Study of Oral HRS-5346 in Adult Patients With Elevated Lipoprotein(a) and High Risk of Cardiovascular Events

StatusNot Yet Recruiting
PhasePhase 2
Started

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Record History

  1. Study First Submitted
This study is designed to evaluate the efficacy and safety of HRS-5346 Tablets in participants with high cardiovascular event risk and elevated Lp(a), and to investigate the appropriate dosage of HRS-5346 Tablets
Trial Details
NCT Number NCT07767513
Lead Sponsor Shandong Suncadia Medicine Co., Ltd.
Conditions
(from sponsor)
Lipoprotein Disorder
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov