Filspari — Blue Cross Blue Shield of Oklahoma
primary immunoglobulin A nephropathy (IgAN)
Initial criteria
- Diagnosis of primary immunoglobulin A nephropathy (IgAN) confirmed by kidney biopsy AND
- Used to slow kidney function decline in a patient at risk for disease progression AND
- ONE of the following: (A) Urine protein-to-creatinine ratio (UPCR) ≥ 0.44 g/g OR (B) Proteinuria ≥ 0.5 g/day AND
- eGFR ≥ 30 mL/min/1.73 m^2 AND
- If the patient has an FDA labeled indication, ONE of the following: (A) Patient’s age is within FDA labeling for the requested indication OR (B) There is support for using the requested agent for the patient’s age for the requested indication AND
- ONE of the following: (A) Tried and had an inadequate response after ≥ 3-month therapy with a maximally tolerated ACE inhibitor (e.g., benazepril, lisinopril) or angiotensin II blocker (e.g., losartan), or a combination containing ACEi or ARB OR (B) Intolerance or hypersensitivity to an ACEi or ARB or a combination containing ACEi or ARB OR (C) FDA labeled contraindication to ALL ACEi or ARB AND
- Will NOT use with an ACEi, ARB, endothelin receptor antagonist (ERA, e.g., bosentan), or aliskiren AND
- Prescriber is a specialist in the area of the patient’s diagnosis (e.g., nephrologist) or has consulted with a specialist AND
- Patient does NOT have any FDA labeled contraindications to the requested agent
Reauthorization criteria
- Patient was previously approved for the requested agent through the plan’s Prior Authorization process AND
- Patient has had clinical benefit with the requested agent AND
- Will NOT use with an ACE inhibitor, ARB, ERA, or aliskiren AND
- Prescriber is a specialist in the area of the patient’s diagnosis (e.g., nephrologist) or has consulted with a specialist AND
- Patient does NOT have any FDA labeled contraindications to the requested agent
Approval duration
12 months