Aqneursa (levacetylleucine) — Blue Cross Blue Shield of Oklahoma
Niemann-Pick disease Type C
Initial criteria
- The patient has a diagnosis of Niemann-Pick disease Type C AND
- Genetic analysis confirms mutation in the NPC1 or NPC2 genes AND
- The patient has disease-related neurological symptoms AND
- The patient weight ≥ 15 kg AND
- The prescriber is a specialist in the area of the patient’s diagnosis (e.g., geneticist) or the prescriber has consulted with a specialist in the area of the patient’s diagnosis AND
- The patient does NOT have any FDA labeled contraindications to the requested agent
Reauthorization criteria
- The patient has been previously approved for the requested agent through the plan’s Prior Authorization process AND
- The patient has had clinical benefit with the requested agent AND
- The prescriber is a specialist in the area of the patient’s diagnosis (e.g., geneticist) or has consulted with a specialist in the area of the patient’s diagnosis AND
- The patient does NOT have any FDA labeled contraindications to the requested agent
Approval duration
BCBSIL plans: 12 months; All other plans: 6 months; Renewal: 12 months