Post-Authorization Long-term Safety Surveillance on Antihypertensive Treatment With Kanarb® (Fimasartan)

NCT02385721 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 601

Last updated 2019-03-06

Study results available
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Summary

Evaluated the incidence and characteristics of adverse events during the treatment for Kanarb tablet.

Conditions

  • Essential Hypertension

Sponsors & Collaborators

  • Boryung Pharmaceutical Co., Ltd

    lead INDUSTRY

Principal Investigators

  • Myung Sook Hong · Boryung Pharmaceutical Co., Ltd

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2017-07-31
Completion
2018-04-30

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02385721 on ClinicalTrials.gov