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Embracing a New Era in Clinical Trials: Learning from the Past for a More Inclusive Future

The journey towards equitable clinical trials in healthcare requires confronting and learning from past transgressions. For those leading patient advocacy in the biotech and pharmaceutical sectors, recognizing these historical challenges is vital to fostering trust and diversity in research.

Henrietta Lacks’ story, where her cells were used without consent, and the Tuskegee Syphilis Study, which exploited African American men, are poignant reminders of past ethical breaches. These incidents have sown deep seeds of mistrust, particularly among minority communities.

Responding to this, the FDA and patient advocacy groups are advocating for trials that better represent the general population, aligning with disease prevalence across demographics. This is more than rectifying past errors; it’s about ensuring the safety and effectiveness of treatments for all.

At Archo Advocacy, we emphasize the role of patient advocates in this transformation. We’re committed to promoting transparency, informed consent, and ethical research practices. Our market research sheds light on patient perspectives in today’s healthcare trust climate, especially regarding clinical trial participation.

We invite you to engage with us at Archo Advocacy. Together, we can contribute to a future where clinical trials are not only scientifically robust but also ethically sound and inclusive.

Join us in turning a new page in healthcare history.

Feel free to reach out to us at hunter.fasanro@archo.io.