Publication:
Drug interactions between dolutegravir and artemether-lumefantrine or artesunate-amodiaquine

dc.contributor.authorStephen I. Walimbwaen_US
dc.contributor.authorMohammed Lamordeen_US
dc.contributor.authorCatriona Waitten_US
dc.contributor.authorJulian Kaboggozaen_US
dc.contributor.authorLaura Elseen_US
dc.contributor.authorPauline Byakika-Kibwikaen_US
dc.contributor.authorAlieu Amaraen_US
dc.contributor.authorJoshua Ginien_US
dc.contributor.authorMarkus Winterbergen_US
dc.contributor.authorJustin Chiongen_US
dc.contributor.authorJoel Tarningen_US
dc.contributor.authorSaye H. Khooen_US
dc.contributor.otherMakerere Universityen_US
dc.contributor.otherUniversity of Liverpoolen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherCollege of Health Sciencesen_US
dc.date.accessioned2020-01-27T10:09:22Z
dc.date.available2020-01-27T10:09:22Z
dc.date.issued2019-02-01en_US
dc.description.abstract© 2019 Walimbwa et al. Across sub-Saharan Africa, patients with HIV on antiretrovirals often get malaria and need cotreatment with artemisinin-containing therapies. We undertook two pharmacokinetic studies in healthy volunteers, using standard adult doses of artemether-lumefantrine or artesunate-amodiaquine given with 50 mg once daily dolutegravir (DTG) to investigate the drug-drug interaction between artemether-lumefantrine or artesunate-amodiaquine and dolutegravir. The dolutegravir/artemether-lumefantrine interaction was evaluated in a two-way crossover study and measured artemether, dihydroartemisinin, lumefantrine, and desbutyl-lumefantrine over 264 h. The dolutegravir/artesunate-amodiaquine interaction was investigated using a parallel study design due to long half-life of the amodiaquine metabolite, desethylamodiaquine and measured artesunate, amodiaquine, and desethylamodiaquine over 624 h. Noncompartmental analysis was performed, and geometric mean ratios and 90% confidence intervals were generated for evaluation of both interactions. Dolutegravir did not significantly change the maximum concentration in plasma, the time to maximum concentration, and the area under the concentration-time curve (AUC) for artemether, dihydroartemisinin, lumefantrine, and desbutyl-lumefantrine, nor did it significantly alter the AUC for artesunate, dihydroartemisinin, amodiaquine, and desethylamodiaquine. Coadministration of dolutegravir with artemether-lumefantrine resulted in a 37% decrease in DTG trough concentrations. Coadministration of dolutegravir with artesunate-amodiaquine resulted in 42 and 24% approximate decreases in the DTG trough concentrations and the AUC, respectively. The significant decreases in DTG trough concentrations with artemether-lumefantrine and artesunate-amodiaquine and dolutegravir exposure with artesunate-amodiaquine are unlikely to be of clinical significance since the DTG trough concentrations were above dolutegravir target concentrations of 300 ng/ml. Study drugs were well tolerated with no serious adverse events. Standard doses of artemether-lumefantrine and artesunate-amodiaquine should be used in patients receiving dolutegravir.en_US
dc.identifier.citationAntimicrobial Agents and Chemotherapy. Vol.63, No.2 (2019)en_US
dc.identifier.doi10.1128/AAC.01310-18en_US
dc.identifier.issn10986596en_US
dc.identifier.issn00664804en_US
dc.identifier.other2-s2.0-85060798453en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/51917
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060798453&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleDrug interactions between dolutegravir and artemether-lumefantrine or artesunate-amodiaquineen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060798453&origin=inwarden_US

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