Comparison between physiologically based pharmacokinetic and population pharmacokinetic modelling to select paediatric doses of gepotidacin in plague

Author:

Nguyen Dung1,Shaik Jafar Sadik1,Tai Guoying1,Tiffany Courtney1,Perry Caroline1,Dumont Etienne1,Gardiner David1,Barth Aline1,Singh Rajendra1,Hossain Mohammad1

Affiliation:

1. GlaxoSmithKline Collegeville PA United States

Funder

Biomedical Advanced Research and Development Authority

GlaxoSmithKline

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference56 articles.

1. World Health Organization.Antibiotic Resistance. November 2017.http://www.who.int/mediacentre/factsheets/antibiotic-resistance/en/Accessed 7 March 2018.

2. In Vitro Activity of Gepotidacin, a Novel Triazaacenaphthylene Bacterial Topoisomerase Inhibitor, against a Broad Spectrum of Bacterial Pathogens

3. Mechanistic and Structural Basis for the Actions of the Antibacterial Gepotidacin against Staphylococcus aureus Gyrase

4. Type IIA topoisomerase inhibition by a new class of antibacterial agents

5. P2.38 Microbiological analysis from a phase II study in adults evaluating single doses of gepotidacin (GSK2140944) in the treatment of uncomplicated urogenital gonorrhoea caused by Neisseria gonorrhoeae;Scangarella‐Oman N;Sex Transm Infect,2017

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