Jesduvroq (daprodustat) — United Healthcare
anemia due to chronic kidney disease (CKD) in adults receiving dialysis for at least four months
Preferred products
- Aranesp (darbepoetin)
- Epogen (epoetin alfa)
- Procrit (epoetin alfa)
- Retacrit (epoetin alfa-epbx)
Initial criteria
- Diagnosis of anemia due to chronic kidney disease (CKD)
- AND Patient has been receiving dialysis for at least four months
- AND Ferritin greater than 100 mcg/L
- AND Transferrin saturation (TSAT) greater than 20%
- AND Hemoglobin level less than 11 g/dL
- AND Trial and failure, contraindication, or intolerance to an erythropoietin stimulating agent (ESA) [e.g., Aranesp (darbepoetin), Epogen (epoetin alfa), Procrit (epoetin alfa), Retacrit (epoetin alfa-epbx)]
- AND Prescribed by or in consultation with a hematologist or nephrologist
Reauthorization criteria
- Documentation of positive clinical response to Jesduvroq therapy (e.g., clinically meaningful increase in hemoglobin level)
- AND Ferritin greater than 100 mcg/L
- AND Transferrin saturation (TSAT) greater than 20%
- AND Hemoglobin level does not exceed 12 g/dL
- AND Patient is not on concurrent treatment with an erythropoietin stimulating agent (ESA) [e.g., Aranesp (darbepoetin), Epogen (epoetin alfa), Procrit (epoetin alfa), Retacrit (epoetin alfa-epbx)]
- AND Prescribed by or in consultation with a hematologist or nephrologist
Approval duration
12 months