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Completed Phase 2 Interventional Results available

A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combination With Ruxolitinib in Participants With Myelofibrosis

ClinicalTrials.gov ID: NCT03222609

Public ClinicalTrials.gov record NCT03222609. 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 21, 2026, 3:27 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 Phase 2 Open-Label Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combination With Ruxolitinib in Subjects With Myelofibrosis (REFINE)

Brief summary

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

This is a Phase 2 open-label, multicenter study evaluating tolerability and efficacy of navitoclax alone or when added to ruxolitinib in participants with myelofibrosis.

Study identification

NCT ID
NCT03222609
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
191 participants

Conditions and interventions

Interventions

Drug

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
Oct 31, 2017 (Actual)
Primary completion
Mar 28, 2022 (Actual)
Completion
Jan 29, 2025 (Actual)
Last update posted
Jan 20, 2026

2017 – 2025

United States locations

U.S. sites
33
U.S. states
19
U.S. cities
30
Facility City State ZIP Site status
UAB Comprehensive Cancer Cente /ID# 165464 Birmingham Alabama 35217 —
TOI Clinical Research /ID# 222546 Cerritos California 90703-2679 —
City of Hope /ID# 221395 Duarte California 91010 —
Moores Cancer Center at UC San Diego /ID# 164084 La Jolla California 92093 —
Long Beach Memorial Medical Ct /ID# 230148 Long Beach California 90806-1701 —
University of Southern California /ID# 164095 Los Angeles California 90033 —
Colorado Blood Cancer Institute /ID# 224250 Denver Colorado 80218 —
Baptist MD Anderson Cancer Center - Jacksonville /ID# 222548 Jacksonville Florida 32207-8432 —
Mayo Clinic /ID# 164201 Jacksonville Florida 32224 —
Moffitt Cancer Center /ID# 164082 Tampa Florida 33612-9416 —
University of Chicago Medicine /ID# 164115 Chicago Illinois 60637-1426 —
Mid Illinois Hematology & Oncology Associates, Ltd /ID# 230536 Normal Illinois 61761 —
Indiana Blood & Marrow Transpl /ID# 165075 Indianapolis Indiana 46237 —
Duplicate_American Oncology Partners of Maryland, PA /ID# 231299 Bethesda Maryland 20817 —
Dana-Farber Cancer Institute /ID# 162675 Boston Massachusetts 02215 —
University of Massachusetts - Worcester /ID# 222547 Worcester Massachusetts 01655 —
Henry Ford Hospital /ID# 162682 Detroit Michigan 48202 —
Ascension Providence Southfield Cancer Center /ID# 223876 Southfield Michigan 48075-3707 —
MidAmerica Division, Inc. /ID# 222058 Kansas City Missouri 64132 —
Weill Cornell Medical College /ID# 162679 New York New York 10065 —
The Ohio State University /ID# 217402 Columbus Ohio 43210-1280 —
Bend Memorial Clinic /ID# 224184 Bend Oregon 97701 —
West Penn Hospital /ID# 222618 Pittsburgh Pennsylvania 15224-1722 —
Duplicate_Medical University of South Carolina /ID# 222597 Charleston South Carolina 29425 —
Prairie Lakes Healthcare System /ID# 224358 Watertown South Dakota 57201 —
Tennessee Oncology-Nashville Centennial /ID# 221410 Nashville Tennessee 37203-1632 —
Texas Oncology - West Texas /ID# 224784 Abilene Texas 79606 —
Texas Oncology- Baylor Charles A. Sammons Cancer Center /ID# 225159 Dallas Texas 75246-2003 —
Oncology Consultants /ID# 230930 Houston Texas 77030-3306 —
MD Anderson Cancer Center at Texas Medical Center /ID# 162683 Houston Texas 77030-4000 —
University of Texas Health San Antonio MD Anderson Cancer Center /ID# 164094 San Antonio Texas 78229 —
Utah Cancer Specialists Salt Lake Clinic /ID# 222806 Salt Lake City Utah 84106 —
University of Utah /ID# 164116 Salt Lake City Utah 84112-5500 —

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 58 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03222609, 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 Jan 20, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03222609 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →