过敏原特异性免疫疗法和证据:欧洲监管视角
Detlef Bartel1, Andreas Bonertz1, Diana Hartenstein1
1Paul-Ehrlich-Institut, Langen, Germany.
Allergologie select
|December 25, 2023
概括
过敏原免疫疗法 (AIT) 已经在一个世纪里发展了. 本审查涉及AIT产品的当前监管标准和挑战,确保其质量,安全性和有效性.
科学领域:
- 免疫学 免疫学 免疫学
- 监管科学 监管科学
- 药物监督 药物监督 药物监督
背景情况:
- 过敏原免疫疗法 (AIT) 在临床应用方面有着悠久的历史.
- 确保AIT产品的质量,安全性和有效性仍然是监管重点之一.
- 保罗-埃里希尔研究所 (PEI) 在评估AIT产品在其整个生命周期中发挥着至关重要的作用.
研究的目的:
- 总结目前对过敏原免疫疗法 (AIT) 的监管标准和挑战.
- 从欧洲的监管角度来看,解决AIT的关键方面.
- 通过严格的评估,确保高质量,安全和有效的AIT产品.
主要方法:
- 对AIT的科学证据和监管要求的审查.
- 分析关键方面,包括产品的特异性,临床疗效和标准化.
- 考虑成人和儿科治疗的推断,以及过敏原暴露室的作用.
主要成果:
- 确定AIT的关键监管方面,包括产品特异性,临床疗效和标准化.
- 讨论与现实世界证据和独立批量发布相关的挑战和好处.
- 强调需要在欧盟一级协调AIT法规.
结论:
- 监管监督对于保持过敏原免疫治疗的高标准至关重要.
- 解决AIT产品开发和评估中的挑战对于患者安全至关重要.
- 协调的监管方法将提高AIT在欧洲的可访问性和一致性.
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