Nivolumab is a human IgG4 monoclonal antibody that targets the PD-1 receptor on T-cells, disrupting its interaction with PD-L1 and PD-L2. This releases the immune inhibition mediated by the PD-1 pathway, enabling T-cells to recognize and destroy cancer cells. When combined with ipilimumab (a CTLA-4 inhibitor), it enhances T-cell activation, promoting a more potent anti-tumor response.
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Proper Packaging
Navigo 40 (Nivolumab) is a PD-1 immune checkpoint inhibitor indicated for the treatment of various cancers, including:
Nivolumab is administered via intravenous infusion. The dosage and schedule vary by indication and may be used alone or in combination with ipilimumab, chemotherapy, or targeted therapy. Common regimens include:
Infusions are given over 30 minutes using a sterile, low protein-binding filter.
Preparation
Dilute with 0.9% Sodium Chloride or 5% Dextrose to a final concentration of 1–10 mg/mL. Do not exceed 160 mL total infusion volume (or 4 mL/kg in patients under 40 kg). Mix gently—do not shake. Administer within 8 hours at room temperature or store up to 7 days at 2–8°C protected from light.
- Pediatric: Not established in patients under 12 years (mCRC) or under 18 for other uses.
- Geriatric: No significant differences in safety or efficacy compared to younger patients.
Keep refrigerated at 2°C to 8°C. Do not freeze. Protect from light and keep out of children's reach.
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