Overview

Fimasartan Achieving SBP Target (FAST) Study

Status:
Completed
Trial end date:
2017-05-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the efficacy and safety of Fimasartan compared to Valsartan and Olmesartan(reference group) in patients with mild to moderate essential hypertension. Patients have 2 weeks of placebo run-in and wash out period, 2 weeks of taking required dose and 4 weeks of taking double dose.
Phase:
Phase 4
Details
Lead Sponsor:
Boryung Pharmaceutical Co., Ltd
Treatments:
Olmesartan
Olmesartan Medoxomil
Valsartan