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Study identifier: NCT05413057 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

An OS to Evaluate Effectiveness and Safety of Fixed-dose Combinations of FMS/AML or FMS/AML/HCTZ

Condition: Hypertension,Essential  ·  Sponsor: Boryung Pharmaceutical Co., Ltd

PhaseN/A
Planned participants20000
Who can joinAll sexes, 19 Years to no upper limit
Healthy volunteersNo

About this study

The main purpose of this observation study is to collect data on the effects and side effects for 12 weeks of the medication administration of the single-pill combinations, which are fimasartan/amlodipine or fimasartan/amlodipine/hydrochlorothiazide, based on fimasartan. (Stage 1). Also, this study will evaluate major cardiovascular events, long-term blood pressure control, and the safety by follow-up of those who consent to the extended study for about 2 years (96 weeks).(Stage 2)

This description comes directly from the study's public registry record.

Talk to the study team

MyungSook Hong  ·  +8227088238  ·  mshong@boryung.co.kr

JiYeon Kim  ·  +8227088128  ·  jiyeonkim@boryung.co.kr

Always discuss trial participation with your own doctor first.

Locations (1)

Seoul National University Bundang HospitalSeoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT05413057