Cipterbin (Inetetamab) | Metastatic Breast Cancer | DengYue

  • Generic Name/Brand Name: ​Inetetamab/Cipterbin
  • Indications: HER2-positive metastatic breast cancer
  • Dosage Form: ​Lyophilized powder for injection
  • Specification: 50 mg or 100 mg x 1 vial
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Inetetamab Application  Scope

Approved in China (June 2020) for HER2-positive metastatic breast cancer, used in combination with chemotherapy (e.g., vinorelbine, HER2 TKIs, pertuzumab)

Inetetamab
Inetetamab

 

Inetetamab Characteristics

  • Ingredients:

    • Active Ingredient: Inetetamab – a recombinant humanized anti-HER2 monoclonal antibody (trastuzumab-like Fab with Fc engineered at positions D359 and L361 for enhanced ADCC)
  • Properties:

    • Pan-HER2-targeting mAb that binds HER2 extracellular domain IV

    • Engineered Fc domain confers about 1.11× stronger ADCC than trastuzumab

  • Packaging Specification:​ Injection vials containing 50 mg or 100 mg inetetamab for IV infusion

  • Storage: Store in original vials at 2–8 °C (refrigerated); do not freeze

  • Expiry Date: ​Generally 24 months from manufacture; exact date printed on vial/carton

  • Executive Standard: ​Complies with China’s NMPA biologics standards; first domestically developed anti-HER2 monoclonal antibody

  • Approval Number: NMPA approval granted in June 2020 for MBC indication; investigational approval (2004 L02352) was secured under NMPA in July 2004

  • Date of Revision: ​Launched in June 2020; clinical updates ongoing through 2024 (e.g., neoadjuvant HOPES trial and real‐world studies)

  • Manufacturer: Developed and marketed by Sunshine Guojian Pharmaceutical (3SBio), a subsidiary of 3SBio in Shanghai

Guidelines for the Use of Inetetamab

  • Dosage and Administration:

    IV Administration: Examples from trials:

    • HOPES regimen – loading dose of 4 mg/kg, then 2 mg/kg weekly with vinorelbine; alternatively 8/6 mg/kg every 3 weeks

    • Standard clinical regimen – 6 mg/kg IV every 3 weeks plus chemotherapy or dual HER2

  • Adverse Reactions:

    • Hematologic: Grade 3–4 neutropenia/leukopenia (~15%)

    • General: Diarrhea, nausea, vomiting, fatigue reported; in one real-world study, any-grade AEs occurred in 96%, with grade ≥3 in ~30% (most commonly diarrhea and myelosuppression)

    • Safety profile: Manageable across regimens; no new safety signals noted

  • Contraindications: No specific contraindications reported; hypersensitivity to inetetamab or excipients presumed as general precaution.

  • Precautions:

    • Infusion reactions & hypersensitivity: Monitor during and after administration

    • Myelosuppression: Regular blood count monitoring and manage neutropenia/leukopenia as needed

    • Diarrhea: Monitor and treat promptly—especially when combined with HER2 TKIs

    • Cardiac/Pulmonary: Although rare, continued vigilance during anti-HER2 therapy is advised

Interactions

  • Drug Interactions:​
  • Combination regimens: Used safely with chemotherapy (vinorelbine, taxanes, carboplatin), TKIs (pyrotinib), and pertuzumab; can be integrated into dual-targeting strategies

  • No significant metabolic drug interactions reported for IV biologics (non-CYP mediated)

 

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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