drugset / Trial / NCT06025773

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

NCT06025773

Phase 1 Completed 24 enrolled Addpharma Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

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

Timeline

Start
2023-09-15
Primary completion
2024-04-19
Completion
2024-04-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Calcium carbonate Other / unclassified 600 mg Oral
Subject Lansoprazole Other / unclassified 15 mg Oral