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Observational Study Evaluating the Efficacy and Safety of Zanubrutinib in Participants With Waldenström Macroglobulinemia

Recruiting · NCT05640102

Conditions: Waldenstrom Macroglobulinemia

At a glance

Research payments reported, 2025
$180,482
U.S. investigators named
16
Sites paid
14
Planned or actual enrollment
111

About the trial

Sponsor
BeiGene
Tested
Zanubrutinib (drug)
Dates
Started 2023-03-03; completion 2027-12
Results posted
Not yet

This is a hybrid (retrospective and prospective) non-interventional registry study to further describe the clinical profile of zanubrutinib in Waldenström macroglobulinemia (WM) participants with and without specific mutations and from racial and ethnic minority groups. Data collected from this registry study will be used to better understand the clinical benefit and safety of zanubrutinib for the treatment of participants in these populations.

From ClinicalTrials.gov, last updated 2026-08-07. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines USA, Inc. reported $180,482 in research payments for this study in 2025 (62 payments).

Products named: Brukinsa

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.