Isturisa (osilodrostat) — Prior Authorization for Endogenous Cushing's Syndrome
This policy governs prior authorization and coverage criteria for Isturisa (osilodrostat tablets) for treatment of endogenous Cushing's syndrome in adults under Cigna-administered health benefit plans.
Patients awaiting surgery and patients awaiting therapeutic response after radiotherapy were added as options for approval.
Endogenous Cushing's syndrome was moved from 'Other Uses with Supportive Evidence' to 'FDA-Approved Indication'.
Requirement for a trial of one previous therapy was removed for the FDA-approved indication.
Cushing's disease is noted to be included within the endogenous Cushing's syndrome indication.
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