This study is being conducted to assess the Safety, Tolerability, and Pharmacokinetics of INCB160058 When Administered Orally to Healthy Adult Participants.
Age range
18 Years – 55 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of participants with Treatment Emergent Adverse Events (TEAEs)
Timeframe: Up to Day 28
INCB160058 pharmacokinetic (PK) when administered as solid tablets in Plasma
Timeframe: Up to Day 5
INCB160058 pharmacokinetic (PK) when administered as a soft gel capsule in Plasma
Timeframe: Up to Day 5
INCB160058 pharmacokinetic (PK) when administered as ASD tablets in Plasma
Timeframe: Up to Day 5
INCB160058 pharmacokinetic (PK) in Plasma to determine the effect of food administered as solid tablets
Timeframe: Up to Day 12
INCB160058 pharmacokinetic (PK) in Plasma to determine the effect of food administered as ASD tablets
Timeframe: Up to Day 12
INCB160058 pharmacokinetic (PK) in Plasma to assess the effect of esomeprazole administered as solid tablets
Timeframe: Up to Day 14
INCB160058 pharmacokinetic (PK) in Plasma to assess the effect of esomeprazole administered as ASD tablets
Timeframe: Up to Day 14
INCB160058 pharmacokinetic (PK) in Plasma to assess the effect of famotidine administered as solid tablets
Timeframe: Up to Day 14
INCB160058 pharmacokinetic (PK) in Plasma to assess the effect of famotidine administered as ASD tablets
Timeframe: Up to Day 14