| Literature DB >> 28475768 |
Helen W Boucher1, Paul G Ambrose2, H F Chambers3, Richard H Ebright4, Amanda Jezek5, Barbara E Murray6, Jason G Newland7, Belinda Ostrowsky8, John H Rex9,10,11.
Abstract
Despite progress in antimicrobial drug development, a critical need persists for new, feasible pathways to develop antibacterial agents to treat people infected with drug-resistant bacteria. Infections due to resistant gram-negative bacilli continue to cause unacceptable morbidity and mortality rates. Antibacterial agents have been historically studied in noninferiority clinical trials that focus on a single site of infection (eg, complicated urinary tract infections, intra-abdominal infections), yet these designs may not be optimal, and often are not feasible, for study of infections caused by drug-resistant bacteria. Over the past several years, multiple stakeholders have worked to develop consensus regarding paths forward with a goal of facilitating timely conduct of antimicrobial development. Here we advocate for a novel and pragmatic approach and, toward this end, present feasible trial designs for antibacterial agents that could enable conduct of narrow-spectrum, organism-specific clinical trials and ultimately approval of critically needed new antibacterial agents.Entities:
Keywords: antibiotic development; antimicrobial resistance
Mesh:
Substances:
Year: 2017 PMID: 28475768 PMCID: PMC5853321 DOI: 10.1093/infdis/jix211
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 7.759