The Next Generation of Gene Editing Therapeutic Technologies

9:00 AM - 10:00 AM (EDT), Thursday, June 8, 2023 ・ Session Room 206AB
Genome Editing therapeutic platforms (e.g. zinc finger nucleases, TALENs, meganucleases) have existed for 25+ years. Since the advent of the CRISPR/Cas9 (“CRISPR 1.0”) Platform, the biomedical research community has developed a Base Editing Platform (“CRISPR 2.0”) and a Prime Editing (“CRISPR 3.0”) – both of which are more precise in their edits and more versatile in treating different types of mutations. In addition, the community has developed other innovations that include RNA Editing Platforms (making temporary rather than permanent gene editing possible) and a Gene Writing Platform (that has the potential to be even more versatile). We seek to provide an overview of next generation platforms with key innovators as they seek to advance the science despite private market, public market, regulatory, and reimbursement challenges.
Moderator
Founding/Managing Partner
Bioluminescence Ventures
Speakers
Chief Medical Officer
Beam Therapeutics
CSO
Tessera Therapeutics
Chief Scientific Officer
Prime Medicine
Chief Executive Officer
Ensoma