Drug-drug Interactions Between DWC202313 and DWC202314 in Healthy Subjects

NCT ID: NCT06119958

Last Updated: 2023-11-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-27

Study Completion Date

2023-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Drug Drug Interaction

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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DWC202313

DWC202313

Group Type EXPERIMENTAL

DWC202313

Intervention Type DRUG

Experimental Drug 1

DWC202314

DWC202314

Group Type EXPERIMENTAL

DWC202314

Intervention Type DRUG

Experimental Drug 2

Interventions

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DWC202313

Experimental Drug 1

Intervention Type DRUG

DWC202314

Experimental Drug 2

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* over 19 year old

Exclusion Criteria

* Galactose intolerance
* Lapp lactase deficiency
Minimum Eligible Age

19 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Daewoong Pharmaceutical Co. LTD.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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H Plus YANGJI Hospital

Seoul, , South Korea

Site Status RECRUITING

Countries

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South Korea

Central Contacts

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Seung-Hyun Kang, MD, Ph D

Role: CONTACT

070-4665-9490

Facility Contacts

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Seung-Hyun Kang, MD, Ph D.

Role: primary

070-4665-9490

Other Identifiers

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DWJ1622101

Identifier Type: -

Identifier Source: org_study_id

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