Iluvien® (fluocinolone acetonide) intravitreal implant (Revised)
Summary
This is a revision to Humana's Iluvien (fluocinolone acetonide) intravitreal implant prior authorization policy, effective June 24, 2026. The policy clarifies coverage for diabetic macular edema (DME) and chronic non-infectious uveitis affecting the posterior segment, requiring prior authorization with specific clinical criteria and exclusions. Key requirement: DME patients must have previous corticosteroid treatment without clinically significant intraocular pressure rise, and advanced glaucoma (cup-to-disc ratio >0.8) is a contraindication for both indications.
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