drugset / Trial / NCT06932705

A Study to Compare to PK Characteristics and Safety Profiles Between PA-111 and PA-111A

NCT06932705 ↗

Phase 1 Recruiting 48 enrolled Addpharma Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of PA-111 in healthy subjects.

Timeline

Start
2025-04
Primary completion
2025-05
Completion
2025-05

Drugs

EvaluationDrugModalityDoseRoute
Subject PA-111 Unknown — Oral
Subject PA-111A Unknown — Oral