Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/73154
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dc.contributor.authorAdrie Bekkeren_US
dc.contributor.authorHelena Rabieen_US
dc.contributor.authorNicolas Salvadorien_US
dc.contributor.authorSamantha Du Toiten_US
dc.contributor.authorKanchana Than-In-Aten_US
dc.contributor.authorMarisa Groenewalden_US
dc.contributor.authorIsabelle Andrieux-Meyeren_US
dc.contributor.authorMukesh Kumaren_US
dc.contributor.authorRatchada Cresseyen_US
dc.contributor.authorJames Nielsenen_US
dc.contributor.authorEdmund Capparellien_US
dc.contributor.authorMarc Lallemanten_US
dc.contributor.authorMark F. Cottonen_US
dc.contributor.authorTim R. Cresseyen_US
dc.date.accessioned2022-05-27T08:36:20Z-
dc.date.available2022-05-27T08:36:20Z-
dc.date.issued2022-03-01en_US
dc.identifier.issn10779450en_US
dc.identifier.issn15254135en_US
dc.identifier.other2-s2.0-85124600719en_US
dc.identifier.other10.1097/QAI.0000000000002871en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124600719&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/73154-
dc.description.abstractBackground:Antiretroviral options for neonates (younger than 28 days) should be expanded. We evaluated the pharmacokinetics, safety, and acceptability of the "4-in-1"fixed-dose pediatric granule formulation of abacavir/lamivudine/lopinavir/ritonavir (30/15/40/10 mg) in neonates.Methods:The PETITE study is an ongoing phase I/II, open-label, single-arm, 2-stage trial conducted in South Africa. In stage 1, term neonates exposed to HIV on standard antiretroviral prophylaxis (nevirapine ± zidovudine) received single dose(s) of the 4-in-1 formulation, followed by intensive pharmacokinetic sampling and safety assessments. At each PK visit, blood was drawn after an observed dose at 1, 2, 4, 8, and 12 hours postdose. In this study, we have reported the planned interim pharmacokinetic and safety analysis after completion of the single-dose administration.Results:Sixteen neonates, with a median (range) birth weight of 3130 g (2790-3590 g), completed 24 pharmacokinetic visits. The 4-in-1 formulation imposed relatively high doses of abacavir [8.6 mg/kg (6.6-11.4)] and lamivudine [4.3 mg/kg (3.3-5.7)] but lower doses of lopinavir [11.5 mg/kg (8.8-15.2)]. The geometric means (GM, 90% CI) AUC0-12of abacavir, lamivudine, and lopinavir were 29.87 (26.29-33.93), 12.61 (10.72-14.83), and 3.49 (2.13-5.72) µg.h/mL, respectively. Lopinavir GM AUC0-12was below the predefined target (20-100 µg.h/mL), and ritonavir concentrations were only detectable in 4 of the 120 (3%) samples. No adverse events were related to study drugs. No neonate had difficulty swallowing the 4-in-1 formulation.Conclusions:The high doses of abacavir and lamivudine (in mg/kg) and AUCs were safe, and the formulation was well tolerated; however, lopinavir/ritonavir exposures were extremely low, preventing its use in neonates use in neonates. Alternative pediatric solid antiretroviral formulations must be studied in neonates.en_US
dc.subjectMedicineen_US
dc.titlePharmacokinetics and Safety of the Abacavir/Lamivudine/Lopinavir/Ritonavir Fixed-Dose Granule Formulation (4-in-1) in Neonates: PETITE Studyen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Acquired Immune Deficiency Syndromesen_US
article.volume89en_US
article.stream.affiliationsCipla Ltd.en_US
article.stream.affiliationsUniversité de Montpellieren_US
article.stream.affiliationsNYU Langone Healthen_US
article.stream.affiliationsUniversity of California, San Diegoen_US
article.stream.affiliationsUniversity of Liverpoolen_US
article.stream.affiliationsStellenbosch Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsDrugs for Neglected Diseases Initiativeen_US
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