Maximizing the benefits of using biosimilars in Egypt
Biosimilars constitute a pathway for sustainable financing of healthcare systems in the era of expensive biologics. However, such a pathway is not free of challenges. Since the biosimilars market is expanding in Egypt, there is an urgent need for a policy framework to optimize their use and diffusio...
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Veröffentlicht in: | Journal of pharmaceutical policy and practice 2023-06, Vol.16 (1), p.79-79 |
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creator | Fasseeh, Ahmad Nader Elezbawy, Baher El-Fass, Kareem Ahmed GamaI, Mary Seyam, Ahmed Hayek, Noha Abdel Rahman, Nagwan Abdelhamid, Sohir Fasseeh, Nader Saad, Amr Shafik Elagamy, Ahmed Mahmoud, Akram Sedrak, Amal Samir Elshazly, Khaled Eldebeiky, Mariam Talaat, Monica Mohamed, Noura Maher Abdelaziz, Rania Ahmed Refaat, Remonda Akeel, Shaimaa Abaza, Sherif Kaló, Zoltán |
description | Biosimilars constitute a pathway for sustainable financing of healthcare systems in the era of expensive biologics. However, such a pathway is not free of challenges. Since the biosimilars market is expanding in Egypt, there is an urgent need for a policy framework to optimize their use and diffusion in the market. We aim to characterize a national framework based on the experiences of other countries and consultation with local experts.
A narrative literature review was conducted to identify biosimilars' policy elements worldwide. A workshop was organized with experts to discuss the narrative review findings and create consensus on recommendations.
The narrative literature review highlighted the need for biosimilar policy actions in four areas: market authorization, pricing, reimbursement, and uptake. Eighteen experts representing the Egyptian healthcare authorities attended the workshop. The most significant conclusions from the workshop included setting the price of the biosimilar at 30-40% less than its originator's price and establishing financing protocols, in which the more expensive biologics with significant price premiums should be excluded from the formulary.
A summarized national framework policy recommendation for biosimilars was created by local experts from the main public healthcare entities in Egypt. These recommendations coincide with the international policies adopted across different countries that aim to improve patient access while sustaining health expenditure. |
doi_str_mv | 10.1186/s40545-023-00581-w |
format | Article |
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A narrative literature review was conducted to identify biosimilars' policy elements worldwide. A workshop was organized with experts to discuss the narrative review findings and create consensus on recommendations.
The narrative literature review highlighted the need for biosimilar policy actions in four areas: market authorization, pricing, reimbursement, and uptake. Eighteen experts representing the Egyptian healthcare authorities attended the workshop. The most significant conclusions from the workshop included setting the price of the biosimilar at 30-40% less than its originator's price and establishing financing protocols, in which the more expensive biologics with significant price premiums should be excluded from the formulary.
A summarized national framework policy recommendation for biosimilars was created by local experts from the main public healthcare entities in Egypt. These recommendations coincide with the international policies adopted across different countries that aim to improve patient access while sustaining health expenditure.</description><identifier>ISSN: 2052-3211</identifier><identifier>EISSN: 2052-3211</identifier><identifier>DOI: 10.1186/s40545-023-00581-w</identifier><identifier>PMID: 37365620</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Biological products ; Drug formularies ; Expenditures ; Experts ; Health care expenditures ; Health care policy ; Health care reform ; Health insurance ; Health services ; Health technology assessment ; Literature reviews ; Markets ; Medical care, Cost of ; Medical policy ; Narratives ; Pharmaceutical industry ; Polls & surveys ; Prices ; Registration ; Reimbursement</subject><ispartof>Journal of pharmaceutical policy and practice, 2023-06, Vol.16 (1), p.79-79</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-c847aa1a184589207d3d9877d63f7c18bb3b6f1c419e760a5433b7e7ace7e9273</citedby><cites>FETCH-LOGICAL-c498t-c847aa1a184589207d3d9877d63f7c18bb3b6f1c419e760a5433b7e7ace7e9273</cites><orcidid>0000-0001-9878-7734</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291771/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291771/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27843,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37365620$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fasseeh, Ahmad Nader</creatorcontrib><creatorcontrib>Elezbawy, Baher</creatorcontrib><creatorcontrib>El-Fass, Kareem Ahmed</creatorcontrib><creatorcontrib>GamaI, Mary</creatorcontrib><creatorcontrib>Seyam, Ahmed</creatorcontrib><creatorcontrib>Hayek, Noha</creatorcontrib><creatorcontrib>Abdel Rahman, Nagwan</creatorcontrib><creatorcontrib>Abdelhamid, Sohir</creatorcontrib><creatorcontrib>Fasseeh, Nader</creatorcontrib><creatorcontrib>Saad, Amr Shafik</creatorcontrib><creatorcontrib>Elagamy, Ahmed</creatorcontrib><creatorcontrib>Mahmoud, Akram</creatorcontrib><creatorcontrib>Sedrak, Amal Samir</creatorcontrib><creatorcontrib>Elshazly, Khaled</creatorcontrib><creatorcontrib>Eldebeiky, Mariam</creatorcontrib><creatorcontrib>Talaat, Monica</creatorcontrib><creatorcontrib>Mohamed, Noura Maher</creatorcontrib><creatorcontrib>Abdelaziz, Rania Ahmed</creatorcontrib><creatorcontrib>Refaat, Remonda</creatorcontrib><creatorcontrib>Akeel, Shaimaa</creatorcontrib><creatorcontrib>Abaza, Sherif</creatorcontrib><creatorcontrib>Kaló, Zoltán</creatorcontrib><title>Maximizing the benefits of using biosimilars in Egypt</title><title>Journal of pharmaceutical policy and practice</title><addtitle>J Pharm Policy Pract</addtitle><description>Biosimilars constitute a pathway for sustainable financing of healthcare systems in the era of expensive biologics. However, such a pathway is not free of challenges. Since the biosimilars market is expanding in Egypt, there is an urgent need for a policy framework to optimize their use and diffusion in the market. We aim to characterize a national framework based on the experiences of other countries and consultation with local experts.
A narrative literature review was conducted to identify biosimilars' policy elements worldwide. A workshop was organized with experts to discuss the narrative review findings and create consensus on recommendations.
The narrative literature review highlighted the need for biosimilar policy actions in four areas: market authorization, pricing, reimbursement, and uptake. Eighteen experts representing the Egyptian healthcare authorities attended the workshop. The most significant conclusions from the workshop included setting the price of the biosimilar at 30-40% less than its originator's price and establishing financing protocols, in which the more expensive biologics with significant price premiums should be excluded from the formulary.
A summarized national framework policy recommendation for biosimilars was created by local experts from the main public healthcare entities in Egypt. 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Zoltán</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maximizing the benefits of using biosimilars in Egypt</atitle><jtitle>Journal of pharmaceutical policy and practice</jtitle><addtitle>J Pharm Policy Pract</addtitle><date>2023-06-26</date><risdate>2023</risdate><volume>16</volume><issue>1</issue><spage>79</spage><epage>79</epage><pages>79-79</pages><issn>2052-3211</issn><eissn>2052-3211</eissn><abstract>Biosimilars constitute a pathway for sustainable financing of healthcare systems in the era of expensive biologics. However, such a pathway is not free of challenges. Since the biosimilars market is expanding in Egypt, there is an urgent need for a policy framework to optimize their use and diffusion in the market. We aim to characterize a national framework based on the experiences of other countries and consultation with local experts.
A narrative literature review was conducted to identify biosimilars' policy elements worldwide. A workshop was organized with experts to discuss the narrative review findings and create consensus on recommendations.
The narrative literature review highlighted the need for biosimilar policy actions in four areas: market authorization, pricing, reimbursement, and uptake. Eighteen experts representing the Egyptian healthcare authorities attended the workshop. The most significant conclusions from the workshop included setting the price of the biosimilar at 30-40% less than its originator's price and establishing financing protocols, in which the more expensive biologics with significant price premiums should be excluded from the formulary.
A summarized national framework policy recommendation for biosimilars was created by local experts from the main public healthcare entities in Egypt. These recommendations coincide with the international policies adopted across different countries that aim to improve patient access while sustaining health expenditure.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37365620</pmid><doi>10.1186/s40545-023-00581-w</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9878-7734</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; PAIS Index; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access; Springer Nature OA Free Journals |
subjects | Biological products Drug formularies Expenditures Experts Health care expenditures Health care policy Health care reform Health insurance Health services Health technology assessment Literature reviews Markets Medical care, Cost of Medical policy Narratives Pharmaceutical industry Polls & surveys Prices Registration Reimbursement |
title | Maximizing the benefits of using biosimilars in Egypt |
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