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A Study Comparing BGB-3111 and Ibrutinib in Participants With Waldenström's Macroglobulinemia (WM)

Completed · Phase 3 · NCT03053440

Conditions: Waldenström's Macroglobulinemia

At a glance

Research payments reported, 2025
$4,843
U.S. investigators named
1
Sites paid
1
Planned or actual enrollment
201

About the trial

Sponsor
BeiGene
Tested
BGB-3111 (drug), Ibrutinib (drug)
Dates
Started 2017-01-25; completion 2022-06-21
Results posted
Yes

This study evaluated the safety, efficacy and clinical benefit of BGB-3111 (zanubrutinib) vs ibrutinib in participants with MYD88 Mutation Waldenström's Macroglobulinemia.

From ClinicalTrials.gov, last updated 2024-10-26. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines USA, Inc. reported $4,843 in research payments for this study in 2025 (1 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.