向其人民提供负担得起的仿制药。其中一种手段是强制许可,它允许非专利制造商生产目前受专利保护的药品。在过去几年中,许多国家都采用了强制许可制度,包括美国、加拿大、印度尼西亚、马来西亚、巴西和泰国。强制许可制度对印度等感染艾滋病毒人数众多的国家尤为重要。本文借鉴其他国家的经验,探讨了在印度现行专利制度下,将强制许可作为一种促进基本药物获取的工具的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An exploration of compulsory licensing as an effective policy tool for antiretroviral drugs in India.

Access to affordable drugs for the treatment of HIV/AIDS and other diseases is increasingly challenging in many developing countries such as Brazil, South Africa, and India. These challenges are in part the result of strengthened patent laws mandated by the 1994 Trade-Related Aspects of Intellectual Property Rights (TRIPS) treaty. However, there are underutilized instruments within TRIPS that governments can use to limit the adverse effects of patent protection and thereby ensure a supply of affordable generic drugs to their people. One such instrument is compulsory licensing, which allows generic manufacturers to produce pharmaceutical products that are currently subject to patent protection. Compulsory licensing has been used by a number of countries in the last few years, including the United States, Canada, Indonesia, Malaysia, Brazil, and Thailand, and is particularly significant for countries such as India, where large numbers of people are infected with HIV. This Article explores the feasibility of compulsory licensing as a tool to facilitate access to essential medicines within the current patent regime in India, drawing on the experiences of other countries.

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