Join this webinar to hear key perspectives from a distinguished panel of experts in rare disease, rare disease clinical trials and diversity.
TORONTO (PRWEB)
August 31, 2022
Rare disease clinical trials are challenging on many levels, from identifying eligible patients, to making it convenient for caregivers, to the outsized expense (over $300k per patient) compared to other therapeutic areas. Not to mention that, in many cases, families are looking to clinical trials as their last, best, or only hope for treatment or a cure — when in reality, clinical trials are more likely to benefit families down the line.
Join this webinar to hear key perspectives from a distinguished panel of experts in rare disease, rare disease clinical trials and diversity.
Featured speaker Daniel Defabio will share the realities of rare disease families — the expectations and hope, frustrations and challenges and importance of maintaining a positive outlook — of participating in rare disease trials.
Featured speaker Dr. Fabian Sandoval will focus on driving diversity in clinical trials — something that is already a patient recruitment challenge without the intersection of rare disease. But diverse patient populations get rare diseases too — so what can be done to serve this community.
Featured speaker Andrea Valente will share trends and solutions that consider the participant experience just as important as the data captured during a trial, and how study sponsors and sites can get the most out of them in 2022 and beyond.
Join Daniel Defabio, Co-Founder and Co-Producer, DISORDER: The Rare Disease Film Festival, Director of Community Engagement, Global Genes; Fabian Sandoval, MD, President & CEO, Emerson Clinical Research Institute; and Andrea Valente, CEO, ClinOne, for the live webinar on Tuesday, September 20, 2022, at 12pm EDT (5pm BST/UK).
For more information, or to register for this event, visit Rare Disease Clinical Trials: Site, Advocate and Technology Insights.
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