Dupilumab Dosing Recommendations
Atopic Dermatitis
For adults with moderate-to-severe atopic dermatitis, administer dupilumab 600 mg initially (two 300 mg injections), followed by 300 mg every 2 weeks. 1
Pediatric Dosing for Atopic Dermatitis
Ages 6 months to 5 years: 1
- 5 to <15 kg: 200 mg every 4 weeks (no loading dose)
- 15 to <30 kg: 300 mg every 4 weeks (no loading dose)
Ages 6 years and older: 1
- 15 to <30 kg: 600 mg loading dose (two 300 mg injections), then 300 mg every 4 weeks
- 30 to <60 kg: 400 mg loading dose (two 200 mg injections), then 200 mg every 2 weeks
- ≥60 kg: 600 mg loading dose (two 300 mg injections), then 300 mg every 2 weeks
Important Considerations for Atopic Dermatitis
- Dupilumab can be used with or without topical corticosteroids 1
- Topical calcineurin inhibitors should be reserved for problem areas only (face, neck, intertriginous and genital areas) 1
- The 300 mg every 2 weeks maintenance regimen is critical for sustained response—longer dosing intervals result in diminished efficacy 2
- For mild disease (Overall Assessment 2.0, <10% BSA), discontinuation with transition to optimized topical therapy is appropriate 3
Asthma
For adults and adolescents ≥12 years with moderate-to-severe eosinophilic asthma, use either 400 mg loading dose (two 200 mg injections) followed by 200 mg every 2 weeks OR 600 mg loading dose (two 300 mg injections) followed by 300 mg every 2 weeks. 1
Special Asthma Populations
For patients with oral corticosteroid-dependent asthma OR co-morbid moderate-to-severe atopic dermatitis OR adults with co-morbid chronic rhinosinusitis with nasal polyps: 600 mg loading dose followed by 300 mg every 2 weeks 1
Pediatric Dosing for Asthma (Ages 6-11 years)
- 15 to <30 kg: 300 mg every 4 weeks (no loading dose) 1
- ≥30 kg: 200 mg every 2 weeks (no loading dose) 1
- If co-morbid moderate-to-severe atopic dermatitis exists, follow the atopic dermatitis dosing table which includes a loading dose 1
Chronic Rhinosinusitis with Nasal Polyps (CRSwNP)
For adults and adolescents ≥12 years with inadequately controlled CRSwNP, administer 300 mg every 2 weeks (no loading dose specified in FDA labeling). 1
Evidence Supporting CRSwNP Dosing
- The SINUS-24 and SINUS-52 trials demonstrated that 300 mg every 2 weeks significantly improved nasal polyp scores, SNOT-22, disease severity, nasal congestion, smell (UPSIT), and CT scores 4
- The Bachert 2016 study used a 600 mg loading dose followed by 300 mg weekly, showing significant improvements at 16 weeks 4, 5
- Improvements occurred regardless of comorbid asthma, NSAID-exacerbated respiratory disease, or previous nasal polyp surgery 6
- All patients should continue intranasal corticosteroids (mometasone 100 μg in each nostril twice daily) concurrently 4
Other Indications
Eosinophilic Esophagitis (Ages ≥1 year, ≥15 kg)
Prurigo Nodularis (Adults)
600 mg loading dose (two 300 mg injections), then 300 mg every 2 weeks 1
Chronic Obstructive Pulmonary Disease (Adults with eosinophilic phenotype)
300 mg every 2 weeks (no loading dose) 1
Chronic Spontaneous Urticaria
Adults: 600 mg loading dose, then 300 mg every 2 weeks 1
Adolescents 12-17 years: 1
- 30 to <60 kg: 400 mg loading dose, then 200 mg every 2 weeks
- ≥60 kg: 600 mg loading dose, then 300 mg every 2 weeks
Bullous Pemphigoid (Adults)
600 mg loading dose, then 300 mg every 2 weeks in combination with a tapering course of oral corticosteroids 1
Administration Guidance
Route and Technique
- Administer subcutaneously into the thigh or abdomen (avoid 2 inches around navel) 1
- Upper arm may be used if a caregiver administers the injection 1
- Rotate injection sites with each dose 1
- Do NOT inject into tender, damaged, bruised, or scarred skin 1
Age-Appropriate Delivery Systems
- Pre-filled pen: approved for ages ≥2 years 1
- Pre-filled syringe: approved for ages ≥6 months 1
- Patients ≥12 years may self-inject under adult supervision 1
- Patients 6 months to <12 years require caregiver administration 1
Vaccination Considerations
Complete all age-appropriate vaccinations per current immunization guidelines prior to initiating dupilumab 1
Safety Profile
Common Adverse Events
- Conjunctivitis (15.6%) and eye dryness (7.8%) are the most concerning ocular side effects—advise patients to report new or worsening eye symptoms 7
- Head and neck dermatitis (19.5%) is the most common dermatologic side effect 7
- Nasopharyngitis, injection site reactions, and headache occur frequently but are generally mild 7, 5
- Most side effects do not require discontinuation 7
Critical Warnings
- Discontinue immediately if hypersensitivity reactions occur (anaphylaxis, AGEP, serum sickness, angioedema) 1
- Do not abruptly discontinue systemic, topical, or inhaled corticosteroids upon dupilumab initiation—taper gradually if appropriate 1
- Monitor for eosinophilic conditions (vasculitic rash, worsening pulmonary symptoms, cardiac complications, kidney injury, neuropathy), especially when reducing oral corticosteroids 1
- Advise patients to report new-onset psoriasis or joint symptoms—consider discontinuation if symptoms persist or worsen 1