Chonbuk National University Hospital
Jeonju, Jeollabuk-do, 561-712, South Korea
NCT Number: NCT02212756
Phase I clinical study to evaluate DW1029M influence the pharmacokinetic profiles of Metformin after oral administration in healthy male volunteer
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Notify Me19 year–55 year
Male
Interventional
Phase 1
Jeonju, Jeollabuk-do, 561-712, South Korea
A Randomized, open-label, multiple-dose, crossover phase I clinical study to evaluate DW1029M influence the pharmacokinetic profiles of Metformin after oral administration in healthy male volunteer
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Metformin 500mg 1 Tablet and DW1029M 300mg 2 Tablets b.i.d. for 7days
Other names: Concomitant of DW1029M 1200mg and Metformin 1000mg
Metformin 500mg b.i.d. for 7 days
Other names: Diabex tab. 500mg
Time frame: 1d/15d, 5d/19d, 6d/20d : Predose(0,morning), 7d/21d: Predose(0), 1, 2, 3, 3.5, 4, 4.5, 5, 5.5, 6, 8, 12 h
Maximum of Concentration(Cmax), Area Under Plasma Concentration-Time Curve(AUC)
Time frame: 1d/15d, 5d/19d, 6d/20d: Predose(0, Morning), 7d/21d: Predose(0), 1, 2, 3, 3.5, 4, 4.5, 5, 5.5, 6, 8, 12 h
Maximum drug concentration time(Tmax), Half-time(t1/2), Apparent renal clearance(CL/F), Apparent volume of distribution(Vd/F), Fluctuation[(Css,max-Css,min)/Css,av], Swing[(Css,max-Css,min)/Css,min]
Dong Wha Pharmaceutical Co. Ltd.
Industry
A Randomized, Open-label, Multiple-dose, Crossover Phase I Clinical Study to Evaluate DW1029M Influence the Pharmacokinetic Profiles of Metformin After Oral Administration in Healthy Male Volunteer
Acronym: PMD
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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