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Pacritinib(Vonjo)

Another NameVonjo、LuciPac、帕克替尼

IndicationsIt is indicated for the treatment of adult patients with intermediate- or high-risk primary or secondary myelofibrosis and a platelet count of less than 50 × 10⁹/L.

  • Reg No.04 L 1337/25

  • Inspection No.758-25

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    Dosage form:capsule

    Specs:100mg*120 capsules

    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 Pacritinib

    Pacritinib, an oral JAK2 inhibitor manufactured by Lucius Pharmaceuticals, provides a targeted treatment option for myelofibrosis patients with low platelet counts.

    Instructions of Pacritinib

    Summary of Key Information for Pacritinib.

    Active Ingredient

    Its main active ingredient is pacritinib.

    Indicated Population

    It is indicated for adult patients with intermediate- or high-risk primary or secondary myelofibrosis and low platelet counts.

    Dosage and Administration

    The recommended dose is 200 mg, administered orally twice daily, with or without food.

    Use in Special Populations

    Dose adjustment is required for patients with severe hepatic impairment. Patients with renal impairment should avoid the use of this drug. Men and women of reproductive potential, as well as lactating women, need to be aware of the relevant risks.

    Drug Overdosage

    Overdose may cause gastrointestinal reactions and myelosuppression, among other adverse effects. There is no specific antidote available.

    Storage Conditions

    Store in the original sealed packaging at room temperature below 30°C, protected from light.

    Pharmacokinetics

    This drug is mainly metabolized by CYP3A4, with a half-life of approximately 28 hours and a high average accumulation rate at steady state.

    FDA,2025.10

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