Independent Researcher, London, United Kingdom.
Treatment Action Group, New York, New York, United States of America.
PLoS One. 2020 Sep 18;15(9):e0239118. doi: 10.1371/journal.pone.0239118. eCollection 2020.
In 2012, bedaquiline became the first new treatment from a novel class to be approved for tuberculosis in nearly five decades and is now a core component of the standard of care for multidrug-resistant tuberculosis. In addition to the originator pharmaceutical company, Janssen, a range of governmental and non-profit entities have contributed to the development of bedaquiline.
We identified various avenues of public investments in the development of bedaquiline: direct funding of clinical trials and a donation programme, tax credits and deductions, and revenues resulting from the priority review voucher (PRV) awarded to the originator. Data on investments were gathered through contact with study leads and/or funders; for non-responses, published average costs were substituted. The originator company's expenses were estimated by similar methods. Tax credits and deductions were calculated based on estimated originator trial costs and donation expenses. The value of the PRV was estimated by application of a published model.
Public contributions through clinical trials funding were estimated at US$109-252 million, tax credits at US$22-36 million, tax deductions at US$8-27 million, administration of a donation programme at US$5 million, PRV revenues at US$300-400 million. Total public investments were US$455-747 million and originator investments were US$90-240 million (if capitalized and risk-adjusted, US$647-1,201 million and US$292-772 million, respectively).
Estimating the investments in the development of a medicine can inform discussions regarding fair pricing and future drug development. We estimated that total public investments exceeded the originator's by a factor of 1.6-5.1.
2012 年,贝达喹啉成为近五十年来首个获准用于结核病治疗的新型药物,也是耐多药结核病标准治疗方案的核心组成部分。除了原研药公司强生公司外,许多政府和非营利组织也为贝达喹啉的研发做出了贡献。
我们确定了公共投资于贝达喹啉研发的各种途径:临床试验的直接资助和捐赠计划、税收抵免和扣除,以及授予原研药的优先审评券(PRV)所产生的收入。通过与研究负责人和/或资助者联系收集投资数据;对于未回复的情况,使用已发表的平均成本进行替代。通过类似的方法估计原研药公司的费用。根据估计的原研药试验成本和捐赠支出计算税收抵免和扣除。应用已发表的模型估算 PRV 的价值。
临床试验资助方面的公共贡献估计为 1.09-2.52 亿美元,税收抵免为 2200-3600 万美元,税收扣除为 800-2700 万美元,捐赠计划管理为 500 万美元,PRV 收入为 3 亿-4 亿美元。公共总投资为 4.55-7.47 亿美元,原研药投资为 9000-2.4 亿美元(如果资本化和风险调整后,分别为 6.47-12.01 亿美元和 2.92-7.72 亿美元)。
估算一种药物研发的投资可以为公平定价和未来药物开发的讨论提供信息。我们估计公共总投资是原研药的 1.6-5.1 倍。