Fasenra (benralizumab) — United Healthcare
Eosinophilic granulomatosis with polyangiitis (EGPA)
Initial criteria
- One of the following:
- 1) All of the following:
- - Patient has been established on therapy with Fasenra under an active UnitedHealthcare medical benefit prior authorization for treatment of EGPA
- - AND Documentation of positive clinical response to Fasenra therapy
- - AND Patient is not receiving Fasenra in combination with any of the following for the same indication: Anti-interleukin 5 therapy [e.g., Cinqair (resilizumab), Nucala (mepolizumab)], Anti-IgE therapy [e.g., Xolair (omalizumab)], Anti-interleukin 4 therapy [e.g., Dupixent (dupilumab)], Thymic stromal lymphopoietin (TSLP) inhibitor therapy [e.g., Tezspire (tezepelumab)]
- OR
- 2) Both of the following:
- - Diagnosis of EGPA
- - AND Patient is not receiving Fasenra in combination with any of the following for the same indication: Anti-interleukin 5 therapy [e.g., Cinqair (resilizumab), Nucala (mepolizumab)], Anti-IgE therapy [e.g., Xolair (omalizumab)], Anti-interleukin 4 therapy [e.g., Dupixent (dupilumab)], Thymic stromal lymphopoietin (TSLP) inhibitor therapy [e.g., Tezspire (tezepelumab)]
Reauthorization criteria
- Both of the following:
- - Documentation of positive clinical response to Fasenra therapy
- - AND Patient is not receiving Fasenra in combination with any of the following for the same indication: Anti-interleukin 5 therapy [e.g., Cinqair, Nucala], Anti-IgE therapy [e.g., Xolair], Anti-interleukin 4 therapy [e.g., Dupixent], Thymic stromal lymphopoietin inhibitor therapy [e.g., Tezspire]
Approval duration
12 months