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Ibrutinib (Induction)

Prof. Dr. M. Dreyling (co-chairman) · Phase 3 active Small molecule

Ibrutinib is a Bruton's tyrosine kinase (BTK) inhibitor that blocks BTK signaling in B cells and other immune cells, leading to reduced proliferation and survival of malignant B cells.

Ibrutinib is a Bruton's tyrosine kinase (BTK) inhibitor that blocks BTK signaling in B cells and other immune cells, leading to reduced proliferation and survival of malignant B cells. Used for Chronic lymphocytic leukemia (CLL), induction phase, Mantle cell lymphoma, induction phase, Waldenström macroglobulinemia, induction phase.

At a glance

Generic nameIbrutinib (Induction)
Also known asImbruvica
SponsorProf. Dr. M. Dreyling (co-chairman)
Drug classBruton's tyrosine kinase (BTK) inhibitor
TargetBTK (Bruton's tyrosine kinase)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Ibrutinib covalently binds to BTK, a key enzyme in the B-cell receptor signaling pathway. By inhibiting BTK, it disrupts downstream signaling cascades that promote B-cell survival and proliferation, making it particularly effective against B-cell malignancies. In the induction phase, it is used as an initial treatment to rapidly reduce tumor burden before consolidation or maintenance therapy.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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