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OncoMatch/Clinical Trials/NCT05294731

Treatment of Chinese Participants With B-Cell Malignancies With BGB-16673, a Bruton Tyrosine Kinase-Targeted Protein-Degrader

Official title: A Phase 1/2, Open-Label, Dose-Escalation and Expansion Study of the Bruton Tyrosine Kinase-Targeted Protein-Degrader BGB-16673 in Chinese Patients With B-Cell Malignancies

Is NCT05294731 recruiting? Yes, currently enrolling (Oct 2026). This Phase 1/2 trial studies Tacabrutideg for b-cell malignancy.

Phase 1/2RecruitingBeOne MedicinesNCT05294731Data as of Oct 2026Location: China

Treatment: Tacabrutideg — This study aims to explore the recommended phase 2 dose and evaluate the safety, tolerability and preliminary antitumor activity of BGB-16673 monotherapy at the recommended Phase 2 dose for the selected B-cell malignancy expansion cohorts

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Extracted eligibility criteria

Treatments studied

Other

Tacabrutideg

Cancer type

Non-Hodgkin Lymphoma

Chronic Lymphocytic Leukemia

Diffuse Large B-Cell Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Lab requirements

Blood counts

Kidney function

Liver function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05294731 currently recruiting?

Yes, this trial is currently recruiting patients.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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