FDA发布治疗性蛋白产品免疫原性评估最终指南（FDA-2013-D-0092）
Immunogenicity Assessment for Therapeutic Protein Products
FDA发布治疗性蛋白产品免疫原性评估最终指南（FDA-2013-D-0092），建议采用基于风险的方式评估和缓解这类产品的免疫应答及免疫相关不良反应。指南由CDER与CBER发布，面向人用治疗性蛋白产品的开发，具体评估方式按个案确定。文件将免疫原性定义为治疗性蛋白产品对自身及相关蛋白产生免疫应答或引发免疫相关不良临床事件的倾向。
该最终指南列出FDA对治疗性蛋白产品免疫原性评估与缓解的风险导向建议框架，便于读者定位相关评估内容。
GUIDANCE DOCUMENT
Final
- Docket Number:
- FDA-2013-D-0092
- Issued by:
-
Guidance Issuing Office
Center for Drug Evaluation and Research
Center for Biologics Evaluation and Research
This guidance is intended to assist manufacturers and clinical investigators involved in the development of therapeutic protein products for human use. In this document, FDA outlines and recommends adoption of a risk-based approach to evaluating and mitigating immune responses to or adverse immunologically related responses associated with therapeutic protein products that affect their safety and efficacy. Any given approach to assessing and mitigating immunogenicity is determined on a case-by-case basis and should take into consideration the risk assessment we describe. For the purposes of this guidance, immunogenicity is defined as the propensity of the therapeutic protein product to generate immune responses to itself and to related proteins or to induce immunologically related adverse clinical events.
Submit Comments
You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))
If unable to submit comments online, please mail written comments to:
Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852
All written comments should be identified with this document's docket number: FDA-2013-D-0092.
来源：FDA Pharmaceutical Quality Documents · fda.gov