Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/9800
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dc.contributor.authorKatongole, Fredrick-
dc.contributor.authorArumugam, Tiyara-
dc.contributor.authorJennings, Angus-
dc.contributor.authorMutata, Constantine-
dc.contributor.authorSsebunya, Patrick-
dc.contributor.authorWamboi, Charity-
dc.contributor.authorGreen, Alexandra-
dc.contributor.authorDangarembizi, Mutsa Bwakura--
dc.contributor.authorKityo, Cissy-
dc.contributor.authorSiika, Abraham-
dc.contributor.authorArchary, Moherndran-
dc.contributor.authorJafta, Lungile-
dc.contributor.authorNamukwaya, Stella-
dc.contributor.authorSeeley, Janet-
dc.contributor.authorMugerwa, Henry-
dc.contributor.authorWalker, Simon-
dc.contributor.authorApoto, Naomi-
dc.contributor.authorThomason, Margaret J.-
dc.contributor.authorFord, Deborah-
dc.contributor.authorPett, Sarah L.-
dc.contributor.authorKekitiinwa, Adeodata R.-
dc.date.accessioned2025-07-03T11:52:12Z-
dc.date.available2025-07-03T11:52:12Z-
dc.date.issued2025-05-29-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/9800-
dc.description.abstractBackground: Novel strategies to improve ART adherence, retention in care and quality of life among adolescents living with HIV (ALHIV) are needed. Short-Cycle Therapy (SCT) with 4/5 sequential days on ART, 2/3 days off ART per week has shown non-inferior virological outcomes and high acceptability, but most data are in adults and are very limited for dolutegravir (DTG)-based SCT. Methods: BREATHER Plus is an ongoing 96-week non-inferiority randomised trial evaluating efficacy, safety and acceptability of SCT (5 sequential days on, 2 days off at the weekend) with DTG/tenofovir (TNV)-based triple ART versus continuous (daily) therapy (CT) in ALHIV. Participants are aged 12 to <20 years in Kenya/South Africa/Uganda/Zimbabwe, virologically suppressed (Viral Load (VL) <50copies/mL) for ≥12 months at enrollment, with no prior treatment failure. Randomisation is 1:1 to SCT versus CT. VL monitoring for clinical management is 6–12 monthly aligning with standard-of-care. The primary outcome is confirmed virological rebound ≥50 copies/mL by 96 weeks. The trial employs the Smooth Away From Expected (SAFE) non-inferiority frontier, where the non-inferiority margin depends on the observed event risk in the CT arm. Secondary out- comes include HIV resistance, toxicities, patient-reported outcomes and cost-effectiveness. Enrolment of 470 participants completed in June 2023. Discussion: BREATHER Plus is the first randomised trial specifically evaluating DTG/TNV-triple based SCT. Rapid roll-out of DTG and a pragmatic approach to VL monitoring mean results will be generalisable to ALHIV across sub-Saharan Africa. If SCT provides non-inferior virological suppression to CT, it may offer choice for ALHIV on how they take their ART.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectClinical trialen_US
dc.subjectDolutegraviren_US
dc.subjectShort-cycleen_US
dc.subjectAntiretroviralen_US
dc.subjectAdolescentsen_US
dc.subjectHIVen_US
dc.titleBREATHER Plus clinical trial design: A randomised non-inferiority trial evaluating the efficacy, safety and acceptability of short cycle (five days on, two days off) dolutegravir/tenofovir-based triple antiretroviral therapy (ART) compared to daily ART in virologically suppressed adolescents living with HIV aged 12 to <20 years in sub-Saharan Africaen_US
dc.typeArticleen_US
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