Drug Drug Interaction
Conditions
Brief summary
This is A two-arm, open-label, single-sequence, multiple oral dosings, crossover study to evaluate the safety and the pharmacokinetic interaction of DWC202313 and DWC202314 in healthy adult volunteers.
Interventions
DRUGDWC202313
Experimental Drug 1
DRUGDWC202314
Experimental Drug 2
Sponsors
Daewoong Pharmaceutical Co. LTD.
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* over 19 year old
Exclusion criteria
* Galactose intolerance * Lapp lactase deficiency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cmax,ss of DWC202313 and DWC202314 | Up to 14 days |
| AUCt,ss of DWC202313 and DWC202314 | Up to 14 days |
Secondary
| Measure | Time frame |
|---|---|
| t1/2 of DWC202313 and DWC202314 | Up to 14 days |
| CLss/F of DWC202313 and DWC202314 | Up to 14 days |
| Tmax,ss of DWC202313 and DWC202314 | Up to 14 days |
| PTF of DWC202313 and DWC202314 | Up to 14 days |
| Vdss/F of DWC202313 and DWC202314 | Up to 14 days |
| Cmin,ss of DWC202313 and DWC202314 | Up to 14 days |
Countries
South Korea
Contacts
Primary ContactSeung-Hyun Kang, MD, Ph D
Outcome results
None listed