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Bimekizumab Shows Promise in Long-Term Management of Hidradenitis Suppurativa

10 months ago3 min read

Key Insights

  • Bimekizumab, a dual IL-17A and IL-17F inhibitor, demonstrates sustained efficacy and durability in treating moderate to severe hidradenitis suppurativa (HS) over 96 weeks.

  • Clinical trials using HiSCR75 showed bimekizumab achieves a higher benchmark in reducing inflammatory nodules and abscesses compared to previous treatments.

  • Long-term data reveals significant reductions in draining tunnels and improvements in patient-reported outcomes, enhancing patients' quality of life.

Bimekizumab is emerging as a promising therapy for the long-term management of hidradenitis suppurativa (HS), a chronic and debilitating skin condition. Recent data from the BE HEARD I and II phase 3 trials, along with open-label extension studies, highlight the drug's sustained efficacy and its potential to significantly improve patients' quality of life.

Sustained Efficacy and Durability

Unlike some existing treatments like TNF inhibitors, which often see waning efficacy over time, bimekizumab has demonstrated durable and consistent results over extended periods. According to Dr. Amit Garg, the 96-week findings provide important direction to patients and physicians in outlining a long-term treatment strategy for HS. The BE HEARD trials leading to bimekizumab’s approval used HiSCR75, a higher efficacy benchmark than HiSCR50, indicating a more clinically meaningful response.

Impact on Draining Tunnels and Patient-Reported Outcomes

One of the most burdensome aspects of HS is the presence of draining tunnels, which contribute to pain, odor, and overall discomfort. Long-term data from bimekizumab trials showed nearly a 75% reduction in draining tunnel count after two years of treatment. This reduction correlated with significant improvements in patient-reported outcomes, with one-third of HS patients reporting no impact on their lives from the disease after two years of bimekizumab treatment.

Addressing Treatment Landscape and Diversity

Bimekizumab offers a new option for patients who may not respond well to existing treatments or who require less frequent dosing. While adalimumab is available, bimekizumab offers a once-monthly administration option. Clinical trials for bimekizumab also incorporated supportive measures to enhance diversity among participants, including travel support and accommodations. This is particularly important given the higher prevalence of HS among individuals with lower socioeconomic status and Black patients.

Safety Profile and Adverse Events

The safety profile of bimekizumab is generally consistent with other IL-17 inhibitors. A notable adverse event is oral thrush, which occurs in approximately 10-15% of patients. However, this condition is typically mild and can be effectively managed with antifungals. According to Dr. Chris Sayed, the benefits of bimekizumab in managing HS far outweigh the risk of short-term thrush for most patients.

Future Directions

The evolving treatment landscape for HS includes numerous drugs in clinical development, offering hope for improved outcomes and expanded options for patients. There is a particular need for treatments specifically studied and approved for patients under 18, as current options are limited in this age group. Bimekizumab represents a significant advancement, potentially raising the bar for what can be expected in HS management and encouraging earlier intervention to prevent irreversible damage.
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