drugset / Trial / NCT02620306

A Randomized, Double-blind, Active Control, Parallel Group, Titration, Multicenter Study to Evaluate the Efficacy and Safety of Fimasartan

NCT02620306

Phase 3 Completed 351 enrolled Boryung Pharmaceutical Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the Efficacy and Safety of Fimasartan in patients with hypertensive diabetic chronic kidney disease.

Timeline

Start
2016-02-11
Primary completion
2019-12-23
Completion
2022-05-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Fimasartan Small molecule 60 mg
Subject Fimasartan Small molecule 120 mg
Comparator Losartan Other / unclassified 50 mg
Comparator Losartan Other / unclassified 100 mg