Genome Editing at the Turning Point—Bringing CRISPR to Clinical Reality
Register Now Laura Sepp-Lorenzino, PhD Former CSO Intellia Therapeutics View Bio Panelist Laura Sepp-Lorenzino, PhD Laura Sepp-Lorenzino, PhD, is scientific advisor and former chief scientific officer at Intellia Therapeutics, a clinical-stage genome editing company developing potential curative CRISPR-based medicines. Previously, she was vice president and head of Nucleic Acid Therapies at Vertex Pharmaceuticals and part of External Innovation. She also held roles at Alnylam Pharmaceuticals and Merck & Co. In addition, she currently serves as the director of the American Society of Gene and Cell Therapy (ASGCT). Close Shengdar Tsai, PhD Associate Member, Department of Hematology St. Jude Children’s Research…
Kathy Vuksanaj ·
Laura Sepp-Lorenzino, PhD
Former CSO Intellia Therapeutics
Shengdar Tsai, PhD
Associate Member, Department of Hematology St. Jude Children’s Research Hospital
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Complex biologics such as bifunctional antibodies are opening new therapeutic possibilities in oncology, but these molecules present CRISPR is now a household term. Stories of genome editing therapies like Casgevy and Baby KJ have been headlines in our inboxes for years. Despite those cases, and the optimism they bring, genome editing has had significant challenges moving into the clinic.
This GEN Live show will bring together a panel of leading experts to break down the latest advances, innovations, and challenges shaping genome editing. The discussion will cover a lot of bases: CRISPR breakthroughs, emerging gene editing platforms, clinical trial milestones, regulatory shifts, access, off-target effects and safety considerations, and the growing role of large-scale population genomics in guiding precision therapies. Please join us to learn more and—because we plan to take questions from the audience—please bring your questions for our panelists, too!