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CompletedNCT02952755Updated Feb 16, 2017

Drug-Drug Interaction Study Between DWC20155 / DWC20156 and DWC20162 in Healthy Volunteers

A Phase 1 interventional study of Co-administration of DWC20155/DWC20156 and DWC20162 in Healthy, sponsored by Daewoong Pharmaceutical Co. LTD.. Completed at 1 site in Korea, Republic of. Open to participants aged 19 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-02-16.

Sponsored by Daewoong Pharmaceutical Co. LTD. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
45
Allocation
Randomized
Ages
19 Years to 45 Years
Sex
All
01

Study summary

A randomized, open label, crossover study to explore drug-drug interactions between DWC20155 / DWC20156 and DWC20162 in Healthy Volunteers

02

Conditions studied

  • Healthy
03

In context

Lead sponsor

Daewoong Pharmaceutical Co. LTD. is the lead sponsor of 196 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Accepts healthy volunteers

Exclusion criteria

Exclusion Criteria:

  • Who has allergy to investigational product
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
45 participants (actual)

Study arms

  • Experimental
    Study effect of DWC20162 on DWC20155/DWC20156 PK

    To study effect of DWC20162 on DWC20155/DWC20156 PK

    Drug: Co-administration of DWC20155/DWC20156 · Drug: DWC20162

  • Experimental
    Study effect of DWC20155/DWC20156 on DWC20162 PK

    To study effect of DWC20155/DWC20156 on DWC20162 PK

    Drug: Co-administration of DWC20155/DWC20156 · Drug: DWC20162

Interventions

  • DrugCo-administration of DWC20155/DWC20156
  • DrugDWC20162
06

What researchers measure

Primary outcomes

  1. Maximum Plasma Concentration (Cmax)

    Time frame: 0 ~ 24 hours

  2. Area under the time versus plasma concentration curve (AUC)

    Time frame: 0 ~ 24 hours

07

Study locations

1 site
  • Bundang CHA Medical Center
    Gyunggi, Korea, Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 16, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02952755
Lead sponsor
Daewoong Pharmaceutical Co. LTD.
Responsible party
Sponsor
First posted
Nov 2, 2016
Start date
Nov 28, 2016
Primary completion
Dec 12, 2016
Completion
Dec 20, 2016
Last update
Feb 16, 2017
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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