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NCT06025773

A Study to Compare PK/PD Characteristics and Safety Profiles Between AD-212-A and AD-2121

Completed Phase 1 Last updated 1 August 2024
What this trial tests

Phase 1 trial testing Lansoprazole 15 mg in Gastro Esophageal Reflux in 24 participants. Completed in 19 April 2024.

Timeline
15 September 2023
Primary endpoint
19 April 2024
19 April 2024

Quick facts

Lead sponsorAddpharma Inc.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment24
Start date15 September 2023
Primary completion19 April 2024
Estimated completion19 April 2024
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Addpharma Inc. — full company profile →

Who can join

19 and older, any sex, with Gastro Esophageal Reflux. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Primary endpoint of this study is to evaluate the pharmacokinetic and pharmacodynamic characteristics of AD-212-A in healthy subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Lansoprazole 15 mg

Trials testing the same drug.

Other recruiting trials for Gastro Esophageal Reflux

Currently open trials in the same condition.

Other Addpharma Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06025773.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing