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How effective is Siliq?: A Comprehensive Review

3 min read

In phase 3 clinical trials, over 83% of patients taking Siliq (brodalumab) achieved at least 75% clear skin within 12 weeks. This impressive statistic shows how effective is Siliq for many individuals with moderate-to-severe plaque psoriasis, but a full understanding requires examining long-term data and side effect profiles.

Quick Summary

Siliq is a highly effective biologic medication for moderate-to-severe plaque psoriasis, demonstrating rapid and sustained skin clearance in many patients, including those who failed other therapies, though it carries notable risks.

Key Points

  • High Clearance Rates: Clinical trials show high percentages of patients achieving 75% or 100% skin clearance (PASI 75 and PASI 100) with Siliq.

  • Long-Lasting Effects: Efficacy has been shown to be sustained over several years of continuous treatment, with many achieving lasting clearance.

  • Unique Mechanism: Siliq blocks the IL-17 receptor, offering a different approach compared to other IL-17 inhibitors that target the cytokine itself.

  • Effective for Biologic Failures: It can be a successful treatment option for patients who have not responded adequately to other biologic therapies.

  • Serious Risks: The medication carries a Boxed Warning for suicidal ideation and behavior, requiring enrollment in a special safety program (REMS).

  • Monitoring Required: Due to potential side effects like serious infections, patients must be closely monitored by their healthcare provider.

In This Article

Siliq, known generically as brodalumab, is a biologic medication used to treat adults with moderate-to-severe plaque psoriasis. It is a prescription injection for patients who haven't responded well to other treatments like systemic therapies or phototherapy. To understand how effective is Siliq, it's helpful to look at clinical trial data, how it works, and how it compares to other treatments.

Understanding How Siliq Works

Siliq's effectiveness comes from its unique action. It's a human monoclonal antibody that targets and blocks the interleukin-17 receptor A (IL-17RA). By doing this, it stops several inflammatory signals, including those from IL-17A and IL-17F, which are involved in psoriasis. This specific way of blocking the receptor is thought to contribute to its effectiveness, especially for those who haven't found success with other treatments.

Clinical Trial Results: A Look at the Evidence

The effectiveness of Siliq has been shown in three large phase 3 clinical trials, called the AMAGINE studies.

High Rates of Skin Clearance

  • PASI 75, PASI 90, and PASI 100: These trials used standard measures of psoriasis severity. At 12 weeks, a significant percentage of patients achieved at least 75% skin clearance (PASI 75). Many patients also saw near or complete clearance (PASI 90 and PASI 100), with some studies showing nearly half reaching PASI 100 at 3 months.
  • sPGA 0/1: This measures clear or almost clear skin according to a physician's assessment. In the AMAGINE trials, a notable percentage of patients had a clear or almost clear score at 12 weeks.

Sustained and Long-Term Efficacy

  • 52-Week Maintenance: Many patients maintained their high level of skin clearance over time. In studies, a significant percentage of patients who achieved complete skin clearance (PASI 100) at 12 weeks kept this level of clearance through 52 weeks.
  • Multi-Year Data: Longer studies also support lasting effectiveness. A long-term study showed that patients with an average of 95% clearance at 3 months maintained over 90% clearance for up to 4.5 years with continued treatment.

How Effective is Siliq Compared to Other Treatments?

Siliq performs well when compared to other treatments, especially in achieving complete skin clearance.

Feature Siliq (Brodalumab) Ustekinumab (Stelara) Other IL-17 Inhibitors
Target IL-17 Receptor (IL-17RA) IL-12 and IL-23 cytokines IL-17A cytokine
Clearance Rates High rates of PASI 75/90/100, can be superior to ustekinumab in achieving complete clearance Effective, but some trials suggest lower complete clearance rates than Siliq Also effective, but Siliq's broader receptor blockade is a key difference
Patient Response Often effective even after other biologics have failed Response can vary, especially after prior biologic use Response can vary, depending on the specific IL-17 pathway dynamics
REMS Program Required due to boxed warning on suicidal ideation Not required Not required

In trials comparing Siliq to ustekinumab, Siliq was statistically better at achieving PASI 90 and PASI 100 at 12 weeks. Many patients also report positive experiences with Siliq, particularly those who didn't get sufficient results from other treatments.

Potential Risks and Special Considerations

Despite its effectiveness, Siliq has notable safety concerns that require careful management.

Serious Warnings and Precautions

  • Suicidal Ideation and Behavior (Boxed Warning): Siliq includes a Boxed Warning about the possibility of suicidal thoughts and behaviors, including suicide. Patients with a history of depression or suicidal tendencies might be more at risk. Because of this, Siliq is only available through a restricted program called the Siliq REMS Program.
  • Serious Infections: Taking Siliq can increase the risk of serious infections. Patients with ongoing or frequent infections need careful evaluation, and treatment should stop if a serious infection occurs.
  • Crohn's Disease: Siliq should not be used by people with Crohn's disease as it can make the condition worse.

Common Side Effects

Common side effects seen in clinical trials include:

  • Joint pain
  • Headache
  • Fatigue
  • Diarrhea
  • Mouth or throat pain
  • Nausea
  • Muscle pain
  • Reactions at the injection site
  • Fungal infections

Conclusion

When considering how effective is Siliq for moderate-to-severe plaque psoriasis, clinical trial data provides strong support. It can lead to rapid, deep, and lasting skin clearance for many patients, including those who haven't responded to other biologics. Its unique way of blocking the IL-17 receptor offers a different approach to managing psoriasis. However, it comes with a serious Boxed Warning about suicidal ideation and requires careful monitoring through a restricted program. For eligible patients and their healthcare providers, who weigh the benefits against the risks, Siliq can be a powerful option for achieving significant skin clearance.


For detailed official prescribing and safety information, please refer to the FDA Siliq Label.

Frequently Asked Questions

Some patients may start to see results in as little as two weeks. However, significant skin clearance, such as a 75% improvement, is typically observed around the 12-week mark in clinical trials.

Yes, clinical data suggests that Siliq can be effective for patients who have not responded to or have lost response to other systemic therapies, including other biologics.

The most serious risk is suicidal ideation and behavior, for which Siliq carries a Boxed Warning. Because of this, it is only available through a restricted distribution program called the Siliq REMS Program.

Siliq is contraindicated in patients with Crohn's disease, as it can worsen the condition. It should also be used with caution in patients with a history of depression or suicidal thoughts.

Siliq is given as a subcutaneous injection. The specific dosing schedule is determined by a healthcare professional and typically involves a period of more frequent initial doses followed by less frequent maintenance doses.

Siliq is unique because it blocks the IL-17 receptor (IL-17RA), inhibiting the activity of several related cytokines. Other IL-17 inhibitors target the IL-17A cytokine directly.

Clinical trials have shown promising results for Siliq in treating psoriatic arthritis symptoms. Some real-world studies also suggest effectiveness against joint issues, but it is primarily indicated for plaque psoriasis.

References

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Medical Disclaimer

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