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VisitFirst Disease Target for CRISPR Therapy
Cancer • 20%
Rare genetic disorders • 20%
Heart disease • 20%
Neurological disorders • 20%
Other • 20%
Clinical trial registries or official announcements from Regeneron and Mammoth Biosciences
Regeneron Invests $100M in Mammoth for CRISPR-Based Gene Editing Therapies
Apr 25, 2024, 11:30 AM
Regeneron Pharmaceuticals has announced a significant expansion into gene editing by partnering with Mammoth Biosciences. The collaboration aims to research, develop, and commercialize CRISPR-based gene editing therapies for various diseases, targeting multiple tissues and cell types. Regeneron will make a substantial financial commitment, including a $5 million upfront payment and a $95 million equity investment in the CRISPR startup, totaling $100 million. This move is part of Regeneron's broader strategy to deepen its capabilities in genetic medicines, including a recent acquisition in cell therapy and ongoing partnerships focused on developing treatments for rare diseases like transthyretin amyloidosis. Mammoth, which previously developed CRISPR technology for COVID-19 diagnostics, has shifted focus to smaller DNA-cutting enzymes that could be more easily delivered into tissues across the body.
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Cancer • 25%
Alzheimer's Disease • 25%
Cystic Fibrosis • 25%
Sickle Cell Disease • 25%
Transthyretin Amyloidosis • 25%
Sickle Cell Disease • 25%
Cystic Fibrosis • 25%
Muscular Dystrophy • 25%
Liver Disease • 25%
Cystic Fibrosis • 25%
Muscular Dystrophy • 25%
Hemophilia • 25%
Skeletal defects • 33%
Inherited retinal diseases • 33%
Another form of blindness • 34%
Neurological disorders • 25%
Muscular disorders • 25%
Metabolic disorders • 25%
No new types • 25%
Yes, for one therapy • 40%
Yes, for more than one therapy • 20%
No • 40%
1-2 diseases • 33%
3-4 diseases • 33%
5 or more diseases • 33%
Approval • 33%
Request for additional data • 33%
Rejection • 33%