Nonclinical Similarity of the Biosimilar Candidate ABP 938 with Aflibercept Reference Product

Introduction ABP 938 is being developed as a biosimilar to Eylea ® (aflibercept reference product [RP]), an anti-vascular endothelial growth factor (VEGF) drug used in the management of retinal diseases. Previously, a comparative analytical similarity assessment demonstrated that ABP 938 and afliber...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Ophthalmology and Therapy 2025, Vol.14 (1), p.85-101
Hauptverfasser: Seo, Neungseon, Kuhns, Scott, Andrews, Dina A., Colbert, Alexander, Chow, Vincent, Liu, Jennifer
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 101
container_issue 1
container_start_page 85
container_title Ophthalmology and Therapy
container_volume 14
creator Seo, Neungseon
Kuhns, Scott
Andrews, Dina A.
Colbert, Alexander
Chow, Vincent
Liu, Jennifer
description Introduction ABP 938 is being developed as a biosimilar to Eylea ® (aflibercept reference product [RP]), an anti-vascular endothelial growth factor (VEGF) drug used in the management of retinal diseases. Previously, a comparative analytical similarity assessment demonstrated that ABP 938 and aflibercept RP have the same amino acid sequence and exhibit similar higher-order structure and biological activity. The nonclinical studies described here were designed to assess the in vitro pharmacology and the in vivo pharmacokinetics (PK), toxicokinetics (TK), and safety profiles of ABP 938 compared to aflibercept RP. Methods In vitro target-binding kinetics and affinity for VEGF-A and placental growth factor (PIGF) isoforms were evaluated using surface plasmon resonance (SPR). Effector functions were assessed by cell-based assays. PK was evaluated in a nonterminal intravitreal (IVT) ocular distribution study in rabbits. Safety was assessed in a 1-month IVT study in cynomolgus monkeys. Results SPR results demonstrated that ABP 938 is similar to aflibercept RP in binding kinetics and affinity for VEGF-A 111 , VEGF-A 121 , VEGF-A 165 , VEGF-A 189 , PlGF-1, and PlGF-2 isoforms. No antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis, or complement-dependent cytotoxicity was observed with ABP 938 and aflibercept RP. Results from the nonterminal ocular distribution study in rabbits indicated that there were no meaningful differences in the distribution kinetics between intravitreally injected ABP 938 and aflibercept RP. Additionally, there was no evidence of ocular or systemic toxicity associated with IVT administration of ABP 938 in a repeat-dose, 1-month toxicology study in cynomolgus monkeys; toxicokinetic and toxicology profiles were similar to aflibercept RP. Conclusions This integrated assessment of results from the in vitro pharmacology assessment and in vivo PK and TK/toxicology profiles formed the nonclinical portion of the totality of evidence demonstrating ABP 938 is a biosimilar to aflibercept RP. Plain Language Summary Biological drugs, commonly referred to as biologics, have transformed the lives of millions of patients. They are made using highly complex manufacturing processes that involve living cells. Biosimilars are comparable to approved “originator” biologics (also known as reference products) in terms of potency, safety, and efficacy. ABP 938 is currently being developed as a biosimilar to aflibercept, an originator b
doi_str_mv 10.1007/s40123-024-01043-5
format Article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_proquest_miscellaneous_3124691538</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A823229411</galeid><doaj_id>oai_doaj_org_article_d6424f7b468d4f1cb5a2db6dfd6714c5</doaj_id><sourcerecordid>A823229411</sourcerecordid><originalsourceid>FETCH-LOGICAL-c461t-c83f70a1a5aa96dd753386ad2d40e1f886c619af9419bc4b5e79b276179298b3</originalsourceid><addsrcrecordid>eNp9kktvEzEUhUcIRKvSP8ACeclmit9jr1Aa8ahUQQXdIsvjR-JoYgfbA-q_x-2Eim6QF7bOPffTvfLputcIXiAIh3eFQoRJDzHtIYKU9OxZd4qRJD1nWDw_vgWm7KQ7L2UHYfMLJil92Z0QySCREp12P76kaKYQg9ET-B72YdI51DuQPKhbBy5DKosI1jraYHV1YHV5AyQR4HeoW7DyUxhdNu5QwTfnXXbROHCTk51NfdW98Hoq7vx4n3W3Hz_crj_3118_Xa1X172hHNXeCOIHqJFmWktu7cAIEVxbbCl0yAvBDUdSe0mRHA0dmRvkiAeOBomlGMlZd7VgbdI7dchhr_OdSjqoByHljdK5BjM5ZTnF1A8j5cJSj8zINLYjt97yAVHDGuv9wjrM495Z42LNenoCfVqJYas26ZdCaMBUYNkIb4-EnH7OrlS1D8W4adLRpbkogjDlEjEimvVisW50my1EnxrStGPdPpgUnQ9NXwlMMG7Lo9aAlwaTUynZ-cfBEFT3uVBLLlTLhXrIhbpf6c2_Kz22_E1BM5DFUFopblxWuzTn2H7sf9g_WmbCkw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3124691538</pqid></control><display><type>article</type><title>Nonclinical Similarity of the Biosimilar Candidate ABP 938 with Aflibercept Reference Product</title><source>DOAJ Directory of Open Access Journals</source><source>Springer Nature OA Free Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Seo, Neungseon ; Kuhns, Scott ; Andrews, Dina A. ; Colbert, Alexander ; Chow, Vincent ; Liu, Jennifer</creator><creatorcontrib>Seo, Neungseon ; Kuhns, Scott ; Andrews, Dina A. ; Colbert, Alexander ; Chow, Vincent ; Liu, Jennifer</creatorcontrib><description>Introduction ABP 938 is being developed as a biosimilar to Eylea ® (aflibercept reference product [RP]), an anti-vascular endothelial growth factor (VEGF) drug used in the management of retinal diseases. Previously, a comparative analytical similarity assessment demonstrated that ABP 938 and aflibercept RP have the same amino acid sequence and exhibit similar higher-order structure and biological activity. The nonclinical studies described here were designed to assess the in vitro pharmacology and the in vivo pharmacokinetics (PK), toxicokinetics (TK), and safety profiles of ABP 938 compared to aflibercept RP. Methods In vitro target-binding kinetics and affinity for VEGF-A and placental growth factor (PIGF) isoforms were evaluated using surface plasmon resonance (SPR). Effector functions were assessed by cell-based assays. PK was evaluated in a nonterminal intravitreal (IVT) ocular distribution study in rabbits. Safety was assessed in a 1-month IVT study in cynomolgus monkeys. Results SPR results demonstrated that ABP 938 is similar to aflibercept RP in binding kinetics and affinity for VEGF-A 111 , VEGF-A 121 , VEGF-A 165 , VEGF-A 189 , PlGF-1, and PlGF-2 isoforms. No antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis, or complement-dependent cytotoxicity was observed with ABP 938 and aflibercept RP. Results from the nonterminal ocular distribution study in rabbits indicated that there were no meaningful differences in the distribution kinetics between intravitreally injected ABP 938 and aflibercept RP. Additionally, there was no evidence of ocular or systemic toxicity associated with IVT administration of ABP 938 in a repeat-dose, 1-month toxicology study in cynomolgus monkeys; toxicokinetic and toxicology profiles were similar to aflibercept RP. Conclusions This integrated assessment of results from the in vitro pharmacology assessment and in vivo PK and TK/toxicology profiles formed the nonclinical portion of the totality of evidence demonstrating ABP 938 is a biosimilar to aflibercept RP. Plain Language Summary Biological drugs, commonly referred to as biologics, have transformed the lives of millions of patients. They are made using highly complex manufacturing processes that involve living cells. Biosimilars are comparable to approved “originator” biologics (also known as reference products) in terms of potency, safety, and efficacy. ABP 938 is currently being developed as a biosimilar to aflibercept, an originator biologic used to treat certain eye diseases. We have conducted studies to compare the characteristics of ABP 938 and aflibercept in laboratory experiments and in animal models. The results from these studies indicate that there are no meaningful differences between ABP 938 and aflibercept reference product. Since then, a study of ABP 938 in humans with age-related macular degeneration has recently been completed, adding to the totality of evidence supporting ABP 938 as a treatment option for healthcare providers and patients in the future.</description><identifier>ISSN: 2193-8245</identifier><identifier>EISSN: 2193-6528</identifier><identifier>DOI: 10.1007/s40123-024-01043-5</identifier><identifier>PMID: 39503991</identifier><language>eng</language><publisher>Cheshire: Springer Healthcare</publisher><subject>ABP 938 ; Aflibercept ; Biosimilar pharmaceuticals ; Comparative analysis ; Dexmedetomidine ; Eye diseases ; Internal Medicine ; Medicine ; Medicine &amp; Public Health ; Nonclinical similarity ; Ophthalmology ; Original Research ; Pharmacology ; Rabbits ; Vascular endothelial growth factor</subject><ispartof>Ophthalmology and Therapy, 2025, Vol.14 (1), p.85-101</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2025 Springer</rights><rights>The Author(s) 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c461t-c83f70a1a5aa96dd753386ad2d40e1f886c619af9419bc4b5e79b276179298b3</cites><orcidid>0000-0001-7308-3191</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/PMC11724829/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11724829/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,27905,27906,41101,42170,51557,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39503991$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seo, Neungseon</creatorcontrib><creatorcontrib>Kuhns, Scott</creatorcontrib><creatorcontrib>Andrews, Dina A.</creatorcontrib><creatorcontrib>Colbert, Alexander</creatorcontrib><creatorcontrib>Chow, Vincent</creatorcontrib><creatorcontrib>Liu, Jennifer</creatorcontrib><title>Nonclinical Similarity of the Biosimilar Candidate ABP 938 with Aflibercept Reference Product</title><title>Ophthalmology and Therapy</title><addtitle>Ophthalmol Ther</addtitle><addtitle>Ophthalmol Ther</addtitle><description>Introduction ABP 938 is being developed as a biosimilar to Eylea ® (aflibercept reference product [RP]), an anti-vascular endothelial growth factor (VEGF) drug used in the management of retinal diseases. Previously, a comparative analytical similarity assessment demonstrated that ABP 938 and aflibercept RP have the same amino acid sequence and exhibit similar higher-order structure and biological activity. The nonclinical studies described here were designed to assess the in vitro pharmacology and the in vivo pharmacokinetics (PK), toxicokinetics (TK), and safety profiles of ABP 938 compared to aflibercept RP. Methods In vitro target-binding kinetics and affinity for VEGF-A and placental growth factor (PIGF) isoforms were evaluated using surface plasmon resonance (SPR). Effector functions were assessed by cell-based assays. PK was evaluated in a nonterminal intravitreal (IVT) ocular distribution study in rabbits. Safety was assessed in a 1-month IVT study in cynomolgus monkeys. Results SPR results demonstrated that ABP 938 is similar to aflibercept RP in binding kinetics and affinity for VEGF-A 111 , VEGF-A 121 , VEGF-A 165 , VEGF-A 189 , PlGF-1, and PlGF-2 isoforms. No antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis, or complement-dependent cytotoxicity was observed with ABP 938 and aflibercept RP. Results from the nonterminal ocular distribution study in rabbits indicated that there were no meaningful differences in the distribution kinetics between intravitreally injected ABP 938 and aflibercept RP. Additionally, there was no evidence of ocular or systemic toxicity associated with IVT administration of ABP 938 in a repeat-dose, 1-month toxicology study in cynomolgus monkeys; toxicokinetic and toxicology profiles were similar to aflibercept RP. Conclusions This integrated assessment of results from the in vitro pharmacology assessment and in vivo PK and TK/toxicology profiles formed the nonclinical portion of the totality of evidence demonstrating ABP 938 is a biosimilar to aflibercept RP. Plain Language Summary Biological drugs, commonly referred to as biologics, have transformed the lives of millions of patients. They are made using highly complex manufacturing processes that involve living cells. Biosimilars are comparable to approved “originator” biologics (also known as reference products) in terms of potency, safety, and efficacy. ABP 938 is currently being developed as a biosimilar to aflibercept, an originator biologic used to treat certain eye diseases. We have conducted studies to compare the characteristics of ABP 938 and aflibercept in laboratory experiments and in animal models. The results from these studies indicate that there are no meaningful differences between ABP 938 and aflibercept reference product. Since then, a study of ABP 938 in humans with age-related macular degeneration has recently been completed, adding to the totality of evidence supporting ABP 938 as a treatment option for healthcare providers and patients in the future.</description><subject>ABP 938</subject><subject>Aflibercept</subject><subject>Biosimilar pharmaceuticals</subject><subject>Comparative analysis</subject><subject>Dexmedetomidine</subject><subject>Eye diseases</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Nonclinical similarity</subject><subject>Ophthalmology</subject><subject>Original Research</subject><subject>Pharmacology</subject><subject>Rabbits</subject><subject>Vascular endothelial growth factor</subject><issn>2193-8245</issn><issn>2193-6528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>DOA</sourceid><recordid>eNp9kktvEzEUhUcIRKvSP8ACeclmit9jr1Aa8ahUQQXdIsvjR-JoYgfbA-q_x-2Eim6QF7bOPffTvfLputcIXiAIh3eFQoRJDzHtIYKU9OxZd4qRJD1nWDw_vgWm7KQ7L2UHYfMLJil92Z0QySCREp12P76kaKYQg9ET-B72YdI51DuQPKhbBy5DKosI1jraYHV1YHV5AyQR4HeoW7DyUxhdNu5QwTfnXXbROHCTk51NfdW98Hoq7vx4n3W3Hz_crj_3118_Xa1X172hHNXeCOIHqJFmWktu7cAIEVxbbCl0yAvBDUdSe0mRHA0dmRvkiAeOBomlGMlZd7VgbdI7dchhr_OdSjqoByHljdK5BjM5ZTnF1A8j5cJSj8zINLYjt97yAVHDGuv9wjrM495Z42LNenoCfVqJYas26ZdCaMBUYNkIb4-EnH7OrlS1D8W4adLRpbkogjDlEjEimvVisW50my1EnxrStGPdPpgUnQ9NXwlMMG7Lo9aAlwaTUynZ-cfBEFT3uVBLLlTLhXrIhbpf6c2_Kz22_E1BM5DFUFopblxWuzTn2H7sf9g_WmbCkw</recordid><startdate>2025</startdate><enddate>2025</enddate><creator>Seo, Neungseon</creator><creator>Kuhns, Scott</creator><creator>Andrews, Dina A.</creator><creator>Colbert, Alexander</creator><creator>Chow, Vincent</creator><creator>Liu, Jennifer</creator><general>Springer Healthcare</general><general>Springer</general><general>Adis, Springer Healthcare</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7308-3191</orcidid></search><sort><creationdate>2025</creationdate><title>Nonclinical Similarity of the Biosimilar Candidate ABP 938 with Aflibercept Reference Product</title><author>Seo, Neungseon ; Kuhns, Scott ; Andrews, Dina A. ; Colbert, Alexander ; Chow, Vincent ; Liu, Jennifer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-c83f70a1a5aa96dd753386ad2d40e1f886c619af9419bc4b5e79b276179298b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>ABP 938</topic><topic>Aflibercept</topic><topic>Biosimilar pharmaceuticals</topic><topic>Comparative analysis</topic><topic>Dexmedetomidine</topic><topic>Eye diseases</topic><topic>Internal Medicine</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Nonclinical similarity</topic><topic>Ophthalmology</topic><topic>Original Research</topic><topic>Pharmacology</topic><topic>Rabbits</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seo, Neungseon</creatorcontrib><creatorcontrib>Kuhns, Scott</creatorcontrib><creatorcontrib>Andrews, Dina A.</creatorcontrib><creatorcontrib>Colbert, Alexander</creatorcontrib><creatorcontrib>Chow, Vincent</creatorcontrib><creatorcontrib>Liu, Jennifer</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Ophthalmology and Therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seo, Neungseon</au><au>Kuhns, Scott</au><au>Andrews, Dina A.</au><au>Colbert, Alexander</au><au>Chow, Vincent</au><au>Liu, Jennifer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonclinical Similarity of the Biosimilar Candidate ABP 938 with Aflibercept Reference Product</atitle><jtitle>Ophthalmology and Therapy</jtitle><stitle>Ophthalmol Ther</stitle><addtitle>Ophthalmol Ther</addtitle><date>2025</date><risdate>2025</risdate><volume>14</volume><issue>1</issue><spage>85</spage><epage>101</epage><pages>85-101</pages><issn>2193-8245</issn><eissn>2193-6528</eissn><abstract>Introduction ABP 938 is being developed as a biosimilar to Eylea ® (aflibercept reference product [RP]), an anti-vascular endothelial growth factor (VEGF) drug used in the management of retinal diseases. Previously, a comparative analytical similarity assessment demonstrated that ABP 938 and aflibercept RP have the same amino acid sequence and exhibit similar higher-order structure and biological activity. The nonclinical studies described here were designed to assess the in vitro pharmacology and the in vivo pharmacokinetics (PK), toxicokinetics (TK), and safety profiles of ABP 938 compared to aflibercept RP. Methods In vitro target-binding kinetics and affinity for VEGF-A and placental growth factor (PIGF) isoforms were evaluated using surface plasmon resonance (SPR). Effector functions were assessed by cell-based assays. PK was evaluated in a nonterminal intravitreal (IVT) ocular distribution study in rabbits. Safety was assessed in a 1-month IVT study in cynomolgus monkeys. Results SPR results demonstrated that ABP 938 is similar to aflibercept RP in binding kinetics and affinity for VEGF-A 111 , VEGF-A 121 , VEGF-A 165 , VEGF-A 189 , PlGF-1, and PlGF-2 isoforms. No antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis, or complement-dependent cytotoxicity was observed with ABP 938 and aflibercept RP. Results from the nonterminal ocular distribution study in rabbits indicated that there were no meaningful differences in the distribution kinetics between intravitreally injected ABP 938 and aflibercept RP. Additionally, there was no evidence of ocular or systemic toxicity associated with IVT administration of ABP 938 in a repeat-dose, 1-month toxicology study in cynomolgus monkeys; toxicokinetic and toxicology profiles were similar to aflibercept RP. Conclusions This integrated assessment of results from the in vitro pharmacology assessment and in vivo PK and TK/toxicology profiles formed the nonclinical portion of the totality of evidence demonstrating ABP 938 is a biosimilar to aflibercept RP. Plain Language Summary Biological drugs, commonly referred to as biologics, have transformed the lives of millions of patients. They are made using highly complex manufacturing processes that involve living cells. Biosimilars are comparable to approved “originator” biologics (also known as reference products) in terms of potency, safety, and efficacy. ABP 938 is currently being developed as a biosimilar to aflibercept, an originator biologic used to treat certain eye diseases. We have conducted studies to compare the characteristics of ABP 938 and aflibercept in laboratory experiments and in animal models. The results from these studies indicate that there are no meaningful differences between ABP 938 and aflibercept reference product. Since then, a study of ABP 938 in humans with age-related macular degeneration has recently been completed, adding to the totality of evidence supporting ABP 938 as a treatment option for healthcare providers and patients in the future.</abstract><cop>Cheshire</cop><pub>Springer Healthcare</pub><pmid>39503991</pmid><doi>10.1007/s40123-024-01043-5</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0001-7308-3191</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2193-8245
ispartof Ophthalmology and Therapy, 2025, Vol.14 (1), p.85-101
issn 2193-8245
2193-6528
language eng
recordid cdi_proquest_miscellaneous_3124691538
source DOAJ Directory of Open Access Journals; Springer Nature OA Free Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects ABP 938
Aflibercept
Biosimilar pharmaceuticals
Comparative analysis
Dexmedetomidine
Eye diseases
Internal Medicine
Medicine
Medicine & Public Health
Nonclinical similarity
Ophthalmology
Original Research
Pharmacology
Rabbits
Vascular endothelial growth factor
title Nonclinical Similarity of the Biosimilar Candidate ABP 938 with Aflibercept Reference Product
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T21%3A09%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nonclinical%20Similarity%20of%20the%20Biosimilar%20Candidate%20ABP%20938%20with%20Aflibercept%20Reference%20Product&rft.jtitle=Ophthalmology%20and%20Therapy&rft.au=Seo,%20Neungseon&rft.date=2025&rft.volume=14&rft.issue=1&rft.spage=85&rft.epage=101&rft.pages=85-101&rft.issn=2193-8245&rft.eissn=2193-6528&rft_id=info:doi/10.1007/s40123-024-01043-5&rft_dat=%3Cgale_doaj_%3EA823229411%3C/gale_doaj_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3124691538&rft_id=info:pmid/39503991&rft_galeid=A823229411&rft_doaj_id=oai_doaj_org_article_d6424f7b468d4f1cb5a2db6dfd6714c5&rfr_iscdi=true