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BCBS TennesseeCommercial · Prior Auth · Medical Policy · TN · Pediatrics, Endocrinology, OB-GYN +1 moreMedium impact

Leuprolide Acetate Depot Suspension (Lupron Depot-Ped®)

Act
by Nov 1, 2026
Effective date
Dec 1, 2026
Identified
Sep 10, 2026

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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What to do

by Nov 1, 2026 · 6 steps
01Billing and prior authorization teams must implement new workflow for Lupron Depot-Ped® claims.
02For CPP cases, require providers to submit laboratory documentation (GnRH agonist test results or pubertal LH levels on third-generation assay) and bone age assessment before authorization.
03For gender dysphoria cases, verify prescriber specialty (pediatric endocrinologist, family medicine, internal medicine, or OB-GYN with mental health collaboration for members under 18) and confirm member meets clinical criteria (Tanner stage 2+, informed consent documented, fertility preservation counseling documented, comorbidities controlled).
04Update authorization system to grant 12-month approvals for initial requests and reauthorizations.
05Flag any requests for members under 18 with gender dysphoria diagnosis for state regulatory review per Tennessee law.
06Train front-desk and authorization staff on new documentation requirements.
If missed: Failure to obtain proper prior authorization will result in claim denials.

Original notice

Leuprolide Acetate Depot Suspension (Lupron Depot-Ped®)
bcbst.com · Always check the source before changing claims.
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