drugset / Trial / NCT06712771

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

NCT06712771 ↗

Phase 3 Active not recruiting 46 enrolled Visirna Therapeutics HK Limited
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2024-11-27
Primary completion
2025-12-31
Completion
2027-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject VSA003 Unknown — Subcutaneous