18-Month efficacy and safety analysis of monthly subcutaneous buprenorphine injection for opioid use disorder: Integrated analysis of phase 3 studies
Few studies investigate the natural history of patients on long-term treatment for opioid use disorder (OUD). We evaluated the long-term efficacy, safety, and tolerability experience of monthly extended-release buprenorphine (BUP-XR) in participants seeking treatment for OUD, via integrated analysis...
Gespeichert in:
Veröffentlicht in: | Journal of substance use and addiction treatment 2023-11, Vol.154, p.209155-209155, Article 209155 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 209155 |
---|---|
container_issue | |
container_start_page | 209155 |
container_title | Journal of substance use and addiction treatment |
container_volume | 154 |
creator | Rutrick, Daniel Learned, Susan M. Boyett, Brent Hassman, David Shinde, Sunita Zhao, Yue |
description | Few studies investigate the natural history of patients on long-term treatment for opioid use disorder (OUD). We evaluated the long-term efficacy, safety, and tolerability experience of monthly extended-release buprenorphine (BUP-XR) in participants seeking treatment for OUD, via integrated analysis of phase 3 studies.
Study 1 was a 24-week randomized, double-blind, placebo-controlled trial of participants receiving monthly injections of BUP-XR (300 mg × 2, 100 mg × 4 [n = 203] or 300 mg × 6 [n = 201]) or placebo (n = 100). Study 2 was a 48-week, open-label trial enrolling 257 participants who completed study 1 and 412 de novo participants, to receive 6 and 12 BUP-XR injections, respectively. Study 3 was a 24-week, open-label extension enrolling 208 participants who completed study 2 for 6 additional injections. We assessed opioid abstinence as the proportion of urine opioid negative participants by visit and the percentage of each participant's negative opioid assessments during the first 6 months.
In total, 916 participants were treated with BUP-XR or placebo. By the end of 18 months, 92.7 % of the de novo cohort and 81.8 % of the study 1 cohort were urine negative for opioids. Among early nonresponders (percentage of abstinence ≤20 %), 73.1 % were urine negative after 18 months. The longer treatment period was well tolerated, with no new safety concerns, and a low incidence of opioid withdrawal signs and symptoms, and hepatic disorder.
Extending BUP-XR treatment beyond 6 months sustained improvement in opioid abstinence and was well tolerated, supporting clinical benefit up to 18 months.
NCT02357901 (study 1); NCT02510014 (study 2); NCT02896296 (study 3).
•Long-term BUP-XR treatment experience for patients with opioid use disorder.•BUP-XR sustained improved opioid abstinence and was well tolerated up to 18 months.•Early nonresponders remaining on treatment had improved abstinence by 18 months. |
doi_str_mv | 10.1016/j.josat.2023.209155 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2860407441</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2949875923002060</els_id><sourcerecordid>2860407441</sourcerecordid><originalsourceid>FETCH-LOGICAL-c261t-c871f5e0f1f9442563c19e0f6124624b906cf808585b54a3792c4110f5e897893</originalsourceid><addsrcrecordid>eNp9UcFO3DAUjKoiFQFf0IuPvWRrO3ZiV-KAUAtIIC5wtrzOc9dR1g5-DtJ-SP-XLOmhXHp5b540M9K8qaqvjG4YZe33YTMktGXDKW-WoZmUn6pTroWuVSf153_wl-oCcaCUct1yKZvT6g9T9UOKZUfA--CsOxAbe4LWQzlCOx4wIEme7I-s8UBw3rq52AhpRrKdpwwx5WkXIpAQB3AlpEh8yiRNIYWezAikD5hyD_kHuYsFfmdboP9gPu3sQmsIlrkPgOfVibcjwsXffVY9__r5dH1b3z_e3F1f3deOt6zUTnXMS6CeeS0El23jmF7OlnHRcrHVtHVeUSWV3Ephm05zJxiji0bpTunmrPq2-k45vcyAxewDOhjHNZ7hqqWCdkKwhdqsVJcTYgZvphz2Nh8Mo-bYgxnMew_m2INZe1hUl6sKlhSvAbJBFyA66ENeXmX6FP6rfwP-c5PL</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2860407441</pqid></control><display><type>article</type><title>18-Month efficacy and safety analysis of monthly subcutaneous buprenorphine injection for opioid use disorder: Integrated analysis of phase 3 studies</title><source>Alma/SFX Local Collection</source><creator>Rutrick, Daniel ; Learned, Susan M. ; Boyett, Brent ; Hassman, David ; Shinde, Sunita ; Zhao, Yue</creator><creatorcontrib>Rutrick, Daniel ; Learned, Susan M. ; Boyett, Brent ; Hassman, David ; Shinde, Sunita ; Zhao, Yue</creatorcontrib><description>Few studies investigate the natural history of patients on long-term treatment for opioid use disorder (OUD). We evaluated the long-term efficacy, safety, and tolerability experience of monthly extended-release buprenorphine (BUP-XR) in participants seeking treatment for OUD, via integrated analysis of phase 3 studies.
Study 1 was a 24-week randomized, double-blind, placebo-controlled trial of participants receiving monthly injections of BUP-XR (300 mg × 2, 100 mg × 4 [n = 203] or 300 mg × 6 [n = 201]) or placebo (n = 100). Study 2 was a 48-week, open-label trial enrolling 257 participants who completed study 1 and 412 de novo participants, to receive 6 and 12 BUP-XR injections, respectively. Study 3 was a 24-week, open-label extension enrolling 208 participants who completed study 2 for 6 additional injections. We assessed opioid abstinence as the proportion of urine opioid negative participants by visit and the percentage of each participant's negative opioid assessments during the first 6 months.
In total, 916 participants were treated with BUP-XR or placebo. By the end of 18 months, 92.7 % of the de novo cohort and 81.8 % of the study 1 cohort were urine negative for opioids. Among early nonresponders (percentage of abstinence ≤20 %), 73.1 % were urine negative after 18 months. The longer treatment period was well tolerated, with no new safety concerns, and a low incidence of opioid withdrawal signs and symptoms, and hepatic disorder.
Extending BUP-XR treatment beyond 6 months sustained improvement in opioid abstinence and was well tolerated, supporting clinical benefit up to 18 months.
NCT02357901 (study 1); NCT02510014 (study 2); NCT02896296 (study 3).
•Long-term BUP-XR treatment experience for patients with opioid use disorder.•BUP-XR sustained improved opioid abstinence and was well tolerated up to 18 months.•Early nonresponders remaining on treatment had improved abstinence by 18 months.</description><identifier>ISSN: 2949-8759</identifier><identifier>EISSN: 2949-8759</identifier><identifier>DOI: 10.1016/j.josat.2023.209155</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>Extended-release buprenorphine ; Integrated analysis ; Long-term safety and efficacy ; Opioid use disorder</subject><ispartof>Journal of substance use and addiction treatment, 2023-11, Vol.154, p.209155-209155, Article 209155</ispartof><rights>2023 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c261t-c871f5e0f1f9442563c19e0f6124624b906cf808585b54a3792c4110f5e897893</cites><orcidid>0000-0003-4297-5781</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Rutrick, Daniel</creatorcontrib><creatorcontrib>Learned, Susan M.</creatorcontrib><creatorcontrib>Boyett, Brent</creatorcontrib><creatorcontrib>Hassman, David</creatorcontrib><creatorcontrib>Shinde, Sunita</creatorcontrib><creatorcontrib>Zhao, Yue</creatorcontrib><title>18-Month efficacy and safety analysis of monthly subcutaneous buprenorphine injection for opioid use disorder: Integrated analysis of phase 3 studies</title><title>Journal of substance use and addiction treatment</title><description>Few studies investigate the natural history of patients on long-term treatment for opioid use disorder (OUD). We evaluated the long-term efficacy, safety, and tolerability experience of monthly extended-release buprenorphine (BUP-XR) in participants seeking treatment for OUD, via integrated analysis of phase 3 studies.
Study 1 was a 24-week randomized, double-blind, placebo-controlled trial of participants receiving monthly injections of BUP-XR (300 mg × 2, 100 mg × 4 [n = 203] or 300 mg × 6 [n = 201]) or placebo (n = 100). Study 2 was a 48-week, open-label trial enrolling 257 participants who completed study 1 and 412 de novo participants, to receive 6 and 12 BUP-XR injections, respectively. Study 3 was a 24-week, open-label extension enrolling 208 participants who completed study 2 for 6 additional injections. We assessed opioid abstinence as the proportion of urine opioid negative participants by visit and the percentage of each participant's negative opioid assessments during the first 6 months.
In total, 916 participants were treated with BUP-XR or placebo. By the end of 18 months, 92.7 % of the de novo cohort and 81.8 % of the study 1 cohort were urine negative for opioids. Among early nonresponders (percentage of abstinence ≤20 %), 73.1 % were urine negative after 18 months. The longer treatment period was well tolerated, with no new safety concerns, and a low incidence of opioid withdrawal signs and symptoms, and hepatic disorder.
Extending BUP-XR treatment beyond 6 months sustained improvement in opioid abstinence and was well tolerated, supporting clinical benefit up to 18 months.
NCT02357901 (study 1); NCT02510014 (study 2); NCT02896296 (study 3).
•Long-term BUP-XR treatment experience for patients with opioid use disorder.•BUP-XR sustained improved opioid abstinence and was well tolerated up to 18 months.•Early nonresponders remaining on treatment had improved abstinence by 18 months.</description><subject>Extended-release buprenorphine</subject><subject>Integrated analysis</subject><subject>Long-term safety and efficacy</subject><subject>Opioid use disorder</subject><issn>2949-8759</issn><issn>2949-8759</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9UcFO3DAUjKoiFQFf0IuPvWRrO3ZiV-KAUAtIIC5wtrzOc9dR1g5-DtJ-SP-XLOmhXHp5b540M9K8qaqvjG4YZe33YTMktGXDKW-WoZmUn6pTroWuVSf153_wl-oCcaCUct1yKZvT6g9T9UOKZUfA--CsOxAbe4LWQzlCOx4wIEme7I-s8UBw3rq52AhpRrKdpwwx5WkXIpAQB3AlpEh8yiRNIYWezAikD5hyD_kHuYsFfmdboP9gPu3sQmsIlrkPgOfVibcjwsXffVY9__r5dH1b3z_e3F1f3deOt6zUTnXMS6CeeS0El23jmF7OlnHRcrHVtHVeUSWV3Ephm05zJxiji0bpTunmrPq2-k45vcyAxewDOhjHNZ7hqqWCdkKwhdqsVJcTYgZvphz2Nh8Mo-bYgxnMew_m2INZe1hUl6sKlhSvAbJBFyA66ENeXmX6FP6rfwP-c5PL</recordid><startdate>202311</startdate><enddate>202311</enddate><creator>Rutrick, Daniel</creator><creator>Learned, Susan M.</creator><creator>Boyett, Brent</creator><creator>Hassman, David</creator><creator>Shinde, Sunita</creator><creator>Zhao, Yue</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4297-5781</orcidid></search><sort><creationdate>202311</creationdate><title>18-Month efficacy and safety analysis of monthly subcutaneous buprenorphine injection for opioid use disorder: Integrated analysis of phase 3 studies</title><author>Rutrick, Daniel ; Learned, Susan M. ; Boyett, Brent ; Hassman, David ; Shinde, Sunita ; Zhao, Yue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c261t-c871f5e0f1f9442563c19e0f6124624b906cf808585b54a3792c4110f5e897893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Extended-release buprenorphine</topic><topic>Integrated analysis</topic><topic>Long-term safety and efficacy</topic><topic>Opioid use disorder</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rutrick, Daniel</creatorcontrib><creatorcontrib>Learned, Susan M.</creatorcontrib><creatorcontrib>Boyett, Brent</creatorcontrib><creatorcontrib>Hassman, David</creatorcontrib><creatorcontrib>Shinde, Sunita</creatorcontrib><creatorcontrib>Zhao, Yue</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of substance use and addiction treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rutrick, Daniel</au><au>Learned, Susan M.</au><au>Boyett, Brent</au><au>Hassman, David</au><au>Shinde, Sunita</au><au>Zhao, Yue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>18-Month efficacy and safety analysis of monthly subcutaneous buprenorphine injection for opioid use disorder: Integrated analysis of phase 3 studies</atitle><jtitle>Journal of substance use and addiction treatment</jtitle><date>2023-11</date><risdate>2023</risdate><volume>154</volume><spage>209155</spage><epage>209155</epage><pages>209155-209155</pages><artnum>209155</artnum><issn>2949-8759</issn><eissn>2949-8759</eissn><abstract>Few studies investigate the natural history of patients on long-term treatment for opioid use disorder (OUD). We evaluated the long-term efficacy, safety, and tolerability experience of monthly extended-release buprenorphine (BUP-XR) in participants seeking treatment for OUD, via integrated analysis of phase 3 studies.
Study 1 was a 24-week randomized, double-blind, placebo-controlled trial of participants receiving monthly injections of BUP-XR (300 mg × 2, 100 mg × 4 [n = 203] or 300 mg × 6 [n = 201]) or placebo (n = 100). Study 2 was a 48-week, open-label trial enrolling 257 participants who completed study 1 and 412 de novo participants, to receive 6 and 12 BUP-XR injections, respectively. Study 3 was a 24-week, open-label extension enrolling 208 participants who completed study 2 for 6 additional injections. We assessed opioid abstinence as the proportion of urine opioid negative participants by visit and the percentage of each participant's negative opioid assessments during the first 6 months.
In total, 916 participants were treated with BUP-XR or placebo. By the end of 18 months, 92.7 % of the de novo cohort and 81.8 % of the study 1 cohort were urine negative for opioids. Among early nonresponders (percentage of abstinence ≤20 %), 73.1 % were urine negative after 18 months. The longer treatment period was well tolerated, with no new safety concerns, and a low incidence of opioid withdrawal signs and symptoms, and hepatic disorder.
Extending BUP-XR treatment beyond 6 months sustained improvement in opioid abstinence and was well tolerated, supporting clinical benefit up to 18 months.
NCT02357901 (study 1); NCT02510014 (study 2); NCT02896296 (study 3).
•Long-term BUP-XR treatment experience for patients with opioid use disorder.•BUP-XR sustained improved opioid abstinence and was well tolerated up to 18 months.•Early nonresponders remaining on treatment had improved abstinence by 18 months.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.josat.2023.209155</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-4297-5781</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2949-8759 |
ispartof | Journal of substance use and addiction treatment, 2023-11, Vol.154, p.209155-209155, Article 209155 |
issn | 2949-8759 2949-8759 |
language | eng |
recordid | cdi_proquest_miscellaneous_2860407441 |
source | Alma/SFX Local Collection |
subjects | Extended-release buprenorphine Integrated analysis Long-term safety and efficacy Opioid use disorder |
title | 18-Month efficacy and safety analysis of monthly subcutaneous buprenorphine injection for opioid use disorder: Integrated analysis of phase 3 studies |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T10%3A26%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=18-Month%20efficacy%20and%20safety%20analysis%20of%20monthly%20subcutaneous%20buprenorphine%20injection%20for%20opioid%20use%20disorder:%20Integrated%20analysis%20of%20phase%203%20studies&rft.jtitle=Journal%20of%20substance%20use%20and%20addiction%20treatment&rft.au=Rutrick,%20Daniel&rft.date=2023-11&rft.volume=154&rft.spage=209155&rft.epage=209155&rft.pages=209155-209155&rft.artnum=209155&rft.issn=2949-8759&rft.eissn=2949-8759&rft_id=info:doi/10.1016/j.josat.2023.209155&rft_dat=%3Cproquest_cross%3E2860407441%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2860407441&rft_id=info:pmid/&rft_els_id=S2949875923002060&rfr_iscdi=true |