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Bioequivalence Study for the Safety and the Pharmacokinetics of DWJ1568 in Healthy Adult Volunteers

Bioequivalence Study for the Safety and the Pharmacokinetics of DWJ1568 in Healthy Adult Volunteers

Recruiting
19 years and older
All
Phase 1
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Overview

This study aims to compare the pharmacokinetics and safety following administration of DWJ1568 and DWC202215 in healthy volunteers

Description

The study design is a Randomized, Open-label, Oral, Single-dose, Four-way crossover study. The patients were randomly assigned to each group. Primary endpoint was Cmax and AUCt of DWJ1568 and DWC202215. Secondary endpoints were AUCinf, Tmax, t1/2 of DWJ1568 and DWC202215.

Eligibility

Inclusion Criteria:

  • over 19 year old

Exclusion Criteria:

  • Galactose intolerance
  • Lapp lactase deficiency

Study details
    Healthy Volunteers

NCT06119945

Daewoong Pharmaceutical Co. LTD.

14 October 2025

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