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Clinical Trials in South Korea / NCT06643130
Recruiting Phase 3

Evaluate the Efficacy and Safety of Co-administration of JW0104+C2402 in Patients With Hypertension and Dyslipidemia

NCT06643130 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 3
Started
2024-12-02
Last updated
2025-09-09

Condition(s) studied

HypertensionDyslipidemia

Investigational drug(s) / intervention(s)

JW0104+C2402JW0104+C2403C2402

JW0104+C2402: For 8 weeks(PO (Per Oral), QD)

JW0104+C2403: For 8 weeks(PO, QD)

C2402: For 8 weeks(PO, QD)

Study summary

A Multi-center, Randomized, Double-blind, Parallel, Phase Ⅲ Clinical Trial to Evaluate the Efficacy and Safety of Co-administration of JW0104+C2402 in Patients with Hypertension and Dyslipidemia

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with hypertension and dyslipidemia Exclusion Criteria: * The subject not meet the specified msBP and LDL-C level

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gangdong Sacred Heart Hospital Seoul South Korea Recruiting

More JW Pharmaceutical trials in South Korea

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06643130 on ClinicalTrials.gov ↗ ← All trials in South Korea