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Bioequivalence (BE) Study Between YHP2205 and YHR2401 in Healthy Volunteers

NCT06775522 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-02-03

No results posted yet for this study

Summary

A randomized, open-label, single-dose, 2-sequence, 2-period, crossover clinical trial to investigate the bioequivalence between YHP2205 and YHR2401 in healthy volunteers

Conditions

  • Healthy Volunteers

Interventions

DRUG

YHP2205

Test drug: YHP2205 Comparator: YHR2401

DRUG

YHR2401

Test drug: YHP2205 Comparator: YHR2401

Sponsors & Collaborators

  • Yuhan Corporation

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-01-11
Primary Completion
2025-01-20
Completion
2025-01-21

Countries

  • South Korea

Study Locations

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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 NCT06775522 on ClinicalTrials.gov