RecruitingPhase 4NCT07169331

A Study to Evaluate the Efficacy and Safety of Zanubrutinib in Chinese Adults With Treatment-Naive Waldenström Macroglobulinemia

Studying Waldenström Macroglobulinemia

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Key facts

Sponsor
BeiGene
Principal Investigator
Study Director
BeiGene
Intervention
Zanubrutinib(drug)
Enrollment
18 enrolled
Eligibility
18 years · All sexes
Timeline
20252028

Study locations (8)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07169331 on ClinicalTrials.gov

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