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dc.rights.licenseopenen_US
dc.contributor.authorELOY, Philippine
dc.contributor.authorLAOUENAN, Cedric
dc.contributor.authorBEAVOGUI, Abdoul Habib
dc.contributor.authorKEITA, Sakoba
dc.contributor.authorMANCHON, Pauline
dc.contributor.authorETARD, Jean-Francois
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSISSOKO, Daouda
dc.contributor.authorMENTRE, France
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierGlobal Health in the Global South [GHiGS]
dc.contributor.authorMALVY, Denis
dc.date.accessioned2022-03-16T08:13:24Z
dc.date.available2022-03-16T08:13:24Z
dc.date.issued2022-02
dc.identifier.issn2214-2509en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/136472
dc.description.abstractEnBACKGROUND: Persistence of Ebola virus (EBOV) in semen remains of deep concern, as sexual transmission of EBOV seems plausible up to 6 months after acute phase of Ebola virus disease (EVD). Favipiravir, a broad spectrum antiviral product, has been evaluated in reducing EVD mortality in Guinea in 2014-2015 in the JIKI trial, the pharmacokinetic results of which suggest that an increase of dose might be necessary to achieve a therapeutically relevant exposure. In FORCE trial, we aimed at evaluating the tolerance and activity of high doses of favipiravir in male EVD survivors with EBOV RNA detection in semen in Guinea. CASE: In 2016, we launched a phase IIa open-labeled multicenter dose escalation study. Male survivors of EVD with EBOV RT-PCR positive on semen received a loading dose of 2400 mg BID of favipiravir on day 1 then a maintenance dose of 1800 mg BID from day 2-14. The primary outcome was the tolerance, assessed daily during period treatment and up to day 90. Unfortunately only two participants were included and the trial was stopped for lack of recruitment. No clinical adverse event of grade 3/4 was reported for both patients. One patient experienced a grade 3 hypocalcemia at day 10 and 14. CONCLUSIONS: High doses of favipiravir were well tolerated in these two participants. Better characterized tolerance and pharmacokinetics of high doses of favipiravir are of utmost importance considering that favipiravir is a candidate treatment for a variety of emerging severe viral diseases with poor prognosis.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subject.enFavipiravir
dc.subject.enEbola survivors
dc.subject.enQTc
dc.subject.enSafety
dc.subject.enSemen
dc.title.enHigh doses of favipiravir in two men survivors of Ebola virus disease carrying Ebola virus in semen in Guinea
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.idcr.2022.e01412en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed35127447en_US
bordeaux.journalIDCasesen_US
bordeaux.volume27en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamGHIGS_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03609928
hal.version1
hal.date.transferred2022-03-16T08:13:27Z
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=IDCases&rft.date=2022-02&rft.volume=27&rft.eissn=2214-2509&rft.issn=2214-2509&rft.au=ELOY,%20Philippine&LAOUENAN,%20Cedric&BEAVOGUI,%20Abdoul%20Habib&KEITA,%20Sakoba&MANCHON,%20Pauline&rft.genre=article


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