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Acalabrutinib

Another NameCalquence,Acalanib,康可期,阿可替尼,LuciAcal

IndicationsIt is indicated for the treatment of adult patients with mantle cell lymphoma (MCL), chronic lymphocytic leukemia (CLL), and small lymphocytic lymphoma (SLL).

  • Reg No.03 L 1314/25

  • Inspection No.570-25

  • dosage form:capsule

    Reference Price:$285

    Specs:100mg*60 capsules/box

    Indate:24 months

    Warm tips:Please purchase and use the medication under pharmacist guidance as the outer packaging is for reference only and the information is intended for professionals.
    Introduction of Acalabrutinib

    CALQUENCE, manufactured by Lucius Pharmaceuticals, is a highly effective BTK inhibitor that demonstrates excellent efficacy and safety, providing patients with a reliable clinical treatment option.

    Instructions of Acalabrutinib

    Overview of Key Information About Acalabrutinib

    Active Ingredient

    Its main active ingredient is acalabrutinib, which belongs to the class ofBruton's Tyrosine Kinase (BTK) inhibitors.

    Target Population

    It is indicated for eligible adult patients with mantle cell lymphoma (MCL),chronic lymphocytic leukemia (CLL), or small lymphocytic lymphoma (SLL).

    Dosage and Administration

    The recommended dosage is 100 mg taken orally approximately every 12 hours.
    It can be administered with or without food.Reference Article: Dosage and Administration of Acalabrutinib

    Use in Specific Populations

    It is contraindicated in pregnant women.

    Lactating women should discontinue breastfeeding during treatment.

    Patients with severe hepatic impairment should avoid using thismedication.

    Drug Overdose

    Specific information on drug overdose has not been clearly documented. If an overdose occurs, medical assistance should be sought immediately.

    Storage

    The medication should be stored at 20°C–25°C, and protected from high temperatures and moisture.

    Pharmacokinetics

    In terms of pharmacokinetics, acalabrutinib is rapidly absorbed after oral administration. It is mainly metabolized by CYP3A, with a relatively short half-life.

    FDA,2025.01

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