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Terminated Phase 3 Interventional Results available

To Evaluate Efficacy and Safety of Parsaclisib and Ruxolitinib in Participants With Myelofibrosis Who Have Suboptimal Response to Ruxolitinib (LIMBER-304)

ClinicalTrials.gov ID: NCT04551053

Public ClinicalTrials.gov record NCT04551053. 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 23, 2026, 7:13 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 Randomized, Double-Blind, Placebo-Controlled Study of the PI3Kδ Inhibitor Parsaclisib Plus Ruxolitinib in Participants With Myelofibrosis Who Have Suboptimal Response to Ruxolitinib

Brief summary

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

The purpose of the study is to compare the efficacy and safety of parsaclisib when combined with ruxolitinb versus placebo combined with ruxolitinib in participants with myelofibrosis who have suboptimal response while receiving ruxolitinib monotherapy.

Study identification

NCT ID
NCT04551053
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Incyte Corporation
Industry
Enrollment
177 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
May 26, 2021 (Actual)
Primary completion
Aug 16, 2023 (Actual)
Completion
Aug 21, 2024 (Actual)
Last update posted
Oct 2, 2025

2021 – 2024

United States locations

U.S. sites
35
U.S. states
18
U.S. cities
30
Facility City State ZIP Site status
Sutter Health Alta Bates Summit Medical Center Absmc Alta Bates Summit Comprehensive Cancer Center Berkeley California 94704 —
CCARE Fresno California 93720 —
California Research Institute (Cri) Los Angeles California 90027-6005 —
Emad Ibrahim Md Inc Redlands California 92373 —
Scripps Clinic San Diego California 92103 —
Coastal Integrated Cancer Care - Cicc San Luis Obispo California 93401 —
Stamford Hospital - Medical Oncology Hematology Stamford Connecticut 06904 —
Georgetown University Washington D.C. District of Columbia 20057 —
Emory University Atlanta Georgia 30322 —
Augusta University - Medical College of Georgia Augusta Georgia 30912 —
Indiana University Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202 —
University of Kansas Hospital Authority Westwood Kansas 66205 —
Tulane University New Orleans Louisiana 70112 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Midamerica Cancer Care Kansas City Missouri 64114 —
New Jersey Hematology Oncology Associates Llc Brick New Jersey 08724 —
Morristown Medical Center - Atlantic Health System Morristown New Jersey 07960 —
Westchester Medical Center Advanced Oncology Hawthorne New York 10532 —
Mount Sinai School of Medicine New York New York 10029 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Montefiore Medical Center The Bronx New York 10467 —
Advent Health Hendersonville Park Ridge Hospital Hendersonville Clyde North Carolina 28721 —
Duke Cancer Center Durham North Carolina 27710 —
Cleveland Clinic Cleveland Ohio 44195 —
Oregon Health & Science University Columbus Ohio 43210 —
Oregon Health & Science University Portland Oregon 97239 —
Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
Baptist Cancer Center Memphis Tennessee 38120 —
Texas Oncology - Medical City Dallas Dallas Texas 75230 —
Texas Oncology - Baylor Sammons Cancer Center Dallas Texas 75246-2092 —
University of Texas Southwestern Medical Center Dallas Texas 75390-8565 —
Renovatio Clinical Houston Texas 77005 —
Kelsey Seybold Clinic Houston Texas 77025 —
Providence Regional Medical Center Everett Everett Washington 98201 —

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 142 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04551053, 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 2, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04551053 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →