FDA 罕见病框架倡议公开会议 10/28/2026
FDA Rare Disease Framework Initiative Public Meeting - 10/28/2026
美国 FDA 与 Reagan-Udall 基金会将于 2026 年 10 月 28 日以线上线下混合形式召开罕见病框架倡议公开会议,就重塑该机构罕见病药物开发路径征求意见。会议面向患者、疾病倡导者、申办方等罕见病社区成员,重点征集基于可及证据的罕见病疗法审评、FDA 监管要求的一致性与可预测性、外部参与审评决策,以及罕见病疗法特有的 CMC 考量等四方面意见。公众意见将用于指导该机构后续工作。
Meeting | Mixed
Event Title
FDA Rare Disease Framework Initiative Public Meeting
- Date:
- October 28, 2026
- Time:
- 1:00 p.m. - 5:00 p.m. ET
Attend
Location
Attend In Person or Online via Zoom
In Person:
FDA White Oak Campus
10903 New Hampshire Avenue
Building 2, Room 2047
Silver Spring, MD 20993
United States
On October 28, 2026, the U.S. Food and Drug Administration, in partnership with the Reagan-Udall Foundation for the FDA, will convene a hybrid public meeting to seek input related to the FDA’s Rare Disease Framework Initiative to reimagine the agency’s approach to rare disease drug development. The intent of this new initiative is to develop a fit-for-purpose Framework that reflects the realities of rare disease drug development by considering the nuances of each disease, patient needs, product type, and the evidence that realistically can be generated in small patient populations.
The public meeting will be an opportunity for members of the rare disease community – including patients, disease advocates, sponsors, and others – to provide input on the direction and focus of the Framework. Insights from the public’s remarks will inform the agency’s upcoming work.
The FDA welcomes all feedback related to the Framework Initiative and in particular seeks input on the following topic areas:
- Fit-for-purpose review of rare disease therapies based on attainable evidence, particular disease state, and population.
- FDA consistency and predictability of drug development and review regulatory requirements.
- FDA engagements with external parties – including patients, disease experts, and researchers – to inform review decision-making.
- Considerations for chemistry, manufacturing, and controls (CMC) specific to rare disease therapies.
来源:FDA 官方药品与生物制品信息 · fda.gov