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Completed Phase 1Phase 2 Interventional Results available

INCB000928 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Anemia Due to Myeloproliferative Disorders

ClinicalTrials.gov ID: NCT04455841

Public ClinicalTrials.gov record NCT04455841. 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 16, 2026, 4:13 PM 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 Phase 1/2 Open-Label, Multicenter Study of INCB000928 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Anemia Due to Myeloproliferative Disorders

Brief summary

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

This Phase 1/2, open-label, dose-finding study is intended to evaluate the safety and tolerability, PK, PD, and efficacy of INCB000928 administered as monotherapy or in combination with ruxolitinib in participants with MF who are transfusion-dependent or presenting with symptomatic anemia. This study will consist of 2 parts: dose escalation and expansion.

Study identification

NCT ID
NCT04455841
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
84 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
Mar 19, 2021 (Actual)
Primary completion
Apr 1, 2025 (Actual)
Completion
Sep 8, 2026 (Actual)
Last update posted
Oct 1, 2026

2021 – 2026

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
City of Hope National Medical Center Duarte California 91010 —
City of Hope Orange County Irvine California 92618 —
Usc Norris Comprehensive Cancer Center Los Angeles California 90089 —
Stanford Cancer Center Palo Alto California 94304 —
Prebys Cancer Center San Diego California 92103 —
Emory University - Winship Cancer Institute Atlanta Georgia 30322 —
Emory University-Winship Cancer Institute Atlanta Georgia 30322 —
Start Midwest Grand Rapids Michigan 49546 —
Washington University School of Medicine St Louis Missouri 63110 —
Weill Cornell Medical Centers New York New York 10065 —
Duke University Medical Center, Department of Hematologic Malignancies and Cellular Therapy Durham North Carolina 27705 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
Md Anderson Cancer Center Houston Texas 77030 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04455841, 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 Oct 1, 2026 · Synced Oct 16, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04455841 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →