Hyftor (sirolimus 0.2% topical gel) — Cigna
Facial angiofibroma associated with tuberous sclerosis
Initial criteria
- Patient is age ≥ 6 years; AND
- Patient has a definitive diagnosis of tuberous sclerosis complex by meeting ONE of the following (a or b):
- a) Identification of a pathogenic variant in the tuberous sclerosis complex 1 (TSC1) gene or tuberous sclerosis complex 2 (TSC2) gene by genetic testing; OR
- b) According to the prescriber, clinical diagnostic criteria suggest a definitive diagnosis of tuberous sclerosis complex by meeting either two major features or one major feature with two minor features; AND
- Patient has three or more facial angiofibromas that are at least 2 mm in diameter with redness in each; AND
- Medication is prescribed by or in consultation with a dermatologist or a physician who specializes in the management of patients with tuberous sclerosis complex
Reauthorization criteria
- Patient is age ≥ 6 years; AND
- Patient has a definitive diagnosis of tuberous sclerosis complex by meeting ONE of the following (a or b):
- a) Identification of a pathogenic variant in the TSC1 or TSC2 gene by genetic testing; OR
- b) According to the prescriber, clinical diagnostic criteria suggest a definitive diagnosis of tuberous sclerosis complex by meeting either two major features or one major feature with two minor features; AND
- Patient has responded to Hyftor as evidenced by a reduction in the size and/or redness of the facial angiofibromas, as determined by the prescriber; AND
- Medication is prescribed by or in consultation with a dermatologist or a physician who specializes in the management of patients with tuberous sclerosis complex
Approval duration
initial 3 months; reauthorization 1 year