Trials / Completed
CompletedNCT01928628
Phase III Clinical Study to Evaluate the Efficacy and Safety of the Combination of Lercanidipine/Valsartan in Hypertensive Patients
A Randomized, Multicenter, Parallel Design Phase III Clinical Study to Evaluate the Efficacy and Safety of the Combination of Lercanidipine/Valsartan in Hypertensive Patients Who Are Not Adequately Controlled on Lercanidipine 10mg Monotherapy.
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 449 (actual)
- Sponsor
- LG Life Sciences · Industry
- Sex
- All
- Age
- 20 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to compare and assess the efficacy and the safety of the combination agent of Lercanidipine and Valsartan and monotherapy of Lercanidipine alone in patients with essential hypertension
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lercanidipine 10mg | |
| DRUG | Lercanidipine10mg /Valsartan 80mg | |
| DRUG | Lercanidipine 10mg /Valsartan 160mg | |
| DRUG | Lercanidipin 10mg Placebo | |
| DRUG | Lercanidipine10mg /Valsartan 80mg Placebo | |
| DRUG | Lercanidipine 10mg /Valsartan 160mg Placebo |
Timeline
- Start date
- 2012-05-01
- Primary completion
- 2013-04-01
- First posted
- 2013-08-27
- Last updated
- 2013-08-28
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01928628. Inclusion in this directory is not an endorsement.