Dupixent (dupilumab) — United Healthcare
Prurigo Nodularis
Initial criteria
- Diagnosis of prurigo nodularis
- Patient has ≥ 20 nodular lesions
- History of failure, contraindication, or intolerance to previous prurigo nodularis treatment(s) (e.g., topical corticosteroids, topical calcineurin inhibitors, topical capsaicin)
- Patient is not receiving Dupixent in combination with either of the following for the same indication: (a) Biologic immunomodulator [e.g., Adbry (tralokinumab-ldrm), Nemluvio (nemolizumab-ilto)] (b) Janus kinase inhibitor [e.g., Rinvoq (upadacitinib), Xeljanz/XR (tofacitinib), Opzelura (topical ruxolitinib), Cibinqo (abrocitinib)]
- Prescribed by dermatologist OR allergist OR immunologist
Reauthorization criteria
- Documentation of positive clinical response to Dupixent therapy
- Patient is not receiving Dupixent in combination with either biologic immunomodulator [e.g., Adbry (tralokinumab-ldrm), Nemluvio (nemolizumab-ilto)] or Janus kinase inhibitor [e.g., Rinvoq (upadacitinib), Xeljanz/XR (tofacitinib), Opzelura (topical ruxolitinib), Cibinqo (abrocitinib)] for the same indication
- Prescribed by dermatologist OR allergist OR immunologist
Approval duration
12 months