Utidelone Injection | Breast Cancer | HongKong DengYue Medicine

  • Generic Name/Brand Name: ​Utidelone/Utidelone Injection
  • Indications:  Metastatic breast cancer
  • Dosage Form: ​IV injection, sterile solution
  • Specification: 5 mL: 50 mg x 1 vial 
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Utidelone Application Scope

  • Treatment of metastatic (recurrent or advanced) breast cancer, especially in patients previously treated with anthracyclines and taxanes.

  • Phase III trials underway for non-small cell lung cancer, gastric cancer, breast cancer neoadjuvant therapy, etc.

utidelone
utidelone

 

Characteristics

  • Ingredients:

    • Active ingredient: Utidelone (epothilone D analogue). Produced via microbial fermentation

    • Excipients: Not publicly listed (refer to full prescribing information/manufacturer

  • Properties:

    • Epothilone-based microtubule stabilizer distinct from taxanes.

    • Overcomes taxane resistance, crosses blood-brain barrier, low hematologic toxicity, tolerable peripheral neuropathy

  • Packaging Specification:​ 5 mL vial containing 50 mg Utidelone per vial

  • Storage: Unknown

  • Expiry Date: ​Unknown

  • Executive Standard: ​Chinese pharmacopoeia and NMPA GMP standards apply; specific number not publicly found.

  • Approval Number: Unknown

  • Date of Revision: ​Unknown

  • Manufacturer: Beijing Biostar Pharmaceuticals (Biostar Pharma)

Guidelines for the Use of Utidelone

  • Dosage and Administration:

    • Typical regimen: 40 mg/m² IV daily on days 1–5 every 21 days (based on NSCLC trials); breast cancer regimens are similar, often combined with capecitabine

    • Infusion administered under medical supervision; pre-treatment lab tests and monitoring recommended

  • Adverse Reactions:

    • Common: peripheral neuropathy (Grade 3 in ~23%), fatigue, diarrhea, nausea, vomiting

    • Hematologic: neutropenia, anemia, myelosuppression (mainly Grade 1–2)

    • Others: myalgia, arthralgia

  • Contraindications: Known hypersensitivity to Utidelone or formulation components; severe pre-existing neuropathy or bone marrow suppression implied.

  • Precautions:

    • Monitor blood counts regularly; manage cytopenias with supportive care.

    • Use caution in patients with liver or kidney impairment

    • Monitor for new or worsening neuropathy.

Interactions

  • Drug Interactions:​ Potential CYP3A4 substrates—use cautiously with strong inhibitors/inducers; may exacerbate hematologic or neurologic toxicity when combined with other myelosuppressive/neurotoxic agents

 

Note:

  • If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
  • It is only for internal discussion among medical staff and does not serve as a basis for medication. For specific medication guidelines, please consult the attending physician.
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