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FEDERAL REGISTER · NOTICENovember 22, 2023NOTICE — NO LEGAL EFFECT

Advancing the Use of Complex Innovative Designs in Clinical Trials: From Pilot to Practice; Public Workshop; Request for Comments

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Document details are published in the U.S. Federal Register; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA or the Office of the Federal Register. The authoritative text is on federalregister.gov.

STATUSNOTICE — NO LEGAL EFFECT
EFFECTIVE—
COMMENTS CLOSEApr 5, 2024 · closed
APPLIES TO · SPEQ TAGDrugBiologicsDevice
Document type
Notice
Agency
Health and Human Services Department
Published
November 22, 2023
Comments close
April 5, 2024
Document number
2023-25854
Docket
FDA-2023-N-4965
ABSTRACT

The Food and Drug Administration (FDA or the Agency) is announcing the following public workshop entitled "Advancing the Use of Complex Innovative Designs in Clinical Trials: From Pilot to Practice." The purpose of the public workshop is to discuss aspects of complex adaptive, Bayesian, and other novel clinical trial designs. This workshop is being conducted to meet the performance goal of convening a public workshop on complex innovative design (CID) included in the seventh authorization of the Prescription Drug User Fee Act (PDUFA VII). The workshop may also inform a draft guidance on the use of Bayesian methodology in clinical trials of drugs and biological products. In conjunction with the workshop, FDA is seeking comments on the use of CID to inform regulatory decision making, including high- level case examples of CIDs and approaches that can advance the use of these designs. The public workshop will be held on March 5, 2024, from 9 a.m. to 3:30 p.m. Eastern Time.

Abstract as published in the Federal Register.

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