IL-17A and IL-17F Inhibitor
Pregnancy: Avoid — insufficient data; animal studies showed no teratogenicity but immunoglobulin-class drugs cross placenta; effective contraception required
Bimekizumab
Brand names: Bimzelx
Adult dose
Dose: 320 mg SC every 4 weeks for 16 weeks; then every 8 weeks (maintenance)
Route: Subcutaneous injection
Frequency: Every 4 weeks (induction) then every 8 weeks (maintenance)
Max: 320 mg per dose
Moderate-severe plaque psoriasis; also licensed for PsA and axial spondyloarthritis; dual IL-17A and IL-17F inhibition
Paediatric dose
Dose: Not established N/A/kg
Route: N/A
Frequency: N/A
Max: N/A
Not licensed in paediatrics
Dose adjustments
Renal
No dose adjustment required
Hepatic
No dose adjustment required
Paediatric weight-based calculator
Not licensed in paediatrics
Clinical pearls
- BE VIVID (NEJM 2021): bimekizumab superior to ustekinumab and placebo — PASI 90 achieved in 85% vs 50% (ustekinumab) at week 16; first head-to-head trial showing superiority over established biologic
- Dual IL-17A and IL-17F inhibition: IL-17F contributes significantly to psoriatic inflammation — blocking both cytokines explains the consistently higher PASI 90/100 response rates vs IL-17A-only inhibitors (secukinumab, ixekizumab)
- MHRA 2023 approved; NICE TA878 for plaque psoriasis; oral candidiasis higher rate vs secukinumab (~20%) — counsel patients, treat topically, rarely requires discontinuation
- Avoid in IBD patients — IL-17 inhibition can worsen Crohn's disease; screen for GI symptoms before starting; if IBD develops, permanently discontinue
- BE RADIANT trial (PsA): high ACR50 and MDA rates — MHRA 2023 extended licence to PsA, positioning bimekizumab as a versatile IL-17 inhibitor across the psoriatic disease spectrum
Contraindications
- Active tuberculosis
- Serious active infections
- Inflammatory bowel disease (may worsen)
- Known hypersensitivity
Side effects
- Nasopharyngitis (most common)
- Upper respiratory tract infections
- Oral candidiasis (higher rate than IL-17A-only inhibitors)
- Injection site reactions
- IBD exacerbation
- Tinea infections
Interactions
- Live vaccines — avoid
- CYP450 substrates — IL-17 inhibition may normalise CYP450 enzyme levels; monitor warfarin, ciclosporin
Monitoring
- TB screening before initiation
- FBC and LFTs (baseline)
- Signs of infection
- IBD symptoms
- Oral candidiasis (each visit)
Reference: BNFc; BNF 90; BE VIVID trial (Reich et al. NEJM 2021); NICE TA878; MHRA SPC Bimzelx 2023; BE RADIANT trial (McInnes et al. Lancet 2023). Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- SMART Risk Score for Recurrent CVD · Cardiovascular Risk
- PCSK9 Inhibitor Eligibility Assessment · Lipid Management
- Immune-Related Adverse Events (irAE) -- GI Toxicity Colitis Grading · Oncology-Related GI
- irAE Hepatitis Grading (CTCAE) · Immunotherapy
- DIPSS — Dynamic International Prognostic Scoring System for Myelofibrosis · Cancer Prognosis
- BALL Score for Relapsed/Refractory CLL · Leukaemia
Pathways
- Suspicious Pigmented Lesion — Melanoma Pathway · NICE NG14 2015 / BAD
- Cellulitis and Erysipelas · NICE NG141 2019 / CREST
- Psoriasis — Severity Assessment and Step-Up Therapy · NICE NG153 2019 / BAD
- Atopic Eczema — Assessment and Step-Up Therapy · NICE NG95 2023
- Urticaria and Angioedema · BSACI / EAACI Guidelines 2022
- Acne Vulgaris — Grading and Treatment · NICE NG198 2021 / BAD