OncRef

Clinical Trial: NCT04116437

Zanubrutinib (BGB-3111) in Participants With Previously Treated B-Cell Lymphoma Intolerant of Prior Bruton Tyrosine Kinase Inhibitor (BTKi) Treatment

Status:

COMPLETED

Phase:

Phase 2

Lead Sponsor:BeiGene
Information Provided By:BeOne Medicines
Last Update Posted:2026-01-28

Study Overview

Brief Summary

The primary objective of this study is to evaluate the safety of zanubrutinib (also known as BGB-3111) in chronic lymphocytic leukemia/small lymphocytic lymphoma, Waldenström macroglobulinemia, mantle cell lymphoma, or marginal zone lymphoma patients who have become intolerant of prior ibrutinib and/or acalabrutinib treatment, by comparing intolerance to adverse event profile as assessed by the recurrence and the change in severity of adverse events.

Official Title

A Phase 2, Multicenter, Single-arm Study of Zanubrutinib (BGB-3111) in Patients With Previously Treated B-Cell Lymphoma Intolerant of Prior Treatment With Ibrutinib and/or Acalabrutinib

Conditions

Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma, Mantle Cell Lymphoma, Marginal Zone Lymphoma, Waldenstrom Macroglobulinemia

Intervention / Treatment

  • Drug: Zanubrutinib

Other Study ID Numbers

  • BGB-3111-215

Start Date (Actual)

2019-10-15

Primary Completion Date (Actual)

2026-01-09

Study Completion Date (Actual)

2026-01-09

Enrollment (Actual)

96

Study Type

Interventional

Phase

Phase 2