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Active Not RecruitingNCT07185776

A Study of HRS-5632 in Adult Participants With Elevated Lipoprotein(a) at High Risk for Cardiovascular Events

A Randomized, Double-Blind, Placebo-Controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of HRS-5632 Injection in Adult Patients at High Risk of Cardiovascular Events With Elevated Lipoprotein(a)

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
203 (actual)
Sponsor
Fujian Shengdi Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to evaluate the efficacy and safety of HRS-5632 in adult participants with elevated Lipoprotein(a) (Lp(a)) at high risk for cardiovascular events.

Conditions

Interventions

TypeNameDescription
DRUGHRS-5632 InjectionHRS-5632 injection.
DRUGHRS-5632 Injection PlaceboHRS-5632 injection placebo.

Timeline

Start date
2025-10-21
Primary completion
2027-04-01
Completion
2027-10-01
First posted
2025-09-22
Last updated
2026-03-05

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07185776. Inclusion in this directory is not an endorsement.