Clinical Trials Center, Seoul National University Hospital
Seoul, 03080, South Korea
NCT Number: NCT02954822
A randomized, open-label, multiple dosing, three treatment, three period, two sequence clinical trial to investigate the pharmacokinetic/pharmacodynamic drug-drug interaction of evogliptin 5 mg and glimepiride 4 mg after oral administration in healthy male subjects
Looking for future studies?
Notify Me19 year–45 year
Male
Interventional
Phase 1
Seoul, 03080, South Korea
A randomized, open-label, multiple-dose, three-treatment, three-period, two-sequence, crossover study
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Evogliptin 5mg will be administered for 7days and then glimepiride 4mg will be added on and administered with Evogliptin 5mg for 2 days. After the washout period for 10 days, Glimepiride 4mg will be administered for 2 days.
Glimepiride : Glimepiride 4mg QD
Evogliptin + Glimepiride : Evogliptin 5mg QD + Glimepiride 4mg QD
Other names: Suganon, Amaryl
After 2 days of administration of Glimepiride 4mg follows the 10-day washout period. Afterwards Evogliptin 5mg will be administered for 7days and then glimepiride 4mg will be added on and administered with Evogliptin 5mg for 2 days.
Other names: Suganon, Amaryl
Time frame: 3 weeks
area under the concentration-time curve
Looking for future studies?
Notify MeDong-A ST Co., Ltd.
Industry
A Randomized, Open-label, Multiple Dosing, Cross-over Clinical Trial to Investigate the Pharmacokinetic/Pharmacodynamic Drug-drug Interaction of Evogliptin 5mg and Glimepiride 4mg After Oral Administration in Healthy Male Subjects
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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