Ilumya (tildrakizumab) vs Bimzelx (bimekizumab-bkzx)

Ilumya (tildrakizumab) vs Bimzelx (bimekizumab-bkzx)

Ilumya (tildrakizumab) and Bimzelx (bimekizumab-bkzx) are both biologic medications approved for the treatment of moderate to severe plaque psoriasis. Ilumya works by targeting IL-23, a cytokine involved in inflammatory processes, and is administered as an injection every 12 weeks after initial doses. Bimzelx, on the other hand, targets both IL-17A and IL-17F, which are also key cytokines in inflammation, and is given as an injection at a frequency determined by the prescribing physician based on the patient's needs. When deciding between the two, a patient should consider factors such as the specific cytokines targeted by the medication, dosing frequency, individual response to treatment, and potential side effects, in consultation with their healthcare provider.

Difference between Ilumya and Bimzelx

Metric Ilumya (tildrakizumab) Bimzelx (bimekizumab-bkzx)
Generic name Tildrakizumab Bimekizumab-bkzx
Indications Plaque psoriasis Plaque psoriasis
Mechanism of action IL-23 inhibitor IL-17A and IL-17F inhibitor
Brand names Ilumya Bimzelx
Administrative route Subcutaneous injection Subcutaneous injection
Side effects Upper respiratory infections, injection site reactions, diarrhea Upper respiratory tract infections, oral candidiasis, injection site reactions
Contraindications Known hypersensitivity to tildrakizumab or excipients Known hypersensitivity to bimekizumab or excipients
Drug class Monoclonal antibody Monoclonal antibody
Manufacturer Sun Pharma UCB Pharma

Efficacy

Efficacy of Ilumya (Tildrakizumab) in Treating Psoriasis

Ilumya, known by its generic name tildrakizumab, is a medication approved for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy or phototherapy. Tildrakizumab is a monoclonal antibody that targets interleukin-23 (IL-23), a cytokine that plays a key role in the inflammation and development of psoriatic plaques. Clinical trials have demonstrated that Ilumya can lead to significant improvement in psoriasis symptoms. In these studies, patients treated with Ilumya showed marked reductions in Psoriasis Area and Severity Index (PASI) scores, a measure of the severity and extent of psoriasis, indicating its efficacy in managing the condition.

The pivotal phase 3 clinical trials, reSURFACE 1 and reSURFACE 2, have provided robust data on the efficacy of Ilumya. These trials have reported that a significant proportion of patients achieved at least a 75% reduction in PASI score (PASI 75) after 12 weeks of treatment, with continued improvement over time. Furthermore, some patients even achieved PASI 90 and PASI 100 responses, representing 90% and 100% improvements in PASI scores, respectively. These results suggest that Ilumya is highly effective in clearing psoriatic lesions and improving patients' quality of life.

Efficacy of Bimzelx (Bimekizumab-bkzx) in Treating Psoriasis

Bimzelx, with the generic name bimekizumab-bkzx, is another biologic therapy recently approved for the treatment of moderate to severe plaque psoriasis in adults. Bimekizumab is a monoclonal antibody that selectively inhibits both interleukin-17A (IL-17A) and interleukin-17F (IL-17F), two key pro-inflammatory cytokines involved in the pathogenesis of psoriasis. By targeting these cytokines, Bimzelx effectively reduces inflammation and the formation of psoriatic plaques. Clinical studies have shown that Bimzelx can lead to rapid and extensive skin clearance in patients with plaque psoriasis.

The efficacy of Bimzelx has been demonstrated in phase 3 clinical trials, including BE VIVID, BE READY, and BE SURE. The results from these studies indicate that a substantial percentage of patients treated with Bimzelx achieved PASI 90 and PASI 100 responses within 16 weeks of treatment initiation. In some cases, improvements were observed as early as the first few weeks of therapy. These findings confirm that Bimzelx is an effective treatment option for patients with moderate to severe plaque psoriasis, providing significant skin clearance and improvement in disease symptoms.

Regulatory Agency Approvals

Ilumya
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Bimzelx
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Ilumya or Bimzelx today

If Ilumya or Bimzelx 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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