Clinical Trial Diversity and Representation
Clinical research contributes to scientific knowledge for treatment options that may potentially benefit patients, physicians, and the broader research community in the future. Equitable access to clinical trials is integral to achieving health equity. Amgen is dedicated to the development of new drugs based on clinical trials, conducted without bias, and with representation of all patients who are afflicted with the disease we are seeking to treat.
In November 2020, Amgen, along with other members of the Pharmaceutical Research and Manufacturers of America (PhRMA), launched industry-wide principles on clinical trial diversity with the goal of addressing the systemic issues that deter people of different races, sexes/genders, socioeconomic circumstances, and other system-level, individual-level, and interpersonal-level barriers from participating in clinical trials. Read more about these principles here.
Achieving diversity and representation in clinical trials is critical work that is the responsibility of all of us at Amgen. A dedicated team, RISE, was launched in 2020 to drive the change and keep progress moving at a steady pace. The extraordinary response from colleagues across the company demonstrates the urgency and our shared commitment to addressing the issue head-on. We all know it's the right one.
Why diversity in clinical trials matters
Volunteer participants make a vital contribution to research and generate valuable information.
When some groups are underrepresented there is a risk of collecting insufficient data to assess effectiveness or safety in those populations.
Racial and/or ethnic background in combination with other interdependent factors can contribute to differences in drug exposure or response.
Equitable access to clinical trials is integral to achieving health equity.
Amgen is driven by six pillars
Evolve the way we design and run clinical trials, focusing on people who have been historically excluded from clinical research.
Partner with clinical trial investigators who are representative of the participants they are aiming to recruit.
Bring the research directly to the communities where people live and work.
Change how researchers communicate with patients, caregivers, and providers.
Enhance precision medicine awareness and improve genetic diversity in translational science.
Collaborate with national and community organizations.
Clinical trials have lacked diversity for decades
Nearly 40% of Americans belong to a racial or ethnic minority, but individuals who participate in clinical trials for new drugs skew heavily White—in some cases, 80 to 90%.
Black/African Americans make up over 13% of the U.S. population, but only 7% of clinical trial participants.1,2
Hispanics/Latinos represent over 18% of the U.S. population, but only 11% of clinical trial participants.1,3
Asian Americans make up 6% of the U.S. population, but make up 1.7% of participants for drugs for which at least 70% of trials were conducted in the U.S.4