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CompletedNCT07382778VICTORYUpdated Feb 3, 2026

Efficacy and Safety of Livalozet® in Hypercholesterolemic Patients With and Without Diabetes

An observational study in Hypercholesterolemia, sponsored by JW Pharmaceutical. Completed at 1 site in South Korea. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-02-03.

Sponsored by JW Pharmaceutical · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,538
Ages
19 Years and older
Sex
All
01

Study summary

A Multi-center, Open-label, Observational Study to Compare and Evaluate the Efficacy and Safety of Livalozet® according to the Presence or Absence of Diabetes Mellitus in Hypercholesterolemia Patients

Read the detailed description

A Multi-center, Open-label, Observational Study

02

Conditions studied

  • Hypercholesterolemia

Keywords

  • hypercholesterolemia
  • Diabetes Mellitus
  • Low Density Lipoprotein Cholesterol
  • Lipid Profile
  • Observational Study
03

In context

Hypercholesterolemia

1,238 studies on the registry are indexed under Hypercholesterolemia; 109 are open to participants now.

This study's enrollment of 1,538 is above the median of 800 across 185 observational studies indexed under Hypercholesterolemia.

Browse Hypercholesterolemia studies →

Lead sponsor

JW Pharmaceutical is the lead sponsor of 75 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Participants will be selected from adult patients aged 19 years or older diagnosed with hypercholesterolemia who are receiving routine clinical care at participating centers. The population includes both patients with and without diabetes mellitus, reflecting real-world treatment practices. Eligible patients must provide informed consent to participate in this observational study.

Inclusion criteria

  • Men and women aged ≥19 years
  • Diagnosed with hypercholesterolemia
  • LDL-C level meets cardiovascular/cerebrovascular risk group classification
  • Willing to participate for 12 months
  • Provided written informed consent

Exclusion criteria

Exclusion Criteria:

- Contraindications to Livalozet®

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,538 participants (actual)
Target follow-up
48 Weeks
Patient registry
Yes

Groups and cohorts

  • Hypercholesterolemia with Diabetes Mellitus

    Observational study; LDL-C and lipid parameters will be followed; no intervention assigned.

  • Hypercholesterolemia without Diabetes Mellitus

    Observational study; LDL-C and lipid parameters will be followed; no intervention assigned.

06

What researchers measure

Primary outcomes

  1. Percent change from baseline in LDL-C level at Week 24

    Time frame: From enrollment to the end of treatment at 24 weeks

07

Study locations

1 site
  • Seoul National University Bundang Hospital
    Seongnam-si, Gyeonggi-do 13496, South Korea
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07382778
Lead sponsor
JW Pharmaceutical
Responsible party
Sponsor
First posted
Feb 3, 2026
Start date
Oct 19, 2022
Primary completion
Jun 13, 2025
Completion
Jun 13, 2025
Last update
Feb 3, 2026

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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