Trials / Completed
CompletedNCT01785472
Efficacy and Safety of LCZ696 in Comparison to Olmesartan in Asian Patients With Essential Hypertension
A Multi-center, Randomized, Double-blind, Active-controlled, 8-week Study to Evaluate the Efficacy and Safety of LCZ696 in Comparison to Olmesartan in Patients With Essential Hypertension
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 1,438 (actual)
- Sponsor
- Novartis Pharmaceuticals · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will assess the efficacy and safety of multiple doses of LCZ696 compared to olmesartan in Asian patients with essential hypertension
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | LCZ696 | LCZ696 200 mg tablet |
| DRUG | Olmesartan | Olmesartan 20 mg capsule |
| DRUG | Placebo of LCZ696 | Placebo tablet of LCZ696 200 mg once daily |
| DRUG | Placebo of Olmesartan | Placebo capsule of olmesartan 20 mg once daily |
Timeline
- Start date
- 2013-04-01
- Primary completion
- 2014-08-01
- Completion
- 2014-08-01
- First posted
- 2013-02-07
- Last updated
- 2016-12-29
- Results posted
- 2015-09-04
Locations
50 sites across 7 countries: China, Hong Kong, Philippines, Singapore, South Korea, Taiwan, Thailand
Source: ClinicalTrials.gov record NCT01785472. Inclusion in this directory is not an endorsement.