Olumiant (baricitinib) vs Kevzara (sarilumab)

Olumiant (baricitinib) vs Kevzara (sarilumab)

Olumiant (baricitinib) is an oral Janus kinase (JAK) inhibitor approved for the treatment of moderate to severe rheumatoid arthritis (RA), while Kevzara (sarilumab) is an injectable interleukin-6 (IL-6) receptor antagonist also used for the treatment of moderate to severe RA. Olumiant's mechanism of action targets enzymes involved in the inflammatory process, potentially offering a broader immunosuppressive effect, whereas Kevzara specifically blocks the IL-6 pathway, which plays a key role in the inflammation associated with RA. The choice between Olumiant and Kevzara should be made in consultation with a healthcare provider, considering factors such as the patient's disease severity, comorbid conditions, route of administration preference, and potential side effects.

Difference between Olumiant and Kevzara

Metric Olumiant (baricitinib) Kevzara (sarilumab)
Generic name Baricitinib Sarilumab
Indications Rheumatoid arthritis, COVID-19 (under Emergency Use Authorization) Moderate to severe rheumatoid arthritis
Mechanism of action Janus kinase (JAK) inhibitor Interleukin-6 (IL-6) receptor antagonist
Brand names Olumiant Kevzara
Administrative route Oral Subcutaneous injection
Side effects Upper respiratory tract infections, nausea, headache, hypertension Infections, neutropenia, injection site reactions, increased liver enzymes
Contraindications Active infection, liver enzyme elevations, thrombosis Active infection, hypersensitivity to sarilumab or excipients
Drug class JAK inhibitor Monoclonal antibody, IL-6 inhibitor
Manufacturer Eli Lilly and Company Sanofi and Regeneron Pharmaceuticals

Efficacy

Introduction to Olumiant (Baricitinib) for Rheumatoid Arthritis

Olumiant (baricitinib) is an oral medication approved for the treatment of adults with moderate to severe 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 plays a key role in the inflammatory process of RA. Clinical trials have demonstrated that baricitinib can reduce the signs and symptoms of RA, improve physical function, and inhibit the progression of structural damage in patients.

Efficacy of Olumiant in Clinical Trials

In pivotal phase III clinical trials, baricitinib has shown significant efficacy in reducing the symptoms of RA compared to placebo. The RA-BEACON study, for example, revealed that patients treated with baricitinib experienced greater improvements in disease activity scores and physical function. Furthermore, the RA-BEGIN and RA-BUILD studies confirmed the drug's efficacy in both methotrexate-naive patients and those with an inadequate response to conventional synthetic disease-modifying antirheumatic drugs (DMARDs), respectively. Baricitinib has also been associated with a rapid onset of action, with some patients experiencing symptom relief as early as the second week of treatment.

Introduction to Kevzara (Sarilumab) for Rheumatoid Arthritis

Kevzara (sarilumab) is an injectable monoclonal antibody specifically designed for the treatment of adult patients with moderately to severely active rheumatoid arthritis who have not responded adequately to one or more disease-modifying antirheumatic drugs (DMARDs). Sarilumab works by targeting and blocking the interleukin-6 (IL-6) receptor, a cytokine implicated in the inflammatory process of RA. Clinical studies have demonstrated that Kevzara can lead to significant improvements in RA symptoms, physical function, and slowing the progression of joint damage.

Efficacy of Kevzara in Clinical Studies

The efficacy of sarilumab was evaluated in several pivotal phase III trials, including the MOBILITY and TARGET studies. In these trials, patients treated with Kevzara in combination with methotrexate or other DMARDs showed a greater reduction in the signs and symptoms of RA compared to those who received placebo. Sarilumab also demonstrated superiority over placebo in achieving clinical remission and improving physical function. The safety and efficacy of Kevzara have supported its use as a treatment option for patients with an inadequate response to or intolerance of TNF inhibitors.

Regulatory Agency Approvals

Olumiant
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Kevzara
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia

Access Olumiant or Kevzara today

If Olumiant or Kevzara 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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