(aflibercept) Injectable Medication Precertification Request (aflibercept) Injectable Medication Pre 2025

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Basel, 04 February 2025 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that the US Food and Drug Administration (FDA) has approved Susvimo (ranibizumab injection) 100 mg/mL for the treatment of diabetic macular edema (DME), a leading cause of vision loss in adults with diabetes, affecting more than 29 million
The recommended dose of EYLEA for Diabetic Retinopathy is 2 mg administered by injection in the eye every 4 weeks (approximately every 28 days, monthly) for the first 5 months, followed by 1 injection every 8 weeks (2 months). Some patients may need every 4-week (monthly) dosing after the first 20 weeks (5 months).
Aflibercept injection is used to treat neovascular (wet) age-related macular degeneration (AMD). AMD is a disorder of the retina in the eye that causes blurred vision or blindness. Aflibercept works by changing the amount of blood that gets to the retina.
The FDA announced that it approved the first 2 biosimilars referencing Eylea (aflibercept) for the treatment of ophthalmic conditions, including neovascular age-related macular degeneration (AMD), macular edema, and diabetic retinopathy.
For diabetic macular edema specifically, 58% of patients had an improvement in their visual acuity measurements at 6 months compared to 6% in the control group. At one year, 80% of patients receiving Eylea improved compared to 15% in the control group.
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(NASDAQ: REGN) today announced that the U.S. Food and Drug Administration (FDA) has approved EYLEA HD (aflibercept) Injection 8 mg for the treatment of patients with wet age-related macular degeneration (wAMD), diabetic macular edema (DME) and diabetic retinopathy (DR).
The cost for Eylea (40 mg/mL) intravitreal solution is around $1,989 for a supply of 0.05 milliliters, depending on the pharmacy you visit. Quoted prices are for cash-paying customers and are not valid with insurance plans.

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