Jyseleca (filgotinib) vs Rinvoq (upadacitinib)

Jyseleca (filgotinib) vs Rinvoq (upadacitinib)

Jyseleca (filgotinib) and Rinvoq (upadacitinib) are both Janus kinase (JAK) inhibitors used to treat conditions such as rheumatoid arthritis, but they target different subtypes of the JAK enzyme, which may influence their effectiveness and side-effect profiles. While Jyseleca selectively inhibits JAK1 and JAK2, Rinvoq is more selective for JAK1, which could theoretically result in fewer side effects related to JAK2 inhibition. The choice between these medications should be based on an individual's specific medical history, the presence of comorbidities, the physician's assessment of potential benefits versus risks, and the patient's response to previous treatments.

Difference between Jyseleca and Rinvoq

Metric Jyseleca (filgotinib) Rinvoq (upadacitinib)
Generic name Filgotinib Upadacitinib
Indications Rheumatoid arthritis, ulcerative colitis Rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, ulcerative colitis, atopic dermatitis
Mechanism of action Selective JAK1 inhibitor Selective JAK1 inhibitor
Brand names Jyseleca Rinvoq
Administrative route Oral Oral
Side effects Nausea, upper respiratory tract infections, anemia, transient liver enzyme elevations Upper respiratory tract infections, nausea, increased liver enzymes, thrombosis
Contraindications Severe liver disease, pregnancy Severe hepatic impairment, pregnancy
Drug class Janus kinase (JAK) inhibitor Janus kinase (JAK) inhibitor
Manufacturer Gilead Sciences AbbVie

Efficacy

Jyseleca (filgotinib) Efficacy in Rheumatoid Arthritis

Jyseleca, also known as filgotinib, is a medication that has demonstrated efficacy in the treatment of adults with moderate to severe rheumatoid arthritis (RA) who have had an inadequate response or intolerance to one or more disease-modifying antirheumatic drugs (DMARDs). Filgotinib is a selective Janus kinase (JAK) inhibitor that targets JAK1, which plays a role in the inflammatory process of RA. Clinical trials have shown that Jyseleca can significantly reduce the signs and symptoms of RA, improve physical function, and inhibit the progression of structural damage as evidenced by X-ray findings in patients with RA.

The FINCH series of clinical trials, which included FINCH 1, FINCH 2, and FINCH 3, provided robust data on the efficacy of filgotinib. In these studies, filgotinib was compared with placebo and, in some cases, with other active treatments. The results consistently demonstrated that patients treated with Jyseleca experienced greater improvements in the American College of Rheumatology (ACR) criteria, which measure the reduction of RA symptoms, compared to those who received placebo or a comparator drug.

Rinvoq (upadacitinib) Efficacy in Rheumatoid Arthritis

Rinvoq, with the generic name upadacitinib, is another JAK inhibitor that has been approved for the treatment of moderate to severe rheumatoid arthritis in adult patients who have had an inadequate response or intolerance to methotrexate. Upadacitinib selectively inhibits JAK1, which is implicated in the pathophysiology of RA. Clinical trials have shown that Rinvoq is effective in reducing the signs and symptoms of RA, achieving clinical remission, and improving physical function in the target patient population.

The SELECT series of phase 3 trials, including SELECT-NEXT, SELECT-BEYOND, SELECT-COMPARE, and SELECT-MONOTHERAPY, have provided evidence of upadacitinib's efficacy. These studies have shown that patients taking Rinvoq had a higher rate of ACR response compared to those on placebo or other DMARDs. Additionally, upadacitinib was found to slow the progression of joint damage, which is a critical aspect of managing RA over the long term. The SELECT-COMPARE trial, in particular, demonstrated the superiority of upadacitinib over adalimumab, a TNF inhibitor, when both were combined with methotrexate, in patients who did not respond adequately to methotrexate alone.

Regulatory Agency Approvals

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

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If Jyseleca or Rinvoq 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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