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Key Takeaways and Learnings 

  • Exclusionary and short-term research practices cost the pharmaceutical industry billions.
  • Community-focused solutions make inclusive research easier by connecting companies to underrepresented communities.
  • Clinical research diversity drives better health outcomes, faster regulatory approvals, and expanded market opportunities.
  • Learn how Acclinate leverages innovative technology to improve representation in clinical trials. 

 

Regulatory bodies are increasingly demanding representation in clinical research. But clinical research diversity is about more than ticking a compliance checkbox—it’s a differentiator that drives better health outcomes for all.

The business returns for inclusive clinical research have never been clearer. Companies that prioritize equitable representation are not only developing safer, more effective treatments. They’re positioning themselves for greater market success, smoother regulatory pathways, and measurable impacts on health equity. 

The True Cost of Exclusionary Research Practices

Clinical research has historically excluded the very communities it has aimed to serve, further perpetuating health disparities and limiting the effectiveness of treatment. But this perpetual issue also presents substantial business risks that many companies are only now beginning to understand.

Research from the University of Southern California’s Schaeffer Center shows that the lack of diversity in clinical trials costs billions of dollars annually. These costs manifest in delayed regulatory approvals, post-market safety issues requiring expensive label modifications, and missed opportunities for broader therapeutic applications. When research isn’t representative of varied populations, companies face increased regulatory scrutiny, extended review periods, and potential requirements for additional studies—all of which extend time to market and increase development costs.

But the regulatory landscape is evolving to address these inequities. The World Health Organization’s recent guidance emphasizes that more effective and equitable clinical trials are essential for developing treatments that serve all communities. It recommends putting community engagement at the forefront of clinical research, making sure trials meet public need and build trust. Demographic inclusion in research is no longer something companies must aspire to, it’s something regulatory bodies—and the public—expect.

The Tangible Results of Inclusive Research 

Pharmaceutical companies that integrate equitable representation into their research strategy from the outset have a competitive advantage that extends far beyond regulatory compliance—they build stronger relationships with the communities they serve. Below, check out the three results forward-thinking companies see from increased clinical research diversity.

  • Comprehensive studies accelerate regulatory pathways: When research includes diverse populations from the beginning, regulatory bodies can more confidently assess a treatment’s safety and efficacy across different communities. This often leads to smoother regulatory reviews and faster approvals. Increasingly, the FDA is prioritizing applications that demonstrate thoughtful consideration of diverse populations, recognizing that these studies provide more robust evidence of real-world effectiveness across all communities.
  • Authentic engagement leads to expanded market opportunities: Inclusive clinical research enables companies to pursue both broader therapeutic applications and market opportunities. When clinical data demonstrates efficacy across different racial and ethnic groups, age, gender, sexuality, and more, companies can serve larger patient populations with confidence. This expanded reach directly translates to increased revenue opportunities and stronger return on investment, while simultaneously advancing health equity.
  • Community-centered understanding enhances product safety: Treatment responses can vary significantly across different populations. By identifying these differences during clinical development rather than after going to market, companies can optimize treatment protocols, develop targeted safety monitoring approaches, and create more comprehensive guidance for prescriptions. This proactive approach reduces the risk of costly post-market safety issues while building physician and patient confidence in new treatments. 

Improving Pharmaceutical Trial Representation Through Community Partnership

The most successful pharmaceutical companies know that meaningful representation in clinical research isn’t achieved through traditional recruitment tactics alone. It requires building authentic relationships based on trust within communities of color and underrepresented populations. This is where affective trust becomes essential. 

Unlike cognitive trust, which is based on competence and reliability, affective trust is built through genuine emotional connections, shared values, and demonstrated commitment to community well-being. Affective trust is particularly crucial when engaging with communities that have historically been exploited by or neglected in medical research. 

Acclinate’s NOWINCLUDED platform puts this shift toward community-centered engagement into action.  By connecting pharmaceutical companies with established community networks and trusted leaders, NOWINCLUDED helps to ensure that clinical research diversity becomes an integrated component of ethical, effective study design and execution. And with the e-DICT platform, companies can access analytics and participant matching capabilities that align with community preferences and values. This allows organizations to identify and connect with diverse participant populations more ethically and efficiently, reducing barriers that have historically excluded underrepresented communities from clinical research. 

3 Ways to Promote Demographic Inclusion in Research

Creating lasting change in clinical research representation demands systemic, organization-wide commitment to health equity. Companies that embrace inclusive research focus on three key strategies.

  1. Integrate representation considerations into clinical development from the earliest stages. Rather than inclusion being an afterthought, it should be a fundamental component of study design, site selection, and protocol development. This proactive approach ensures that goals for equitable research are achievable and woven into all aspects of research execution. For example, COPD disproportionately impacts Black and African American communities. So Acclinate partnered with a leading biotechnology research company to address this disparity through community engagement using the NOWINCLUDED platform. This entailed creating a dedicated lung health circle on the platform, participating in 26 community events to establish trust, and presenting over 8,000 NOWINCLUDED members with a trial opportunity. In doing so, Acclinate increased not just awareness and education, but participation in COPD research.
  2. Invest in long-term community partnerships rather than transactional recruitment efforts. Building affective trust with underrepresented communities requires consistent engagement, transparent communication, and a demonstrated commitment to addressing health disparities. Companies that embrace this approach often find that their representation efforts become more authentic and effective over time. Acclinate’s work with BIPOC communities to improve maternal and fetal health, and the resulting engagement and mobilization, highlights the power of community investment.
  3. Leverage technology and community insights to identify and address barriers to participation. By analyzing demographic patterns, geographic distribution, and socioeconomic factors, companies can design more inclusive protocols and select sites that can successfully serve diverse populations through meaningful pharmaceutical trial representation. Acclinate’s NOWINCLUDED and e-DICT platforms allow companies to effectively increase participation in clinical trials from underrepresented communities through trust and connection. 

Representation Can Be Your Trial’s Greatest Asset

Weaving equity into the fabric of clinical research isn’t just the right thing to do—it’s essential for business success. So as regulatory expectations continue to evolve and market competition intensifies, pharmaceutical companies that invest in clinical research diversity will have a clear advantage. And the advantages of representative research will go on to benefit patients, companies, and entire communities alike.

Ready to sharpen your company’s competitive advantage by using a community-based approach? Schedule a 1:1 meeting with our team.

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