| Literature DB >> 33940253 |
Melinda Rottas1, Peter Thadeio2, Rachel Simons2, Raven Houck2, David Gruben2, David Keller2, David Scholfield3, Koshika Soma2, Brian Corrigan2, Annette Schettino4, Patrick J McCann2, Marie-Pierre Hellio2, Kannan Natarajan4, Rob Goodwin2, Judy Sewards5, Peter Honig6, Rod MacKenzie5.
Abstract
The approval of new medicinal agents requires robust efficacy and safety clinical trial data demonstrated to be applicable to population subgroups. Limited data have previously been reported by drug sponsors on the topic of clinical trial diversity. In order to establish a baseline of diversity in our clinical trials that can be used by us and other sponsors, an analysis of clinical trial diversity was conducted covering race, ethnicity, sex, and age. This analysis includes Pfizer interventional clinical trials that initiated enrollment between 2011 through 2020. The data set comprises 213 trials with 103,103 US participants. The analysis demonstrated that overall trial participation of Black or African American individuals was at the US census level (14.3% vs 13.4%), participation of Hispanic or Latino individuals was below US census (15.9% vs 18.5%), and female participation was at US census (51.1% vs 50.8%). The analysis also examined the percentage of trials that achieved racial and ethnic distribution levels at or above census levels. Participant levels above census were achieved in 56.1% of Pfizer trials for Black or African American participants, 51.4% of trials for White participants, 16.0% of trials for Asian participants, 14.2% of trials for Native Hawaiian and Pacific Islander participants, 8.5% of trials for American Indian and Alaska Native participants, and 52.3% of trials for Hispanic or Latino participants. The results presented here provide a baseline upon which we can quantify the impact of our ongoing efforts to improve racial and ethnic diversity in clinical trials.Entities:
Keywords: Clinical trials; Diversity; Ethnicity; Pfizer; Race; Representation
Mesh:
Year: 2021 PMID: 33940253 DOI: 10.1016/j.cct.2021.106421
Source DB: PubMed Journal: Contemp Clin Trials ISSN: 1551-7144 Impact factor: 2.226