Efficacy, Safety and Pharmacodynamic/Pharmacokinetic Study of Fimasartan (BR-A-657•K)

PHASE2CompletedINTERVENTIONAL
Enrollment

81

Participants

Timeline

Start Date

April 30, 2005

Primary Completion Date

June 30, 2006

Study Completion Date

June 30, 2006

Conditions
Essential Hypertension
Interventions
DRUG

Placebo

Placebo

DRUG

Fimasartan (BR-A-657•K) 20 mg

Fimasartan 20 mg, 1 tablet + placebo, 2 tablets

DRUG

Fimasartan (BR-A-657•K) 60 mg

Fimasartan 20 mg, 1 tablet + 40 mg, 1 tablet + placebo 1 tablet

DRUG

Fimasartan (BR-A-657•K) 180 mg

Fimasartan 20 mg, 1 tablet + 80 mg, 1 tablet + 80 mg 1 tablet

All Listed Sponsors
lead

Boryung Pharmaceutical Co., Ltd

INDUSTRY