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IL-17A and IL-17F Inhibitor

Bimekizumab

Brand names: Bimzelx

Bimekizumab is a humanised monoclonal antibody and a systemic biologic for moderate-to-severe plaque psoriasis, also used in psoriatic arthritis and axial spondyloarthritis, given by subcutaneous injection.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It selectively binds and neutralises both interleukin-17A and interleukin-17F, two pro-inflammatory cytokines central to the keratinocyte activation and inflammation that drive psoriatic plaques.

Prescribing in practice

  • Dual IL-17 inhibition carries a notable risk of mucocutaneous candidiasis (especially oral candidiasis), and the patient should be screened and treated if infection occurs.
  • Screen for active and latent tuberculosis and exclude active infection before starting, and avoid live vaccines during treatment.
  • Use with caution in patients with a history of inflammatory bowel disease, as IL-17 inhibition has been associated with new or worsening IBD.

Monitoring

Monitor for signs of infection, candidiasis and new or worsening inflammatory bowel symptoms throughout treatment and review response against psoriasis severity scores.

Counselling the patient

  • Report sore mouth, white patches, or other signs of thrush, as well as any signs of infection.
  • Tell the team about any new or worsening bowel symptoms such as diarrhoea or abdominal pain.
  • Avoid live vaccines while on treatment and discuss vaccination needs in advance.

Evidence & guidelines

NICE has recommended bimekizumab for moderate-to-severe plaque psoriasis, supported by the BE VIVID and BE RADIANT phase 3 trials.

Reference: BE VIVID trial (Reich et al. NEJM 2021); NICE TA878; MHRA SPC Bimzelx 2023; BE RADIANT trial (McInnes et al. Lancet 2023); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.