A new oral delivery system for 5‐ASA: Preliminary clinical findings for MMx
Background: Multi‐matrix (MMx), a new delivery system for mesalazine, seems to release 5‐aminosalicyclic acid (5‐ASA) preferentially in the sigmoid colon. This study had 2 objectives: (1) to evaluate the therapeutic response to MMx in patients with active left‐sided disease and (2) to gain additiona...
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Veröffentlicht in: | Inflammatory bowel diseases 2005-05, Vol.11 (5), p.421-427 |
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creator | Prantera, Cosimo Viscido, Angelo Biancone, Livia Francavilla, Antonio Giglio, Lucio Campieri, Massimo |
description | Background: Multi‐matrix (MMx), a new delivery system for mesalazine, seems to release 5‐aminosalicyclic acid (5‐ASA) preferentially in the sigmoid colon. This study had 2 objectives: (1) to evaluate the therapeutic response to MMx in patients with active left‐sided disease and (2) to gain additional insights as to how the therapy would compare with topical 5‐ASA.
Methods: Patients received either 1.2 g of 5‐ASA MMx three times per day plus placebo enema or 4 g of 5‐ASA enema plus placebo tablets for 8 weeks. The primary endpoint was clinical remission (clinical activity index ≤4) at 8 weeks. Secondary endpoints were endoscopic and histologic remissions.
Results: Seventy‐nine patients were enrolled. Clinical remission rates at 4 and 8 weeks were 57.5% and 60.0% for patients treated with MMx and 68.4% and 50.0% for patients randomized to 5‐ASA enemas, respectively (95% confidence interval for the difference at 8 weeks, −12 to +32). Endoscopic remission was achieved by 45.0% of patients on 5‐ASA MMx and by 36.8% of those on enema, whereas 15.0% and 8% of patients, respectively, showed histologic remission. Compliance was 97.0% for oral and 87.5% for topical therapy. In the enema group, compliance was 88.0% for the patients in remission and 65.5% for those with active disease.
Conclusions: Preliminary studies suggest that similar rates for induction of remission can be expected from 5‐ASA enemas and MMx for patients with left‐sided ulcerative colitis. |
doi_str_mv | 10.1097/01.MIB.0000158386.25660.1e |
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Methods: Patients received either 1.2 g of 5‐ASA MMx three times per day plus placebo enema or 4 g of 5‐ASA enema plus placebo tablets for 8 weeks. The primary endpoint was clinical remission (clinical activity index ≤4) at 8 weeks. Secondary endpoints were endoscopic and histologic remissions.
Results: Seventy‐nine patients were enrolled. Clinical remission rates at 4 and 8 weeks were 57.5% and 60.0% for patients treated with MMx and 68.4% and 50.0% for patients randomized to 5‐ASA enemas, respectively (95% confidence interval for the difference at 8 weeks, −12 to +32). Endoscopic remission was achieved by 45.0% of patients on 5‐ASA MMx and by 36.8% of those on enema, whereas 15.0% and 8% of patients, respectively, showed histologic remission. Compliance was 97.0% for oral and 87.5% for topical therapy. In the enema group, compliance was 88.0% for the patients in remission and 65.5% for those with active disease.
Conclusions: Preliminary studies suggest that similar rates for induction of remission can be expected from 5‐ASA enemas and MMx for patients with left‐sided ulcerative colitis.</description><identifier>ISSN: 1078-0998</identifier><identifier>EISSN: 1536-4844</identifier><identifier>DOI: 10.1097/01.MIB.0000158386.25660.1e</identifier><identifier>PMID: 15867580</identifier><language>eng</language><publisher>Philadelphia: Lippincott Williams & Wilkins, Inc</publisher><subject>5‐aminosalicyclic acid ; 5‐aminosalicyclic acid multi‐matrix ; Administration, Oral ; Adult ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Colitis, Ulcerative - drug therapy ; Colitis, Ulcerative - pathology ; Colon ; Colonoscopy ; Double-Blind Method ; Drug Carriers ; Enema ; Female ; Humans ; Inflammatory bowel diseases ; left‐sided ulcerative colitis ; Male ; mesalamine ; Mesalamine - administration & dosage ; Middle Aged ; Patient Compliance ; Remission ; Tablets ; Treatment Outcome ; Ulcerative colitis</subject><ispartof>Inflammatory bowel diseases, 2005-05, Vol.11 (5), p.421-427</ispartof><rights>Copyright © 2005 Crohn's & Colitis Foundation of America, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4111-c4437d311c0858a9c0d33d6e2364d2b38902a9e0e11e44267be7ca1519e027933</citedby><cites>FETCH-LOGICAL-c4111-c4437d311c0858a9c0d33d6e2364d2b38902a9e0e11e44267be7ca1519e027933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2F01.MIB.0000158386.25660.1e$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2F01.MIB.0000158386.25660.1e$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15867580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Prantera, Cosimo</creatorcontrib><creatorcontrib>Viscido, Angelo</creatorcontrib><creatorcontrib>Biancone, Livia</creatorcontrib><creatorcontrib>Francavilla, Antonio</creatorcontrib><creatorcontrib>Giglio, Lucio</creatorcontrib><creatorcontrib>Campieri, Massimo</creatorcontrib><title>A new oral delivery system for 5‐ASA: Preliminary clinical findings for MMx</title><title>Inflammatory bowel diseases</title><addtitle>Inflamm Bowel Dis</addtitle><description>Background: Multi‐matrix (MMx), a new delivery system for mesalazine, seems to release 5‐aminosalicyclic acid (5‐ASA) preferentially in the sigmoid colon. This study had 2 objectives: (1) to evaluate the therapeutic response to MMx in patients with active left‐sided disease and (2) to gain additional insights as to how the therapy would compare with topical 5‐ASA.
Methods: Patients received either 1.2 g of 5‐ASA MMx three times per day plus placebo enema or 4 g of 5‐ASA enema plus placebo tablets for 8 weeks. The primary endpoint was clinical remission (clinical activity index ≤4) at 8 weeks. Secondary endpoints were endoscopic and histologic remissions.
Results: Seventy‐nine patients were enrolled. Clinical remission rates at 4 and 8 weeks were 57.5% and 60.0% for patients treated with MMx and 68.4% and 50.0% for patients randomized to 5‐ASA enemas, respectively (95% confidence interval for the difference at 8 weeks, −12 to +32). Endoscopic remission was achieved by 45.0% of patients on 5‐ASA MMx and by 36.8% of those on enema, whereas 15.0% and 8% of patients, respectively, showed histologic remission. Compliance was 97.0% for oral and 87.5% for topical therapy. In the enema group, compliance was 88.0% for the patients in remission and 65.5% for those with active disease.
Conclusions: Preliminary studies suggest that similar rates for induction of remission can be expected from 5‐ASA enemas and MMx for patients with left‐sided ulcerative colitis.</description><subject>5‐aminosalicyclic acid</subject><subject>5‐aminosalicyclic acid multi‐matrix</subject><subject>Administration, Oral</subject><subject>Adult</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Colitis, Ulcerative - drug therapy</subject><subject>Colitis, Ulcerative - pathology</subject><subject>Colon</subject><subject>Colonoscopy</subject><subject>Double-Blind Method</subject><subject>Drug Carriers</subject><subject>Enema</subject><subject>Female</subject><subject>Humans</subject><subject>Inflammatory bowel diseases</subject><subject>left‐sided ulcerative colitis</subject><subject>Male</subject><subject>mesalamine</subject><subject>Mesalamine - administration & dosage</subject><subject>Middle Aged</subject><subject>Patient Compliance</subject><subject>Remission</subject><subject>Tablets</subject><subject>Treatment Outcome</subject><subject>Ulcerative colitis</subject><issn>1078-0998</issn><issn>1536-4844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkE1OwzAQhS0EglK4AopYwKplJk5sh135r0QEErC20mSCjPIDcQt0xxE4IydhaCuxQ8KWPJbf98b2E2IfYYiQ6CPAYTo-GQIPjI00ahjGSrFIa6KHsVSDyETROu9BmwEkidkS294_AYQ8k02xxTalYwM9kY6Cht6CtsuqoKDKvVI3D_zcT6kOyrYL4q-Pz9Hd6Di47VitXZOxnleucTk7StcUrnn0CzRN33fERplVnnZXtS8eLs7vT68G1zeX49PR9SCPEJHXSOpCIuZgYpMlORRSFopCqaIinEiTQJglBIRIURQqPSGdZxgjn4U6kbIvDpd9n7v2ZUZ-amvnc6qqrKF25i37pVSgNJMHf5JKa8O5GAaPl2Detd53VNrnztX8W4tgf2K3gJZjt7-x20XsFonNe6tbZpOail_rKmcGzpfAm6to_o_WdnxyJvmJiBADym-w1JBZ</recordid><startdate>200505</startdate><enddate>200505</enddate><creator>Prantera, Cosimo</creator><creator>Viscido, Angelo</creator><creator>Biancone, Livia</creator><creator>Francavilla, Antonio</creator><creator>Giglio, Lucio</creator><creator>Campieri, Massimo</creator><general>Lippincott Williams & Wilkins, Inc</general><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>7T5</scope><scope>H94</scope></search><sort><creationdate>200505</creationdate><title>A new oral delivery system for 5‐ASA: Preliminary clinical findings for MMx</title><author>Prantera, Cosimo ; Viscido, Angelo ; Biancone, Livia ; Francavilla, Antonio ; Giglio, Lucio ; Campieri, Massimo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4111-c4437d311c0858a9c0d33d6e2364d2b38902a9e0e11e44267be7ca1519e027933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>5‐aminosalicyclic acid</topic><topic>5‐aminosalicyclic acid multi‐matrix</topic><topic>Administration, Oral</topic><topic>Adult</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Colitis, Ulcerative - drug therapy</topic><topic>Colitis, Ulcerative - pathology</topic><topic>Colon</topic><topic>Colonoscopy</topic><topic>Double-Blind Method</topic><topic>Drug Carriers</topic><topic>Enema</topic><topic>Female</topic><topic>Humans</topic><topic>Inflammatory bowel diseases</topic><topic>left‐sided ulcerative colitis</topic><topic>Male</topic><topic>mesalamine</topic><topic>Mesalamine - administration & dosage</topic><topic>Middle Aged</topic><topic>Patient Compliance</topic><topic>Remission</topic><topic>Tablets</topic><topic>Treatment Outcome</topic><topic>Ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prantera, Cosimo</creatorcontrib><creatorcontrib>Viscido, Angelo</creatorcontrib><creatorcontrib>Biancone, Livia</creatorcontrib><creatorcontrib>Francavilla, Antonio</creatorcontrib><creatorcontrib>Giglio, Lucio</creatorcontrib><creatorcontrib>Campieri, Massimo</creatorcontrib><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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Inflammatory bowel diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prantera, Cosimo</au><au>Viscido, Angelo</au><au>Biancone, Livia</au><au>Francavilla, Antonio</au><au>Giglio, Lucio</au><au>Campieri, Massimo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new oral delivery system for 5‐ASA: Preliminary clinical findings for MMx</atitle><jtitle>Inflammatory bowel diseases</jtitle><addtitle>Inflamm Bowel Dis</addtitle><date>2005-05</date><risdate>2005</risdate><volume>11</volume><issue>5</issue><spage>421</spage><epage>427</epage><pages>421-427</pages><issn>1078-0998</issn><eissn>1536-4844</eissn><abstract>Background: Multi‐matrix (MMx), a new delivery system for mesalazine, seems to release 5‐aminosalicyclic acid (5‐ASA) preferentially in the sigmoid colon. This study had 2 objectives: (1) to evaluate the therapeutic response to MMx in patients with active left‐sided disease and (2) to gain additional insights as to how the therapy would compare with topical 5‐ASA.
Methods: Patients received either 1.2 g of 5‐ASA MMx three times per day plus placebo enema or 4 g of 5‐ASA enema plus placebo tablets for 8 weeks. The primary endpoint was clinical remission (clinical activity index ≤4) at 8 weeks. Secondary endpoints were endoscopic and histologic remissions.
Results: Seventy‐nine patients were enrolled. Clinical remission rates at 4 and 8 weeks were 57.5% and 60.0% for patients treated with MMx and 68.4% and 50.0% for patients randomized to 5‐ASA enemas, respectively (95% confidence interval for the difference at 8 weeks, −12 to +32). Endoscopic remission was achieved by 45.0% of patients on 5‐ASA MMx and by 36.8% of those on enema, whereas 15.0% and 8% of patients, respectively, showed histologic remission. Compliance was 97.0% for oral and 87.5% for topical therapy. In the enema group, compliance was 88.0% for the patients in remission and 65.5% for those with active disease.
Conclusions: Preliminary studies suggest that similar rates for induction of remission can be expected from 5‐ASA enemas and MMx for patients with left‐sided ulcerative colitis.</abstract><cop>Philadelphia</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>15867580</pmid><doi>10.1097/01.MIB.0000158386.25660.1e</doi><tpages>7</tpages></addata></record> |
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subjects | 5‐aminosalicyclic acid 5‐aminosalicyclic acid multi‐matrix Administration, Oral Adult Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Colitis, Ulcerative - drug therapy Colitis, Ulcerative - pathology Colon Colonoscopy Double-Blind Method Drug Carriers Enema Female Humans Inflammatory bowel diseases left‐sided ulcerative colitis Male mesalamine Mesalamine - administration & dosage Middle Aged Patient Compliance Remission Tablets Treatment Outcome Ulcerative colitis |
title | A new oral delivery system for 5‐ASA: Preliminary clinical findings for MMx |
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