Rinvoq (upadacitinib) vs Simlandi (adalimumab-ryvk)

Rinvoq (upadacitinib) vs Simlandi (adalimumab-ryvk)

Rinvoq (upadacitinib) is a selective JAK inhibitor taken orally, designed to interfere with the JAK-STAT signaling pathway, which is implicated in the pathogenesis of many inflammatory and autoimmune diseases. Simlandi (adalimumab-ryvk), a biosimilar to Humira (adalimumab), is a TNF inhibitor administered through subcutaneous injection, which blocks the pro-inflammatory cytokine TNF-alpha to reduce inflammation. When choosing between the two, considerations should include the specific condition being treated, the patient's response to previous therapies, potential side effects, the route of administration preference, and the advice of a healthcare professional.

Difference between Rinvoq and Simlandi

Metric Rinvoq (upadacitinib) Simlandi (adalimumab-ryvk)
Generic name Upadacitinib Adalimumab-ryvk
Indications Rheumatoid arthritis, Psoriatic arthritis, Ankylosing spondylitis, Atopic dermatitis, Ulcerative colitis Rheumatoid arthritis, Juvenile idiopathic arthritis, Psoriatic arthritis, Ankylosing spondylitis, Crohn's disease, Ulcerative colitis, Plaque psoriasis
Mechanism of action JAK inhibitor, specifically inhibiting Janus kinase 1 (JAK1) TNF inhibitor, binds to tumor necrosis factor-alpha (TNFα)
Brand names Rinvoq Simlandi
Administrative route Oral Subcutaneous injection
Side effects Upper respiratory infections, nausea, increased blood creatinine phosphokinase, cough Injection site reactions, upper respiratory infections, headache, rash
Contraindications Active tuberculosis, serious infections, severe hepatic impairment Active tuberculosis, serious infections, moderate to severe heart failure
Drug class JAK inhibitor TNF blocker
Manufacturer AbbVie Inc. AbbVie Inc.

Efficacy

Rinvoq (Upadacitinib) Efficacy in Rheumatoid Arthritis

Rinvoq (upadacitinib) is a selective and reversible Janus kinase (JAK) inhibitor approved by the FDA for the treatment of adults with moderate to severe rheumatoid arthritis (RA) who have had an inadequate response or intolerance to methotrexate. Clinical trials have demonstrated that Rinvoq can significantly reduce the signs and symptoms of RA, including tender and swollen joints, pain, and physical function. In pivotal phase 3 studies, such as the SELECT-COMPARE trial, Rinvoq met primary and key secondary endpoints, showing superiority over placebo and, in some measures, over adalimumab when used in combination with methotrexate.

Patients treated with Rinvoq have also experienced improvements in disease activity scores and physical function as measured by the Health Assessment Questionnaire Disability Index (HAQ-DI). The drug has been shown to inhibit the progression of structural damage in patients with RA, which is a critical aspect of managing the disease long-term. The efficacy of Rinvoq has been sustained over time, with continued response rates in long-term extension studies.

Simlandi (Adalimumab-ryvk) Efficacy in Rheumatoid Arthritis

Simlandi (adalimumab-ryvk) is a biosimilar to the reference product adalimumab, a tumor necrosis factor (TNF) inhibitor widely used in the treatment of rheumatoid arthritis. Biosimilars are highly similar to and have no clinically meaningful differences from an existing FDA-approved reference product. Simlandi is approved for all indications of its reference product, including the treatment of moderate to severe rheumatoid arthritis. Clinical studies have shown that Simlandi is equivalent in efficacy to the reference adalimumab in patients with RA, providing similar reductions in disease activity and improvement in physical function.

Patients receiving Simlandi have reported outcomes consistent with those of the reference product, including the achievement of ACR20, ACR50, and ACR70 responses, which represent 20%, 50%, and 70% improvements in RA symptoms, respectively. The biosimilar has also been effective in slowing the progression of joint damage, as evidenced by radiographic assessments. As with other TNF inhibitors, Simlandi's efficacy has been observed in both methotrexate-naive patients and those who have had an inadequate response to methotrexate or other disease-modifying antirheumatic drugs (DMARDs).

Regulatory Agency Approvals

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

Access Rinvoq or Simlandi today

If Rinvoq or Simlandi 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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