The US Food and Drug Administration's Complex Innovative Trial Design Pilot Meeting Program: Progress to date

被引:12
|
作者
Price, Dionne [1 ]
Scott, John [1 ]
机构
[1] US FDA, 10903 New Hampshire Ave, Silver Spring, MD 20993 USA
关键词
Food and Drug Administration; complex innovative trial designs; pilot program;
D O I
10.1177/17407745211050580
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background The Center for Drug Evaluation and Research and the Center for Biologics Evaluation and Research of the U.S. Food and Drug Administration have been leaders in advancing science to protect and promote public health by ensuring that safe and effective drugs and biological products are available to those who need them. Recently, new therapeutic discoveries, increased understanding of disease mechanisms, the need for innovation to optimally use resources, and global public health crises have led to an evolving drug development landscape. As a result, the U.S. Food and Drug Administration and medical product developers are faced with unique challenges and opportunities. The U.S. Food and Drug Administration is proactively meeting the challenges of this evolving landscape through various efforts, including the Complex Innovative Trial Design Pilot Meeting Program. Our focus, here, will be on the pilot meeting program. Methods The U.S. Food and Drug Administration has defined a process to facilitate the implementation of the Complex Innovative Trial Design Pilot Meeting Program. The process is transparent and outlines the steps and timeline for submission, review, and meetings. Results Five submitted meeting requests have been selected for participation in the Complex Innovative Trial Design Pilot Meeting Program. Conclusion The pilot meeting program has been successful in further educating stakeholders on the potential uses of complex innovative designs in trials intended to provide substantial evidence of effectiveness. The selected submissions, thus far, have all utilized a Bayesian framework. The reasons for the use of Bayesian approaches may be due to the flexibility provided, the ability to incorporate multiple sources of evidence, and a desire to better understand the U.S. Food and Drug Administration perspective on such approaches. We are confident the pilot meeting program will have continued success and impact the collective goal of bringing safe and effective medical products to patients.
引用
收藏
页码:706 / 710
页数:5
相关论文
共 50 条
  • [1] The US Food and Drug Administration's Model-Informed Drug Development Meeting Program: From Pilot to Pathway
    Madabushi, Rajanikanth
    Benjamin, Jessica
    Zhu, Hao
    Zineh, Issam
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2024, 116 (02) : 278 - 281
  • [2] The US Food and Drug Administration's Model-Informed Drug Development Paired Meeting Pilot Program: Early Experience and Impact
    Madabushi, Rajanikanth
    Benjamin, Jessica M.
    Grewal, Renmeet
    Pacanowski, Michael A.
    Strauss, David G.
    Wang, Yaning
    Zhu, Hao
    Zineh, Issam
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2019, 106 (01) : 74 - 78
  • [3] Evaluation of epinephrine's expiration date: A US Food and Drug Administration's perspective
    Lan, Jennifer
    Paterniti, Miya
    Bertha, Craig
    Pinto, Julia
    Randazzo, Giuseppe
    Sood, Ramesh
    Seymour, Sally
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2019, 7 (08): : 2948 - 2948
  • [4] Methodology for the US food and drug administration's radionuclides in foods program
    Baratta, EJ
    JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, 1998, 236 (1-2) : 139 - 144
  • [5] FINDING VALUE IN THE US FOOD AND DRUG ADMINISTRATION'S FAST TRACK PROGRAM
    Reichert, J. M.
    Rochon, S. L.
    Zhang, B. D.
    DRUG NEWS & PERSPECTIVES, 2009, 22 (01) : 53 - 58
  • [6] US Food and Drug Administration Regulatory Programs for Innovative Technologies
    Brodie, Frank
    Nguyen, Tieuvi
    Eydelman, Malvina
    JAMA OPHTHALMOLOGY, 2019, 137 (12) : 1349 - 1350
  • [7] US Food and Drug Administration and Design of Drug Approval Studies
    Woloshin, Steven
    Schwartz, Lisa M.
    Frankel, Brittney
    Faerber, Adrienne
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2014, 312 (20): : 2163 - 2165
  • [8] Biomarker qualification pilot process at the US food and drug administration
    Goodsaid, Federico
    Frueh, Felix
    AAPS JOURNAL, 2007, 9 (01): : E105 - E108
  • [9] Biomarker qualification pilot process at the US Food and Drug Administration
    Federico Goodsaid
    Felix Frueh
    The AAPS Journal, 9
  • [10] US Food and Drug Administration Precertification Pilot Program for Digital Health Software: Weighing the Benefits and Risks
    Lee, Theodore T.
    Kesselheim, Aaron S.
    ANNALS OF INTERNAL MEDICINE, 2018, 168 (10) : 730 - +