Effect of Cefiderocol, a Siderophore Cephalosporin, on QT/QTc Interval in Healthy Adult Subjects

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 repolari...

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Veröffentlicht in:Clinical therapeutics 2019-09, Vol.41 (9), p.1724-1736.e4
Hauptverfasser: Sanabria, Carlos, Migoya, Elizabeth, Mason, Jay W., Stanworth, Stephanie H., Katsube, Takayuki, Machida, Mitsuaki, Narukawa, Yukitoshi, Den Nagata, Tsutae
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container_end_page 1736.e4
container_issue 9
container_start_page 1724
container_title Clinical therapeutics
container_volume 41
creator Sanabria, Carlos
Migoya, Elizabeth
Mason, Jay W.
Stanworth, Stephanie H.
Katsube, Takayuki
Machida, Mitsuaki
Narukawa, Yukitoshi
Den Nagata, Tsutae
description 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. 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. All point estimates for the ddQTcF interval were
doi_str_mv 10.1016/j.clinthera.2019.07.006
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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. All point estimates for the ddQTcF interval were &lt;5 ms and the upper bound of the 90% CIs were &lt;10 ms at each timepoint after the initiation of the cefiderocol 3-hour infusion. Concentration-effect modeling showed a slightly negative slope and predicted modestly negative values of the ddQTcF interval at the Cmax of cefiderocol. Both doses of cefiderocol were well tolerated. All adverse events were mild in severity, with no deaths or serious adverse events reported. 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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. 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. 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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. 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. All point estimates for the ddQTcF interval were &lt;5 ms and the upper bound of the 90% CIs were &lt;10 ms at each timepoint after the initiation of the cefiderocol 3-hour infusion. Concentration-effect modeling showed a slightly negative slope and predicted modestly negative values of the ddQTcF interval at the Cmax of cefiderocol. Both doses of cefiderocol were well tolerated. All adverse events were mild in severity, with no deaths or serious adverse events reported. Overall, therapeutic and supratherapeutic doses of cefiderocol had no apparent clinically significant effect on the QTcF.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31378318</pmid><doi>10.1016/j.clinthera.2019.07.006</doi><oa>free_for_read</oa></addata></record>
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subjects Adult
Anti-Bacterial Agents - pharmacology
Antibiotics
carbapenem resistance
Cefiderocol
Cephalosporins
Cephalosporins - adverse effects
Cephalosporins - blood
Cephalosporins - pharmacokinetics
Cephalosporins - pharmacology
Cross-Over Studies
Double-Blind Method
Drug dosages
EKG
Electrocardiography - drug effects
Female
Gram-negative bacteria
gram-negative bacterial infection
Healthy Volunteers
Heart
Heart - drug effects
Heart - physiology
Heart Rate - drug effects
Humans
Laboratories
Male
Moxifloxacin
Moxifloxacin - pharmacology
Multidrug resistance
Pain
siderophore
Siderophores - adverse effects
Siderophores - blood
Siderophores - pharmacokinetics
Siderophores - pharmacology
Upper bounds
Young Adult
title Effect of Cefiderocol, a Siderophore Cephalosporin, on QT/QTc Interval in Healthy Adult Subjects
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