Rinvoq — United Healthcare
Atopic dermatitis
Initial criteria
- Patient is currently on Rinvoq therapy as documented by claims history or submission of medical records (document date and duration of therapy)
- Patient has not received a manufacturer supplied sample at no cost in the prescriber’s office, or any form of assistance from the Abbvie sponsored Rinvoq Complete program as a means to establish as a current user of Rinvoq
- Patient is not receiving Rinvoq in combination with either of the following: (a) Targeted immunomodulator [e.g., Adbry (tralokinumab-ldrm), Dupixent (dupilumab), Cibinqo (abrocitinib), Ebglyss (lebrikizumab-lbkz), Nemluvio (nemolizumab-ilto), Xeljanz/XR (tofacitinib), Olumiant (baricitinib), Opzelura (topical ruxolitinib)] OR (b) Potent immunosuppressant (e.g., azathioprine, cyclosporine, mycophenolate mofetil)
- Prescribed by a dermatologist OR allergist OR immunologist
Reauthorization criteria
- Documentation of positive clinical response to Rinvoq therapy
- Patient is not receiving Rinvoq in combination with either of the following: (a) Targeted immunomodulator [same list as above] OR (b) Potent immunosuppressant (e.g., azathioprine, cyclosporine, mycophenolate mofetil)
- Prescribed by or in consultation with a dermatologist OR allergist OR immunologist
Approval duration
12 months