Investigative Ophthalmology & Visual Science Cover Image for Volume 64, Issue 8
June 2023
Volume 64, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2023
The Biosimilar Paradox: How Anti-VEGF Biosimilars will Increase Patient and Overall Healthcare Costs
Author Affiliations & Notes
  • Casey Zhang
    Grossman School of Medicine, NYU Langone Health, New York, New York, United States
  • Scott Friedman
    Florida Retina Consultants, Lakeland, Florida, United States
  • Prithvi Mruthyunjaya
    Stanford University, Stanford, California, United States
  • Ravi Parikh
    Grossman School of Medicine, NYU Langone Health, New York, New York, United States
  • Footnotes
    Commercial Relationships   Casey Zhang None; Scott Friedman Amgen, Bayer, Chengdu Kanghong, EyePoint, Kodiak Science, Ophthea, Regeneron, RegenxBio, Code F (Financial Support); Prithvi Mruthyunjaya Alcon, Aura Biosciences, Castle Biosciences, Code C (Consultant/Contractor), Genentech, Code F (Financial Support); Ravi Parikh Apellis, Anthem Blue Cross Blue Shield, Code R (Recipient)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2023, Vol.64, 3695. doi:
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      Casey Zhang, Scott Friedman, Prithvi Mruthyunjaya, Ravi Parikh; The Biosimilar Paradox: How Anti-VEGF Biosimilars will Increase Patient and Overall Healthcare Costs. Invest. Ophthalmol. Vis. Sci. 2023;64(8):3695.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Anti-vascular endothelial growth factor (anti-VEGF) medications have a major and increasing cost on healthcare and patients. Biosimilar use may be a means to reducing these costs. However, the impending approval of an ophthalmic biosimilar formulation of bevacizumab, bevacizumab-vikg, may paradoxically increase the cost burden of intravitreal anti-VEGF, as “off-label” compounded drug may no longer be an option. We aim to investigate the impact of biosimilars on health system and patient costs in the US.

Methods : All data presented is current publicly available Medicare data and previously published market share data. Average sales price (ASP) of ranibizumab, aflibercept, and bevacizumab are calculated from Medicare allowable payments and a previously published representative Medicare administrative contractor allowable. ASPs of biosimilars are calculated from wholesale acquisition costs from a representative distributor. The cost of an intraocular bevacizumab formulation is modeled at $500 and $900 per injection, increased from $84.91 per injection with current off-label use.

Results : If an intraocular bevacizumab were to be priced at $500, costs to Medicare would increase by $457 million from $3.01 billion to $3.47 billion (an increase of 15.2%). Patient responsibility would increase by $117 million from $768 million to $884 million. Similarly, if intraocular bevacizumab were priced at $900, Medicare costs would increase by $897 million to $3.91 billion (an increase of 29.8%), and patient responsibility would increase by $229 million to $997 million. Theoretically, use of ranibizumab and aflibercept biosimilars may offset the increased cost of bevacizumab, reducing the overall costs. However, were the price of bevacizumab to increase to $500, switching all patients currently on ranibizumab or aflibercept to respective biosimilars would only compensate for 28.1% of the increased cost.

Conclusions : The eyecare sector faces a potential drastic increase in costs following the approval of an intraocular bevacizumab biosimilar and must find a way to keep intravitreal anti-VEGF injections accessible.

This abstract was presented at the 2023 ARVO Annual Meeting, held in New Orleans, LA, April 23-27, 2023.

 

Pricing an intraocular bevacizumab biosimilar at $500 per injection would result in a 15.2% increase in Medicare costs. Switching all patients currently on ranibizumab or aflibercept to respective biosimilars would only compensate for 28.1% of this increased cost.

Pricing an intraocular bevacizumab biosimilar at $500 per injection would result in a 15.2% increase in Medicare costs. Switching all patients currently on ranibizumab or aflibercept to respective biosimilars would only compensate for 28.1% of this increased cost.

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