Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy

Elexacaftor-tezacaftor-ivacaftor is a newly approved triple-combination cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapy that contains 2 correctors and a potentiator of the CFTR channel. Its labeled indication for use is for persons 12 years of age and older with at leas...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The journal of pediatric pharmacology and therapeutics 2020, Vol.25 (3), p.192-197
Hauptverfasser: Ridley, Kaden, Condren, Michelle
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 197
container_issue 3
container_start_page 192
container_title The journal of pediatric pharmacology and therapeutics
container_volume 25
creator Ridley, Kaden
Condren, Michelle
description Elexacaftor-tezacaftor-ivacaftor is a newly approved triple-combination cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapy that contains 2 correctors and a potentiator of the CFTR channel. Its labeled indication for use is for persons 12 years of age and older with at least 1 F508del mutation for the gene. This drug combination provides potential therapy to many patients who had previously been excluded from CFTR modulation therapy due to the nature of their genetic mutations. The efficacy demonstrated in clinical trials surpasses the currently available therapies related to lung function, quality of life, sweat chloride reduction, and reducing exacerbations. The most common adverse events seen in clinical trials included rash and headache, and laboratory monitoring is recommended to evaluate liver function. Continued evaluation of patient data is needed to confirm its long-term safety and efficacy. Elexacaftor-tezacaftor-ivacaftor is a monumental and encouraging therapy for cystic fibrosis; however, approximately 10% of the CF population are not candidates for this or any other CFTR modulation therapy.
doi_str_mv 10.5863/1551-6776-25.3.192
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7134581</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2387690357</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3172-8d15be1c6dbf2dc78a2c751076c2f16d311c9c1b3ded17ad391af2158f10b5d03</originalsourceid><addsrcrecordid>eNpVkc1O3DAUha0KVEaUF-iiypJNpr52bCddIKEIKBJVJTRI7CzHdgZXSTzYCWLY8951xDACb-6x7rmffw5C3wEvWcnpT2AMci4Ezwlb0iVU5AtaEEohp0V5f4AWe8MROonxH06rKARmxVd0RAnhjGOyQK8XnX1WWrWjD_nKvrzL66ed-pWtHmx26UIcs1Vwm87mte8bN6jR-SGrt3F0OvWb4KOLyaKG2Nu-SdVmtR_MpEc1aJvd2vXUqUTM_ngzKzesZ3ZQm-03dNiqLtqTXT1Gd5cXq_p3fvP36ro-v8k1BUHy0gBrLGhumpYYLUpFtGCABdekBW4ogK40NNRYA0IZWoFqCbCyBdwwg-kxOnvjbqamt0bbYQyqk5vgehW20isnP3cG9yDX_kkKoAUrIQFOd4DgHycbR9m7qG3Xpdf6KUpCS8ErTJlIVvJm1elnYrDt_hjAco5QzgnJOSFJmEzbiqShHx8vuB95D4z-Bz0VmyA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2387690357</pqid></control><display><type>article</type><title>Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Ridley, Kaden ; Condren, Michelle</creator><creatorcontrib>Ridley, Kaden ; Condren, Michelle</creatorcontrib><description>Elexacaftor-tezacaftor-ivacaftor is a newly approved triple-combination cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapy that contains 2 correctors and a potentiator of the CFTR channel. Its labeled indication for use is for persons 12 years of age and older with at least 1 F508del mutation for the gene. This drug combination provides potential therapy to many patients who had previously been excluded from CFTR modulation therapy due to the nature of their genetic mutations. The efficacy demonstrated in clinical trials surpasses the currently available therapies related to lung function, quality of life, sweat chloride reduction, and reducing exacerbations. The most common adverse events seen in clinical trials included rash and headache, and laboratory monitoring is recommended to evaluate liver function. Continued evaluation of patient data is needed to confirm its long-term safety and efficacy. Elexacaftor-tezacaftor-ivacaftor is a monumental and encouraging therapy for cystic fibrosis; however, approximately 10% of the CF population are not candidates for this or any other CFTR modulation therapy.</description><identifier>ISSN: 1551-6776</identifier><identifier>EISSN: 2331-348X</identifier><identifier>DOI: 10.5863/1551-6776-25.3.192</identifier><identifier>PMID: 32265602</identifier><language>eng</language><publisher>United States: Pediatric Pharmacy Advocacy Group</publisher><subject>Reviews</subject><ispartof>The journal of pediatric pharmacology and therapeutics, 2020, Vol.25 (3), p.192-197</ispartof><rights>Copyright Pediatric Pharmacy Association. All rights reserved. For permissions, email: mhelms@pediatricpharmacy.org 2020.</rights><rights>Pediatric Pharmacy Association. All rights reserved. For permissions, email: 2020 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3172-8d15be1c6dbf2dc78a2c751076c2f16d311c9c1b3ded17ad391af2158f10b5d03</citedby><cites>FETCH-LOGICAL-c3172-8d15be1c6dbf2dc78a2c751076c2f16d311c9c1b3ded17ad391af2158f10b5d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134581/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134581/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32265602$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ridley, Kaden</creatorcontrib><creatorcontrib>Condren, Michelle</creatorcontrib><title>Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy</title><title>The journal of pediatric pharmacology and therapeutics</title><addtitle>J Pediatr Pharmacol Ther</addtitle><description>Elexacaftor-tezacaftor-ivacaftor is a newly approved triple-combination cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapy that contains 2 correctors and a potentiator of the CFTR channel. Its labeled indication for use is for persons 12 years of age and older with at least 1 F508del mutation for the gene. This drug combination provides potential therapy to many patients who had previously been excluded from CFTR modulation therapy due to the nature of their genetic mutations. The efficacy demonstrated in clinical trials surpasses the currently available therapies related to lung function, quality of life, sweat chloride reduction, and reducing exacerbations. The most common adverse events seen in clinical trials included rash and headache, and laboratory monitoring is recommended to evaluate liver function. Continued evaluation of patient data is needed to confirm its long-term safety and efficacy. Elexacaftor-tezacaftor-ivacaftor is a monumental and encouraging therapy for cystic fibrosis; however, approximately 10% of the CF population are not candidates for this or any other CFTR modulation therapy.</description><subject>Reviews</subject><issn>1551-6776</issn><issn>2331-348X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVkc1O3DAUha0KVEaUF-iiypJNpr52bCddIKEIKBJVJTRI7CzHdgZXSTzYCWLY8951xDACb-6x7rmffw5C3wEvWcnpT2AMci4Ezwlb0iVU5AtaEEohp0V5f4AWe8MROonxH06rKARmxVd0RAnhjGOyQK8XnX1WWrWjD_nKvrzL66ed-pWtHmx26UIcs1Vwm87mte8bN6jR-SGrt3F0OvWb4KOLyaKG2Nu-SdVmtR_MpEc1aJvd2vXUqUTM_ngzKzesZ3ZQm-03dNiqLtqTXT1Gd5cXq_p3fvP36ro-v8k1BUHy0gBrLGhumpYYLUpFtGCABdekBW4ogK40NNRYA0IZWoFqCbCyBdwwg-kxOnvjbqamt0bbYQyqk5vgehW20isnP3cG9yDX_kkKoAUrIQFOd4DgHycbR9m7qG3Xpdf6KUpCS8ErTJlIVvJm1elnYrDt_hjAco5QzgnJOSFJmEzbiqShHx8vuB95D4z-Bz0VmyA</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Ridley, Kaden</creator><creator>Condren, Michelle</creator><general>Pediatric Pharmacy Advocacy Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2020</creationdate><title>Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy</title><author>Ridley, Kaden ; Condren, Michelle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3172-8d15be1c6dbf2dc78a2c751076c2f16d311c9c1b3ded17ad391af2158f10b5d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Reviews</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ridley, Kaden</creatorcontrib><creatorcontrib>Condren, Michelle</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of pediatric pharmacology and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ridley, Kaden</au><au>Condren, Michelle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy</atitle><jtitle>The journal of pediatric pharmacology and therapeutics</jtitle><addtitle>J Pediatr Pharmacol Ther</addtitle><date>2020</date><risdate>2020</risdate><volume>25</volume><issue>3</issue><spage>192</spage><epage>197</epage><pages>192-197</pages><issn>1551-6776</issn><eissn>2331-348X</eissn><abstract>Elexacaftor-tezacaftor-ivacaftor is a newly approved triple-combination cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapy that contains 2 correctors and a potentiator of the CFTR channel. Its labeled indication for use is for persons 12 years of age and older with at least 1 F508del mutation for the gene. This drug combination provides potential therapy to many patients who had previously been excluded from CFTR modulation therapy due to the nature of their genetic mutations. The efficacy demonstrated in clinical trials surpasses the currently available therapies related to lung function, quality of life, sweat chloride reduction, and reducing exacerbations. The most common adverse events seen in clinical trials included rash and headache, and laboratory monitoring is recommended to evaluate liver function. Continued evaluation of patient data is needed to confirm its long-term safety and efficacy. Elexacaftor-tezacaftor-ivacaftor is a monumental and encouraging therapy for cystic fibrosis; however, approximately 10% of the CF population are not candidates for this or any other CFTR modulation therapy.</abstract><cop>United States</cop><pub>Pediatric Pharmacy Advocacy Group</pub><pmid>32265602</pmid><doi>10.5863/1551-6776-25.3.192</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1551-6776
ispartof The journal of pediatric pharmacology and therapeutics, 2020, Vol.25 (3), p.192-197
issn 1551-6776
2331-348X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7134581
source EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Reviews
title Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T23%3A04%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Elexacaftor-Tezacaftor-Ivacaftor:%20The%20First%20Triple-Combination%20Cystic%20Fibrosis%20Transmembrane%20Conductance%20Regulator%20Modulating%20Therapy&rft.jtitle=The%20journal%20of%20pediatric%20pharmacology%20and%20therapeutics&rft.au=Ridley,%20Kaden&rft.date=2020&rft.volume=25&rft.issue=3&rft.spage=192&rft.epage=197&rft.pages=192-197&rft.issn=1551-6776&rft.eissn=2331-348X&rft_id=info:doi/10.5863/1551-6776-25.3.192&rft_dat=%3Cproquest_pubme%3E2387690357%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2387690357&rft_id=info:pmid/32265602&rfr_iscdi=true