Tremfya (guselkumab) vs Sotyktu (deucravacitinib)

Tremfya (guselkumab) vs Sotyktu (deucravacitinib)

Tremfya (guselkumab) is a biologic medication that targets interleukin-23 (IL-23), a protein involved in the inflammatory process, and is approved for the treatment of moderate to severe plaque psoriasis and active psoriatic arthritis. Sotyktu (deucravacitinib), on the other hand, is an oral medication that inhibits TYK2, a Janus kinase involved in the signaling pathways of several pro-inflammatory cytokines, and is approved for the treatment of moderate to severe plaque psoriasis. When deciding between the two, it is important to consider factors such as the route of administration (injection for Tremfya vs oral for Sotyktu), the specific indications approved for each drug, potential side effects, and how they may interact with other medications or health conditions the patient may have.

Difference between Tremfya and Sotyktu

Metric Tremfya (guselkumab) Sotyktu (deucravacitinib)
Generic name Guselkumab Deucravacitinib
Indications Plaque psoriasis, Psoriatic arthritis Plaque psoriasis
Mechanism of action IL-23 inhibitor Tyrosine kinase 2 (TYK2) inhibitor
Brand names Tremfya Sotyktu
Administrative route Subcutaneous injection Oral
Side effects Upper respiratory infections, headache, injection site reactions Nasopharyngitis, upper respiratory tract infection, headache, diarrhea
Contraindications Active tuberculosis or other severe infections Not yet fully established
Drug class Monoclonal antibody Small molecule
Manufacturer Janssen Biotech, Inc. Bristol Myers Squibb

Efficacy

Tremfya (Guselkumab) for Psoriasis

Tremfya, with the active ingredient guselkumab, is a biologic medication approved by the U.S. Food and Drug Administration (FDA) 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 designed to selectively block 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 significant skin clearance in a majority of patients. The VOYAGE 1 and 2 trials, pivotal phase 3 studies, showed that over 70% of patients treated with guselkumab achieved at least a 90% improvement in the Psoriasis Area and Severity Index (PASI 90) by week 16, which was maintained through week 48.

Sotyktu (Deucravacitinib) for Psoriasis

Sotyktu, with the active ingredient deucravacitinib, is an oral medication that has shown efficacy in the treatment of moderate to severe plaque psoriasis. As a selective tyrosine kinase 2 (TYK2) inhibitor, Sotyktu modulates the signaling pathways that contribute to the inflammatory process in psoriasis. The drug's efficacy was evaluated in clinical trials, including the phase 3 POETYK PSO-1 and PSO-2 trials. These trials demonstrated that a significant proportion of patients achieved PASI 75, which represents at least a 75% reduction in PASI score, indicating substantial improvement in psoriatic lesions. The results were sustained over a period of 52 weeks with continuous treatment.

Comparing the efficacy of Tremfya and Sotyktu, both medications have shown to be highly effective in the treatment of psoriasis, with differences in their mechanisms of action and administration routes. Guselkumab, as a subcutaneous injection, has a well-established safety and efficacy profile, with long-term data supporting its use. Deucravacitinib, as an oral medication, offers a novel mechanism of action and the convenience of an oral route, which may be preferred by some patients. The choice between these medications may depend on individual patient factors, preferences, and the clinical judgment of the healthcare provider.

It is important to note that while these medications have been proven to be effective for psoriasis, they may have different safety profiles and contraindications. Healthcare providers should consider the full clinical picture when prescribing these treatments, including the severity of the disease, comorbid conditions, patient preference, and potential side effects. Patients should be monitored regularly to assess the efficacy and safety of the treatment and to make any necessary adjustments to their therapeutic regimen.

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
Sotyktu
  • Food and Drug Administration (FDA), USA

Access Tremfya or Sotyktu today

If Tremfya or Sotyktu 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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