Info
acalabrutinib
Acalabrutinib is a targeted cancer drug used to treat various types of B-cell non-Hodgkin lymphoma, including mantle cell lymphoma (MCL) and chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) [1][3][4].
Key points about acalabrutinib
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It is a Bruton tyrosine kinase (BTK) inhibitor that prevents the proliferation, trafficking, chemotaxis, and adhesion of B cells [1][2].
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Acalabrutinib is more selective and potent than the first-in-class BTK inhibitor ibrutinib, with a better safety profile and reduced adverse effects like bleeding risk and severe diarrhea [3][5].
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In the EU, acalabrutinib is approved for previously untreated and relapsed/refractory CLL, either as monotherapy or with obinutuzumab. In the US, it is approved for relapsed/refractory MCL and CLL/SLL [3][4].
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Common side effects include headache, diarrhea, and weight gain. Serious side effects like atrial fibrillation, infections, and bleeding can occur [1][3][4].
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Acalabrutinib is taken orally as capsules twice daily, with or without food. Dose adjustments may be needed for certain drug interactions [1][4].
In summary, acalabrutinib is an effective targeted therapy for B-cell malignancies that offers improved selectivity and tolerability compared to earlier BTK inhibitors like ibrutinib [1][3][4][5].
Citations: [1] https://go.drugbank.com/drugs/DB11703 [2] https://pubchem.ncbi.nlm.nih.gov/compound/Acalabrutinib [3] https://en.wikipedia.org/wiki/Acalabrutinib [4] https://www.cancerresearchuk.org/about-cancer/treatment/drugs/acalabrutinib [5] https://pubmed.ncbi.nlm.nih.gov/34055635/
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