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
| Type | Name | Description |
|---|---|---|
| DRUG | Exforge tab. 10/160mg | |
| DRUG | Lodivixx 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.