Tremfya (guselkumab) vs Skyrizi (risankizumab)

Tremfya (guselkumab) vs Skyrizi (risankizumab)

Tremfya (guselkumab) and Skyrizi (risankizumab) are both injectable biologic medications approved for the treatment of moderate to severe plaque psoriasis in adults, but they target different proteins involved in the inflammatory process. Tremfya works by blocking interleukin-23 (IL-23), a cytokine that plays a key role in chronic inflammation and autoimmune diseases, and is administered once every 8 weeks after two starter doses. Skyrizi targets interleukin-23 (IL-23) as well, but it is typically administered at week 0, week 4, and then every 12 weeks thereafter, which may be a consideration for patients looking for a less frequent dosing schedule.

Difference between Tremfya and Skyrizi

Metric Tremfya (guselkumab) Skyrizi (risankizumab)
Generic name Guselkumab Risankizumab
Indications Plaque psoriasis, Psoriatic arthritis Plaque psoriasis, Psoriatic arthritis
Mechanism of action IL-23 inhibitor IL-23 inhibitor
Brand names Tremfya Skyrizi
Administrative route Subcutaneous injection Subcutaneous injection
Side effects Upper respiratory infections, headache, injection site reactions Upper respiratory infections, headache, injection site reactions
Contraindications Known hypersensitivity to guselkumab or excipients Known hypersensitivity to risankizumab or excipients
Drug class Monoclonal antibody Monoclonal antibody
Manufacturer Janssen Biotech, Inc. AbbVie Inc.

Efficacy

Efficacy of Tremfya (Guselkumab) for Psoriasis

Tremfya, with the active ingredient guselkumab, is a medication approved for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy or phototherapy. Guselkumab is a human monoclonal antibody that selectively blocks the protein interleukin-23 (IL-23), which plays a key role in the pathogenesis of psoriasis. Clinical trials have demonstrated that Tremfya is effective in achieving clear or almost clear skin. The majority of patients treated with Tremfya in clinical studies experienced significant improvement in their psoriasis symptoms, as measured by the Psoriasis Area and Severity Index (PASI) scores.

Efficacy of Skyrizi (Risankizumab) for Psoriasis

Skyrizi, containing the active substance risankizumab, is another biologic medication used for the treatment of moderate to severe plaque psoriasis in adults who may benefit from systemic therapy or phototherapy. Risankizumab is a humanized monoclonal antibody that also targets the IL-23 pathway but binds with high affinity to the p19 subunit of IL-23, inhibiting its interaction with the IL-23 receptor. In pivotal phase 3 trials, Skyrizi has shown high levels of skin clearance, with a significant proportion of patients achieving PASI 90 and PASI 100 responses, indicating 90% and 100% reductions in PASI scores respectively.

Comparative Efficacy in Clinical Trials

Comparative studies and head-to-head trials have been conducted to evaluate the efficacy of different IL-23 inhibitors, including Tremfya and Skyrizi. These studies have generally shown that both medications are highly effective for the treatment of plaque psoriasis with favorable safety profiles. While direct comparisons in clinical practice may vary, the data from clinical trials suggest that both Tremfya and Skyrizi are valuable treatment options for achieving and maintaining clear skin in patients with psoriasis.

Long-Term Efficacy and Considerations

Long-term data for both Tremfya and Skyrizi are important for understanding the sustainability of treatment response in psoriasis. Extension studies for both medications have shown that the efficacy is maintained over time, with a significant percentage of patients continuing to experience clear or almost clear skin after several years of treatment. Physicians consider various factors, including the efficacy, safety, dosing frequency, and patient preferences when selecting the most appropriate treatment for psoriasis. Both Tremfya and Skyrizi have emerged as strong contenders in the long-term management of moderate to severe plaque psoriasis.

Regulatory Agency Approvals

Tremfya
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
Skyrizi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia

Access Tremfya or Skyrizi today

If Tremfya or Skyrizi 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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