Blincyto | Leukemia | HK DengYueMedicine

  • Generic Name/Brand Name: Blinatumomab/Blincyto
  • Indications: Relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL) in both adult and pediatric patients.
  • Dosage Form: Lyophilized powder 
  • Specification: Single-use vials available in 35 µg and 140 µg strengths
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Blincyto Application Scope

Blincyto (blinatumomab) is indicated for the treatment of relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL) in both adult and pediatric patients.

Blincyto Blinatumomab
Blincyto Blinatumomab

 

Blincyto Characteristics

  • Ingredients: Blinatumomab (a bispecific T-cell engager [BiTE] antibody construct).

  • Properties: A recombinant fusion protein that binds CD19 on B cells and CD3 on T cells, facilitating T-cell mediated cytotoxicity against malignant B cells.

  • Specification: Supplied as a lyophilized powder for reconstitution.

  • Packaging Specification: Provided in single-use vials (e.g., 35 µg/vial or 140 µg/vial); refer to the latest packaging details.

  • Storage: Store at 2°C to 8°C and protect from light.

  • Expiry Date: As specified on the product label (typically 36 months from the manufacturing date).

  • Executive Standard: Manufactured under current Good Manufacturing Practices (cGMP) and relevant pharmacopeial standards.

  • Approval Number: For example, US FDA NDA No. 208871 (subject to regional variations).

  • Date of Revision: Refer to the most recent product labeling.

  • Manufacturer: Amgen Inc.

Guidelines For The Use Of Blincyto

  • Dosage and Administration: Administered as a continuous intravenous infusion over 28 days per treatment cycle with a stepwise dosing regimen (e.g., an initial lower dose followed by a higher maintenance dose). Specific dosing should be confirmed with the official prescribing information.

  • Adverse Reactions: Common adverse events include cytokine release syndrome, neurological events, infections, and fever. Patients must be monitored closely.

  • Contraindications: Contraindicated in patients with known hypersensitivity to blinatumomab or any of its components.

  • Precautions: Monitor for cytokine release syndrome and neurotoxicity; dose adjustments may be necessary based on patient response.

Blincyto Interactions

Drug Interactions: Use caution when co-administering with immunosuppressants or other agents that affect T-cell function.

 

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.
  • Prescription drugs must be purchased from designated suppliers with a doctor’s prescription.
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