Key result
Therapeutic and supratherapeutic doses of cefiderocol had no apparent clinically significant effect on the QTcF interval in healthy adults.
Why the study?
This study was conducted to assess the tolerability of single-ascending doses of cefiderocol and its effect on cardiac repolarization, assessed using QTcF and other ECG parameters, in healthy adult subjects.
Does cefiderocol prolong the QT/QTc interval in healthy adult subjects?
RCT
double-blind
randomized
Does cefiderocol prolong the QT/QTc interval in healthy adult subjects?
Cefiderocol does not cause clinically significant QT prolongation at therapeutic or supratherapeutic doses.
Cefiderocol shows no clinically significant QTcF effect at therapeutic or supratherapeutic doses; extends cardiac safety data for this novel agent in gram-negative infections.
PURPOSE: Cefiderocol is a novel siderophore cephalosporin with potent activity against gram-negative bacteria, including multidrug-resistant strains. This Phase I study was conducted to assess the tolerability of single-ascending doses of cefiderocol (part 1) and the effect of cefiderocol on cardiac repolarization, assessed using the electrocardiographic corrected QT interval (QTcF) and other ECG parameters (part 2), in healthy adult subjects. METHODS: Part 1 was a randomized, double-blind, placebo-controlled, single-ascending dose study in healthy adult male and female subjects. Part 2 was a 4-period crossover study in which subjects received a single 2-g dose of cefiderocol (therapeutic dose), a single 4-g dose of cefiderocol (supratherapeutic dose), or saline (placebo), each infused over 3 hours, and a single oral 400-mg dose of moxifloxacin. In each treatment period, continuous cardiac monitoring was used to assess the effects of cefiderocol on ECG parameters. The QT interval corrected using the Fridericia formula (QTcF) was the primary ECG parameter; the time-matched placebo- and baseline-adjusted (dd)-QTcF interval was the primary end point. The plasma pharmacokinetic properties of cefiderocol were calculated on the basis of concentration-time profiles in all evaluable subjects. FINDINGS: of cefiderocol. Both doses of cefiderocol were well tolerated. All adverse events were mild in severity, with no deaths or serious adverse events reported. IMPLICATIONS: Overall, therapeutic and supratherapeutic doses of cefiderocol had no apparent clinically significant effect on the QTcF.
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Sanabria et al. (2019) conducted an RCT in Healthy. Cefiderocol vs. Placebo (saline) and moxifloxacin was evaluated on time-matched placebo- and baseline-adjusted (dd)-QTcF interval. Therapeutic and supratherapeutic doses of cefiderocol had no apparent clinically significant effect on the QTcF interval in healthy adults.
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