Dupixent (dupilumab) — United Healthcare
moderate-to-severe asthma
Initial criteria
- Diagnosis of moderate-to-severe asthma
- Asthma classified as uncontrolled/inadequately controlled (poor symptom control, ≥2 systemic corticosteroid bursts, emergency treatment, airflow limitation, or oral corticosteroid dependence)
- Eosinophilic phenotype (baseline eosinophil level ≥150 cells/μL) OR oral corticosteroid dependence
- Dupixent used in combination with one of the following: (a) maximally dosed combination ICS/LABA [e.g., Advair/AirDuo, Symbicort, Breo Ellipta] OR (b) maximally dosed ICS plus one additional controller (LABA, LTRA, or theophylline)
- Not used in combination with anti-IL5 therapy [e.g., Nucala, Cinqair, Fasenra], anti-IgE therapy [e.g., Xolair], or TSLP inhibitor [e.g., Tezspire]
- Prescribed by an Allergist, Immunologist, or Pulmonologist
Reauthorization criteria
- Positive clinical response (reduction in exacerbations, decreased rescue med use, improved FEV1, reduced symptoms, or reduced corticosteroid requirements)
- Continued use in combination with an ICS-containing maintenance medication [e.g., Advair/AirDuo, Breo Ellipta, Symbicort, Trelegy Ellipta]
- Not used with anti-IL5, anti-IgE, or TSLP inhibitors
- Prescribed by an Allergist, Immunologist, or Pulmonologist
Approval duration
12 months