Active, not recruitingPhase 3NCT06712771

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

Studying Homozygous familial hypercholesterolemia

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Key facts

Sponsor
Visirna Therapeutics HK Limited
Intervention
VSA003(drug)
Enrollment
46 enrolled
Eligibility
12 years · All sexes
Timeline
20242027

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06712771 on ClinicalTrials.gov

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