Olumiant (baricitinib) — United Healthcare
Rheumatoid Arthritis
Initial criteria
- Diagnosis of moderately to severely active rheumatoid arthritis
- History of failure, contraindication, or intolerance to at least one TNF antagonist therapy
- Patient is not receiving Olumiant in combination with either of the following:
- Targeted immunomodulator [e.g., adalimumab, Cimzia (certolizumab), Enbrel (etanercept), Orencia (abatacept), Rinvoq (upadacitinib), Simponi (golimumab), Xeljanz (tofacitinib)]
- Potent immunosuppressant (e.g., azathioprine or cyclosporine)
Reauthorization criteria
- Documentation of positive clinical response to Olumiant therapy
- Patient is not receiving Olumiant in combination with either of the following:
- Targeted immunomodulator [e.g., adalimumab, Cimzia (certolizumab), Enbrel (etanercept), Orencia (abatacept), Rinvoq (upadacitinib), Simponi (golimumab), Xeljanz (tofacitinib)]
- Potent immunosuppressant (e.g., azathioprine or cyclosporine)
Approval duration
12 months