Bioequivalence Study of AG2202

NCT06549504 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2024-08-14

No results posted yet for this study

Summary

The objective of this study is to evaluate the human bioequivalence of AG2202T and AG2202R.

Conditions

  • Bioequivalence Study

Interventions

DRUG

AG2202T

AG2202T Single-dose

DRUG

AG2202R

AG2202R Single-dose

Sponsors & Collaborators

  • Ahn-Gook Pharmaceuticals Co.,Ltd

    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
2024-08-31
Primary Completion
2024-09-30
Completion
2024-09-30

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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 NCT06549504 on ClinicalTrials.gov