Contact SCGE




Clinical Trial Report

Gene Therapy Trial Report

Summary

A Study of VERVE-101 in Patients With Familial Hypercholesterolemia and Cardiovascular Disease


NCTID NCT05398029 (View at clinicaltrials.gov)
Description
Indication Familial Hypercholesterolemia, Heterozygous
Compound Name VERVE-101
Sponsor Verve Therapeutics, Inc.
Funder Type Industry
Status
Active not recruiting
Enrollment Count 44

Therapy Information


Target Gene/Variant PCSK9
Therapy Type Gene editing
Therapy Route In-vivo
Mechanism of Action Gene inactivation
Route of Administration Intravenous
Drug Product Type MRNA, LNP
Target Tissue/Cell Hepatocyte
Delivery System Lipid encapsulation
Vector Type LDLR
Editor Type ABE8.8m
Dose 1 0.1 mg/kg
Dose 2 0.3 mg/kg
Dose 3 0.45 mg/kg
Dose 4 0.6 mg/kg
Dose 5

Study Record Dates


Current Stage Phase1
Submit Date 2022-05-19
Completion Date 2024-12
Last Update 2024-04-08

Participation Criteria


Eligible Age 18 Years - 75 Years
Standard Ages Adult, Older adult
Eligible Sex ALL

Locations


No.of Trial Sites 3
Locations New Zealand,United Kingdom

Regulatory Information


Has US IND True
Recent Updates Update given during ASGCT 2024 on the off-target assessments done by VERVE

Resources/Links