Tarlatamab-Dlle|Extensive-Stage Small Cell Lung Cancer

  • Generic Name/Brand Name: Tarlatamab-dlle / Imdelltra
  • Indications: Extensive-Stage Small Cell Lung Cancer
  • Dosage Form: Injection for intravenous use
  • Specification: 1mg/vial

Tarlatamab-Dlle Application Scope

Imdelltra is indicated for the treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC) who have experienced disease progression on or after platinum-based chemotherapy.​

tarlatamab-dlle

Tarlatamab-dlle Characteristics

  • Specification: Supplied as a kit containing a vial of tarlatamab-dlle and an IV solution stabilizer

  • Ingredients: Tarlatamab-dlle is a bispecific delta-like ligand 3 (DLL3)-directed CD3 T-cell engager

  • Properties: Designed to redirect T-cells to target and kill DLL3-expressing tumor cells

  • Packaging Specification: Packaged as a kit with necessary components for intravenous administration

  • Storage: Store in a refrigerator at 2°C to 8°C (36°F to 46°F); do not freeze

  • Expiry Date: Dependent on the shortest expiration date of any component in the kit

  • Executive Standard: Approved under FDA Accelerated Approval Program

  • Approval Number: Biologics License Application (BLA) 761344

  • Date of Revision: May 16, 2024

  • Manufacturer: Amgen Inc.​

Guidelines for the Use of Tarlatamab-dlle

Dosage and Administration:
Administered intravenously with a step-up dosing schedule to mitigate the risk of cytokine release syndrome (CRS). The recommended dosing is 3.2 mg/m² every 21 days until disease progression or unacceptable toxicity.

Adverse Reactions:

  • Common: Fatigue, pyrexia (fever), musculoskeletal pain

  • Serious: Cytokine release syndrome (CRS), neurologic toxicity including immune effector cell-associated neurotoxicity syndrome (ICANS), hepatotoxicity, hypersensitivity reactions during infusion, cytopenias (neutropenia, thrombocytopenia, anemia)

Contraindications:
Patients with known hypersensitivity to tarlatamab-dlle or any of its components.

Precautions:

  • Monitor for signs of CRS and neurologic toxicity; manage promptly.

  • Assess liver function tests before and during treatment.

  • Advise patients to avoid driving or operating machinery if experiencing dizziness, confusion, or other neurologic symptoms.

Interactions

Drug Interactions:
Has known interactions with 356 drugs, including 55 major and 301 moderate interactions. Notably, strong CYP3A inhibitors and inducers may affect tarlatamab-dlle metabolism.

 

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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