欧洲里瓦洛克萨班长期许可后安全研究计划的挑战和经验教训
Gunnar Brobert1, Ana Ruigomez2, Tania Schink3
1Bayer AG, Berlin, Germany gunnar.brobert@gmail.com.
BMJ open
|March 26, 2024
概括
本研究详细介绍了利瓦洛克萨班安全性制药流行病学研究的挑战,并提出了诸如共同数据模型和适应性设计等策略,以改善基于人口的研究以满足监管需求.
科学领域:
- 药学流行病学 药学流行病学
- 观测研究 观测研究
- 药品安全 药品安全
背景情况:
- 里瓦罗克萨班许可后安全研究 (PASS) 计划涉及四项药物流行病学数据库研究.
- 这项研究是作为对欧洲药物署的监管批准后承诺的一部分进行的.
研究的目的:
- 描述基于人口的观测研究中的机遇和挑战.
- 提出方法来最大限度地提高这种研究在满足监管要求的价值.
主要方法:
- 在德国,荷兰,瑞典和英国使用了特定的国家电子健康记录数据库.
- 包括355,152名患者被处方里瓦罗克萨班和338,199名患者被处方维生素K抗剂.
主要成果:
- 关键的挑战包括在药物吸收已知之前完成研究设计,并在研究期间解决新的研究问题.
- 这些挑战源于各国特定的数据库编码结构和不断变化的处方环境.
结论:
- 倡导共同的数据模型,以便在不同数据库中实现一致的分析工具.
- 建议早期监管机构沟通,适应不确定性设计,并为研究目标设定里程碑.
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