This study is being conducted to assess the Safety, Tolerability, and Pharmacokinetics of INCB160058 When Administered Orally to Healthy Adult Participants.
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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