drugset / Trial / NCT02466490

Efficacy and Safety of Fimasartan Alone or Combined With HCTZ in Mexican Patients With Essential Hypertension

NCT02466490

Phase 3 Completed 272 enrolled Stendhal Americas, S.A.
RandomizedParallel-groupOpen-labelTreatment

Summary

Fimasartan (FMS) is an AT1 receptor antagonist indicated for once a day administration, currently approved for the treatment of essential hypertension in Corea and Mexico. As the safety and efficacy of FMS was initially demonstrated in Korea only, it was necessary to address the potential for ethnic factors to have an effect on the drug´s efficacy and safety in the Mexican population. To address this need, a cohort of 272 Mexican subjects with grades 1-2 essential hypertension were sequentially treated on a treat to target basis (target: sitting Diastolic Blood Pressure (sDBP) \<90 mmHg) with 60 mg FMS once a day (8 weeks), either 120 mg FMS or 60 mg FMS+12.5 mg HCTZ once a day (randomized 4 week treatment period) and 120 mg FMS once a day (during 12 weeks) for a total treatment period of 24 weeks.

Timeline

Start
2013-04
Primary completion
2014-02
Completion
2014-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fimasartan Small molecule 60 mg Oral
Subject Fimasartan Small molecule 120 mg Oral
Subject Hydrochlorothiazide Unknown 12.5 mg Oral