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dc.rights.licenseopenen_US
dc.contributor.authorCOSTA, Enrico
dc.contributor.authorGIROTTI, Silvia
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMATHIEU, Clement
dc.contributor.authorCASTELLANI, Carlo
dc.contributor.authorROSS, Joseph S
dc.contributor.authorTAYLOR-COUSAR, Jennifer L
dc.contributor.authorLEUFKENS, Hubert G M
dc.date.accessioned2024-10-10T10:06:31Z
dc.date.available2024-10-10T10:06:31Z
dc.date.issued2024-08-24
dc.identifier.issn1873-5010en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202379
dc.description.abstractEnBACKGROUND: The objective of this study was to assess the differential times of submission and approval of CFTR modulators in the United States (US) and the European Union (EU). METHODS: By collecting publicly available data from the websites of the Food and Drug Administration and the European Medicines Agency, we quantified differential times in submission, review duration, and approvals of initial marketing authorization and variation of indications of CFTR modulators in the US and the EU by December 31, 2023. RESULTS: Applications regarding marketing of 4 CFTR modulators were submitted 103 (SD ±143) days later in the EU than in the US: 31 (SD ±39) days later for initial approval, and 124 (SD ±155) days for supplemental indications. The regulatory review process was completed in 181 days [IQR, 179 - 182] in the US and 325 days [IQR, 276 - 382] in the EU: 167 days [IQR, 102 - 232] in the US and 346 days [IQR, 302 - 400] in the EU for first approvals, 181 days [IQR, 181 - 182] in the US and 324 days [IQR, 264 - 382] in the EU for supplemental indication approvals. CFTR modulators were approved 267 (SD 143) days later in the EU than in the US: 220 (SD ±76) days for initial approval and 280 (SD ±157) days for supplemental indications. CONCLUSION: We found significant differences in times of submission and for approval of CFTR modulators between the US and EU, whereby initial approvals and subsequent indication approvals were always first granted in the US.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enCFTR modulators
dc.subject.enEuropean Medicines Agency
dc.subject.enFood and Drug Administration
dc.subject.enTimes of approval
dc.subject.enTimes of submission
dc.title.enDifferential times of submission and approval of CFTR modulators for the treatment of Cystic Fibrosis in the United States and the European Union
dc.title.alternativeJ Cyst Fibrosen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.jcf.2024.08.002en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed39183127en_US
bordeaux.journalJournal of Cystic Fibrosisen_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDNational Institutes of Healthen_US
hal.identifierhal-04730151
hal.version1
hal.date.transferred2024-10-10T10:06:33Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Cystic%20Fibrosis&rft.date=2024-08-24&rft.eissn=1873-5010&rft.issn=1873-5010&rft.au=COSTA,%20Enrico&GIROTTI,%20Silvia&MATHIEU,%20Clement&CASTELLANI,%20Carlo&ROSS,%20Joseph%20S&rft.genre=article


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