Sogroya (somapacitan-beco) — CareFirst (Caremark)
Adult growth hormone deficiency
Preferred products
- Norditropin
Initial criteria
- ANY of the following:
- 1. Member had 2 pretreatment pharmacologic provocative GH tests with both demonstrating deficient GH responses defined as:
- • Insulin tolerance test (ITT) peak GH ≤ 5 ng/mL OR
- • Macrilen peak GH < 2.8 ng/mL OR
- • Glucagon stimulation test peak GH ≤ 3.0 ng/mL in BMI ≤ 30 kg/m2 and high pretest probability of GHD or BMI < 25 kg/m2 OR
- • Glucagon stimulation test peak GH ≤ 1.0 ng/mL in BMI ≥ 25 kg/m2 and low pretest probability of GHD or BMI > 30 kg/m2
- AND pretreatment IGF-1 level 0 to 2 SD below mean for age and gender
- 2. Member had 1 pretreatment pharmacologic GH test demonstrating deficient GH response per above and pretreatment IGF-1 level > 2 SD below mean for age/gender
- 3. Organic hypothalamic-pituitary disease (e.g., suprasellar mass with surgery and cranial irradiation) with ≥ 3 documented pituitary hormone deficiencies and pretreatment IGF-1 level > 2 SD below mean for age/gender
- 4. Genetic or congenital structural hypothalamic-pituitary defects
- 5. Childhood-onset GH deficiency with congenital abnormality of CNS, hypothalamus, or pituitary
Reauthorization criteria
- Member currently receiving the requested medication or another growth hormone product (e.g., Norditropin) for adult GH deficiency
- ANY of the following:
- • Current IGF-1 level not elevated for age/gender
- • Organic hypothalamic-pituitary disease with ≥ 3 pituitary hormone deficiencies
- • Genetic or congenital structural hypothalamic-pituitary defects
- • Childhood-onset GH deficiency with congenital abnormality of CNS, hypothalamus, or pituitary
Approval duration
12 months