Somavert 2097 A Sgm P2023
Policy governs prior authorization, documentation, initial and continuation coverage criteria for Somavert (pegvisomant) for treatment of acromegaly. Only FDA-approved indication covered; all other uses considered experimental/investigational and not medically necessary.
No material clinical/coverage changes
Coverage Summary
Policy 2097-A (Somavert (pegvisomant) for acromegaly) governs prior authorization, documentation, and initial and continuation coverage criteria for Somavert. The policy covers the FDA-approved indication: treatment of acromegaly in patients who have had an inadequate response to surgery or radiation therapy or for whom these therapies are not appropriate. Coverage is with criteria — initial and continuation approvals require submission of specific documentation (laboratory reports and chart notes). All other uses beyond the FDA-approved acromegaly indication are considered experimental/investigational and not medically necessary.