A Study of VERVE-102 in Patients With Familial Hypercholesterolemia or Premature Coronary Artery Disease

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

OPEN-LABEL, PHASE LB, SINGLE ASCENDING DOSE STUDY TO EVALUATE THE SAFETY OF VERVE-102 ADMINISTERED TO PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR PREMATURE CORONARY ARTERY DISEASE WHO REQUIRE ADDITIONAL LOWERING OF LOW-DENSITY LIPOPROTEIN CHOLESTEROL

Intervention/treatment:
VERVE-102
Medical condition:
HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Protocol code:
VT-10201
Control number:
283095
Status:
Recruiting
Approved:
February 22, 2024
Trial phase:
Phase 1
For more information:
ClinicalTrials.gov - NCT06164730
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 70 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
Role
CONTACT
Phone:
317-615-4559
Name
Physicians interested in becoming principal investigators please contact
Role
CONTACT
Sponsor
VERVE THERAPEUTICS, INC., A WHOLLY OWNED SUBSIDIARY OF ELI LILLY AND COMPANY

Locations

Clinical Study Center
Chicoutimi
Recruiting
Clinical Study Center
Hamilton
Recruiting
Clinical Study Center
Montreal
Recruiting
Clinical Study Center
Québec
Recruiting
Clinical Study Center
Toronto
Recruiting
Clinical Study Center
Vancouver
Recruiting
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