Safety and Pharmacokinetics Study of DWC20155 and DWC20156 in Healthy Subjects
Sponsor
Daewoong Pharmaceutical Co. LTD. (Industry)
Overall Status
Completed
CT.gov ID
NCT02952547
Collaborator
(none)
52
1
2
2.4
22
Study Details
Study Description
Brief Summary
The purpose of this study to Compare the safety and pharmacokinetics between co-administration and fixed dose combination of DWC20155 and DWC20156 in healthy subjects
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Phase 1 |
Study Design
Study Type:
Interventional
Actual Enrollment
:
52 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Randomized, Open-label, Oral Dose, Crossover Study to Compare the Safety and Pharmacokinetics Between Co-administration and Fixed Dose Combination of DWC20155 and DWC20156 in Healthy Subjects
Actual Study Start Date
:
Oct 30, 2016
Actual Primary Completion Date
:
Nov 26, 2016
Actual Study Completion Date
:
Jan 10, 2017
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Test / Reference Drug DWJ1366 Tab. followed by co-administration of DWC20155 and DWC20156 Tab. |
Drug: Co-administration of DWC20155 and DWC20156
Drug: DWJ1366 Tab.
|
Experimental: Reference / Test Drug Co-administration of DWC20155 and DWC20156 Tab. followed by DWJ1366 Tab. |
Drug: Co-administration of DWC20155 and DWC20156
Drug: DWJ1366 Tab.
|
Outcome Measures
Primary Outcome Measures
- Maximum Plasma Concentration (Cmax) [0-24 hours]
- Area under the plasma concentration versus time curve (AUC) [0-24 hours]
Eligibility Criteria
Criteria
Ages Eligible for Study:
19 Years
to 55 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
-
BMI ≥ 18.5 and ≤ 27.0 kg/m2.
-
No clinically significant findings
-
Age 19-55 years at screening
Exclusion Criteria:
- Who has allergy to investigational product
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Busan Paik Hospital | Busan | Korea, Republic of |
Sponsors and Collaborators
- Daewoong Pharmaceutical Co. LTD.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Daewoong Pharmaceutical Co. LTD.
ClinicalTrials.gov Identifier:
NCT02952547
Other Study ID Numbers:
- DW_DWJ1366002
First Posted:
Nov 2, 2016
Last Update Posted:
Feb 16, 2017
Last Verified:
Feb 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No