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BREATHER 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 Africa

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dc.contributor.author Katongole, Fredrick
dc.contributor.author Arumugam, Tiyara
dc.contributor.author Jennings, Angus
dc.contributor.author Mutata, Constantine
dc.contributor.author Ssebunya, Patrick
dc.contributor.author Wamboi, Charity
dc.contributor.author Green, Alexandra
dc.contributor.author Dangarembizi, Mutsa Bwakura-
dc.contributor.author Kityo, Cissy
dc.contributor.author Siika, Abraham
dc.contributor.author Archary, Moherndran
dc.contributor.author Jafta, Lungile
dc.contributor.author Namukwaya, Stella
dc.contributor.author Seeley, Janet
dc.contributor.author Mugerwa, Henry
dc.contributor.author Walker, Simon
dc.contributor.author Apoto, Naomi
dc.contributor.author Thomason, Margaret J.
dc.contributor.author Ford, Deborah
dc.contributor.author Pett, Sarah L.
dc.contributor.author Kekitiinwa, Adeodata R.
dc.date.accessioned 2025-07-03T11:52:12Z
dc.date.available 2025-07-03T11:52:12Z
dc.date.issued 2025-05-29
dc.identifier.uri http://ir.mu.ac.ke:8080/jspui/handle/123456789/9800
dc.description.abstract Background: 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.iso en en_US
dc.publisher Elsevier en_US
dc.subject Clinical trial en_US
dc.subject Dolutegravir en_US
dc.subject Short-cycle en_US
dc.subject Antiretroviral en_US
dc.subject Adolescents en_US
dc.subject HIV en_US
dc.title BREATHER 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 Africa en_US
dc.type Article en_US


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