Zanubrutinib — Active Pharmaceutical Ingredient

Zanubrutinib is an active pharmaceutical ingredient found in 1 FDA-approved drug product. Forms: CAPSULE, TABLET. Routes: ORAL.

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Zanubrutinib (1 brand name, 2 dosage forms, 1 route)

Available dosage forms: CAPSULE, TABLET.

Routes of administration: ORAL.

Brand Names

  • BRUKINSA

Contraindications

None.

Adverse Reactions

The following clinically significant adverse reactions are discussed in more detail in other sections of the labeling: Hemorrhage [see Warnings and Precautions (5.1)] Infections [see Warnings and Precautions (5.2)] Cytopenias [see Warnings and Precautions (5.3)] Second Primary Malignancies [see Warnings and Precautions (5.4)] Cardiac Arrhythmias [see Warnings and Precautions (5.5)] Hepatotoxicity, including DILI [see Warnings and Precautions (5.6)]

Mechanism of Action

Zanubrutinib is a small-molecule inhibitor of Bruton’s tyrosine kinase (BTK). Zanubrutinib forms a covalent bond with a cysteine residue in the BTK active site, leading to inhibition of BTK activity. BTK is a signaling molecule of the B-cell antigen receptor (BCR) and cytokine receptor pathways. In B-cells, BTK signaling results in activation of pathways necessary for B-cell proliferation, trafficking, chemotaxis, and adhesion. In nonclinical studies, zanubrutinib inhibited malignant B-cell proliferation and reduced tumor growth.

⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional before taking any medication.