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LBL-007

BeiGene · Phase 3 active Small molecule

LBL-007 is a Bruton's tyrosine kinase (BTK) inhibitor that blocks BTK signaling to suppress B-cell and myeloid cell activation in hematologic malignancies.

LBL-007 is a Bruton's tyrosine kinase (BTK) inhibitor that blocks BTK signaling to suppress B-cell and myeloid cell activation in hematologic malignancies. Used for Chronic lymphocytic leukemia (CLL), Small lymphocytic lymphoma (SLL).

At a glance

Generic nameLBL-007
Also known asAlcestobart, LBL-007
SponsorBeiGene
Drug classBruton's tyrosine kinase (BTK) inhibitor
TargetBTK
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

BTK is a critical signaling molecule in B-cell receptor and toll-like receptor pathways. By inhibiting BTK, LBL-007 reduces proliferation and survival of malignant B cells and suppresses the tumor microenvironment. This mechanism has demonstrated efficacy in chronic lymphocytic leukemia and other B-cell lymphomas.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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