Agenda Details

Learn more about sessions and presentations at the 26th Annual Meeting

Detailed Program

N=1 and Beyond: Small Patient Studies to Enable New Therapies for Genetic Disorders

Rapidly evolving advances in gene and cell therapy have led to scientific democratization of therapeutic possibilities to treat genetic disorders, even for N=1 indications. This session will overview selected aspects of developing treatments for ultra rare disorders, including clinical examples, regulatory considerations, and models to support the development of gene therapy for orphan indications. The presentation will be followed by a panel discussion led by clinical and regulatory experts, with audience engagement encouraged.

Session Details

Co-Chair

Rebecca Ahrens-Nicklas, PhD, MD. Children's Hospital of Philadelphia, Philadelphia, PA

Co-Chair

Gerald S.. Lipshutz, MD. University of California, Los Angeles, Los Angeles, CA

From Mila to Millions: Opportunities for Individualized Medicines

Julia Vitarello. Mila's Miracle Foundation, Longmont, CO

N=1 and Milosen

Timothy Yu, MD, PhD. Boston Children's Hospital, Boston, MA

Bespoke Program

PJ Brooks, PhD. NIH / NCATS, MD

Panelist - N=1 and Beyond: Small Patient Studies to Enable New Therapies for Genetic Disorders

Kevin Whittlesey. Dark Horse Consulting Group, Walnut Creek, CA

Panelist - N=1 and Beyond: Small Patient Studies to Enable New Therapies for Genetic Disorders

Amanda Haidet-Phillips, PhD. Sarepta Therapeutics, Columbus, OH

Panelist - N=1 and Beyond: Small Patient Studies to Enable New Therapies for Genetic Disorders

Petra Kaufmann, MD. Affinia Therapeutics, Inc., MD

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