FDA Approves YolTech’s Application for YOLT-101 to Treat Heterozygous Familial Hypercholesterolemia

The U.S. Food and Drug Administration (FDA) has approved YolTech’s investigational new drug application for YOLT-101, a treatment targeting heterozygous familial hypercholesterolemia (HeFH). The approval marks a significant step in the development of therapies aimed at addressing this genetic condition, which is characterized by elevated cholesterol levels and an increased risk of cardiovascular disease.

Heterozygous familial hypercholesterolemia affects approximately one in 250 individuals globally and results from inherited mutations that impair the body’s ability to regulate cholesterol levels. YOLT-101 is designed to address these underlying genetic factors, offering potential therapeutic benefits for patients living with HeFH. With the FDA’s clearance, YolTech can now proceed with clinical trials to evaluate the safety and efficacy of YOLT-101 in treating this condition.

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Source: GO-AI-ne1

Date: June 9, 2025

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Author

Mark Chiang