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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