drugset / Trial / NCT06916130

A Study to Compare PK/PD Characteristics and Safety Profiles Between AD-120 and AD-120A

NCT06916130 ↗

Phase 1 Not yet recruiting 48 enrolled Addpharma Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

Primary endpoint of this study is to evaluate the pharmacokinetic and pharmacodynamic characteristics of AD-120 in healthy subjects.

Timeline

Start
2025-04-21
Primary completion
2025-09-01
Completion
2025-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject AD-120 Unknown — Oral
Subject AD-120A Unknown — Oral