Kaitanni (Cadonilimab Injection) – Oncologic immunotherapy | HongKong DengYue Medicine

  • Generic Name/Brand Name: Cadonilimab/Kaitanni
  • Indications: Non-small cell lung cancer (NSCLC), hepatocellular carcinoma (HCC), esophageal squamous cell carcinoma (ESCC), pancreatic cancer
  • Dosage Form: ​Injection (sterile concentrate for intravenous infusion)
  • Specification: 125 mg/10 mL × 1 vial

Cadonilimab Injection Application Scope

It is a recombinant humanized bispecific monoclonal antibody that simultaneously targets and blocks two immune checkpoint pathways: PD-1 (Programmed Cell Death Protein 1) and CTLA-4 (Cytotoxic T-Lymphocyte-Associated Protein 4).

kaitanni cadonilimab
kaitanni cadonilimab

Cadonilimab Injection Characteristics

  • Ingredients: Cadonilimab

  • Properties:​ Clear, colorless to light yellow liquid

  • Packaging Specification:​ 125 mg/10 mL/vial

  • Storage: Store refrigerated at 2–8°C (36–46°F). Keep in original carton to protect from light. Do not freeze

  • Expiry Date: 24 months from manufacturing date

  • Executive Standard: ​National Drug Standard

  • Approval Number: National Drug Approval Number S20220018

  • Date of Revision: 9.July.2025 (Please refer to the latest version of the package insert for the most current information)

  • Manufacturer: Zhongshan Kangfang Biopharmaceutical Co., Ltd

Guidelines for the Use of Cadonilimab Injection

  • Dosage and Administration:

    • Recommended Dose:

      • For Cervical Cancer: The recommended dosage is 6 mg/kg body weight, administered via intravenous infusion every 2 weeks (Q2W) until disease progression or unacceptable toxicity occurs.

      • For Gastric or GEJ Adenocarcinoma: Please consult the latest official prescribing information for the specific recommended dosage regimen for this indication, as it may involve combination therapy.

    • Administration: Administer as an intravenous infusion over approximately 60 minutes (±10 minutes). Do not administer as an intravenous push or bolus. Use a sterile, pyrogen-free, low-protein-binding in-line filter (pore size 0.22 or 0.2 μm) during infusion. Do not co-administer other drugs through the same infusion line.

    • Missed Dose:​ If a dose is missed, administer it as soon as possible. Subsequently, adjust the dosing schedule to maintain the regular interval. Consult the treating physician for specific guidance.

  • Adverse Reactions:

    • Common Adverse Reactions:

      • Fatigue: Reported in clinical trials

      • Rash: Skin reactions observed

      • Diarrhea: Gastrointestinal disturbances

      • Pruritus: Itching

    • Serious Adverse Reactions:

      • Infusion-Related Reactions (IRRs): Symptoms include fever, chills, rash, and hypotension

      • Immune-Related Adverse Events (irAEs): Such as pneumonitis, hepatitis, colitis, and endocrinopathies

  • Contraindications:

    • Hypersensitivity: Known allergy to cadonilimab or any component of the formulation

    • Active Infections: Uncontrolled infections

    • Autoimmune Disorders: Patients with active autoimmune diseases

  • Precautions:

    • Monitoring: Regular monitoring for adverse reactions during treatment

    • Pre-medication: Consideration for pre-medication to reduce the risk of infusion-related reactions

    • Discontinuation: Discontinue if severe adverse reactions occur

Cadonilimab Injection Interactions

  • Concomitant Use: Use with other immunosuppressive agents may increase the risk of adverse reactions

  • Vaccinations: Avoid live vaccines during treatmen

 

Note:

  • If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
  •  This content is for reference only. Prescription drugs must be used under a doctor’s guidance and purchased from authorized sources.
Contact Us
Contact Form Demo