定义可持续全球生物类药物市场的框架,利用有针对性的文献审查的结果
Joshua A Roth1,2, Victoria W Dayer3,4, Mireia Jofre-Bonet5
1Pfizer, Inc., New York, NY, USA. Joshua.Roth@Pfizer.com.
概括
生物类药物市场的可持续性面临着威胁药物可用性和创新的挑战. 本研究确定了关键的维度和利益相关者考虑,以确保生物类似药市场的长期可行性.
科学领域:
- 药物经济学 药物经济学
- 卫生政策 卫生政策
- 制药市场分析 制药市场分析
背景情况:
- 生物类药物为参考生物制品提供了替代品,但市场的可持续性受到各种挑战的威胁.
- 缺乏系统框架阻碍了评估和采取行动来应对这些威胁.
- 其后果包括潜在的药物短缺,竞争减少和创新减少.
研究的目的:
- 通过文献审查,确定生物类似药市场可持续性的关键维度.
- 确定关键的利益相关者群体和普遍的可持续性因素.
- 制定一个框架,确保生物类似药市场的长期可行性.
主要方法:
- 全球生物类似物文献的当代,有针对性的审查.
- 识别和分析通常引用的利益相关者群体.
- 在文献中讨论的普遍可持续性维度的分析.
主要成果:
- 关键的利益相关者包括付款人,监管机构,提供者,制造商,患者和购买者.
- 普遍存在的可持续性维度包括定价,成本节约,监管障碍,制造商流程,供应商选择,知识和采购.
- 这些发现被合成为生物类似药市场可持续性的框架.
结论:
- 考虑多个利益相关者的观点的全面框架对于生物类似药市场的可持续性至关重要.
- 解决定价,监管和访问障碍对于长期可行性至关重要.
- 这一框架有助于利益相关者确保生物类似药的持续可用性和创新.
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