School of Public Health, Faculty of Medicine, Imperial College London, United Kingdom.
School of Public Health, Faculty of Medicine, Imperial College London, United Kingdom.
J Cyst Fibros. 2022 Sep;21(5):866-872. doi: 10.1016/j.jcf.2022.04.007. Epub 2022 Apr 16.
While the clinical benefits of CFTR modulators are clear, their high prices render them inaccessible outside of the world's richest countries. Despite this, there is currently limited evidence regarding global access to these transformative therapies. Therefore, this study aims to estimate the minimum costs of production of CFTR modulators, assuming robust generic competition, and to compare them with current list prices to evaluate the feasibility of increased global access to treatment.
Minimum costs of production for CFTR modulators were estimated via an algorithm validated in previous literature and identification of cost-limiting key starting materials from published routes of chemical synthesis. This algorithm utilised per kilogram active pharmaceutical ingredient costs obtained from global import/export data. Estimated production costs were compared with published list prices in a range of countries.
Costs of production for elexacaftor/tezacaftor/ivacaftor are estimated at $5,676 [$4,628-6,723] per year, over 90% lower than the US list price. Analysis of chemical structure and published synthetic pathways for elexacaftor/tezacaftor/ivacaftor revealed relatively straightforward routes of synthesis related to currently available products. Total cost of triple therapy for all eligible diagnosed CF patients worldwide would be $489 million per year. Comparatively, the annual cost at US list price would be $31.2 billion.
Elexacaftor/tezacaftor/ivacaftor could be produced via generic companies for a fraction of the list price. The current pricing model restricts access to the best available therapy, thereby exacerbating existing inequalities in CF care. Urgent action is needed to increase the availability of triple combination treatment worldwide. One strategy based on previous success is originator-issued voluntary licenses.
虽然 CFTR 调节剂的临床益处显而易见,但由于价格高昂,这些药物在世界上最富裕的国家之外都无法获得。尽管如此,目前关于这些变革性疗法在全球范围内的可及性的证据有限。因此,本研究旨在估计 CFTR 调节剂在假设强大的仿制药竞争下的最低生产成本,并将其与当前的标价进行比较,以评估增加全球获得治疗的可行性。
通过在先前文献中验证的算法和从已发表的化学合成路线中确定成本限制的关键起始材料来估计 CFTR 调节剂的最低生产成本。该算法利用从全球进出口数据中获得的每公斤活性药物成分成本。将估计的生产成本与一系列国家的已发表标价进行比较。
elexacaftor/tezacaftor/ivacaftor 的生产成本估计为每年 5676 美元(4628-6723 美元),比美国标价低 90%以上。对 elexacaftor/tezacaftor/ivacaftor 的化学结构和已发表的合成途径进行分析,发现与现有产品相关的合成途径相对简单。全球所有符合条件的诊断 CF 患者的三联疗法总成本将为每年 4.89 亿美元。相比之下,按美国标价计算,每年的成本为 312 亿美元。
仿制药公司可以以标价的一小部分生产 elexacaftor/tezacaftor/ivacaftor。目前的定价模式限制了获得最佳可用疗法的机会,从而加剧了 CF 护理方面现有的不平等。需要采取紧急行动来增加全球范围内三联疗法的可及性。基于以往成功经验的一个策略是原始制造商发布自愿许可。