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A Study to Compare PK, PD and Safety of the AD-213-B and AD-2132

NCT04755985 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2021-08-06

No results posted yet for this study

Summary

A study to compare safety, pharmacokinetics and pharmacodynamics of AD-213-B to AD-2132 in healthy volunteers.

Conditions

  • Gastroesophagus Reflux Disease

Interventions

DRUG

AD-213-B

1 tablet administered before the breakfast during 5 days

DRUG

AD-2132

1 tablet administered before the breakfast during 5 days

Sponsors & Collaborators

  • Addpharma Inc.

    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
2021-03-21
Primary Completion
2021-05-13
Completion
2021-07-23

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 NCT04755985 on ClinicalTrials.gov