A Study to Compare PK, PD and Safety of the AD-213-A and AD-2131
NCT04690868 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 43
Last updated 2022-04-27
Summary
A study to compare safety, pharmacokinetics and pharmacodynamics of AD-213-A to AD-2131 in healthy volunteers.
Conditions
- Gastroesophagus Reflux Disease
Interventions
- DRUG
-
AD-213-A
1 tablet administered before the breakfast during 5 days
- DRUG
-
AD-2131
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
- 2021-10-15
- Primary Completion
- 2021-12-11
- Completion
- 2021-12-21
Countries
- South Korea
Study Locations
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