Trials / Completed
CompletedNCT01599104
Efficacy and Safety of LCZ696 in Comparison to Olmesartan in Japanese 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 Japanese Patients With Essential Hypertension
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 1,161 (actual)
- Sponsor
- Novartis Pharmaceuticals · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
This study assessed the efficacy of LCZ696 in Japanese patients with essential hypertension
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | LCZ696 | 200 mg (one tablet) or 400 mg (2 tablets of 200mg) once daily |
| DRUG | Olmesartan | Olmesartan 20 mg capsule one daily |
| DRUG | Placebo | Placebo to LCZ696 or Olmesartan |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2013-04-01
- Completion
- 2013-04-01
- First posted
- 2012-05-15
- Last updated
- 2015-10-16
- Results posted
- 2015-08-06
Locations
61 sites across 1 country: Japan
Source: ClinicalTrials.gov record NCT01599104. Inclusion in this directory is not an endorsement.