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ACTIVE NOT RECRUITING
NCT06712771
PHASE3

A Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of VSA003 in Chinese HoFH Patients

Sponsor: Visirna Therapeutics HK Limited

View on ClinicalTrials.gov

Summary

Significant reduction in ANGPLT3 levels is expected to reduce plasma LDL-C and TG levels and may lead to the reduction of risk of coronary heart disease and cardiovascular events associated with hypertriglyceridemia and LDL-C in subjects with persistent dyslipidemia. In this clinical study, the efficacy and safety of VSA003, an RNAi-based therapeutic targeting ANGPTL3, will be evaluated in subjects with HoFH.

Official title: A Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of VSA003 Injection in Chinese Adolescents and Adults With Homozygous Familial Hypercholesterolaemia (HoFH)

Key Details

Gender

All

Age Range

12 Years - Any

Study Type

INTERVENTIONAL

Enrollment

46

Start Date

2024-11-27

Completion Date

2027-12-30

Last Updated

2026-05-05

Healthy Volunteers

No

Interventions

DRUG

VSA003

subcutaneous injections

DRUG

Placebo

subcutaneous injections

Locations (1)

Peking Union Medical College Hospital

Beijing, China