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Budget impact analysis of the introduction of ranibizumab’s biosimilar to the Jordanian joint procurement system

Bibliographic Data

ID22068960
AuthorsJalal Abu Hamida (University of Jordan), Nimer S Alkhatib (0000-0001-5071-9257, Program for Appropriate Technology in Health), Khawla Abu Hammour (0000-0002-7861-1958, University of Jordan), Shiraz Halloush (Therapeutics Clinical Research), Amanj Kurdi (0000-0001-5036-1988, University of Strathclyde), Bander Balkhi (0000-0003-3801-5497, King Saud University), Osamah M Alfayez (0000-0003-4362-6508, Qassim University), Rimal Mousa (0000-0002-1788-0281, University of Jordan)
Year2026
Volume14
Pages1800784-1800784
Publication date2026-05-07
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueFrontiers in Public Health (JOURNAL)
Journal identifiersISSN: 2296-2565 • E-ISSN: 2296-2565
PublisherFrontiers Media SA (PUBLISHER • CH)
DOI10.3389/fpubh.2026.1800784
PMID42245378
OpenAlexW7160536651
LanguageEN
References cited32

Introduction: The adoption of biologic therapies imposes a substantial financial burden on the Jordanian healthcare system. ranibizumab is prescribed for various retinal disorders, and its associated costs are considerable. The introduction of biosimilars is beneficial in retaining desired clinical parameters while providing cost relief and enhanced access to patients. Objective: To examine the budget impact and expanded access of switching to ranibizumab's biosimilar for the management of retinal diseases in guideline-based practice and in real-world practice in Jordan. Method: A 4-year budget impact analysis from Jordanian public sector payer's sector was performed (2023 to 2026) that included patient prevalence and incidence, average ranibizumab dose per year, and anticipated shifts in the market share of ranibizumab and aflibercept. The model took into account the anticipated price erosion of the biosimilar in 2025 and 2026. Sensitivity analyses were performed to assess the effect of changes in uptake rates, price, and market share. Results: The annual cost savings per patient when switching from aflibercept to ranibizumab's biosimilar were from 20.55 JOD (Jordanian Dinar) to 1519.93 JOD, translating to a percentage saving of 2.68 to 35.12% across the various scenarios and indications. The total budget impact ranged widely from 6.9 M JOD to 21.2 M JOD based on treatment regimens adjusted to current practice, PRN (Pro re nata), or T&E (Treat and extend). Patient access improved between 2.75 to 124.76% in the different scenarios. Conclusion: The introduction of ranibizumab's biosimilar significantly reduces the expenditures and enhances treatment access

Aflibercept · Biosimilar · Market share · Procurement · Ranibizumab · Reimbursement · Biosimilars and Bioanalytical Methods · Health Systems, Economic Evaluations, Quality of Life · Pharmaceutical Economics and Policy

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