Oral treatment for multiple sclerosis
Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs...
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Veröffentlicht in: | Lancet neurology 2011-11, Vol.10 (11), p.1026-1034 |
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description | Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs. |
doi_str_mv | 10.1016/S1474-4422(11)70228-9 |
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Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.</description><identifier>ISSN: 1474-4422</identifier><identifier>EISSN: 1474-4465</identifier><identifier>DOI: 10.1016/S1474-4422(11)70228-9</identifier><identifier>PMID: 22014437</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject><![CDATA[Administration, Oral ; Attention ; cladribine ; Cladribine - administration & dosage ; Cladribine - therapeutic use ; Clinical trials ; Clinical Trials as Topic ; Crotonates - administration & dosage ; Crotonates - therapeutic use ; Cytokines ; Data processing ; Dimethyl Fumarate ; Drug dosages ; Drugs ; FDA approval ; Fingolimod Hydrochloride ; Fumarates - administration & dosage ; Fumarates - therapeutic use ; Humans ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - therapeutic use ; Interferon ; Lymphocytes ; Multiple sclerosis ; Multiple Sclerosis, Relapsing-Remitting - drug therapy ; Neurology ; Neuroprotection ; Propylene Glycols - administration & dosage ; Propylene Glycols - therapeutic use ; Quinolones - administration & dosage ; Quinolones - therapeutic use ; Sphingosine - administration & dosage ; Sphingosine - analogs & derivatives ; Sphingosine - therapeutic use ; Toluidines - administration & dosage ; Toluidines - therapeutic use]]></subject><ispartof>Lancet neurology, 2011-11, Vol.10 (11), p.1026-1034</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Nov 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-bc08ac6686ca35d40e111b40bf59148c92621452cf60675ae2d0ba6cfc34acc93</citedby><cites>FETCH-LOGICAL-c478t-bc08ac6686ca35d40e111b40bf59148c92621452cf60675ae2d0ba6cfc34acc93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/900472684?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974,64362,64364,64366,72216</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22014437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Killestein, Joep, Dr</creatorcontrib><creatorcontrib>Rudick, Richard A, Prof</creatorcontrib><creatorcontrib>Polman, Chris H, Prof</creatorcontrib><title>Oral treatment for multiple sclerosis</title><title>Lancet neurology</title><addtitle>Lancet Neurol</addtitle><description>Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.</description><subject>Administration, Oral</subject><subject>Attention</subject><subject>cladribine</subject><subject>Cladribine - administration & dosage</subject><subject>Cladribine - therapeutic use</subject><subject>Clinical trials</subject><subject>Clinical Trials as Topic</subject><subject>Crotonates - administration & dosage</subject><subject>Crotonates - therapeutic use</subject><subject>Cytokines</subject><subject>Data processing</subject><subject>Dimethyl Fumarate</subject><subject>Drug dosages</subject><subject>Drugs</subject><subject>FDA approval</subject><subject>Fingolimod Hydrochloride</subject><subject>Fumarates - administration & dosage</subject><subject>Fumarates - therapeutic use</subject><subject>Humans</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Interferon</subject><subject>Lymphocytes</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis, Relapsing-Remitting - drug therapy</subject><subject>Neurology</subject><subject>Neuroprotection</subject><subject>Propylene Glycols - administration & dosage</subject><subject>Propylene Glycols - therapeutic use</subject><subject>Quinolones - administration & dosage</subject><subject>Quinolones - therapeutic use</subject><subject>Sphingosine - administration & dosage</subject><subject>Sphingosine - analogs & derivatives</subject><subject>Sphingosine - therapeutic use</subject><subject>Toluidines - administration & dosage</subject><subject>Toluidines - therapeutic use</subject><issn>1474-4422</issn><issn>1474-4465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkE1P3DAQhq2qqHz1J7RaVUKUQ2DGcZzkAkKrUpCQOEDPljOZSKZOsrUTJP49ye52D1zaky3r8TvzPkJ8QThHQH3xiCpXiVJSfkc8y0HKIik_iIPts84-7u5S7ovDGJ8BJKoCP4l9KQGVSvMDcfIQrF8Mge3Qcjcsmj4s2tEPbuV5Eclz6KOLx2KvsT7y5-15JH7d_Hha3ib3Dz_vltf3Cam8GJKKoLCkdaHJplmtgBGxUlA1WTlNplLqaYNMUqNB55llWUNlNTWUKktUpkfidJO7Cv2fkeNgWheJvbcd92M0JShVFjIt_oMEnUKqYCK_vSOf-zF0U40ZUrnUhZqgbAPR1DcGbswquNaGV4NgZt9m7dvMMg2iWfs288Jft-Fj1XK9-_VX8ARcbQCetL04DiaS4464doFpMHXv_jni8l0Cedc5sv43v3LclUETpYFNyJyBuE4o0zeq_KGP</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Killestein, Joep, Dr</creator><creator>Rudick, Richard A, Prof</creator><creator>Polman, Chris H, Prof</creator><general>Elsevier Ltd</general><general>Elsevier Limited</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>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20111101</creationdate><title>Oral treatment for multiple sclerosis</title><author>Killestein, Joep, Dr ; 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Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22014437</pmid><doi>10.1016/S1474-4422(11)70228-9</doi><tpages>9</tpages></addata></record> |
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subjects | Administration, Oral Attention cladribine Cladribine - administration & dosage Cladribine - therapeutic use Clinical trials Clinical Trials as Topic Crotonates - administration & dosage Crotonates - therapeutic use Cytokines Data processing Dimethyl Fumarate Drug dosages Drugs FDA approval Fingolimod Hydrochloride Fumarates - administration & dosage Fumarates - therapeutic use Humans Immunosuppressive Agents - administration & dosage Immunosuppressive Agents - therapeutic use Interferon Lymphocytes Multiple sclerosis Multiple Sclerosis, Relapsing-Remitting - drug therapy Neurology Neuroprotection Propylene Glycols - administration & dosage Propylene Glycols - therapeutic use Quinolones - administration & dosage Quinolones - therapeutic use Sphingosine - administration & dosage Sphingosine - analogs & derivatives Sphingosine - therapeutic use Toluidines - administration & dosage Toluidines - therapeutic use |
title | Oral treatment for multiple sclerosis |
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