Back to Search Start Over

Working Together to Address Women's Health in Research and Drug Development: Summary of the 2017 Women's Health Congress Preconference Symposium

Authors :
Pamela E. Scott
Marjorie R. Jenkins
Irwin M. Feuerstein
Michael S. Lauer
Stephanie A. Devaney
Tonse N.K. Raju
Janine A. Clayton
Milena Lolic
Susan G. Kornstein
Marsha Henderson
Tamara Johnson
Source :
Journal of Women's Health. 27:1195-1203
Publication Year :
2018
Publisher :
Mary Ann Liebert Inc, 2018.

Abstract

Historically, women have been underrepresented in clinical research, requiring physicians to extrapolate medical recommendations for women from clinical research done in cohorts consisting predominantly of male participants. While government-funded clinical research has achieved gender parity in phase-3 clinical trials across many biomedical disciplines, improvements are still needed in several facets of women's health research, such as the inclusion of women in early-phase clinical trials, the inclusion of pregnant women and women with physical and intellectual disabilities, the consideration of sex as a biological variable in preclinical research, and the analysis and reporting of sex and gender differences across the full biomedical research continuum. The National Institutes of Health (NIH) Office of Research on Women's Health and the Office of Women's Health of the U.S. Food and Drug Administration (FDA) cosponsored a preconference symposium at the 25th Annual Women's Health Congress, held in Arlington, VA in April, 2017, to highlight gains made and remaining needs regarding the representation of women in clinical research, to introduce innovative procedures and technologies, and to outline revised policy for future studies. Six speakers presented information on a range of subjects related to the representation of women in clinical research and federal initiatives to advance precision medicine. Topics included the following: the return on investment from the NIH-funded Women's Health Initiative; progress in including women in clinical trials for FDA-approved drugs and products; the importance of clinical trials in pregnant women; FDA initiatives to report drug safety during pregnancy; the NIH-funded All of Us Research Program; and efforts to enhance FDA transparency and communications, including the introduction of Drug Trials Snapshots. This article summarizes the major points of the presentations and the discussions that followed.

Details

ISSN :
1931843X and 15409996
Volume :
27
Database :
OpenAIRE
Journal :
Journal of Women's Health
Accession number :
edsair.doi.dedup.....8c900285becb26d43db920c418d2b82b
Full Text :
https://doi.org/10.1089/jwh.2018.29019.pcss