A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of INCB160058 When Administered Orally to Healthy Adult Participant

PHASE1CompletedINTERVENTIONAL
Enrollment

137

Participants

Timeline

Start Date

March 14, 2024

Primary Completion Date

August 19, 2025

Study Completion Date

August 19, 2025

Conditions
Healthy Participants
Interventions
DRUG

INCB160058

Oral; Immediate release solid tablet

DRUG

Placebo

Oral; Tablet

DRUG

Esomeprazole

Oral; Delayed-release capsule or tablet

DRUG

Famotidine

Oral; Tablet

Trial Locations (1)

03004

Nucleus Network Pty Ltd, Melbourne

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Incyte Corporation

INDUSTRY