Examples of using Ipilimumab in English and their translations into Italian
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Pregnant monkeys received ipilimumab every 3 weeks from the onset of organogenesis in the first trimester through delivery, at exposure(AUC) levels either similar to or higher than those associated with the clinical dose of 3 mg/kg of ipilimumab.
were reported with concurrent administration of ipilimumab(3 mg/kg) and vemurafenib 960 mg BID or 720 mg BID.
CD8+ T cells also was observed after treatment with ipilimumab.
before starting ipilimumab, should be avoided because of their potential interference with the pharmacodynamic activity and efficacy of ipilimumab. .
Patients who were given Opdivo plus ipilimumab lived for another 11.5 months without their disease getting worse and patients given only
were reported with concurrent administration of ipilimumab(3 mg/kg)
For patients who received ipilimumab 3 mg/kg monotherapy in MDX010-20,
A drug-interaction study of ipilimumab administered alone and in combination with chemotherapy(dacarbazine
In patients who received ipilimumab 3 mg/kg monotherapy in MDX010-20,
In patients who received ipilimumab 3 mg/kg monotherapy in MDX010-20,
Ipilimumab clearance increased with increasing body weight and with increasing LDH at baseline;
The study included adult patients who had progressed on or after ipilimumab and if BRAF V600 mutation positive had also progressed on
Patients were randomized in a 3:1:1 ratio to receive ipilimumab 3 mg/kg+ an investigational gp100 peptide vaccine(gp100), ipilimumab 3 mg/kg monotherapy, or gp100 alone.
systemic anti-cancer therapy and increased with higher ipilimumab Cminss plasma concentrations.
have been reported in< 2% of patients treated with ipilimumab 3 mg/kg monotherapy:
Permanent discontinuation of treatment was required in a greater proportion of patients receiving nivolumab in combination with ipilimumab than in those receiving nivolumab monotherapy for immune-related colitis(16% and 0.7%, respectively), immune-related hepatitis(9% and 0.9%), and immune-related endocrinopathies 2.5% and 0.1.
In MDX010-20(see section 5.1), ipilimumab at 3 mg/kg with
Ipilimumab must be permanently discontinued in patients with severe(Grade 3
The safety profile of ipilimumab 3 mg/kg in chemotherapy-naive patients pooled across Phase 2
the scheduled dose of ipilimumab should be withheld see section 4.2.