First conditional marketing authorization approval in the European Union for hemophilia "A" gene therapy

dc.contributor.authorVandenDriessche, Thierry
dc.contributor.authorPipe, Steven W.
dc.contributor.authorPierce, Glenn F.
dc.contributor.authorKaczmarek, Radoslaw
dc.contributor.departmentPediatrics, School of Medicine
dc.date.accessioned2024-04-17T10:36:24Z
dc.date.available2024-04-17T10:36:24Z
dc.date.issued2022
dc.eprint.versionFinal published version
dc.identifier.citationVandenDriessche T, Pipe SW, Pierce GF, Kaczmarek R. First conditional marketing authorization approval in the European Union for hemophilia "A" gene therapy. Mol Ther. 2022;30(11):3335-3336. doi:10.1016/j.ymthe.2022.09.020
dc.identifier.urihttps://hdl.handle.net/1805/40073
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.ymthe.2022.09.020
dc.relation.journalMolecular Therapy
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectDrug approval
dc.subjectGenetic therapy
dc.subjectHemophilia A
dc.titleFirst conditional marketing authorization approval in the European Union for hemophilia "A" gene therapy
dc.typeArticle
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637642/
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