Document
Advancing the Development of Pediatric Therapeutics Complex Innovative Trial Design; Public Workshop
The Food and Drug Administration (FDA) is announcing the following public workshop entitled "Advancing the Development of Pediatric Therapeutics (ADEPT 7) Complex Innovative Tri...
SUPPLEMENTARY INFORMATION:
I. Background
Over the last two decades, great advances have been made in pediatric drug development. In addition, there is a growing recognition that complex and innovative trial designs have the potential to optimize drug development in small populations. Innovations that have been proposed include Bayesian and other methods of utilizing external historical information from previous pediatric trials or other populations (such as adults), adaptive designs, bridging biomarkers, etc. These designs tend to require more extensive discussion and collaboration between drug developers and regulators to implement effectively.
The Complex Innovative Trial Design Pilot Meeting Program (CID Program) facilitates and advances the use of these types of designs by providing for increased interactions between staff in the Center for Drug Evaluation and Research and the Center for Biologics Evaluation and Research and sponsors accepted into the program. Several pediatric study designs have been accepted into the CID Program. This workshop is being organized in collaboration with the CID Program.
II. Topics for Discussion at the Public Workshop
The main objective of the “Advancing the Development of Pediatric Therapeutics (ADEPT 7) Complex Innovative Trial Design” workshop is to discuss opportunities for leveraging complex and innovative trial designs, understand the challenges with their applications, and develop solutions on how challenges in the designs can be overcome. The workshop will specifically focus on two topics of interest: Bridging biomarkers in pediatric extrapolation and Bayesian techniques in pediatric studies. In addition, the workshop will allow for an open dialogue around the use of these approaches among regulators, industry, academia, and patient organizations.
III. Participating in the Public Workshop
Registration:
To register for the public workshop, please visit the following website:
https://go.umd.edu/ADEPT7. Please provide complete contact information for each attendee, including name, title, affiliation, address, email, and telephone.
Registration is free and based on space availability, with priority given to early registrants. Early registration is recommended because space is limited; therefore, FDA may limit the number of participants from each organization.
If you need special accommodations due to a disability, please contact
Evangela Covert or Denise Pica-Branco (see
FOR FURTHER INFORMATION CONTACT
) no later than August 18, 2021, by 5 p.m. Eastern Time.
Streaming Webcast of the Public Workshop:
This public workshop will also be webcast at the following site:
https://collaboration.fda.gov/adept7.
If you have never attended a Connect Pro event before, test your connection at
https://collaboration.fda.gov/common/help/en/support/meeting_test.htm. To get a quick overview of the Connect Pro program, visit
https://www.adobe.com/go/connectpro_overview. FDA has verified the website addresses in this document, as of the date this document publishes in the
Federal Register
, but websites are subject to change over time.
Dated: August 2, 2021.
Lauren K. Roth,
Associate Commissioner for Policy.