This document provides new general guidelines for the design and execution of studies evaluat-ing anti-infective drugs for the prevention or treatment of infectious diseases. The first step in evaluation is the determination of in vitro microbial susceptibility. Next, studies are conducted in animals. Several animal models provide information useful in the prediction of appropriate dosing and activity in humans. If the results of these studies are favorable, staged clinical trials are then conducted. These guidelines reflect changes in the practice of medicine, dealing with topics such as the switch from parenteral to oral drug administration during a course of therapy, treatment in settings other than acute-care hospitals, and the use of a...
The research carried out to find a better treatment, improve healthcare, and benefit the current med...
Increasing rates of antimicrobial-resistant infections and the dwindling pipeline of new agents nece...
The early preclinical development of an antiviral agent is accomplished essentially in two stages. T...
Evaluating new antimicrobial agents is governed mostly by interaction between the phar-maceutical in...
In February 2017 the World Health Organization first published the list of antibiotic-resistant «pri...
The process of drug development involves non-clinical and clinical studies. Non-clinical studies are...
For clinical trials of anti-infective drugs for the treatment of vascular access device—related bloo...
These guidelines describe the design and implementation of clinical trials to assess the safety and ...
The need for careful testing of new drugs in animal models before study in humans has been recognise...
Preclinical studies and testing strategies with and without the use of animal testing methods have t...
This guideline describes the preclinical documentation required for a new drug active against human ...
The working group focused on defining exploratory trials on medicinal products and developing recom...
The vast majority of medical interventions introduced into clinical development prove unsafe or inef...
The transition from laboratory testing to evaluation in humans marks an important stage in vaccine d...
BackgroundAntimicrobial use in food-producing animals selects for antimicrobial resistance that can ...
The research carried out to find a better treatment, improve healthcare, and benefit the current med...
Increasing rates of antimicrobial-resistant infections and the dwindling pipeline of new agents nece...
The early preclinical development of an antiviral agent is accomplished essentially in two stages. T...
Evaluating new antimicrobial agents is governed mostly by interaction between the phar-maceutical in...
In February 2017 the World Health Organization first published the list of antibiotic-resistant «pri...
The process of drug development involves non-clinical and clinical studies. Non-clinical studies are...
For clinical trials of anti-infective drugs for the treatment of vascular access device—related bloo...
These guidelines describe the design and implementation of clinical trials to assess the safety and ...
The need for careful testing of new drugs in animal models before study in humans has been recognise...
Preclinical studies and testing strategies with and without the use of animal testing methods have t...
This guideline describes the preclinical documentation required for a new drug active against human ...
The working group focused on defining exploratory trials on medicinal products and developing recom...
The vast majority of medical interventions introduced into clinical development prove unsafe or inef...
The transition from laboratory testing to evaluation in humans marks an important stage in vaccine d...
BackgroundAntimicrobial use in food-producing animals selects for antimicrobial resistance that can ...
The research carried out to find a better treatment, improve healthcare, and benefit the current med...
Increasing rates of antimicrobial-resistant infections and the dwindling pipeline of new agents nece...
The early preclinical development of an antiviral agent is accomplished essentially in two stages. T...