Phase 1b Study of VERVE-201 in Patients With Refractory Hyperlipidemia

Recruiting now · Phase 1

Conditions studied: Hypercholesterolemia, Hypertriglyceridemia, Refractory Hyperlipidemia

In brief

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.

Key facts

Study ID
NCT06451770
Run by
Verve Therapeutics, Inc.
People needed
36
Starts
2024-10-30
Expected to finish
2027-12-01
Last updated by the study team
2026-07-17

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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