Verve Gets OK from FDA to Test Gene Editing, Expands Lilly Relationship
- Posted by ISPE Boston
- On November 2, 2023
Verve Therapeutics has announced the lifting of the clinical hold and clearance of its Investigational New Drug (IND) application by the FDA to conduct a clinical trial evaluating Verve-101 for the treatment of heterozygous familial hypercholesterolemia (HeFH). Verve-101 is an investigational, in vivo base editing medicine designed to be a single-course treatment that inactivates the […]
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