Leuprolide Acetate Depot Suspension (Lupron Depot-Ped®)
Summary
BlueCross BlueShield of Tennessee is establishing new medical policy for Leuprolide Acetate Depot Suspension (Lupron Depot-Ped®) effective December 1, 2026, covering two indications: FDA-approved use for central precocious puberty (CPP) in pediatric patients, and compendial use for gender dysphoria in adolescents seeking gender-affirming care. The policy requires specific prior authorization criteria, provider specialties, and documentation for both indications, with 12-month authorization periods for initial and continuation therapy.
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