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We aimed to evaluate the clinical pharmacokinetics (PK) and pharmacodynamics of dalbavancin in a prospective, randomized, open-label, crossover PK study of adult patients with end-stage renal disease ESRD who were receiving PD. Sampling occurred prior to a single 30-min infusion of dalbavancin at 1,500\u2009mg and at 1, 2, 3, 4, and 6\u2009h and 7 and 14 days postadministration.<\/jats:p>","DOI":"10.1128\/aac.02089-19","type":"journal-article","created":{"date-parts":[[2020,2,29]],"date-time":"2020-02-29T10:11:43Z","timestamp":1582971103000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":13,"title":["Intravenous and Intraperitoneal Pharmacokinetics of Dalbavancin in Peritoneal Dialysis Patients"],"prefix":"10.1128","volume":"64","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9125-9509","authenticated-orcid":false,"given":"E. 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