Clinical Trials Directory

Trials / Terminated

TerminatedNCT07039929

Study to Assess the Safety, Tolerability, and Pharmacokinetics of INCB000631 When Administered Orally to Healthy Adult Participants

A Phase 1, Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose, Dose-Escalation Study to Assess the Safety, Tolerability, and Pharmacokinetics of INCB000631 When Administered Orally to Healthy Adult Participants

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Incyte Corporation · Industry
Sex
All
Age
19 Years – 55 Years
Healthy volunteers
Accepted

Summary

This study will be conducted to assess the safety, tolerability, and pharmacokinetics of INCB000631 when administered orally to healthy adult participants.

Conditions

Interventions

TypeNameDescription
DRUGINCB000631Oral; Tablet
DRUGPlaceboOral; Tablet

Timeline

Start date
2025-07-28
Primary completion
2025-10-11
Completion
2025-10-11
First posted
2025-06-26
Last updated
2025-10-29

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07039929. Inclusion in this directory is not an endorsement.

Study to Assess the Safety, Tolerability, and Pharmacokinetics of INCB000631 When Administered Orally to Healthy Adult P (NCT07039929) · Clinical Trials Directory