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1000 Titel
  • A pharmacokinetics study of proposed bevacizumab biosimilar MYL-1402O vs EU-bevacizumab and US-bevacizumab
1000 Autor/in
  1. Hummel, Matthew |
  2. Bosje, Tjerk |
  3. Shaw, Andrew |
  4. Liu, Mark Shiyao |
  5. Barve, Abhijit |
  6. Kothekar, Mudgal |
  7. Socinski, Mark A. |
  8. Waller, Cornelius |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-17
1000 Erschienen in
1000 Quellenangabe
  • 148(2):487-496
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00432-021-03628-0 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800899/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!Bevacizumab is a recombinant humanized monoclonal antibody that inhibits vascular endothelial growth factor-specific angiogenesis in some cancers. MYL-1402O is a proposed bevacizumab biosimilar.!##!Methods!#!The primary objective of this single-center, randomized, double-blind, three-arm, parallel-group, phase 1 study in healthy male volunteers was to evaluate bioequivalence of MYL-1402O to EU and US-reference bevacizumab, and EU-reference bevacizumab to US-reference bevacizumab. The primary pharmacokinetic parameter was area under the serum concentration-time curve from 0 extrapolated to infinity (AUC!##!Results!#!Of 111 enrolled subjects, 110 were included in the pharmacokinetic analysis (MYL-1402O, n = 37; EU-reference bevacizumab, n = 36; US-reference bevacizumab, n = 37). Bioequivalence was demonstrated between MYL-1402O and EU-reference bevacizumab, MYL-1402O and US-reference bevacizumab, and between EU- and US-reference bevacizumab where least squares mean ratios of AUC!##!Conclusion!#!MYL-1402O was well tolerated and demonstrated pharmacokinetic and safety profiles similar to EU-reference bevacizumab and US-reference bevacizumab in healthy male volunteers. No new significant safety issues emerged (ClinicalTrials.gov, NCT02469987; ClinicalTrialsRegister.eu EudraCT, 2014-005621-12; June 12, 2015).
1000 Sacherschließung
lokal Adolescent [MeSH]
lokal Double-Blind Method [MeSH]
lokal Europe [MeSH]
lokal Therapeutic Equivalency [MeSH]
lokal Cancer
lokal United States [MeSH]
lokal Adult [MeSH]
lokal Original Article – Clinical Oncology
lokal Biosimilar Pharmaceuticals/pharmacokinetics [MeSH]
lokal Humans [MeSH]
lokal Bevacizumab/pharmacokinetics [MeSH]
lokal Monoclonal antibody
lokal Middle Aged [MeSH]
lokal Bevacizumab/chemistry [MeSH]
lokal Male [MeSH]
lokal Drug Compounding/standards [MeSH]
lokal Pharmacokinetics
lokal Healthy Volunteers [MeSH]
lokal Young Adult [MeSH]
lokal Phase 1
lokal Drug Compounding/methods [MeSH]
lokal Netherlands [MeSH]
lokal Bioequivalence
lokal Biosimilar Pharmaceuticals/chemistry [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/SHVtbWVsLCBNYXR0aGV3|https://frl.publisso.de/adhoc/uri/Qm9zamUsIFRqZXJr|https://frl.publisso.de/adhoc/uri/U2hhdywgQW5kcmV3|https://frl.publisso.de/adhoc/uri/TGl1LCBNYXJrIFNoaXlhbw==|https://frl.publisso.de/adhoc/uri/QmFydmUsIEFiaGlqaXQ=|https://frl.publisso.de/adhoc/uri/S290aGVrYXIsIE11ZGdhbA==|https://frl.publisso.de/adhoc/uri/U29jaW5za2ksIE1hcmsgQS4=|https://orcid.org/0000-0002-5777-0212
1000 Hinweis
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1000 Erstellt am 2023-05-09T10:28:11.073+0200
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1000 Zuletzt bearbeitet Sat Oct 21 02:10:50 CEST 2023
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