Rinvoq (upadacitinib) vs Ilaris (canakinumab)

Rinvoq (upadacitinib) vs Ilaris (canakinumab)

Rinvoq (upadacitinib) is a Janus kinase (JAK) inhibitor used for treating conditions such as rheumatoid arthritis, psoriatic arthritis, and ankylosing spondylitis, working by modulating the immune system to reduce inflammation. Ilaris (canakinumab) is a monoclonal antibody that targets interleukin-1 beta (IL-1β), a cytokine that causes inflammation, and is used to treat rare auto-inflammatory conditions like Cryopyrin-Associated Periodic Syndromes (CAPS) and systemic juvenile idiopathic arthritis. When deciding between Rinvoq and Ilaris, it is crucial to consider the specific condition being treated, as each medication is approved for different indications and has a distinct mechanism of action, and the decision should be made in consultation with a healthcare provider.

Difference between Rinvoq and Ilaris

Metric Rinvoq (upadacitinib) Ilaris (canakinumab)
Generic name Upadacitinib Canakinumab
Indications Rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, atopic dermatitis, ulcerative colitis Cryopyrin-associated periodic syndromes, systemic juvenile idiopathic arthritis, adult-onset Still's disease, familial Mediterranean fever, gouty arthritis
Mechanism of action Selective Janus kinase (JAK) inhibitor, specifically inhibiting JAK1 Monoclonal antibody targeting interleukin-1 beta (IL-1β)
Brand names Rinvoq Ilaris
Administrative route Oral Subcutaneous injection
Side effects Upper respiratory infections, nausea, increased blood creatine phosphokinase, cough, pyrexia, and others Infections, vertigo, injection site reactions, weight gain, and others
Contraindications Active serious infections, hypersensitivity to upadacitinib Active infections, hypersensitivity to canakinumab or any component of the formulation
Drug class Janus kinase inhibitor Interleukin-1 beta blocker
Manufacturer AbbVie Inc. Novartis Pharmaceuticals Corporation

Efficacy

Rinvoq (Upadacitinib) for Rheumatoid Arthritis

Rinvoq (upadacitinib) is a Janus kinase (JAK) inhibitor that has been approved for the treatment of moderate to severe rheumatoid arthritis (RA) in adult patients who have had an inadequate response or intolerance to methotrexate. The efficacy of Rinvoq in rheumatoid arthritis was demonstrated in several pivotal clinical trials, where it was shown to reduce symptoms and improve physical function. Patients receiving Rinvoq experienced significant improvements in joint swelling and tenderness, which are key markers of disease activity in RA.

In these clinical trials, Rinvoq also demonstrated the ability to inhibit the progression of structural damage to joints, which is a critical aspect of managing the disease over the long term. The medication has been evaluated as both a monotherapy and in combination with other disease-modifying antirheumatic drugs (DMARDs), showing a consistent efficacy profile. The American College of Rheumatology (ACR) criteria, which measure the percentage of improvement in RA symptoms, were used as a benchmark, and Rinvoq achieved ACR20/50/70 responses, indicating 20%, 50%, and 70% improvement respectively.

Ilaris (Canakinumab) for Rheumatoid Arthritis

Ilaris (canakinumab) is an interleukin-1 beta (IL-1β) blocker that has been studied for its efficacy in rheumatoid arthritis, although it is not primarily approved for this condition. Canakinumab targets the IL-1 pathway, which is known to play a role in the inflammatory process of rheumatoid arthritis. In clinical trials, canakinumab has been assessed for its potential to reduce the signs and symptoms of RA and improve physical function in patients with the disease.

While Ilaris has shown some potential in clinical studies, its use in rheumatoid arthritis remains off-label, and further research is necessary to fully establish its efficacy and safety profile for this indication. It is important for patients and healthcare providers to consider the evidence and weigh the benefits and risks when considering Ilaris for the off-label management of rheumatoid arthritis. As with any medication, the decision to use Ilaris should be made in the context of an individual patient's overall treatment plan and in consultation with a healthcare professional who is knowledgeable about the patient's specific condition and history.

Regulatory Agency Approvals

Rinvoq
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Ilaris
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Rinvoq or Ilaris today

If Rinvoq or Ilaris are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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