Bimekizumab Impact on Flare in Hidradenitis Suppurativa Over 2 Years: Data from BE HEARD EXT

Introduction: Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease characterised by recurrent nodules, abscesses and draining tunnels, with patients often experiencing periodic worsening of symptoms, known as flares.1 Achieving disease control is important to reduce flare frequency.1 Bimekizumab (BKZ) is a humanised monoclonal IgG1 antibody which selectively inhibits interleukin (IL)-17A and F.2 We report the proportion of patients who experienced a flare at a given visit and the cumulative proportion of patients who remained flare-free up to Weeks (Wks)48 and 96, from the BE HEARD I&II trials and their OLE, BE HEARD EXT, in patients with moderate-to-severe HS.3,4 Procedure: Data pooled from the BE HEARD I&II studies and BE HEARD EXT. Wk48 completers could enroll in BE HEARD EXT and receive open-label BKZ 320 mg Q2W/Q4W based on ≥90% HS Clinical Response (averaged from BE HEARD I&II Wks36, 40 and 44). Patients randomised to receive BKZ from baseline in BE HEARD I&II and who entered BE HEARD EXT were included (BKZ Total). Flare defined as ≥25% increase in abscess and inflammatory nodule (AN) count with an absolute increase in AN count of ≥2 relative to baseline. Proportion of patients who experienced a flare at the given visit (single point) and cumulative proportion (any visit up to and including the given timepoint) who remained flare-free up to Wks48 and 96 are reported as OC. Results: 556 patients randomised to BKZ in BE HEARD I&II completed Wk48 and entered BE HEARD EXT; 446 of these completed a lesion count assessment at Wk96. At Wk48, (12/556 [2.2%]) patients in BKZ Total experienced a flare. This low rate was maintained at Wk96 (5/446 [1.1%]). Most (466/556 [83.8%]) patients in BKZ Total remained flare-free to Wk48; this was maintained through Wk96 (372/446 [83.4%]). Conclusion: The majority of patients with moderate-to-severe HS treated with bimekizumab did not experience a flare at any given study visit and remained flare-free through 2 years. Funding: UCB. Medical writing provided by Costello Medical. Previously submitted to EHSF 2025.

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SKIN The Journal of Cutaneous Medicine
Published
2025-03-17
DOI
https://doi.org/10.25251/skin.10.supp.568
Primary Topic
Hidradenitis Suppurativa and Treatments
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article
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article

Bimekizumab Impact on Flare in Hidradenitis Suppurativa Over 2 Years: Data from BE HEARD EXT

Haley B. Naik, Leah Davis, Sayaka Yamaguchi, Pablo Fernández‐Peñas et al.
SKIN The Journal of Cutaneous Medicine
Hidradenitis Suppurativa and Treatments
article

Bimekizumab Impact on Flare in Hidradenitis Suppurativa Over 2 Years: Data from BE HEARD EXT

Haley B. Naik, Leah Davis, Sayaka Yamaguchi, Pablo Fernández‐Peñas, Antonio Martorell, Errol Prospero Prens, Steven Daveluy, Bartosz Lukowski, Z. Reguiaï, Christina Crater
article en

Abstract

Introduction: Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease characterised by recurrent nodules, abscesses and draining tunnels, with patients often experiencing periodic worsening of symptoms, known as flares.1 Achieving disease control is important to reduce flare frequency.1 Bimekizumab (BKZ) is a humanised monoclonal IgG1 antibody which selectively inhibits interleukin (IL)-17A and F.2 We report the proportion of patients who experienced a flare at a given visit and the cumulative proportion of patients who remained flare-free up to Weeks (Wks)48 and 96, from the BE HEARD I&II trials and their OLE, BE HEARD EXT, in patients with moderate-to-severe HS.3,4 Procedure: Data pooled from the BE HEARD I&II studies and BE HEARD EXT. Wk48 completers could enroll in BE HEARD EXT and receive open-label BKZ 320 mg Q2W/Q4W based on ≥90% HS Clinical Response (averaged from BE HEARD I&II Wks36, 40 and 44). Patients randomised to receive BKZ from baseline in BE HEARD I&II and who entered BE HEARD EXT were included (BKZ Total). Flare defined as ≥25% increase in abscess and inflammatory nodule (AN) count with an absolute increase in AN count of ≥2 relative to baseline. Proportion of patients who experienced a flare at the given visit (single point) and cumulative proportion (any visit up to and including the given timepoint) who remained flare-free up to Wks48 and 96 are reported as OC. Results: 556 patients randomised to BKZ in BE HEARD I&II completed Wk48 and entered BE HEARD EXT; 446 of these completed a lesion count assessment at Wk96. At Wk48, (12/556 [2.2%]) patients in BKZ Total experienced a flare. This low rate was maintained at Wk96 (5/446 [1.1%]). Most (466/556 [83.8%]) patients in BKZ Total remained flare-free to Wk48; this was maintained through Wk96 (372/446 [83.4%]). Conclusion: The majority of patients with moderate-to-severe HS treated with bimekizumab did not experience a flare at any given study visit and remained flare-free through 2 years. Funding: UCB. Medical writing provided by Costello Medical. Previously submitted to EHSF 2025.

SKIN The Journal of Cutaneous MedicineVol. 9(2)
The University of Sydney (AU), University of California, San Francisco (US), Wayne State University (US), Erasmus MC (NL), Westmead Hospital (AU), University of the Ryukyus (JP), Hospital de Manises (ES), Polyclinique de Franche Comté (FR), Hidradenitis Suppurativa Foundation (US)
Openalex Percentile: Top 90%
Hidradenitis Suppurativa and Treatments
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