Dupilumab
Brand names: Dupixent
Dupilumab is a fully human monoclonal antibody used as a subcutaneous biologic for moderate-to-severe atopic dermatitis and other type 2 inflammatory conditions such as asthma and chronic rhinosinusitis with nasal polyps.
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 binds the shared alpha subunit of the interleukin-4 receptor, blocking signalling of both IL-4 and IL-13, the key cytokines driving type 2 inflammation.
Prescribing in practice
- Conjunctivitis and keratitis are recognised class effects; advise patients to report new or worsening eye symptoms and refer for ophthalmology assessment if severe or persistent.
- It is given by subcutaneous injection and, in atopic dermatitis, is typically reserved for disease inadequately controlled by topical therapy or where systemic treatment is indicated.
- Avoid initiating in the presence of active infection and ensure age-appropriate vaccinations are up to date before starting; live vaccines should generally be avoided during treatment.
Monitoring
Routine laboratory monitoring is not generally mandated, but patients should be reviewed for treatment response, injection-site and hypersensitivity reactions, and ocular symptoms.
Counselling the patient
- Report any new or worsening eye redness, irritation or visual change promptly.
- Patients or carers can be trained to self-administer the subcutaneous injection at home.
- Continue prescribed emollients and topical treatments alongside dupilumab unless told otherwise.
Evidence & guidelines
NICE has issued technology appraisal guidance supporting dupilumab for moderate-to-severe atopic dermatitis, supported by the pivotal SOLO and CHRONOS randomised trials.
Reference: NICE TA534; BAD Dupilumab Guidelines; EADV Guidelines; 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.
- EASI — Eczema Area and Severity Index · Diagnosis
- PASI Score (Psoriasis Area and Severity Index) · Psoriasis
- DLQI (Dermatology Life Quality Index) · Quality of Life
- EASI Score (Eczema Area and Severity Index) · Atopic Dermatitis
- Eosinophilic Oesophagitis Endoscopic Reference Score (EREFS) · Upper GI
- Index of Severity for Eosinophilic Oesophagitis (I-SEE) · Oesophageal Disease
- 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