Active Ingredient: Ipilimumab
Ipilimumab in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma.
For this indication, competent medicine agencies globally authorize below treatments:
Intravenous
1 - 1 mg per kg of body weight
From 1 To 1 mg per kg of body weight once every 21 day(s) for 84 day(s)
The recommended dose is 1 mg/kg ipilimumab in combination with 3 mg/kg nivolumab administered intravenously every 3 weeks for the first 4 doses. This is then followed by a second phase in which nivolumab monotherapy is administered intravenously at either 240 mg every 2 weeks or at 480 mg every 4 weeks, as presented in the following table. For the monotherapy phase, the first dose of nivolumab should be administered;
Recommended doses and infusion times for intravenous administration of ipilimumab in combination with nivolumab:
| Combination phase, every 3 weeks for 4 dosing cycles | Monotherapy phase | |
|---|---|---|
| Nivolumab | 3 mg/kg over 30 minutes | 240 mg every 2 weeks over 30 minutes or 480 mg every 4 weeks over 60 minutes |
| Ipilimumab | 1 mg/kg over 30 minutes | - |
Treatment with ipilimumab in combination with nivolumab, should be continued for the four doses of combination therapy as long as clinical benefit is observed or until treatment is no longer tolerated by the patient. Atypical responses (i.e. an initial transient increase in tumour size or small new lesions within the first few months followed by tumour shrinkage) have been observed. It is recommended to continue treatment with ipilimumab in combination with nivolumab for clinically stable patients with initial evidence of disease progression until disease progression is confirmed.
Liver function tests (LFTs) and thyroid function tests should be evaluated at baseline and before each dose of ipilimumab. In addition, any signs or symptoms of immune-related adverse reactions, including diarrhoea and colitis, must be assessed during treatment with ipilimumab.
The recommended infusion period is 30 or 90 minutes, depending on the dose.
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