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Denosumab Products: (Prolia®); Denosumab-nxxp (Bildyos®); Denosumab-kyqq (Bosaya™); Denosumab-bnht (Conexxence®); Denosumab-qbde (Enoby™); enosumab-bbdz (Jubbonti®); Denosumab-dssb (Ospomyv™); Denosumab-bmwo (Stoboclo®)

BCBS Tennessee·Endocrinology, Rheumatology, Oncology +3 more·Medical Policy
Effective date
Jun 30, 2026
We identified it
Jun 17, 2026
Days to comply
13 days

Summary

New comprehensive medical policy covering Denosumab products (Prolia and 7 biosimilars) for osteoporosis and cancer-related bone loss, establishing prior authorization criteria, documentation requirements, and quantity limits. Policy takes effect June 30, 2026, replacing current coverage guidelines.

Action Required

Before Jun 30, 2026
Before June 30, 2026: Update prior authorization workflows for all Denosumab products including biosimilars (Bildyos, Bosaya, Conexxence, Enoby, Jubbonti, Ospomyv, Stoboclo). Billing team must program 12-month authorization limits and 60mg every 6 months quantity restrictions. Providers must document T-scores, FRAX scores, fracture history, and bisphosphonate trial history in medical records. Update encounter forms to capture required documentation elements. Claims will require prior authorization and proper documentation for approval.