Secukinumab
Brand names: Cosentyx
Secukinumab is a fully human monoclonal antibody targeting interleukin-17A, used for moderate-to-severe plaque psoriasis, psoriatic arthritis, axial spondyloarthritis and hidradenitis suppurativa.
Adult dose
Dose adjustments
Not studied in renal or hepatic impairment — no dose recommendations can be made.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance or to any of the excipients
- Clinically important, active infection, e.g. active tuberculosis
Side effects
- Upper respiratory tract infections — very common (17.1%), most frequently nasopharyngitis and rhinitis
- Oral herpes — common
- Headache — common
- Diarrhoea and nausea — common
- Eczema and fatigue — common; rhinorrhoea — common
- Rare: anaphylactic reactions, angioedema, exfoliative dermatitis, hypersensitivity vasculitis; uncommon: neutropenia, oral candidiasis, inflammatory bowel disease
Interactions
- Live vaccines — the UK SPC §4.5 interaction text was not captured in the retrieved extract; verify vaccination advice against the full SPC
- Certain CYP450 substrates (from US prescribing information §7, not present in the retrieved UK SPC extract): raised cytokines during chronic inflammation may suppress CYP enzyme formation, so on starting or stopping secukinumab consider monitoring the effect or concentration of concomitant CYP450 substrates with a narrow therapeutic margin and adjust their dose as needed
Clinical monograph
How it works
It binds and neutralises interleukin-17A, a key pro-inflammatory cytokine driving keratinocyte activation and inflammation in psoriasis and related conditions.
Prescribing in practice
- Screen for active and latent tuberculosis and active infection before starting, as IL-17 inhibition increases infection risk.
- Use with caution in patients with inflammatory bowel disease, which may be triggered or exacerbated.
- Increased susceptibility to mucocutaneous candidiasis should be anticipated and managed.
Monitoring
No mandatory routine bloods are required, but monitor clinically for infection, new or worsening inflammatory bowel disease and treatment response.
Counselling the patient
- Report signs of infection or new or worsening bowel symptoms such as diarrhoea or abdominal pain.
- Patients can be trained to self-inject using the pre-filled device.
- Avoid live vaccines while on treatment.
Evidence & guidelines
NICE recommends secukinumab as an option for severe plaque psoriasis, with efficacy shown in the ERASURE and FIXTURE trials.
Reference: NICE TA350; CLEAR Trial; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Revised Original International Autoimmune Hepatitis Score (IAIHG) · Autoimmune Liver Disease
- Ho Index for Predicting Response to Medical Therapy in IBD · Inflammatory Bowel Disease
- Rh(D) Immune Globulin Dosage for Maternal-Fetal Haemorrhage · Haematology in Pregnancy
- AREDS Classification of Age-related Macular Degeneration · Macular Degeneration
- Diabetic Macular Oedema (DMO) Classification · Diabetic Retinopathy
- Retinopathy of Prematurity — International Classification (ICROP3) · Paediatric Retina
- 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