Olumiant (baricitinib) vs Nanozora (ozoralizumab)

Olumiant (baricitinib) vs Nanozora (ozoralizumab)

Olumiant (baricitinib) is an oral Janus kinase (JAK) inhibitor approved for the treatment of moderate to severe rheumatoid arthritis and has been studied for its potential benefits in other inflammatory conditions. Nanozora (ozoralizumab), on the other hand, is a nanobody-based biologic therapy targeting TNF-alpha, which is under investigation for similar indications but is not yet widely approved or available. When deciding between these medications, it is important to consider factors such as the specific condition being treated, the medication's safety profile, the route of administration, and the guidance of a healthcare provider.

Difference between Olumiant and Nanozora

Metric Olumiant (baricitinib) Nanozora (ozoralizumab)
Generic name Baricitinib Ozoralizumab
Indications Rheumatoid arthritis, COVID-19 (under Emergency Use Authorization) Rheumatoid arthritis (investigational)
Mechanism of action JAK inhibitor Anti-TNF nanobody
Brand names Olumiant Nanozora (not yet commercially available)
Administrative route Oral Subcutaneous (anticipated)
Side effects Upper respiratory tract infections, nausea, headaches, hypertension Currently under investigation; not fully characterized
Contraindications Active tuberculosis, serious infections, severe hepatic impairment Not yet established
Drug class Janus kinase (JAK) inhibitor Monoclonal antibody
Manufacturer Eli Lilly and Company Not yet determined

Efficacy

Olumiant (Baricitinib) Efficacy in 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 critical 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 with RA.

In pivotal phase III studies, such as the RA-BEAM and RA-BUILD trials, baricitinib showed significant efficacy compared to placebo and active comparators. The RA-BEAM trial, for instance, revealed that baricitinib was superior to adalimumab, a commonly used TNF inhibitor, in improving the American College of Rheumatology 20 (ACR20) response rates at week 12. Moreover, baricitinib-treated patients experienced a rapid onset of action, with symptom improvements noted as early as the first week of treatment.

Nanozora (Ozoralizumab) Efficacy in Rheumatoid Arthritis

Nanozora (ozoralizumab) is an investigational monoclonal antibody being studied for the treatment of rheumatoid arthritis. As a nanobody, ozoralizumab targets and neutralizes TNF-alpha, a cytokine that plays a central role in the inflammation and joint destruction associated with RA. While ozoralizumab is not yet approved for use, clinical studies have shown promise in its efficacy for treating RA.

Early clinical trials have indicated that ozoralizumab can lead to significant improvements in RA symptoms. In these studies, patients treated with ozoralizumab experienced reductions in disease activity scores and improved physical function. The drug has been observed to have a rapid onset of action, with some patients reporting symptom relief within days of treatment initiation. However, it is important to note that as of the knowledge cutoff date, ozoralizumab is still undergoing clinical evaluation, and more data is needed to fully assess its efficacy and safety profile for the treatment of RA.

Regulatory Agency Approvals

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

Access Olumiant or Nanozora today

If Olumiant or Nanozora 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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