Bioepuivalence Study for the Safety and the Pharmacokinetics of DWJ1589 and DWC202315

NCT06592495 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2024-09-23

No results posted yet for this study

Summary

This study aims to evaluate the safety and pharmacokinetic characteristics after administration of DWJ1589 and DWC202315 in healty adult volunteers.

Conditions

  • Healthy Volunteers

Interventions

DRUG

Period 1

DWJ1589 or DWC202315

DRUG

Period 2

DWJ1589 or DWC202315

DRUG

Period 3

DWJ1589 or DWC202315

DRUG

Period 4

DWJ1589 or DWC202315

Sponsors & Collaborators

  • Daewoong Pharmaceutical Co. LTD.

    lead INDUSTRY

Principal Investigators

  • KANG, MD, PhD · H Plus Yangji Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-31
Primary Completion
2025-01-31
Completion
2025-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06592495 on ClinicalTrials.gov