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

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JW Pharmaceutical

Status

Completed

Conditions

Hypercholesterolemia

Study type

Observational

Funder types

Industry

Identifiers

NCT07382778
JW21403

Details and patient eligibility

About

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

Full description

A Multi-center, Open-label, Observational Study

Enrollment

1,538 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

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

- Contraindications to Livalozet®

Trial design

1,538 participants in 2 patient groups

Hypercholesterolemia with Diabetes Mellitus
Description:
Observational study; LDL-C and lipid parameters will be followed; no intervention assigned.
Hypercholesterolemia without Diabetes Mellitus
Description:
Observational study; LDL-C and lipid parameters will be followed; no intervention assigned.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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