With the availability of multiple approved products for the treatment of diabetic macular edema (DME) in the EU5, including Bayer HealthCare’s Eylea, Novartis’s Lucentis, Allergan’s Ozurdex, and Alimera Sciences’ Iluvien, as well as the noteworthy use of off-label Avastin (Roche) in some countries, treatment decisions for DME are highly nuanced. They are affected not only by clinical considerations but also by the reimbursement environment in each country. Factoring in the anticipated availability of biosimilars of Lucentis and Eylea, as well as emerging therapies for DME, EU5 payers and prescribers must carefully balance clinical superiority with cost-effectiveness, and drug marketers must be well prepared to navigate a complex road to reimbursement.
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PRODUCT DESCRIPTION
Access & Reimbursement: Provides in-depth insight regarding the impact of payer policy on physician prescribing behavior so that clients can build their market access strategy and optimize their brand positioning.
Markets covered: EU5: France, Germany, Italy, Spain, United Kingdom.
Primary research:
Key companies: Roche, Bayer HealthCare, Alimera Sciences, Allergan, Allegro Ophthalmics, Novartis
Key drugs: Avastin, Eylea, Lucentis, Iluvien, Ozurdex, abicipar pegol, RG-7716, Luminate
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