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ADVANCING INCLUSIVE RESEARCH®

Always Design with Patient Inclusion in Mind

Conducting scientifically representative research requires that clinical trials reflect the broader patient population that we endeavor to benefit. By doing so, we aim to optimize health outcomes for everyone.

WHY INCLUSIVE RESEARCH?

More must be done to ensure clinical trial participants are representative of the entire patient population.

  • <10% Today, fewer than 10% of U.S. patients participate in clinical trials and of those only 5-15% are non-European.1
  • ~50% Yet, approximately half of the U.S. population is projected to be non-white by 2044.2
  • >94% More than 94% of genomic material available to scientists is of European ancestry.3

STRATEGIC FOCUS AREAS

REIMAGINING CLINICAL STUDIES

EMPOWERING PATIENTS & PROVIDERS

COLLABORATING WITH EXTERNAL PARTNERS

Click each dropdown to see our impact in action:

ADVANCING INCLUSIVE RESEARCH® SITE ALLIANCE


The U.S. Advancing Inclusive Research Site Alliance is a coalition of clinical research sites in oncology and ophthalmology that partner with Genentech to:

  • Ensure that our research studies include a broad spectrum of patients, reflective of those who experience the diseases we are studying.
  • Test recruitment and retention approaches.
  • Establish best practices that can be leveraged across the industry to help ensure that as many relevant patients as possible can benefit from potentially transformative medicines.

Meet our site alliance champions.

At Roche and Genentech, we believe that improving health outcomes for all patients is core to our mission, and we are committed to being industry leaders in delivering improved health outcomes for all...

Click here to read Roche's position on Race, Ethnicity and Genetic Ancestry in Clinical Research.


REFERENCES
1 Nabhan C, Choueiri TK, Mato AR. Rethinking Clinical Trials Reform During the COVID-19 Pandemic. JAMA Oncol. 2020;6(9):1327-1329. doi:10.1001/jamaoncol.2020.3142; for non-Caucasian participation (Hispanic and Latino): Coakley M, Fadiran EO, Parrish LJ, Griffith RA, Weiss E, Carter C. Dialogues on diversifying clinical trials: successful strategies for engaging women and minorities in clinical trials . J Womens Health (Larchmt). Jul 2012;21(7):713-6. doi:10.1089/jwh.2012.3733
2 Colby SL, Ortman JM. Rethinking Projections of the Size and Composition of the U.S. Population: 2014 to 2060.
3 Genomic Data Source: Rethinking Total GWAS Participants Diversity. GWAS Diversity Monitor.
4 Hittle M, et al. Population-Based Estimates for the Prevalence of Multiple Sclerosis in the United States by Race, Ethnicity, Age, Sex, and Geographic Region. JAMA Neurol. 2023;80(7):693-701.