LcuiPirto (Pirtobrutinib)

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  • Model Number:
    RL3120250101
  • Brand Name:
    LcuiPirto
  • Origin:
    Generic drug,Laos
  • Small Orders:
    Small batches also available
  • Tags:
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Poster
  • Details
  • Description
  • Packaging Size
    30t/bottle
  • Strength
    50mg
  • Compositon
    Pirtobrutinib
  • Treatment
    Mantle Cell Lymphoma, Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
  • Form
    Tablet
  • Brand
    LcuiPirto
  • Quantity Unit
    50mg*30T/Box
  • Manufacturer
    Lucius Pharmaceuticals (Lao) Co.,Ltd

About Pirtobrutinib 

Pirtobrutinib is an inhibits B cell lymphocyte proliferation and survival by binding and inhibiting Bruton's tyrosine kinase (BTK).

Mantle Cell Lymphoma

Indicated for relapsed or refractory mantle cell lymphoma (MCL) after at least 2 lines of systemic therapy, including a Bruton tyrosine kinase (BTK) inhibitor

200 mg PO qDay

Continue until disease progression or unacceptable toxicity

Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Indicated for chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) in adults who have received at ≥2 prior lines of therapy, including a BTK inhibitor and a BCL-2 inhibitor

200 mg PO qDay

Continue until disease progression or unacceptable toxicity

Dosage Modifications

Asymptomatic lymphocytosis: Dose modification not recommended

Asymptomatic lipase increase: May not necessarily warrant a dose modification

Hematologic toxicities

  • NOTE: Based on starting dose of 200 mg qDay
  • Absolute neutrophil count (ANC) 0.5 to <1 x 109/L with fever and/or infection
  • ANC <0.5 x 109/L lasting ≥7 days
  • Platelet count 25 to <50 x 109/L with bleeding
  • Platelet count <25 x 109/L
  • Modification

    • First occurrence: Interrupt therapy until recovery to Grade 1 or baseline; restart at original dose (200 mg qDay)
    • Second occurrence: Interrupt therapy until recovery to Grade 1 or baseline; restart at 100 mg qDay
    • Third occurrence: Interrupt therapy until recovery to Grade 1 or baseline; restart at 50 mg qDay
    • Fourth occurrence: Discontinue treatment

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