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Anti-IL-23p19 monoclonal antibody

Tildrakizumab

Brand names: Ilumetri

Tildrakizumab is a humanised monoclonal antibody targeting the p19 subunit of interleukin-23, used for moderate-to-severe plaque psoriasis.

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 the p19 subunit of interleukin-23, blocking IL-23-driven differentiation and activation of T-helper 17 cells and the downstream inflammation that produces psoriatic plaques.

Prescribing in practice

  • Screen for active and latent tuberculosis and exclude clinically important active infection before starting treatment.
  • Avoid initiation during a serious active infection and treat infections that arise during therapy.
  • Avoid live vaccines during treatment.

Monitoring

No mandatory routine laboratory monitoring is required; monitor clinically for infection and assess psoriasis response to guide continuation.

Counselling the patient

  • Treatment is given by subcutaneous injection, typically every few months after initial doses.
  • Report signs of infection such as fever or persistent cough.
  • Tell clinicians you are on this medicine before receiving any vaccinations.

Evidence & guidelines

NICE recommends tildrakizumab for severe plaque psoriasis, with efficacy demonstrated in the reSURFACE 1 and 2 trials.

Reference: NICE TA575; SmPC; 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.