Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow‐up in the SELECTION open‐label long‐term extension study
Summary Background Filgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis. Aims The aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term ext...
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creator | Feagan, Brian G. Matsuoka, Katsuyoshi Rogler, Gerhard Laharie, David Vermeire, Séverine Danese, Silvio Loftus, Edward V. Beales, Ian Schreiber, Stefan Kim, Hyo Jong Faes, Margaux Haas, Angela Masior, Tomasz Rudolph, Christine Peyrin‐Biroulet, Laurent |
description | Summary
Background
Filgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.
Aims
The aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).
Methods
In this interim analysis of SELECTIONLTE, SELECTION completers (week 10 responders to filgotinib who completed the maintenance study) continued their assigned treatment (double‐blind filgotinib 200 mg [FIL200] or filgotinib 100 mg) and SELECTION week 10 non‐responders received open‐label FIL200. We assessed safety by adverse events (AEs), and efficacy by partial Mayo Clinic Score (pMCS), inflammatory biomarkers and health‐related quality of life (HRQoL). We compared safety and efficacy between achievers and non‐achievers of a multi‐component endpoint, comprehensive disease control (CDC), comprising symptomatic, endoscopic, inflammatory biomarker and HRQoL improvements.
Results
Data for completers (n = 250) and non‐responders (n = 372) were reported for ≤202 weeks. AE occurrences were low and consistent with previous analyses. The as‐observed proportion of FIL200‐treated patients in pMCS, biomarker and HRQoL remission during SELECTIONLTE remained high among completers (week 144: 80.0%, 86.4% and 86.0%, respectively) and increased among non‐responders (week 192: 62.1%, 76.7% and 59.3%, respectively). Significantly higher proportions of CDC achievers at SELECTION week 58 achieved pMCS, IBDQ and corticosteroid‐free pMCS remission than non‐achievers, up to LTE week 96.
Conclusions
Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results showed a proven long‐term benefit–risk profile. FIL200‐treated CDC achievers had better long‐term outcomes than non‐achievers.
This interim analysis aimed to assess the safety and efficacy of continued filgotinib therapy in moderately to severely active ulcerative colitis over ~4 years in SELECTIONLTE (NCT02914535). Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results demonstrated its proven long‐term benefit–risk profile. |
doi_str_mv | 10.1111/apt.18158 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3086956854</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3086956854</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2158-7328cc0066856ece2bf57c287f0ea2de090e5fa81156928475de183f4511cec03</originalsourceid><addsrcrecordid>eNp1UcFu1DAUtBCILoUDP4B8pIe0trNOHG7VaoGVVhSJ5Rx5nedi5NjBdlpy65Ub31h-BGe3IC744ifNeOZ5BqGXlJzTfC7kkM6poFw8QgtaVrxgpKweowVhVVMwQcsT9CzGr4SQqibsKTopGyIqWpIF-rX17vr-7meC0OMoNaQJS9dh0NooqSbsNdbGXvtknNlj7QNOXwCnADL14NKM976DIBPYCSePI9xAmGepkrkBPFo1o_OovDXJxDd447Kf6bOTtFM0EevgezwO8_vl_d2PCWSIB2tvrb_N-2XMuIP1p_V2vdptrj5gP4DLkJV7sNj-8w_4nsBF4x2Oaeym5-iJljbCi4f7FH1-u96t3hfbq3eb1eW2UCxnV9QlE0rljCrBK1DA9prXiolaE5CsA9IQ4FoKSnnVMLGseQdUlHrJKVWgSHmKXh91h-C_jRBT25uowFrpwI-xLXPoDc_qy0w9O1JV8DEG0O2Q85Bhailp507b3Gl76DRzXz3Ijvseur_MPyVmwsWRcGssTP9Xai8_7o6SvwF57rTT</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3086956854</pqid></control><display><type>article</type><title>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow‐up in the SELECTION open‐label long‐term extension study</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Feagan, Brian G. ; Matsuoka, Katsuyoshi ; Rogler, Gerhard ; Laharie, David ; Vermeire, Séverine ; Danese, Silvio ; Loftus, Edward V. ; Beales, Ian ; Schreiber, Stefan ; Kim, Hyo Jong ; Faes, Margaux ; Haas, Angela ; Masior, Tomasz ; Rudolph, Christine ; Peyrin‐Biroulet, Laurent</creator><creatorcontrib>Feagan, Brian G. ; Matsuoka, Katsuyoshi ; Rogler, Gerhard ; Laharie, David ; Vermeire, Séverine ; Danese, Silvio ; Loftus, Edward V. ; Beales, Ian ; Schreiber, Stefan ; Kim, Hyo Jong ; Faes, Margaux ; Haas, Angela ; Masior, Tomasz ; Rudolph, Christine ; Peyrin‐Biroulet, Laurent</creatorcontrib><description>Summary
Background
Filgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.
Aims
The aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).
Methods
In this interim analysis of SELECTIONLTE, SELECTION completers (week 10 responders to filgotinib who completed the maintenance study) continued their assigned treatment (double‐blind filgotinib 200 mg [FIL200] or filgotinib 100 mg) and SELECTION week 10 non‐responders received open‐label FIL200. We assessed safety by adverse events (AEs), and efficacy by partial Mayo Clinic Score (pMCS), inflammatory biomarkers and health‐related quality of life (HRQoL). We compared safety and efficacy between achievers and non‐achievers of a multi‐component endpoint, comprehensive disease control (CDC), comprising symptomatic, endoscopic, inflammatory biomarker and HRQoL improvements.
Results
Data for completers (n = 250) and non‐responders (n = 372) were reported for ≤202 weeks. AE occurrences were low and consistent with previous analyses. The as‐observed proportion of FIL200‐treated patients in pMCS, biomarker and HRQoL remission during SELECTIONLTE remained high among completers (week 144: 80.0%, 86.4% and 86.0%, respectively) and increased among non‐responders (week 192: 62.1%, 76.7% and 59.3%, respectively). Significantly higher proportions of CDC achievers at SELECTION week 58 achieved pMCS, IBDQ and corticosteroid‐free pMCS remission than non‐achievers, up to LTE week 96.
Conclusions
Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results showed a proven long‐term benefit–risk profile. FIL200‐treated CDC achievers had better long‐term outcomes than non‐achievers.
This interim analysis aimed to assess the safety and efficacy of continued filgotinib therapy in moderately to severely active ulcerative colitis over ~4 years in SELECTIONLTE (NCT02914535). Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results demonstrated its proven long‐term benefit–risk profile.</description><identifier>ISSN: 0269-2813</identifier><identifier>ISSN: 1365-2036</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/apt.18158</identifier><identifier>PMID: 39086130</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Colitis, Ulcerative - drug therapy ; Double-Blind Method ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Pyridines - administration & dosage ; Pyridines - adverse effects ; Pyridines - therapeutic use ; Quality of Life ; Severity of Illness Index ; Treatment Outcome ; Triazoles - administration & dosage ; Triazoles - adverse effects ; Triazoles - therapeutic use ; Young Adult</subject><ispartof>Alimentary pharmacology & therapeutics, 2024-09, Vol.60 (5), p.563-584</ispartof><rights>2024 The Author(s). published by John Wiley & Sons Ltd.</rights><rights>2024 The Author(s). Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2158-7328cc0066856ece2bf57c287f0ea2de090e5fa81156928475de183f4511cec03</cites><orcidid>0000-0003-2254-7771 ; 0000-0003-2536-6618 ; 0000-0003-1923-3237 ; 0000-0001-7341-1351 ; 0000-0002-4753-6676 ; 0000-0001-7199-6851</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fapt.18158$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fapt.18158$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39086130$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feagan, Brian G.</creatorcontrib><creatorcontrib>Matsuoka, Katsuyoshi</creatorcontrib><creatorcontrib>Rogler, Gerhard</creatorcontrib><creatorcontrib>Laharie, David</creatorcontrib><creatorcontrib>Vermeire, Séverine</creatorcontrib><creatorcontrib>Danese, Silvio</creatorcontrib><creatorcontrib>Loftus, Edward V.</creatorcontrib><creatorcontrib>Beales, Ian</creatorcontrib><creatorcontrib>Schreiber, Stefan</creatorcontrib><creatorcontrib>Kim, Hyo Jong</creatorcontrib><creatorcontrib>Faes, Margaux</creatorcontrib><creatorcontrib>Haas, Angela</creatorcontrib><creatorcontrib>Masior, Tomasz</creatorcontrib><creatorcontrib>Rudolph, Christine</creatorcontrib><creatorcontrib>Peyrin‐Biroulet, Laurent</creatorcontrib><title>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow‐up in the SELECTION open‐label long‐term extension study</title><title>Alimentary pharmacology & therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary
Background
Filgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.
Aims
The aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).
Methods
In this interim analysis of SELECTIONLTE, SELECTION completers (week 10 responders to filgotinib who completed the maintenance study) continued their assigned treatment (double‐blind filgotinib 200 mg [FIL200] or filgotinib 100 mg) and SELECTION week 10 non‐responders received open‐label FIL200. We assessed safety by adverse events (AEs), and efficacy by partial Mayo Clinic Score (pMCS), inflammatory biomarkers and health‐related quality of life (HRQoL). We compared safety and efficacy between achievers and non‐achievers of a multi‐component endpoint, comprehensive disease control (CDC), comprising symptomatic, endoscopic, inflammatory biomarker and HRQoL improvements.
Results
Data for completers (n = 250) and non‐responders (n = 372) were reported for ≤202 weeks. AE occurrences were low and consistent with previous analyses. The as‐observed proportion of FIL200‐treated patients in pMCS, biomarker and HRQoL remission during SELECTIONLTE remained high among completers (week 144: 80.0%, 86.4% and 86.0%, respectively) and increased among non‐responders (week 192: 62.1%, 76.7% and 59.3%, respectively). Significantly higher proportions of CDC achievers at SELECTION week 58 achieved pMCS, IBDQ and corticosteroid‐free pMCS remission than non‐achievers, up to LTE week 96.
Conclusions
Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results showed a proven long‐term benefit–risk profile. FIL200‐treated CDC achievers had better long‐term outcomes than non‐achievers.
This interim analysis aimed to assess the safety and efficacy of continued filgotinib therapy in moderately to severely active ulcerative colitis over ~4 years in SELECTIONLTE (NCT02914535). Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results demonstrated its proven long‐term benefit–risk profile.</description><subject>Adult</subject><subject>Colitis, Ulcerative - drug therapy</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pyridines - administration & dosage</subject><subject>Pyridines - adverse effects</subject><subject>Pyridines - therapeutic use</subject><subject>Quality of Life</subject><subject>Severity of Illness Index</subject><subject>Treatment Outcome</subject><subject>Triazoles - administration & dosage</subject><subject>Triazoles - adverse effects</subject><subject>Triazoles - therapeutic use</subject><subject>Young Adult</subject><issn>0269-2813</issn><issn>1365-2036</issn><issn>1365-2036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1UcFu1DAUtBCILoUDP4B8pIe0trNOHG7VaoGVVhSJ5Rx5nedi5NjBdlpy65Ub31h-BGe3IC744ifNeOZ5BqGXlJzTfC7kkM6poFw8QgtaVrxgpKweowVhVVMwQcsT9CzGr4SQqibsKTopGyIqWpIF-rX17vr-7meC0OMoNaQJS9dh0NooqSbsNdbGXvtknNlj7QNOXwCnADL14NKM976DIBPYCSePI9xAmGepkrkBPFo1o_OovDXJxDd447Kf6bOTtFM0EevgezwO8_vl_d2PCWSIB2tvrb_N-2XMuIP1p_V2vdptrj5gP4DLkJV7sNj-8w_4nsBF4x2Oaeym5-iJljbCi4f7FH1-u96t3hfbq3eb1eW2UCxnV9QlE0rljCrBK1DA9prXiolaE5CsA9IQ4FoKSnnVMLGseQdUlHrJKVWgSHmKXh91h-C_jRBT25uowFrpwI-xLXPoDc_qy0w9O1JV8DEG0O2Q85Bhailp507b3Gl76DRzXz3Ijvseur_MPyVmwsWRcGssTP9Xai8_7o6SvwF57rTT</recordid><startdate>202409</startdate><enddate>202409</enddate><creator>Feagan, Brian G.</creator><creator>Matsuoka, Katsuyoshi</creator><creator>Rogler, Gerhard</creator><creator>Laharie, David</creator><creator>Vermeire, Séverine</creator><creator>Danese, Silvio</creator><creator>Loftus, Edward V.</creator><creator>Beales, Ian</creator><creator>Schreiber, Stefan</creator><creator>Kim, Hyo Jong</creator><creator>Faes, Margaux</creator><creator>Haas, Angela</creator><creator>Masior, Tomasz</creator><creator>Rudolph, Christine</creator><creator>Peyrin‐Biroulet, Laurent</creator><scope>24P</scope><scope>WIN</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>7X8</scope><orcidid>https://orcid.org/0000-0003-2254-7771</orcidid><orcidid>https://orcid.org/0000-0003-2536-6618</orcidid><orcidid>https://orcid.org/0000-0003-1923-3237</orcidid><orcidid>https://orcid.org/0000-0001-7341-1351</orcidid><orcidid>https://orcid.org/0000-0002-4753-6676</orcidid><orcidid>https://orcid.org/0000-0001-7199-6851</orcidid></search><sort><creationdate>202409</creationdate><title>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow‐up in the SELECTION open‐label long‐term extension study</title><author>Feagan, Brian G. ; Matsuoka, Katsuyoshi ; Rogler, Gerhard ; Laharie, David ; Vermeire, Séverine ; Danese, Silvio ; Loftus, Edward V. ; Beales, Ian ; Schreiber, Stefan ; Kim, Hyo Jong ; Faes, Margaux ; Haas, Angela ; Masior, Tomasz ; Rudolph, Christine ; Peyrin‐Biroulet, Laurent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2158-7328cc0066856ece2bf57c287f0ea2de090e5fa81156928475de183f4511cec03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Colitis, Ulcerative - drug therapy</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pyridines - administration & dosage</topic><topic>Pyridines - adverse effects</topic><topic>Pyridines - therapeutic use</topic><topic>Quality of Life</topic><topic>Severity of Illness Index</topic><topic>Treatment Outcome</topic><topic>Triazoles - administration & dosage</topic><topic>Triazoles - adverse effects</topic><topic>Triazoles - therapeutic use</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feagan, Brian G.</creatorcontrib><creatorcontrib>Matsuoka, Katsuyoshi</creatorcontrib><creatorcontrib>Rogler, Gerhard</creatorcontrib><creatorcontrib>Laharie, David</creatorcontrib><creatorcontrib>Vermeire, Séverine</creatorcontrib><creatorcontrib>Danese, Silvio</creatorcontrib><creatorcontrib>Loftus, Edward V.</creatorcontrib><creatorcontrib>Beales, Ian</creatorcontrib><creatorcontrib>Schreiber, Stefan</creatorcontrib><creatorcontrib>Kim, Hyo Jong</creatorcontrib><creatorcontrib>Faes, Margaux</creatorcontrib><creatorcontrib>Haas, Angela</creatorcontrib><creatorcontrib>Masior, Tomasz</creatorcontrib><creatorcontrib>Rudolph, Christine</creatorcontrib><creatorcontrib>Peyrin‐Biroulet, Laurent</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Alimentary pharmacology & therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feagan, Brian G.</au><au>Matsuoka, Katsuyoshi</au><au>Rogler, Gerhard</au><au>Laharie, David</au><au>Vermeire, Séverine</au><au>Danese, Silvio</au><au>Loftus, Edward V.</au><au>Beales, Ian</au><au>Schreiber, Stefan</au><au>Kim, Hyo Jong</au><au>Faes, Margaux</au><au>Haas, Angela</au><au>Masior, Tomasz</au><au>Rudolph, Christine</au><au>Peyrin‐Biroulet, Laurent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow‐up in the SELECTION open‐label long‐term extension study</atitle><jtitle>Alimentary pharmacology & therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2024-09</date><risdate>2024</risdate><volume>60</volume><issue>5</issue><spage>563</spage><epage>584</epage><pages>563-584</pages><issn>0269-2813</issn><issn>1365-2036</issn><eissn>1365-2036</eissn><abstract>Summary
Background
Filgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.
Aims
The aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).
Methods
In this interim analysis of SELECTIONLTE, SELECTION completers (week 10 responders to filgotinib who completed the maintenance study) continued their assigned treatment (double‐blind filgotinib 200 mg [FIL200] or filgotinib 100 mg) and SELECTION week 10 non‐responders received open‐label FIL200. We assessed safety by adverse events (AEs), and efficacy by partial Mayo Clinic Score (pMCS), inflammatory biomarkers and health‐related quality of life (HRQoL). We compared safety and efficacy between achievers and non‐achievers of a multi‐component endpoint, comprehensive disease control (CDC), comprising symptomatic, endoscopic, inflammatory biomarker and HRQoL improvements.
Results
Data for completers (n = 250) and non‐responders (n = 372) were reported for ≤202 weeks. AE occurrences were low and consistent with previous analyses. The as‐observed proportion of FIL200‐treated patients in pMCS, biomarker and HRQoL remission during SELECTIONLTE remained high among completers (week 144: 80.0%, 86.4% and 86.0%, respectively) and increased among non‐responders (week 192: 62.1%, 76.7% and 59.3%, respectively). Significantly higher proportions of CDC achievers at SELECTION week 58 achieved pMCS, IBDQ and corticosteroid‐free pMCS remission than non‐achievers, up to LTE week 96.
Conclusions
Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results showed a proven long‐term benefit–risk profile. FIL200‐treated CDC achievers had better long‐term outcomes than non‐achievers.
This interim analysis aimed to assess the safety and efficacy of continued filgotinib therapy in moderately to severely active ulcerative colitis over ~4 years in SELECTIONLTE (NCT02914535). Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results demonstrated its proven long‐term benefit–risk profile.</abstract><cop>England</cop><pmid>39086130</pmid><doi>10.1111/apt.18158</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0003-2254-7771</orcidid><orcidid>https://orcid.org/0000-0003-2536-6618</orcidid><orcidid>https://orcid.org/0000-0003-1923-3237</orcidid><orcidid>https://orcid.org/0000-0001-7341-1351</orcidid><orcidid>https://orcid.org/0000-0002-4753-6676</orcidid><orcidid>https://orcid.org/0000-0001-7199-6851</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Colitis, Ulcerative - drug therapy Double-Blind Method Female Follow-Up Studies Humans Male Middle Aged Pyridines - administration & dosage Pyridines - adverse effects Pyridines - therapeutic use Quality of Life Severity of Illness Index Treatment Outcome Triazoles - administration & dosage Triazoles - adverse effects Triazoles - therapeutic use Young Adult |
title | Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow‐up in the SELECTION open‐label long‐term extension study |
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