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DIA 2018 Global Annual Meeting


Sex Considerations in the FDA Drug Review Pipeline: The Where, When, and How

    Session Chair(s)
      Pamela Elizabeth Scott, PhD, MA

      Pamela Elizabeth Scott, PhD, MA

      • Deputy Director and Director of R&D, Office of Women's Health, OC
      • FDA, United States
    There has been considerable progress in how sex differences are incorporated into both clinical trial development and how FDA reviews this data. The FDA has published several regulations and guidance in regard to women and sex and gender inclusion and incorporation into the review process. This forum will walk through the impact of these requirements and recommendations on the inclusion of women in clinical trials and comprehensive review of sex differences in clinical trials. It will dive further into the drug approval timeline focusing on the role of pharmacological and toxicology reviewers at the FDA. Participants will have the ability to test their knowledge on the drug approval process as well as walk through case study examples of drugs approved or rejected from the market. Presenters will begin with a brief overview of the regulatory history of the inclusion of women in research activities and clinical trials. In addition, presenters will discuss the evaluation of potential sex differences throughout the process of drug development including the pre-clinical and clinical phases.
    Learning Objective : Recognize the impact of regulatory requirements and policy on the inclusion of women in clinical trials; State the requirements for the use of male and female animals in preclinical toxicity studies; Identify when and how sex is considered in the FDA drug review and approval process; Identify at least one method which FDA utilizes to communicate findings regarding sex differences to the public
    Speaker(s)
      Pamela Elizabeth Scott, PhD, MA

      Inclusion and Analysis of Sex and Gender Differences in Clinical Trials Supporting Drug Approvals

      Pamela Elizabeth Scott, PhD, MA

      • Deputy Director and Director of R&D, Office of Women's Health, OC
      • FDA, United States
      Representative Invited

      Sex Considerations in Drug Development: A Nonclinical Perspective

      Representative Invited

      • FDA, United States
      Representative Invited

      Clinical Evaluation of a New Drug: Looking for Sex Differences

      Representative Invited

      • FDA, United States