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Gene-editing drug VERVE-102 shows promise in reducing bad cholesterol in early trial

The gene-editing drug VERVE-102 has demonstrated safety and efficacy in reducing bad cholesterol by 62% in a small Phase I trial involving 35 patients. The findings suggest potential long-term benefits in lowering cardiovascular disease risk, although further data is needed for conclusive results.

An experimental gene-editing therapy, VERVE-102, has shown positive results in a Phase I safety trial aimed at lowering bad cholesterol after a single infusion. Researchers published interim results this week from a study involving 35 patients in the New England Journal of Medicine. The findings indicate that VERVE-102 is safe, with no serious adverse events reported, although a mild increase in a liver enzyme was noted, suggesting minor liver injury. Participants receiving the highest dose experienced a 62% reduction in low-density lipoprotein (LDL) cholesterol, dropping to a mean of 78 mg per deciliter. This level of reduction could potentially lower the risk of cardiovascular disease significantly if maintained over a long period. The trial has provided up to 18 months of follow-up data, showing sustained LDL reductions across all subgroups.

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Original Headline

Bad cholesterol slashed 62% by single dose of gene-editing drug in small trial

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Gene-editing drug VERVE-102 shows promise in reducing bad cholesterol in early trial