Seoul National University Hospital
Seoul, South Korea
NCT Number: NCT01148368
The purpose of this study is to compare and evaluate the pharmacokinetic characteristics and the safety of fimasartan in renal impairment patients and healthy volunteers.
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Notify Me20 year–65 year
All sexes
Interventional
Phase 1
Seoul, South Korea
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
<Renal impairment patient>
<Healthy volunteer>
Exclusion criteria
single administration of fimasartan 120mg
Time frame: 0, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 32, 48h
AUC, Cmax, Tmax, T1/2, and CL/F of fimasartan
Boryung Pharmaceutical Co., Ltd
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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