Fierce Biotech April 25, 2024
Regeneron is signing another major deal in gene editing—and, this time, it’s Mammoth.
Mammoth Biosciences, that is. The companies will collaborate on in vivo CRISPR-based gene editing therapies in a deal worth $100 million upfront plus $370 million in milestones per target, according to a Thursday press release.
Regeneron will bring its adeno-associated viral vectors (AAVs) that use antibody-based targeting to deliver genetic medicine payloads. Mammoth’s ultracompact nucleases and associated gene editing systems will complement the delivery mechanism.
“After years spent developing our next-generation delivery approaches, we are eager to combine them with Mammoth’s gene editing systems to better match payload, delivery system and disease type,” said Christos Kyratsous, Ph.D., senior vice president and co-head of Regeneron Genetic Medicines.
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