| Literature DB >> 28739794 |
Abdullah Alsultan1,2, Jennifer J Furin3, Jeannine Du Bois4, Elana van Brakel4, Phalkun Chheng3, Amour Venter5, Bonnie Thiel3, Sara A Debanne6, W Henry Boom3, Andreas H Diacon4,5, John L Johnson3, Charles A Peloquin7.
Abstract
AZD-5847 is a new oxazolidinone derivative under development for the treatment of tuberculosis (TB). Here we describe the population pharmacokinetics (PK) of AZD-5847 in patients with tuberculosis based on a recently completed phase II study. The study included 60 patients with drug-susceptible TB. Patients were randomized to four dosages (500 mg once daily, 1,200 mg once daily, 500 mg twice daily, and 800 mg twice daily). Patients were intensively sampled on days 1 and 14. AZD-5847 pharmacokinetics were best described with a two-compartment model with lag time (Tlag) for absorption. AZD-5847 bioavailability was nonlinear and plateaued at 800 mg. We performed deterministic simulation to compare the PK/pharmacodynamics (PD) of AZD-5847, linezolid, and sutezolid. AZD-5847 PK/PD in terms of both area under the concentration-time curve for the free, unbound fraction (fAUC)/MIC and time the free concentration was above the MIC (fT>MIC) were less favorable than those for linezolid and sutezolid. This could help explain the poor bactericidal activity of AZD-5847 in the recent phase II study.Entities:
Keywords: AZD-5847; pharmacokinetics; tuberculosis
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Year: 2017 PMID: 28739794 PMCID: PMC5610519 DOI: 10.1128/AAC.01066-17
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191