drugset / Trial / NCT03156842

Combination of Fimasartan/Amlodipine/Rosuvastatin in Patients With Essential Hypertension and Dyslipidemia

NCT03156842

Phase 3 Completed 138 enrolled Boryung Pharmaceutical Co., Ltd
RandomizedParallel-groupTriple-blindTreatment

Summary

The objective of this clinical study is to evaluate the efficacy and safety by comparing the fimasartan/amlodipine/rosuvastatin treatment group to the fimasartan/amlodipine treatment group and the fimasartan/rosuvastatin treatment group respectively at Week 8 in patients with essential hypertension and dyslipidemia who fail to respond to the fimasartan monotherapy.

Timeline

Start
2017-05-29
Primary completion
2018-12-07
Completion
2018-12-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Amlodipine Other / unclassified 10 mg
Comparator Fimasartan Small molecule 60 mg
Comparator Rosuvastatin Small molecule 20 mg