Lucibelu (Belumosudil)

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  • Model Number:
    RL362025062201
  • Brand Name:
    Lucibelu
  • Origin:
    Generic drug,Laos
  • Small Orders:
    Small batches also available
  • Tags:
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Poster
  • Details
  • Description
  • Packaging Size
    30t/bottle
  • Strength
    200mg
  • Compositon
    Belumosudil
  • Treatment
    chronic graft versus host disease (cGvHD)
  • Form
    Tablet
  • Brand
    Lucibelu
  • Quantity Unit
    200mg*30t/Box
  • Manufacturer
    Lucius Pharmaceuticals (Lao) Co.,Ltd

About Belumosudil

Belumosudil is a medication used for the treatment of chronic graft versus host disease (cGvHD).It is in the class of drugs known as serine/threonine kinase inhibitors. Specifically, it is an inhibitor of Rho-associated coiled-coil kinase 2 (ROCK2; ROCK-II).ROCK2-mediated signaling pathways are major players in pro- and anti-inflammatory immune cell responses. A study in cultured human cells demonstrated that the drug also has effects on oxidative phosphorylation, WNT signaling, angiogenesis, and KRAS signaling.

Graft Versus Host Disease

Indicated for chronic graft versus host disease (GVHD) in adults and adolescents aged ≥12 years after failure of at least 2 prior lines of systemic therapy

200 mg PO qDay

Continue until progression of chronic GVHD requires new systemic therapy

Dosage Modifications

Hepatotoxicity

  • Grade 3 AST or ALT (5-20x ULN) or Grade 2 bilirubin (1.5-3x ULN): Hold until recovery of bilirubin, AST, and ALT to Grade 0-1, then resume at recommended dose
  • Grade 4 AST or ALT (>20x ULN) or Grade ≥3 bilirubin (>3x ULN): Permanently discontinue

Other adverse reactions

  • Grade 3: Hold until recovery to Grade 0-1, then resume at recommended dose level
  • Grade 4: Permanently discontinue

Renal impairment

  • Mild-to-moderate (≥30 to <90 mL/min/1.72 m2): No dosage adjustment necessary
  • Severe (<30 mL/min/1.72 m2): Not studied
  • Patients with preexisting severe renal impairment: Not studied; consider risks and potential benefits before initiating treatment

Hepatic impairment

  • Mild Hepatic impairment (Child-Pugh A): No dosage adjustment recommended
  • Moderate or severe hepatic impairment IChild-Pugh B or C): Avoid use

Strong CYP3A4 inducers

  • If coadministered, increase to 200 mg PO BID

Proton pump inhibitors

  • If coadministered, increase to 200 mg PO BID

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