Clinical Trials Directory

Trials / Completed

CompletedNCT01819779

Clinical Trial to Assess the Pharmacokinetic Characteristics of Lodivixx Tab. 5/160mg in Healthy Male Subjects (N=60)

Clinical Trial to Assess the Pharmacokinetic Characteristics of Lodivixx Tab. 5/160mg in Healthy Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
53 (actual)
Sponsor
Hanlim Pharm. Co., Ltd. · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

To assess the pharmacokinetic characteristics of valsartan and S-amlodipine after single oral administration of Exforge tab. 10/160mg, a combination formulation of valsartan and amlodipine as reference drug and Lodivixx tab

Detailed description

The purpose of this study is to assess the pharmacokinetic characteristics of valsartan and S-amlodipine after single oral administration of Exforge tab. 10/160mg, a combination formulation of valsartan and amlodipine as reference drug and Lodivixx tab. 5/160mg, a combination formulation of valsartan and S-amlodipine as test drug in healthy male adults. Additionally the safety and tolerability of two drugs will be evaluated.

Conditions

Interventions

TypeNameDescription
DRUGExforge tab. 10/160mg
DRUGLodivixx tab. 5/160mg

Timeline

Start date
2013-03-01
Primary completion
2013-05-01
Completion
2013-11-01
First posted
2013-03-28
Last updated
2018-08-03

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01819779. Inclusion in this directory is not an endorsement.