Bimekizumab Maintenance of Response at Every Visit Over 4 Years in Patients with Psoriasis Achieving Clear Skin at Week 16: Results from Four Phase 3 Trials

Introduction: Achieving and maintaining skin clearance is key for patients with psoriasis.1,2 However, loss of disease control over time is often seen with biologics; therefore, evaluating whether high efficacy levels are maintained at every visit in the long term is important.3 Here, we assess whether bimekizumab (BKZ)-treated patients, who achieved complete skin clearance (PASI 100; 100% improvement in Psoriasis Area and Severity Index) after 16 weeks, maintained BSA (body surface area) ≤1% and PASI 90/75 (≥90/75% improvement in PASI) responses at every visit over 4 years. Procedure/study: Data were pooled from the 52/56-week BE VIVID/BE SURE/BE READY trials and their 144-week open-label extension (OLE) BE BRIGHT.4–7 Included patients received BKZ 320 mg every 4 weeks (Q4W) to Week16, then Q4W or Q8W into the OLE; all received BKZ Q8W from Week100/104 or next scheduled visit. Dose groups were pooled for all analyses. Proportions of patients achieving PASI 100 at Week16 who maintained BSA ≤1%/PASI 90/PASI 75 at every subsequent study visit (29/30 further visits [study-dependent]) up to Year4 (Week196/200) are reported. Proportions who maintained their response at every visit except at most 1 and at most 2 are also reported. Patients discontinuing treatment due to lack of efficacy/treatment-related adverse events were considered non-responders at subsequent timepoints; last observation carried forward was used for other missing data (mNRI-LOCF). Results: Of 989 BKZ-randomized patients, 62.7% achieved PASI 100 at Week16 (non-responder imputation). 503 Week16 PASI 100 responders received continuous BKZ and entered the OLE. Among these patients, BSA ≤1%, PASI 90, and PASI 75 responses were maintained at every study visit from Week16–Year4 by 69.4%, 80.9%, and 93.0% of patients, respectively (at every visit except at most 1: 79.5%, 87.5%, and 95.2%; at every visit except at most 2: 84.1%, 91.8%, and 96.8%). Conclusion: High proportions of Week16 PASI 100 responders maintained BSA ≤1%/PASI 90/PASI 75 at every visit through 4 years. The vast majority maintained these responses at every visit except at most 2 visits through 4 years. Funding: UCB. Medical writing support: Costello Medical.

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Journal
SKIN The Journal of Cutaneous Medicine
Published
2025-03-17
DOI
https://doi.org/10.25251/skin.10.supp.526
Primary Topic
Psoriasis: Treatment and Pathogenesis
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article
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article

Bimekizumab Maintenance of Response at Every Visit Over 4 Years in Patients with Psoriasis Achieving Clear Skin at Week 16: Results from Four Phase 3 Trials

Peter Foley, Naiem Tony Issa, Bengt Hoepken, April Wang Armstrong et al.
SKIN The Journal of Cutaneous Medicine
Psoriasis: Treatment and Pathogenesis
article

Bimekizumab Maintenance of Response at Every Visit Over 4 Years in Patients with Psoriasis Achieving Clear Skin at Week 16: Results from Four Phase 3 Trials

Peter Foley, Naiem Tony Issa, Bengt Hoepken, April Wang Armstrong, Mark Lebwohl, Balint Szilagyi, Richard G. Langley, Georgios Kokolakis, Richard Bruce Warren, Rhys Warham, Heather Herr
article en

Abstract

Introduction: Achieving and maintaining skin clearance is key for patients with psoriasis.1,2 However, loss of disease control over time is often seen with biologics; therefore, evaluating whether high efficacy levels are maintained at every visit in the long term is important.3 Here, we assess whether bimekizumab (BKZ)-treated patients, who achieved complete skin clearance (PASI 100; 100% improvement in Psoriasis Area and Severity Index) after 16 weeks, maintained BSA (body surface area) ≤1% and PASI 90/75 (≥90/75% improvement in PASI) responses at every visit over 4 years. Procedure/study: Data were pooled from the 52/56-week BE VIVID/BE SURE/BE READY trials and their 144-week open-label extension (OLE) BE BRIGHT.4–7 Included patients received BKZ 320 mg every 4 weeks (Q4W) to Week16, then Q4W or Q8W into the OLE; all received BKZ Q8W from Week100/104 or next scheduled visit. Dose groups were pooled for all analyses. Proportions of patients achieving PASI 100 at Week16 who maintained BSA ≤1%/PASI 90/PASI 75 at every subsequent study visit (29/30 further visits [study-dependent]) up to Year4 (Week196/200) are reported. Proportions who maintained their response at every visit except at most 1 and at most 2 are also reported. Patients discontinuing treatment due to lack of efficacy/treatment-related adverse events were considered non-responders at subsequent timepoints; last observation carried forward was used for other missing data (mNRI-LOCF). Results: Of 989 BKZ-randomized patients, 62.7% achieved PASI 100 at Week16 (non-responder imputation). 503 Week16 PASI 100 responders received continuous BKZ and entered the OLE. Among these patients, BSA ≤1%, PASI 90, and PASI 75 responses were maintained at every study visit from Week16–Year4 by 69.4%, 80.9%, and 93.0% of patients, respectively (at every visit except at most 1: 79.5%, 87.5%, and 95.2%; at every visit except at most 2: 84.1%, 91.8%, and 96.8%). Conclusion: High proportions of Week16 PASI 100 responders maintained BSA ≤1%/PASI 90/PASI 75 at every visit through 4 years. The vast majority maintained these responses at every visit except at most 2 visits through 4 years. Funding: UCB. Medical writing support: Costello Medical.

SKIN The Journal of Cutaneous MedicineVol. 9(2)
Dalhousie University (CA), University of Miami (US), University of California, Los Angeles (US), The University of Melbourne (AU), George Washington University (US), Manchester Academic Health Science Centre (GB), Northern Health and Social Care Trust (GB), Humboldt-Universität zu Berlin (DE), St Vincent's Hospital Melbourne (AU), Manchester University NHS Foundation Trust (GB), Forefront of Dermatology (US), UCB Pharma (United Kingdom) (GB), NIHR Manchester Biomedical Research Centre (GB), Skin Health Institute (AU), UCB Pharma (Germany) (DE), Freie Universität Berlin (DE), Charité - Universitätsmedizin Berlin (DE), Icahn School of Medicine at Mount Sinai (US)
Openalex Percentile: Top 95%
Psoriasis: Treatment and Pathogenesis
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