Skip to main content

A Study to Investigate Safety and Effectiveness of Tacabrutideg (BGB-16673) in Combination With Other Agents in Participants With Relapsed or Refractory B-Cell Malignancies

Recruiting · Phase 1, Phase 2 · NCT06634589

Conditions: B-cell Malignancy, Relapsed Cancer, Refractory Cancer, B-cell Lymphoma

At a glance

Research payments reported, 2025
$3.3M
U.S. investigators named
15
Sites paid
18
Planned or actual enrollment
80

About the trial

Sponsor
BeOne Medicines
Tested
Tacabrutideg (drug), Sonrotoclax (drug), Zanubrutinib (drug), Mosunetuzumab (drug), Glofitamab (drug), Obinutuzumab (drug)
Dates
Started 2024-11-27; completion 2029-12-02
Results posted
Not yet

The purpose of this study is to measure the safety, preliminary antitumor activity, pharmacokinetics, and pharmacodynamics with tacabrutideg in combination with other agents in participants with relapsed or refractory (R/R) B-cell malignancies. This study is structured as a master protocol with separate substudies. This study currently includes four substudies, and more substudies may be added as other combination agents are identified.

From ClinicalTrials.gov, last updated 2026-09-11. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines Ltd. reported $3.3M in research payments for this study in 2025 (243 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.