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Completed Phase 1 Interventional

Study of Itacitinib in Combination With Corticosteroids for the Treatment of Acute GVHD

ClinicalTrials.gov ID: NCT02614612

Public ClinicalTrials.gov record NCT02614612. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 4:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Parallel-Cohort Phase 1 Study of Itacitinib in Combination With Corticosteroids for the Treatment of Acute Graft Versus Host Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To determine if Itacitinib in combination with corticosteroids is safe and tolerable in patients with Grade IIB-IVD acute graft-versus-host disease (GVHD).

Study identification

NCT ID
NCT02614612
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Incyte Corporation
Industry
Enrollment
31 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2015 (Type not available)
Primary completion
Jun 2016 (Actual)
Completion
Aug 2018 (Actual)
Last update posted
Mar 8, 2019

2015 – 2018

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
Not listed Duarte California — —
Not listed La Jolla California — —
Not listed Los Angeles California — —
Not listed Denver Colorado — —
Not listed Coral Gables Florida — —
Not listed Atlanta Georgia — —
Not listed Chicago Illinois — —
Not listed Kansas City Kansas — —
Not listed Westwood Kansas — —
Not listed New Orleans Louisiana — —
Not listed Boston Massachusetts — —
Not listed Detroit Michigan — —
Not listed St Louis Missouri — —
Not listed Omaha Nebraska — —
Not listed New York New York — —
Not listed Rochester New York — —
Not listed Cincinnati Ohio — —
Not listed Cleveland Ohio — —
Not listed Portland Oregon — —
Not listed Hershey Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed San Antonio Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02614612, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 8, 2019 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02614612 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →