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FDA places clinical hold on Verve Therapeutics gene-editing treatment

Summary by Ground News
Verve Therapeutics says its experimental gene-editing treatment for a common form of heart disease was placed on clinical hold by the FDA. The Cambridge, Mass.-based biotech had submitted a request to the FDA in October to allow participants in the U.S. to receive the CRISPR-based treatment.

2 Articles

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FDA places clinical hold on Verve Therapeutics gene-editing treatment

The therapy, VERVE-101, uses a form of CRISPR to treat familial hypercholesterolemia, a relatively common form of high cholesterol.

·Boston, United States
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GEN - Genetic Engineering and Biotechnology News…GEN - Genetic Engineering and Biotechnology News…

FDA Places Clinical Hold on Verve's Cardio Base Editing Therapy

FDA places clinical hold on Verve Therapeutics' IND application for lead candidate VERVE-101 for Heterozygous Familial Hypercholesterolemia.

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STAT broke the news in Boston, United States on Monday, November 7, 2022.
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