Discover how Natera and ENYO Pharma accelerated clinical trial enrollment with a data-informed approach to Alport Syndrome patient recruitment.
This real-world case study will explore the successful utilization of Natera’s proprietary Clinical Trial Support service, including:
ENYO Pharma will provide their perspective on:
Bryce Powerman is a healthcare professional, patient advocate, and survivor of DOCK8 deficiency, an ultra-rare primary immunodeficiency. Diagnosed at the National Institutes of Health (NIH) after a lengthy diagnostic odyssey, he eventually underwent a life-saving pediatric bone marrow transplant in a first-in-human trial. Bryce serves as the Director of Business Development at Natera, a leading genetic testing company in the renal space, where he champions early genetic testing and proactive education as critical tools for improving patient outcomes.
Pete Leone is a seasoned life sciences entrepreneur with over 30 years of success in biopharmaceuticals and medical devices, spanning public and private sectors. He has played a key role in high-value deals, such as a $1.7 billion potential agreement between Bicycle Therapeutics and Genentech and a $3.7 billion partnership for hepatitis B therapies at Arrowhead Pharmaceuticals. Pete has founded three venture backed companies, including Mersana Therapeutics, and has extensive experience in orphan diseases, oncology and other therapeutic areas. A Dartmouth College and Stanford MBA graduate, he has also contributed as a board member for corporate and nonprofit organizations like SeromYx and NPH USA.
Libby Valenti is a board-certified genetic counselor with over two decades of clinical experience in genetic counseling. Currently, she serves as the Director of Clinical Strategy and Development at Natera, where she leads Clinical Trial Support programs, including patient matching. Her deep understanding of patient needs and clinical nuances has been instrumental in creating a robust framework that aligns patients with the most suitable clinical trials. Her commitment to personalized care is a key driver in successfully connecting patients with new treatment avenues and advancing medical research in the field of genetics.