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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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 |
format | Article |
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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 <5 ms and the upper bound of the 90% CIs were <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.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2019.07.006</identifier><identifier>PMID: 31378318</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Clinical therapeutics, 2019-09, Vol.41 (9), p.1724-1736.e4</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>2019. The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-a9bd08717544664d628a14fe13bf0b865b7c9b146419c0557b2abd01498309e03</citedby><cites>FETCH-LOGICAL-c514t-a9bd08717544664d628a14fe13bf0b865b7c9b146419c0557b2abd01498309e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0149291819303492$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31378318$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sanabria, Carlos</creatorcontrib><creatorcontrib>Migoya, Elizabeth</creatorcontrib><creatorcontrib>Mason, Jay W.</creatorcontrib><creatorcontrib>Stanworth, Stephanie H.</creatorcontrib><creatorcontrib>Katsube, Takayuki</creatorcontrib><creatorcontrib>Machida, Mitsuaki</creatorcontrib><creatorcontrib>Narukawa, Yukitoshi</creatorcontrib><creatorcontrib>Den Nagata, Tsutae</creatorcontrib><title>Effect of Cefiderocol, a Siderophore Cephalosporin, on QT/QTc Interval in Healthy Adult Subjects</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><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 <5 ms and the upper bound of the 90% CIs were <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.</description><subject>Adult</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotics</subject><subject>carbapenem resistance</subject><subject>Cefiderocol</subject><subject>Cephalosporins</subject><subject>Cephalosporins - adverse effects</subject><subject>Cephalosporins - blood</subject><subject>Cephalosporins - pharmacokinetics</subject><subject>Cephalosporins - pharmacology</subject><subject>Cross-Over Studies</subject><subject>Double-Blind Method</subject><subject>Drug dosages</subject><subject>EKG</subject><subject>Electrocardiography - drug effects</subject><subject>Female</subject><subject>Gram-negative bacteria</subject><subject>gram-negative bacterial infection</subject><subject>Healthy Volunteers</subject><subject>Heart</subject><subject>Heart - drug effects</subject><subject>Heart - physiology</subject><subject>Heart Rate - drug effects</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Male</subject><subject>Moxifloxacin</subject><subject>Moxifloxacin - pharmacology</subject><subject>Multidrug resistance</subject><subject>Pain</subject><subject>siderophore</subject><subject>Siderophores - adverse effects</subject><subject>Siderophores - blood</subject><subject>Siderophores - pharmacokinetics</subject><subject>Siderophores - pharmacology</subject><subject>Upper bounds</subject><subject>Young Adult</subject><issn>0149-2918</issn><issn>1879-114X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkE9r3DAQxUVpaLZpv0Ir6DV2ZmxZf47LkjaBQAjZQm-qLMusjGO5kh3It4_STXPtaRjmvTe8HyFfEUoE5BdDaUc_LQcXTVkBqhJECcDfkQ1KoQpE9us92QAyVVQK5Sn5mNIAALVqqg_ktMZayBrlhvy-7HtnFxp6unO971wMNozn1ND7v8t8CNHl03wwY0hziH46p2Gid_uLu72l19Pi4qMZqZ_olTPjcnii224dF3q_tkMOTp_ISW_G5D6_zjPy8_vlfndV3Nz-uN5tbwrbIFsKo9oOpEDRMMY563glDbLeYd320EretMKqFhlnqCw0jWgrkx25oKxBOajPyLdj7hzDn9WlRQ9hjVN-qatK8UZygCqrxFFlY0gpul7P0T-Y-KQR9AtZPeg3svqFrAahM9ns_PKav7YPrnvz_UOZBdujwOWWj95Fnax3k3WdjxmE7oL_75Nndm2Mrw</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Sanabria, Carlos</creator><creator>Migoya, Elizabeth</creator><creator>Mason, Jay W.</creator><creator>Stanworth, Stephanie H.</creator><creator>Katsube, Takayuki</creator><creator>Machida, Mitsuaki</creator><creator>Narukawa, Yukitoshi</creator><creator>Den Nagata, Tsutae</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201909</creationdate><title>Effect of Cefiderocol, a Siderophore Cephalosporin, on QT/QTc Interval in Healthy Adult Subjects</title><author>Sanabria, Carlos ; Migoya, Elizabeth ; Mason, Jay W. ; Stanworth, Stephanie H. ; Katsube, Takayuki ; Machida, Mitsuaki ; Narukawa, Yukitoshi ; Den Nagata, Tsutae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c514t-a9bd08717544664d628a14fe13bf0b865b7c9b146419c0557b2abd01498309e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibiotics</topic><topic>carbapenem resistance</topic><topic>Cefiderocol</topic><topic>Cephalosporins</topic><topic>Cephalosporins - adverse effects</topic><topic>Cephalosporins - blood</topic><topic>Cephalosporins - pharmacokinetics</topic><topic>Cephalosporins - pharmacology</topic><topic>Cross-Over Studies</topic><topic>Double-Blind Method</topic><topic>Drug dosages</topic><topic>EKG</topic><topic>Electrocardiography - drug effects</topic><topic>Female</topic><topic>Gram-negative bacteria</topic><topic>gram-negative bacterial infection</topic><topic>Healthy Volunteers</topic><topic>Heart</topic><topic>Heart - drug effects</topic><topic>Heart - physiology</topic><topic>Heart Rate - drug effects</topic><topic>Humans</topic><topic>Laboratories</topic><topic>Male</topic><topic>Moxifloxacin</topic><topic>Moxifloxacin - pharmacology</topic><topic>Multidrug resistance</topic><topic>Pain</topic><topic>siderophore</topic><topic>Siderophores - adverse effects</topic><topic>Siderophores - blood</topic><topic>Siderophores - pharmacokinetics</topic><topic>Siderophores - pharmacology</topic><topic>Upper bounds</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanabria, Carlos</creatorcontrib><creatorcontrib>Migoya, Elizabeth</creatorcontrib><creatorcontrib>Mason, Jay W.</creatorcontrib><creatorcontrib>Stanworth, Stephanie H.</creatorcontrib><creatorcontrib>Katsube, Takayuki</creatorcontrib><creatorcontrib>Machida, Mitsuaki</creatorcontrib><creatorcontrib>Narukawa, Yukitoshi</creatorcontrib><creatorcontrib>Den Nagata, Tsutae</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanabria, Carlos</au><au>Migoya, Elizabeth</au><au>Mason, Jay W.</au><au>Stanworth, Stephanie H.</au><au>Katsube, Takayuki</au><au>Machida, Mitsuaki</au><au>Narukawa, Yukitoshi</au><au>Den Nagata, Tsutae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Cefiderocol, a Siderophore Cephalosporin, on QT/QTc Interval in Healthy Adult Subjects</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2019-09</date><risdate>2019</risdate><volume>41</volume><issue>9</issue><spage>1724</spage><epage>1736.e4</epage><pages>1724-1736.e4</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>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 <5 ms and the upper bound of the 90% CIs were <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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