Satisfaction with the Injection Experience of a New, Citrate-Free Formulation of Ixekizumab
Introduction A new, citrate-free ixekizumab formulation, which is bioequivalent to the original formulation, was associated with significant reduction in injection site pain. This study evaluates patient satisfaction with the first injection experience of citrate-free ixekizumab in a real-world sett...
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Veröffentlicht in: | Advances in therapy 2024-04, Vol.41 (4), p.1672-1684 |
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description | Introduction
A new, citrate-free ixekizumab formulation, which is bioequivalent to the original formulation, was associated with significant reduction in injection site pain. This study evaluates patient satisfaction with the first injection experience of citrate-free ixekizumab in a real-world setting.
Methods
A non-interventional, observational, web-based survey of adults (≥ 18 years) with psoriasis, psoriatic arthritis, or axial spondyloarthritis was conducted between August 2022 and March 2023. Patients enrolled in the Taltz US Customer Support Program were identified as receiving either the original ixekizumab or initiating citrate-free ixekizumab. Patients receiving original ixekizumab completed one survey at baseline to assess satisfaction with the formulation and one survey after switching to assess satisfaction, willingness to continue using and recommending citrate-free ixekizumab, and formulation preference. Participants previously exposed to ixekizumab completed one survey to assess their satisfaction and willingness to continue using and recommending citrate-free ixekizumab. Descriptive and comparative statistics are reported for patients that switched from original to citrate-free ixekizumab (
n
= 361); and descriptive statistics are reported for patients not previously exposed to ixekizumab (
n
= 90).
Results
A total of 451 patients were included in the analysis. Significantly more patients were satisfied with their first injection with citrate-free ixekizumab compared to original ixekizumab (83.9% vs. 71.7% respectively;
p
= 0.0001). Almost all patients who switched from original ixekizumab were definitely or mostly willing to continue using and recommending citrate-free ixekizumab (93.9% and 93.4%, respectively). Additionally, 94.2% of patients who switched from original to citrate-free ixekizumab preferred citrate-free ixekizumab or had no preference. Three-fourths of patients not previously exposed to ixekizumab were satisfied with their first injection with citrate-free ixekizumab and 94.5% were definitely or mostly willing to continue using citrate-free ixekizumab.
Conclusion
The citrate-free ixekizumab formulation was preferred and well accepted by most patients who switched from the original ixekizumab formulation. Similar findings were seen for those newly initiating citrate-free ixekizumab. |
doi_str_mv | 10.1007/s12325-024-02812-1 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10960761</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2938285282</sourcerecordid><originalsourceid>FETCH-LOGICAL-c398t-16e9f070419edffa349d1d89b0ef79de2fd079cc73eb5f5143fa7e263a8b85463</originalsourceid><addsrcrecordid>eNp9kU1P3DAQhq2qqCzQP9BDlWMPDfgrsX2qqtUurITgQCsh9WA5yZj1NokXOykfvx5DANELh5Elz-N3Rn4Q-kLwIcFYHEVCGS1yTHkqSWhOPqAZkWWRp6If0QwLTnLK5OUu2otxgzHFopCf0C6TnLOSFzP058IMLlpTD8732Y0b1tmwhmzVb2C6WtxuITjoa8i8zUx2Bjffs7kbghkgXwaAbOlDN7bmiU7I6hb-uvuxM9UB2rGmjfD5-dxHv5eLX_OT_PT8eDX_eZrXTMkhJyUoiwXmREFjrWFcNaSRqsJghWqA2gYLVdeCQVXYgnBmjQBaMiMrWfCS7aMfU-52rDpoaujTdq3eBteZcKe9cfr_Tu_W-sr_0wSrEouSpIRvzwnBX48QB925WEPbmh78GDVVTFJZUEkTSie0Dj7GAPZ1DsH6UYuetOikRT9p0Y_5X99u-PrkxUMC2ATE1OqvIOiNH0Offu292Af-85oZ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2938285282</pqid></control><display><type>article</type><title>Satisfaction with the Injection Experience of a New, Citrate-Free Formulation of Ixekizumab</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Chabra, Sanjay ; Birt, Julie ; Bolce, Rebecca ; Lisse, Jeffrey ; Malatestinic, William N. ; Zhu, Baojin ; Kimel, Miriam ; McCormack, Julie ; Stefan, Marissa ; Cragun, W. Chad</creator><creatorcontrib>Chabra, Sanjay ; Birt, Julie ; Bolce, Rebecca ; Lisse, Jeffrey ; Malatestinic, William N. ; Zhu, Baojin ; Kimel, Miriam ; McCormack, Julie ; Stefan, Marissa ; Cragun, W. Chad</creatorcontrib><description>Introduction
A new, citrate-free ixekizumab formulation, which is bioequivalent to the original formulation, was associated with significant reduction in injection site pain. This study evaluates patient satisfaction with the first injection experience of citrate-free ixekizumab in a real-world setting.
Methods
A non-interventional, observational, web-based survey of adults (≥ 18 years) with psoriasis, psoriatic arthritis, or axial spondyloarthritis was conducted between August 2022 and March 2023. Patients enrolled in the Taltz US Customer Support Program were identified as receiving either the original ixekizumab or initiating citrate-free ixekizumab. Patients receiving original ixekizumab completed one survey at baseline to assess satisfaction with the formulation and one survey after switching to assess satisfaction, willingness to continue using and recommending citrate-free ixekizumab, and formulation preference. Participants previously exposed to ixekizumab completed one survey to assess their satisfaction and willingness to continue using and recommending citrate-free ixekizumab. Descriptive and comparative statistics are reported for patients that switched from original to citrate-free ixekizumab (
n
= 361); and descriptive statistics are reported for patients not previously exposed to ixekizumab (
n
= 90).
Results
A total of 451 patients were included in the analysis. Significantly more patients were satisfied with their first injection with citrate-free ixekizumab compared to original ixekizumab (83.9% vs. 71.7% respectively;
p
= 0.0001). Almost all patients who switched from original ixekizumab were definitely or mostly willing to continue using and recommending citrate-free ixekizumab (93.9% and 93.4%, respectively). Additionally, 94.2% of patients who switched from original to citrate-free ixekizumab preferred citrate-free ixekizumab or had no preference. Three-fourths of patients not previously exposed to ixekizumab were satisfied with their first injection with citrate-free ixekizumab and 94.5% were definitely or mostly willing to continue using citrate-free ixekizumab.
Conclusion
The citrate-free ixekizumab formulation was preferred and well accepted by most patients who switched from the original ixekizumab formulation. Similar findings were seen for those newly initiating citrate-free ixekizumab.</description><identifier>ISSN: 0741-238X</identifier><identifier>EISSN: 1865-8652</identifier><identifier>DOI: 10.1007/s12325-024-02812-1</identifier><identifier>PMID: 38443645</identifier><language>eng</language><publisher>Cheshire: Springer Healthcare</publisher><subject>Adult ; Antibodies, Monoclonal, Humanized - therapeutic use ; Arthritis, Psoriatic ; Cardiology ; Citrates ; Citric Acid ; Endocrinology ; Humans ; Internal Medicine ; Medicine ; Medicine & Public Health ; Oncology ; Original Research ; Personal Satisfaction ; Pharmacology/Toxicology ; Psoriasis ; Rheumatology ; Treatment Outcome</subject><ispartof>Advances in therapy, 2024-04, Vol.41 (4), p.1672-1684</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c398t-16e9f070419edffa349d1d89b0ef79de2fd079cc73eb5f5143fa7e263a8b85463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12325-024-02812-1$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12325-024-02812-1$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38443645$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chabra, Sanjay</creatorcontrib><creatorcontrib>Birt, Julie</creatorcontrib><creatorcontrib>Bolce, Rebecca</creatorcontrib><creatorcontrib>Lisse, Jeffrey</creatorcontrib><creatorcontrib>Malatestinic, William N.</creatorcontrib><creatorcontrib>Zhu, Baojin</creatorcontrib><creatorcontrib>Kimel, Miriam</creatorcontrib><creatorcontrib>McCormack, Julie</creatorcontrib><creatorcontrib>Stefan, Marissa</creatorcontrib><creatorcontrib>Cragun, W. Chad</creatorcontrib><title>Satisfaction with the Injection Experience of a New, Citrate-Free Formulation of Ixekizumab</title><title>Advances in therapy</title><addtitle>Adv Ther</addtitle><addtitle>Adv Ther</addtitle><description>Introduction
A new, citrate-free ixekizumab formulation, which is bioequivalent to the original formulation, was associated with significant reduction in injection site pain. This study evaluates patient satisfaction with the first injection experience of citrate-free ixekizumab in a real-world setting.
Methods
A non-interventional, observational, web-based survey of adults (≥ 18 years) with psoriasis, psoriatic arthritis, or axial spondyloarthritis was conducted between August 2022 and March 2023. Patients enrolled in the Taltz US Customer Support Program were identified as receiving either the original ixekizumab or initiating citrate-free ixekizumab. Patients receiving original ixekizumab completed one survey at baseline to assess satisfaction with the formulation and one survey after switching to assess satisfaction, willingness to continue using and recommending citrate-free ixekizumab, and formulation preference. Participants previously exposed to ixekizumab completed one survey to assess their satisfaction and willingness to continue using and recommending citrate-free ixekizumab. Descriptive and comparative statistics are reported for patients that switched from original to citrate-free ixekizumab (
n
= 361); and descriptive statistics are reported for patients not previously exposed to ixekizumab (
n
= 90).
Results
A total of 451 patients were included in the analysis. Significantly more patients were satisfied with their first injection with citrate-free ixekizumab compared to original ixekizumab (83.9% vs. 71.7% respectively;
p
= 0.0001). Almost all patients who switched from original ixekizumab were definitely or mostly willing to continue using and recommending citrate-free ixekizumab (93.9% and 93.4%, respectively). Additionally, 94.2% of patients who switched from original to citrate-free ixekizumab preferred citrate-free ixekizumab or had no preference. Three-fourths of patients not previously exposed to ixekizumab were satisfied with their first injection with citrate-free ixekizumab and 94.5% were definitely or mostly willing to continue using citrate-free ixekizumab.
Conclusion
The citrate-free ixekizumab formulation was preferred and well accepted by most patients who switched from the original ixekizumab formulation. Similar findings were seen for those newly initiating citrate-free ixekizumab.</description><subject>Adult</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Arthritis, Psoriatic</subject><subject>Cardiology</subject><subject>Citrates</subject><subject>Citric Acid</subject><subject>Endocrinology</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Original Research</subject><subject>Personal Satisfaction</subject><subject>Pharmacology/Toxicology</subject><subject>Psoriasis</subject><subject>Rheumatology</subject><subject>Treatment Outcome</subject><issn>0741-238X</issn><issn>1865-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU1P3DAQhq2qqCzQP9BDlWMPDfgrsX2qqtUurITgQCsh9WA5yZj1NokXOykfvx5DANELh5Elz-N3Rn4Q-kLwIcFYHEVCGS1yTHkqSWhOPqAZkWWRp6If0QwLTnLK5OUu2otxgzHFopCf0C6TnLOSFzP058IMLlpTD8732Y0b1tmwhmzVb2C6WtxuITjoa8i8zUx2Bjffs7kbghkgXwaAbOlDN7bmiU7I6hb-uvuxM9UB2rGmjfD5-dxHv5eLX_OT_PT8eDX_eZrXTMkhJyUoiwXmREFjrWFcNaSRqsJghWqA2gYLVdeCQVXYgnBmjQBaMiMrWfCS7aMfU-52rDpoaujTdq3eBteZcKe9cfr_Tu_W-sr_0wSrEouSpIRvzwnBX48QB925WEPbmh78GDVVTFJZUEkTSie0Dj7GAPZ1DsH6UYuetOikRT9p0Y_5X99u-PrkxUMC2ATE1OqvIOiNH0Offu292Af-85oZ</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Chabra, Sanjay</creator><creator>Birt, Julie</creator><creator>Bolce, Rebecca</creator><creator>Lisse, Jeffrey</creator><creator>Malatestinic, William N.</creator><creator>Zhu, Baojin</creator><creator>Kimel, Miriam</creator><creator>McCormack, Julie</creator><creator>Stefan, Marissa</creator><creator>Cragun, W. Chad</creator><general>Springer Healthcare</general><scope>C6C</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><scope>5PM</scope></search><sort><creationdate>20240401</creationdate><title>Satisfaction with the Injection Experience of a New, Citrate-Free Formulation of Ixekizumab</title><author>Chabra, Sanjay ; Birt, Julie ; Bolce, Rebecca ; Lisse, Jeffrey ; Malatestinic, William N. ; Zhu, Baojin ; Kimel, Miriam ; McCormack, Julie ; Stefan, Marissa ; Cragun, W. Chad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-16e9f070419edffa349d1d89b0ef79de2fd079cc73eb5f5143fa7e263a8b85463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Arthritis, Psoriatic</topic><topic>Cardiology</topic><topic>Citrates</topic><topic>Citric Acid</topic><topic>Endocrinology</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Original Research</topic><topic>Personal Satisfaction</topic><topic>Pharmacology/Toxicology</topic><topic>Psoriasis</topic><topic>Rheumatology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chabra, Sanjay</creatorcontrib><creatorcontrib>Birt, Julie</creatorcontrib><creatorcontrib>Bolce, Rebecca</creatorcontrib><creatorcontrib>Lisse, Jeffrey</creatorcontrib><creatorcontrib>Malatestinic, William N.</creatorcontrib><creatorcontrib>Zhu, Baojin</creatorcontrib><creatorcontrib>Kimel, Miriam</creatorcontrib><creatorcontrib>McCormack, Julie</creatorcontrib><creatorcontrib>Stefan, Marissa</creatorcontrib><creatorcontrib>Cragun, W. Chad</creatorcontrib><collection>Springer Nature OA/Free Journals</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Advances in therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chabra, Sanjay</au><au>Birt, Julie</au><au>Bolce, Rebecca</au><au>Lisse, Jeffrey</au><au>Malatestinic, William N.</au><au>Zhu, Baojin</au><au>Kimel, Miriam</au><au>McCormack, Julie</au><au>Stefan, Marissa</au><au>Cragun, W. Chad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Satisfaction with the Injection Experience of a New, Citrate-Free Formulation of Ixekizumab</atitle><jtitle>Advances in therapy</jtitle><stitle>Adv Ther</stitle><addtitle>Adv Ther</addtitle><date>2024-04-01</date><risdate>2024</risdate><volume>41</volume><issue>4</issue><spage>1672</spage><epage>1684</epage><pages>1672-1684</pages><issn>0741-238X</issn><eissn>1865-8652</eissn><abstract>Introduction
A new, citrate-free ixekizumab formulation, which is bioequivalent to the original formulation, was associated with significant reduction in injection site pain. This study evaluates patient satisfaction with the first injection experience of citrate-free ixekizumab in a real-world setting.
Methods
A non-interventional, observational, web-based survey of adults (≥ 18 years) with psoriasis, psoriatic arthritis, or axial spondyloarthritis was conducted between August 2022 and March 2023. Patients enrolled in the Taltz US Customer Support Program were identified as receiving either the original ixekizumab or initiating citrate-free ixekizumab. Patients receiving original ixekizumab completed one survey at baseline to assess satisfaction with the formulation and one survey after switching to assess satisfaction, willingness to continue using and recommending citrate-free ixekizumab, and formulation preference. Participants previously exposed to ixekizumab completed one survey to assess their satisfaction and willingness to continue using and recommending citrate-free ixekizumab. Descriptive and comparative statistics are reported for patients that switched from original to citrate-free ixekizumab (
n
= 361); and descriptive statistics are reported for patients not previously exposed to ixekizumab (
n
= 90).
Results
A total of 451 patients were included in the analysis. Significantly more patients were satisfied with their first injection with citrate-free ixekizumab compared to original ixekizumab (83.9% vs. 71.7% respectively;
p
= 0.0001). Almost all patients who switched from original ixekizumab were definitely or mostly willing to continue using and recommending citrate-free ixekizumab (93.9% and 93.4%, respectively). Additionally, 94.2% of patients who switched from original to citrate-free ixekizumab preferred citrate-free ixekizumab or had no preference. Three-fourths of patients not previously exposed to ixekizumab were satisfied with their first injection with citrate-free ixekizumab and 94.5% were definitely or mostly willing to continue using citrate-free ixekizumab.
Conclusion
The citrate-free ixekizumab formulation was preferred and well accepted by most patients who switched from the original ixekizumab formulation. Similar findings were seen for those newly initiating citrate-free ixekizumab.</abstract><cop>Cheshire</cop><pub>Springer Healthcare</pub><pmid>38443645</pmid><doi>10.1007/s12325-024-02812-1</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Adult Antibodies, Monoclonal, Humanized - therapeutic use Arthritis, Psoriatic Cardiology Citrates Citric Acid Endocrinology Humans Internal Medicine Medicine Medicine & Public Health Oncology Original Research Personal Satisfaction Pharmacology/Toxicology Psoriasis Rheumatology Treatment Outcome |
title | Satisfaction with the Injection Experience of a New, Citrate-Free Formulation of Ixekizumab |
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