DOI: 10.1128/JCM.01270-19
ABSTRACT
There are now several new antibiotics available to treat multidrug-resistant pathogens, and susceptibility testing methods for these drugs are increasingly available at the time of drug approval. However, lack of clarity regarding verification requirements remains a formidable barrier to introducing such testing in clinical laboratories, making these drugs practically unavailable for patient use. We propose a change in the framework for bringing in testing for new antibiotics, focusing on quality control rather than underpowered verification studies.
The views expressed in this article do not necessarily reflect the views of the journal or of ASM.
- Copyright © 2019 American Society for Microbiology.
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