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Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet Versus Best Available Therapy to Assess Change in Spleen Volume in Adult Participants With Relapsed/Refractory Myelofibrosis

Active, not recruiting · Phase 3 · NCT04468984

Conditions: Myelofibrosis (MF)

At a glance

Research payments reported, 2025
$96,283
U.S. investigators named
16
Sites paid
16
Planned or actual enrollment
330

About the trial

Sponsor
AbbVie
Tested
Navitoclax (drug), Ruxolitinib (drug), Best Available Therapy (BAT) (drug)
Dates
Started 2020-08-31; completion 2026-12
Results posted
Not yet

Myelofibrosis (MF) is a rare blood cancer, notable for scarring of the bone marrow (the spongy tissue inside bones) and the spleen becoming larger. The purpose of this study is to assess safety and change in spleen volume when navitoclax is given in combination with ruxolitinib, compared to best available therapy, for adult participants with MF. Navitoclax is an investigational drug (not yet approved) being developed for the treatment of MF. Participants in this study will be randomly selected (like picking numbers out of a hat) to be in 1 of 2 treatment arms. Neither participants nor the study doctor will be able to pick which treatment arm a participants enters. In Arm A, participants w…

From ClinicalTrials.gov, last updated 2026-01-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $96,283 in research payments for this study in 2025 (31 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.