drugset / Trial / NCT06858865

A Study to Evaluate the Safety and Pharmacokinetics of AD-228A Compared to Coadministration of AD-2281 and AD-2282

NCT06858865 ↗

Phase 1 Completed 60 enrolled Addpharma Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-228A in healthy subjects.

Timeline

Start
2025-07-12
Primary completion
2025-08-14
Completion
2025-08-14

Drugs

EvaluationDrugModalityDoseRoute
Subject AD-2281 Unknown — Oral
Subject AD-2282 Unknown — Oral
Subject AD-228A Unknown — Oral

Indications