Diabetic Macular Edema / Diabetic Retinopathy – Access & Reimbursement – Detailed, Expanded Analysis (EU5)
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.
QUESTIONS ANSWERED
- How do reimbursement terms for current DME therapies vary across the EU5? How do payers regulate the prescribing of premium-priced agents?
- What are payer and physician perspectives of promising but costly emerging therapies for DME, such as Allergan’s abicipar pegol, Allergo Ophthalmics’ Luminate, and Roche’s RG-7716? What strategies can drug developers use to optimize market access to their emerging DME and DR agents in the EU5?
- What key market access challenges do novel DME and diabetic retinopathy (DR) agents face? What lessons have been learned, and what market access levers can drug developers use to optimize the positioning of their products?
- How will market access barriers for branded DME agents evolve when the first biosimilars of Lucentis and Eylea are approved?
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:
- Survey of ophthalmologists/retinal specialists across the EU5 (~50 per country).
- Interviews with 10 EU5 payers (2 per country).
Key companies: Roche, Bayer HealthCare, Alimera Sciences, Allergan, Allegro Ophthalmics, Novartis
Key drugs: Avastin, Eylea, Lucentis, Iluvien, Ozurdex, abicipar pegol, RG-7716, Luminate
Content highlights:
- Actionable recommendations to optimize market access.
- Market access success and stumbles.
- Market access roadblocks.
- Reimbursement dynamics.
- The impact of pricing and reimbursement, policy, and coverage on prescribing.
- Market access outlook for emerging therapies.
Table of contents
- Diabetic Macular Edema / Diabetic Retinopathy - Access & Reimbursement - Detailed, Expanded Analysis (EU5)
- Access & Reimbursement - Diabetic Macular Edema/Diabetic Retinopathy EU5 [August 2018]
Yulia Privolnev, M.A., is a manager on the Global Market Access Insights team at DRG, part of Clarivate. She focuses on European market access. She holds a bachelor’s degree from the University of Toronto and a master’s degree from the London School of Economics.
Himanshu Jain, M.S.(Pharm.), is a manager on the CNS/Ophthalmology Disorders team at Clarivate. He has authored content for ophthalmology (retinal / nonretinal) and psychiatry indications, including age-related macular degeneration, diabetic retinopathy / diabetic macular edema, glaucoma, uveitis, and schizophrenia. He has more than ten years of experience working in market research and consulting firms. He earned his master’s degree from the National Institute of Pharmacological Education and Research and holds an Executive Post-Graduate Diploma in international business from the Indian Institute of Foreign Trade.