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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03005223
Other study ID # DW_DWJ1366005
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received December 26, 2016
Last updated February 14, 2017
Start date January 4, 2017
Est. completion date June 2017

Study information

Verified date February 2017
Source Daewoong Pharmaceutical Co. LTD.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized, open label, crossover study to explore drug-drug interactions between DWC20155 / DWC20156 and DWC20163 in Healthy Volunteers


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 52
Est. completion date June 2017
Est. primary completion date May 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 19 Years to 45 Years
Eligibility Inclusion Criteria:

- Accepts healthy volunteers

Exclusion Criteria:

- Who has allergy to investigational product

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Co-administration of DWC20155/DWC20156

DWC20163


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Daewoong Pharmaceutical Co. LTD.

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum Plasma Concentration (Cmax) 0 ~ 24 hours
Primary Area under the time versus plasma concentration curve (AUC) 0 ~ 24 hours
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