ilaris
ilaris
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Ilaris is a prescription medication containing canakinumab, a human monoclonal antibody that targets and neutralises interleukin‑1β (IL‑1β), used to treat various rare auto inflammatory conditions and gout flares.
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5-7 dayIn Stock
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Source Canadian PharmacyIlaris (canakinumab) is a fully human IgG1 monoclonal antibody designed to bind selectively to IL‑1β and block its interaction with IL‑1 receptors, thereby dampening inflammatory pathways driven by this cytokine Administered as a subcutaneous injection (typically 150 mg or weight-based dosing), it has a half-life of approximately 26 days with peak blood concentrations reached around one week post-injection
Approved Uses Include:
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Cryopyrin-Associated Periodic Syndromes (CAPS): Muckle-Wells syndrome, Neonatal-Onset Multisystem Inflammatory Disease (NOMID/CINCA), familial cold urticaria
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Tumour Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS)
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Hyperimmunoglobulin D Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD)
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Familial Mediterranean Fever (FMF)
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Still’s Disease: Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged ≥ 2 years
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Gout Flares: For adults with frequent attacks who do not respond to or cannot tolerate NSAIDs, colchicine, or steroids
 
Mechanism & Benefits:
Ilaris intercepts IL‑1β, a key inflammatory mediator, reducing symptoms like fever, joint pain, rashes, fatigue, and systemic inflammation. Clinical trials show rapid improvement—typically within 7 days—with over 70% of CAPS patients responding fully by this time and 97% by eight weeks
Administration & Safety Profile:
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Given under the skin by a healthcare provider every 4–8 weeks, depending on indication
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Common side effects include upper respiratory infections, injection-site reactions, headache, nausea, abdominal pain, and sometimes vertigo
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Serious risks include increased susceptibility to infections (including TB) and rare hypersensitivity events. Live vaccines are contraindicated during treatment, and TB screening is required before starting therapy
 
Pharmacokinetics & Efficacy Monitoring:
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Peak serum levels occur ~7 days post-dose; half‑life ~26 days; bioavailability ~66%
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Biomarkers like C‑reactive protein (CRP) and Serum Amyloid A (SAA) typically normalise within days of treatment