Kyungpook National University Hospital
Daegu, Samdeok-dong, 2-ga 50, Samdeok-dong, 2-ga 50 Jung-gu, 700-721, South Korea
NCT Number: NCT02250833
A randomized, open-label, single-dose, two-period, two-way, crossover study to compare the pharmacokinetics and safety CKD-828 (Fixed Dose Combination Tablet) to coadministration telmisartan and s-amlodipine in health volunteers.
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Notify Me19 year–55 year
Male
Interventional
Phase 1
Daegu, Samdeok-dong, 2-ga 50, Samdeok-dong, 2-ga 50 Jung-gu, 700-721, South Korea
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Telmisartan 80mg /S-Amlodipine 5mg(FDC) Tablet, Oral, Once Daily
Other names: Telminuvo
Other names: Micardis
Other names: Anydipine s
Time frame: up to 168 hours post dose
Time frame: up to 168 hours post dose
Time frame: up to 168 hours post dose
Time frame: up to 168 hours post dose
Time frame: up to 168 hours post dose
Time frame: up to 31days post dose
Chong Kun Dang Pharmaceutical
Industry
To Compare the Pharmacokinetics and Safety of CKD-828 80/5mg to Coadministration of Telmisartan 80mg and S-amlodipine 5mg in Healthy Male Volunteers
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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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