Cinryze — Medica
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency – treatment of acute attacks
Initial criteria
- Patient has HAE type I or type II as confirmed by BOTH: low levels of functional C1-INH protein (< 50% of normal) at baseline AND lower than normal serum C4 levels at baseline [documentation required]
- A diagnosis of HAE with normal C1-INH (HAE type III) does NOT satisfy this requirement
- Medication is prescribed by or in consultation with an allergist/immunologist or a physician who specializes in the treatment of HAE or related disorders
Reauthorization criteria
- Patient has a diagnosis of HAE type I or type II [documentation required]
- A diagnosis of HAE with normal C1-INH (HAE type III) does NOT satisfy this requirement
- According to the prescriber, the patient has had a favorable clinical response with Berinert or Cinryze treatment (e.g., decrease in duration of attacks, quick onset of symptom relief, complete resolution of symptoms, or decreased attack frequency/severity)
- Medication is prescribed by or in consultation with an allergist/immunologist or a physician who specializes in the treatment of HAE or related disorders
Approval duration
1 year