Skilarence (dimethyl fumarate) vs Wezlana (ustekinumab-auub)

Skilarence (dimethyl fumarate) vs Wezlana (ustekinumab-auub)

Skilarence (dimethyl fumarate) is an oral medication primarily used for the treatment of moderate to severe plaque psoriasis, working by modulating the immune system to reduce inflammation. Wezlana (ustekinumab-auub), on the other hand, is a biologic injectable medication that targets specific proteins in the immune system, interleukin-12 and interleukin-23, and is used to treat moderate to severe plaque psoriasis, psoriatic arthritis, and Crohn's disease. When deciding between the two, patients should consider factors such as the severity of their condition, route of administration preference, potential side effects, and any pre-existing health conditions that may affect treatment efficacy or safety.

Difference between Skilarence and Wezlana

Metric Skilarence (dimethyl fumarate) Wezlana (ustekinumab-auub)
Generic name Dimethyl fumarate Ustekinumab
Indications Psoriasis, Multiple Sclerosis Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, Ulcerative Colitis
Mechanism of action Activates the Nrf2 pathway, which protects cells from oxidative stress Targets interleukin-12 and interleukin-23 to modulate the immune response
Brand names Skilarence, Tecfidera Wezlana, Stelara
Administrative route Oral Subcutaneous, Intravenous
Side effects Flushing, gastrointestinal issues, lymphopenia Upper respiratory infections, headache, fatigue, injection site reactions
Contraindications Known hypersensitivity to dimethyl fumarate or its excipients Known hypersensitivity to ustekinumab or its excipients
Drug class Fumaric acid ester Monoclonal antibody
Manufacturer Almirall, Biogen Janssen Biotech

Efficacy

Efficacy of Skilarence (Dimethyl Fumarate) in Psoriasis

Skilarence, containing the active ingredient dimethyl fumarate, is an oral medication approved for the treatment of moderate to severe plaque psoriasis. Psoriasis is a chronic, immune-mediated skin condition characterized by red, scaly patches. Clinical trials have demonstrated that Skilarence can significantly reduce the severity of skin lesions and improve the quality of life for patients with psoriasis. The drug's efficacy is measured by the Psoriasis Area and Severity Index (PASI) score, which assesses the extent and severity of psoriasis. In pivotal studies, a significant number of patients treated with Skilarence achieved a 75% reduction in PASI score (PASI 75) compared to placebo, indicating a substantial improvement in their skin condition.

Efficacy of Wezlana (Ustekinumab-auub) in Psoriasis

Wezlana, with the active substance ustekinumab-auub, is a biologic medication administered via subcutaneous injection and is indicated for the treatment of moderate to severe plaque psoriasis. Ustekinumab targets interleukin-12 and interleukin-23, cytokines involved in the inflammatory processes of psoriasis. The efficacy of Wezlana has been established through extensive clinical trials. Patients receiving Wezlana have shown a significant improvement in their PASI scores, with many achieving PASI 75, PASI 90, and even PASI 100, which represents complete clearance of psoriatic lesions. The response to Wezlana is typically rapid, with patients often observing improvements within the first few weeks of treatment.

Comparison of Efficacy in Psoriasis Treatment

When comparing Skilarence and Wezlana, both medications have demonstrated efficacy in the treatment of psoriasis, albeit through different mechanisms of action. Skilarence, as an oral treatment, may be preferred by patients who are averse to injections. However, Wezlana, as a biologic, may be more suitable for patients with more severe disease or those who have not responded adequately to traditional systemic therapies. The choice between these medications should be individualized, taking into account the patient's medical history, the severity of psoriasis, and the presence of comorbidities.

Considerations and Conclusion

In conclusion, both Skilarence and Wezlana have been shown to be effective treatments for moderate to severe plaque psoriasis. The efficacy of these medications has been validated in clinical trials, which have highlighted their potential to significantly reduce the burden of psoriasis on patients. It is important for healthcare providers to consider the individual needs and preferences of patients, as well as the safety profiles and potential side effects of these medications, when recommending a treatment plan for psoriasis.

Regulatory Agency Approvals

Skilarence
  • European Medical Agency (EMA), European Union
Wezlana
  • Food and Drug Administration (FDA), USA

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If Skilarence or Wezlana 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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