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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
Conditions
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