Clinical Trials Directory

Trials / Completed

CompletedNCT04322266

A Study to Compare the Pharmacokinetics, Safety and Tolerability Between Fixed-Dose Combination and Co-Administration of HGP0904, HGP0608 and HCP1306 Tablets in Healthy Male Subjects.

An Open-Label, Randomized, Single-Dose Crossover Study to Compare the Pharmacokinetics, Safety and Tolerability Between Fixed-Dose Combination and Co-Administration of HGP0904, HGP0608 and HCP1306 Tablets in Healthy Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
61 (actual)
Sponsor
Hanmi Pharmaceutical Company Limited · Industry
Sex
Male
Age
19 Years – 45 Years
Healthy volunteers
Accepted

Summary

An Open-Label, Randomized, Single-Dose Crossover Study to Compare the Pharmacokinetics, Safety and Tolerability Between Fixed-Dose Combination and Co-Administration of HGP0904, HGP0608 and HCP1306 Tablets in Healthy Male Subjects

Conditions

Interventions

TypeNameDescription
DRUGHCP1701Ezetimibe / Rosuvastatin / Amlodipine / Losartan potassium
DRUGHCP1306Ezetimibe /Rosuvastatin
DRUGHGP0904Amlodipine
DRUGHGP0608Losartan potassium

Timeline

Start date
2018-12-21
Primary completion
2019-02-13
Completion
2019-02-13
First posted
2020-03-26
Last updated
2020-03-26

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04322266. Inclusion in this directory is not an endorsement.