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What is Bimzelx similar to?: A Comparative Look at Biologic Therapies

3 min read

As the first dual inhibitor of both IL-17A and IL-17F, Bimzelx (bimekizumab) offers a unique mechanism of action that differentiates it from many other biologic therapies. For patients and healthcare providers considering treatment for inflammatory conditions such as psoriasis and psoriatic arthritis, understanding what is Bimzelx similar to is crucial for informed decision-making.

Quick Summary

Bimzelx, a dual IL-17A and IL-17F inhibitor, is compared to other similar biologics for conditions like psoriasis, including other IL-17 inhibitors, TNF inhibitors, and IL-23 inhibitors. Differences in mechanisms, efficacy, and potential side effects are explored.

Key Points

  • Dual Inhibition of IL-17A and IL-17F: Bimzelx uniquely targets both IL-17A and IL-17F, offering broader inflammatory suppression than other IL-17 inhibitors that target only IL-17A.

  • Superior Efficacy in Trials: Head-to-head clinical trials have shown Bimzelx to be superior to Cosentyx (secukinumab), Humira (adalimumab), and Stelara (ustekinumab) in achieving high levels of skin clearance in psoriasis patients.

  • Comparable IL-17 Inhibitors: Other biologics in the IL-17 class include Cosentyx and Taltz (IL-17A blockers), and Siliq (IL-17 receptor blocker), which differ in their specific targets.

  • Alternative Biologic Classes: Beyond IL-17 inhibitors, similar biologics include TNF inhibitors (e.g., Humira), IL-23 inhibitors (e.g., Skyrizi, Tremfya), and IL-12/23 inhibitors (e.g., Stelara), each with distinct mechanisms.

  • Distinct Side Effect Profile: Bimzelx has a higher reported rate of oral candidiasis compared to other IL-17A inhibitors, though its overall safety profile is considered comparable.

  • Personalized Treatment Decisions: The best biologic choice depends on individual factors like condition severity, previous treatment history, comorbidities, efficacy expectations, and convenience of administration.

In This Article

Bimzelx (bimekizumab) is a type of biologic medication that targets interleukin-17A (IL-17A) and interleukin-17F (IL-17F), two inflammatory proteins involved in conditions like plaque psoriasis and psoriatic arthritis. By blocking both of these proteins, Bimzelx aims to reduce the inflammation associated with these diseases. This approach is distinct from some earlier biologics that target only IL-17A.

Understanding Bimzelx's Unique Mechanism

Bimzelx's dual targeting of both IL-17A and IL-17F is based on research suggesting that while IL-17A is potent, IL-17F is also significantly present in inflamed tissues. Blocking both may lead to more complete control of inflammation. Clinical trials have supported this, showing high rates of skin clearance in patients treated with Bimzelx.

Comparison with Other Interleukin-17 (IL-17) Inhibitors

Other biologics that target IL-17 are considered similar to Bimzelx, although their specific mechanisms differ.

  • Cosentyx (secukinumab): This was the first approved IL-17A inhibitor. Trials have shown Bimzelx to be more effective than Cosentyx in achieving complete skin clearance in plaque psoriasis, but Bimzelx is associated with a higher incidence of oral candidiasis.
  • Taltz (ixekizumab): Another IL-17A inhibitor, Taltz is also effective for psoriasis and psoriatic arthritis. While both Taltz and Bimzelx are effective, Bimzelx may offer an advantage in efficacy, though both have similar overall safety profiles, except for Bimzelx's increased risk of oral candidiasis.
  • Siliq (brodalumab): This biologic targets the IL-17 receptor, blocking several IL-17 subunits. Siliq carries a warning regarding suicidal ideation and should not be used in patients with Crohn's disease.

Comparison with Other Biologic Classes

Several other classes of biologics are used to treat inflammatory conditions.

  • TNF Inhibitors: Medications like adalimumab (Humira), etanercept (Enbrel), and infliximab (Remicade) block TNF-α. In head-to-head trials, Bimzelx has shown superior skin clearance compared to Humira.
  • IL-23 Inhibitors: Skyrizi (risankizumab) and Tremfya (guselkumab) target IL-23. These are effective options, but studies suggest Bimzelx may lead to a faster and more profound response.
  • IL-12/23 Inhibitors: Stelara (ustekinumab) blocks both IL-12 and IL-23. Bimzelx has demonstrated faster and better skin clearance rates in comparative trials.

Comparing Biologic Mechanisms and Features

Feature Bimzelx (bimekizumab) Cosentyx (secukinumab) Skyrizi (risankizumab) Humira (adalimumab)
Mechanism Dual IL-17A and IL-17F inhibitor IL-17A inhibitor IL-23 inhibitor TNF-alpha inhibitor
Efficacy in Trials Superior to Cosentyx, Humira, and Stelara in achieving high levels of skin clearance Established efficacy, though potentially less effective than Bimzelx for complete clearance Highly effective for psoriasis, but Bimzelx may be faster Effective, but surpassed by Bimzelx in head-to-head trial
Key Safety Note Higher risk of oral candidiasis compared to other IL-17A inhibitors Risk of upper respiratory infections and inflammatory bowel disease Risk of infections, including liver issues Risk of serious infections (e.g., TB), worsening heart failure

Considering Your Treatment Options

Choosing a biologic treatment is a personal decision made with a healthcare provider, taking into account factors like the specific condition, its severity, your medical history, and potential side effects.

Important discussion points with your doctor include:

  • Mechanism: Bimzelx's dual targeting may benefit patients who haven't responded well to biologics with single targets.
  • Efficacy: Trial data comparing Bimzelx to other biologics can inform expectations about skin clearance and how quickly a response might occur.
  • Administration: The frequency and method of receiving the medication are important considerations in managing a chronic condition.
  • Co-existing conditions: Certain biologics may be more or less suitable depending on other health issues you may have, such as inflammatory bowel disease or a history of infections.
  • Side effects: The increased risk of oral candidiasis with Bimzelx should be considered alongside the side effect profiles of other treatments.

Conclusion

Bimzelx is a notable biologic treatment, employing a dual approach by inhibiting both IL-17A and IL-17F. Clinical trials indicate high efficacy, potentially exceeding some established therapies. However, selecting a biologic involves a careful evaluation of its mechanism, effectiveness, safety profile, and convenience for each patient. While Bimzelx is comparable to other IL-17 inhibitors and biologics, its dual action and trial results suggest it may be particularly effective for rapid and complete skin clearance in certain individuals. Always consult with a healthcare provider to determine the most suitable treatment plan.

For further information on the dual inhibition of IL-17A and IL-17F, you can review this article from the NIH.

Frequently Asked Questions

While Cosentyx (secukinumab) and Taltz (ixekizumab) block only the IL-17A protein, Bimzelx (bimekizumab) is the first to block both IL-17A and IL-17F, a unique dual-inhibition mechanism.

Both medications carry an increased risk of infections, including upper respiratory tract infections. A key difference is that Bimzelx has a higher rate of oral thrush (oral candidiasis) compared to Cosentyx.

Head-to-head studies in psoriasis patients have shown Bimzelx to be superior to Cosentyx, Humira (adalimumab), and Stelara (ustekinumab) in achieving specific measures of skin clearance, such as PASI 100, at week 16.

Besides other IL-17 inhibitors, alternative biologic classes include TNF inhibitors (e.g., Humira, Enbrel), IL-23 inhibitors (e.g., Skyrizi, Tremfya), and IL-12/23 inhibitors (e.g., Stelara).

The frequency of administration for Bimzelx in the treatment of moderate-to-severe plaque psoriasis involves an initial phase followed by a maintenance phase. A healthcare professional can provide the specific schedule.

Yes. Bimzelx is approved for several inflammatory conditions, including psoriatic arthritis, ankylosing spondylitis, non-radiographic axial spondyloarthritis, and hidradenitis suppurativa.

You should discuss the potential risk of infections, be screened for tuberculosis (TB), and review any history of inflammatory bowel disease (IBD) or depression/suicidal ideation. Your doctor will consider these alongside the drug's efficacy and administration convenience.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.