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Study identifier: NCT05914662 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Zanubrutinib Plus BR in Newly Diagnosed Symptomatic WM

Condition: Waldenstrom Macroglobulinemia  ·  Sponsor: Institute of Hematology & Blood Diseases Hospital, China

PhasePhase 2
Planned participants42
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to evaluate the long-term efficacy of BTK inhibitor Zanubrutinib combined bendamustine and rituximab (ZBR) for time-limited treatment of Waldenstrom macroglobulinemia, The combination therapy is expected to improve the remission depth, prolong the remission time, and improve the progression-free survival and overall survival of newly diagnosed WM patients. On the one hand, the patients have to bear a long-term economic burden, which is often difficult for some patients to adhere to for a long time. On the other hand, in the course of long-term treatment of BTKi, drug resistance and intolerable side effects are prone to occur. At the same time, it can prevent the disease rebound after the withdrawal of BTKi, so as to achieve the phased withdrawal of WM

This description comes directly from the study's public registry record.

Talk to the study team

Shuhua Yi, Dr.  ·  86-22-23909106  ·  yishuhua@ihcams.ac.cn

Lugui Qiu, Dr.  ·  86-22-23909172  ·  qiulg@ihcams.ac.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Institute of Hematology & Blood Diseases HospitalTianjin, Tianjin Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05914662