The brief
- YOLT-101, a PCSK9 base editor, showed 50% LDL-C and 76% PCSK9 reduction in Phase I trials.
- Raised $115M across Series B and C funding through May 2026.
- First in vivo base editor for cardiovascular disease to enter clinical trials in China and the U.S.
Technical approach
Base editing, not cutting
Single-letter DNA changes without double-strand breaks
Base editing converts one DNA letter to another without cutting both DNA strands, reducing immune activation and off-target edits compared to CRISPR cutting.
In vivo delivery
Editing happens inside living cells, in one dose
LNP delivery carries base-editing machinery to liver cells intravenously. Cells retain the edit permanently.
PCSK9 disruption
Permanently lowers cholesterol
Disrupting PCSK9 in liver cells increases LDL clearance, mimicking drugs but from one treatment.
