Status: Recruiting
Phase 1b Study of VERVE-201 in Patients With Refractory Hyperlipidemia
VT-20101 is an Open-label, Phase 1b, Single-ascending dose study that will evaluate the safety of VERVE-201 administered to patients with Refractory Hyperlipidemia. VERVE-201 uses base-editing technology designed to inactivate the expression of the ANGPTL3 gene in the liver and lower circulating low-density lipoprotein cholesterol (LDL-C) and triglycerides. This study is designed to determine the safety and pharmacodynamic profile of VERVE-201 in this patient population.
Participants needed: 36
Trial details
Phase: Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: Verve Therapeutics, Inc.Updated: Apr 28, 2026Locations: 10
Eligibility criteria
Refractory hypercholesterolemia [+1]
Active or history of chronic liver disease [+2]