Olumiant (baricitinib) vs Adbry (tralokinumab-ldrm)

Olumiant (baricitinib) vs Adbry (tralokinumab-ldrm)

Olumiant (baricitinib) is an oral Janus kinase (JAK) inhibitor used primarily for the treatment of moderate to severe rheumatoid arthritis and has also been authorized for emergency use to treat COVID-19 in hospitalized adults. Adbry (tralokinumab-ldrm), on the other hand, is a subcutaneous monoclonal antibody designed to specifically target and neutralize interleukin-13 (IL-13), and it is indicated for the treatment of moderate-to-severe atopic dermatitis in adults. When deciding between these medications, it is important to consider the specific condition being treated, as Olumiant is not indicated for atopic dermatitis, and Adbry is not used for rheumatoid arthritis or COVID-19, thus the choice is highly dependent on the individual's diagnosis and the recommendation of their healthcare provider.

Difference between Olumiant and Adbry

Metric Olumiant (baricitinib) Adbry (tralokinumab-ldrm)
Generic name Baricitinib Tralokinumab-ldrm
Indications Rheumatoid arthritis, COVID-19 (under Emergency Use Authorization) Atopic dermatitis
Mechanism of action Janus kinase (JAK) inhibitor, interferes with the JAK-STAT signaling pathway Interleukin-13 (IL-13) inhibitor, blocks the action of IL-13
Brand names Olumiant Adbry
Administrative route Oral Subcutaneous injection
Side effects Upper respiratory tract infections, nausea, headaches, hypertension Injection site reactions, eye and eyelid inflammation, cold sores
Contraindications Active tuberculosis, serious infections, severe hepatic impairment Known hypersensitivity to tralokinumab or excipients
Drug class JAK inhibitor Monoclonal antibody
Manufacturer Eli Lilly and Company LEO Pharma

Efficacy

Efficacy of Olumiant (Baricitinib) for Atopic Dermatitis

Olumiant (baricitinib) is an oral medication that has been shown to be effective in the treatment of moderate-to-severe atopic dermatitis (AD) in adults. It belongs to a class of drugs known as Janus kinase (JAK) inhibitors, which work by interfering with the signaling pathway that leads to inflammation. Clinical trials have demonstrated that baricitinib, in combination with topical corticosteroids, significantly improves the signs and symptoms of atopic dermatitis, including itch, extent, and severity of the disease, compared to placebo.

Studies such as BREEZE-AD1 and BREEZE-AD2 have reported that patients treated with baricitinib achieved a clear or almost clear skin as assessed by the Investigator's Global Assessment (IGA) score, which is a significant measure of efficacy in AD treatments. Additionally, improvements in the Eczema Area and Severity Index (EASI) scores were observed, indicating a reduction in the overall disease severity. The onset of action for baricitinib is relatively rapid, with some patients experiencing relief from symptoms as early as one to two weeks after starting treatment.

Efficacy of Adbry (Tralokinumab-ldrm) for Atopic Dermatitis

Adbry (tralokinumab-ldrm) is a monoclonal antibody designed to specifically target and neutralize interleukin-13 (IL-13), a key cytokine involved in the pathogenesis of atopic dermatitis. As a biologic medication administered by subcutaneous injection, Adbry has been approved for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy. Clinical trials, including ECZTRA 1, 2, and 3, have shown that Adbry significantly improves disease severity, with a substantial proportion of patients achieving at least a 75% reduction in the EASI score (EASI-75) from baseline.

In addition to improvements in EASI scores, patients receiving Adbry have also reported enhanced quality of life and reduced itch, which are critical considerations in the management of atopic dermatitis. The efficacy of Adbry has been maintained with continued treatment, and the safety profile remains favorable, making it a promising long-term option for patients with this chronic inflammatory skin disease. It is important to note that the response to treatment can vary among individuals, and a healthcare provider can help determine the most appropriate therapy based on the patient's specific condition and medical history.

Regulatory Agency Approvals

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

Access Olumiant or Adbry today

If Olumiant or Adbry 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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