Olumiant (baricitinib) vs Jyseleca (filgotinib)

Olumiant (baricitinib) vs Jyseleca (filgotinib)

Olumiant (baricitinib) and Jyseleca (filgotinib) are both oral medications classified as Janus kinase (JAK) inhibitors, used to treat conditions like rheumatoid arthritis by modulating the immune system. Baricitinib is approved for the treatment of moderate to severe rheumatoid arthritis in adults who have had an inadequate response to one or more tumor necrosis factor (TNF) antagonist therapies, and may also be used in certain cases for COVID-19, while filgotinib is specifically indicated for the treatment of moderate to severe rheumatoid arthritis. When choosing between the two, it is important to consider individual patient factors such as disease severity, previous treatments, potential side effects, and any other health conditions that may influence the drug's efficacy and safety profile.

Difference between Olumiant and Jyseleca

Metric Olumiant (baricitinib) Jyseleca (filgotinib)
Generic name Baricitinib Filgotinib
Indications Rheumatoid arthritis, COVID-19 (under Emergency Use Authorization) Rheumatoid arthritis
Mechanism of action Janus kinase (JAK) inhibitor Janus kinase (JAK) inhibitor
Brand names Olumiant Jyseleca
Administrative route Oral Oral
Side effects Upper respiratory tract infections, nausea, headache, hypertension Nausea, respiratory tract infections, elevated liver enzymes, headache
Contraindications Severe liver impairment, active serious infections Severe liver impairment, active serious infections
Drug class JAK inhibitor JAK inhibitor
Manufacturer Eli Lilly and Company Gilead Sciences

Efficacy

Introduction to Olumiant (Baricitinib) in Rheumatoid Arthritis Treatment

Olumiant (baricitinib) is an oral medication approved for the treatment of adults with moderately to severely active rheumatoid arthritis (RA) who have had an inadequate response to one or more tumor necrosis factor (TNF) antagonist therapies. As a Janus kinase (JAK) inhibitor, baricitinib works by interfering with the JAK-STAT signaling pathway, which is known to play a key role in the inflammatory process of RA. Clinical trials have demonstrated that baricitinib can reduce symptoms and improve physical function in patients with RA, and it may also slow the progression of joint damage.

Efficacy of Olumiant (Baricitinib) in Clinical Studies

The efficacy of Olumiant in the treatment of rheumatoid arthritis has been established through various clinical trials. The RA-BEACON study, for example, showed that baricitinib significantly improved clinical response and physical function compared to placebo in patients with previously inadequate responses to biologic DMARDs. Furthermore, the RA-BEGIN and RA-BUILD studies found that baricitinib was effective in patients who were methotrexate-naive or had an inadequate response to methotrexate, respectively. Patients treated with baricitinib often experienced improvement in disease activity scores and a reduction in the progression of joint damage as observed in radiographic analyses.

Introduction to Jyseleca (Filgotinib) in Rheumatoid Arthritis Management

Jyseleca (filgotinib) is another JAK inhibitor that has been approved for the treatment of adults with moderate to severe rheumatoid arthritis. Similar to baricitinib, filgotinib targets the JAK-STAT signaling pathway to exert its anti-inflammatory effects. It is indicated for patients who have had an inadequate response or intolerance to one or more DMARDs. Clinical trials have shown that filgotinib can lead to significant improvements in signs and symptoms of RA, enhance physical function, and potentially slow the radiographic progression of the disease.

Efficacy of Jyseleca (Filgotinib) in Clinical Trials

The efficacy of Jyseleca in the treatment of rheumatoid arthritis has been supported by data from multiple clinical trials, including the FINCH 1, FINCH 2, and FINCH 3 studies. These trials collectively evaluated the efficacy of filgotinib in diverse RA patient populations, ranging from methotrexate-naive patients to those with prior inadequate responses to biologic DMARDs. The results consistently showed that filgotinib provided significant improvements in disease activity scores and physical function. Additionally, filgotinib was associated with a reduction in the rate of joint damage progression, as measured by X-ray, which is a critical aspect of managing the long-term outcomes of RA.

Regulatory Agency Approvals

Olumiant
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Jyseleca
  • European Medical Agency (EMA), European Union
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Olumiant or Jyseleca today

If Olumiant or Jyseleca 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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