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RECRUITING
NCT06932705
PHASE1

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

Sponsor: Addpharma Inc.

View on ClinicalTrials.gov

Summary

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

Official title: An Open-label, Randomized, Single-dose, 2-sequence, 2-period, Crossover Study to Evaluate the Safety and the Pharmacokinetics of PA-111 Compared to PA-111A in Healthy Adult Volunteers Under Fed State Conditions

Key Details

Gender

All

Age Range

19 Years - Any

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2025-04

Completion Date

2025-05

Last Updated

2025-04-17

Healthy Volunteers

Yes

Interventions

DRUG

PA-111

PA-111 1Tab., Per Oral

DRUG

PA-111A

PA-111A 1Capsule., Per Oral

Locations (1)

H Plus Yangji Hospital

Seoul, South Korea