Neovastat—a novel antiangiogenic drug for cancer therapy
Neovastat (Æ-941) is an antiangiogenic drug isolated from marine cartilage. It interferes with several steps associated with the development of angiogenesis through its ability to induce endothelial cell apoptosis, and to inhibit matrix metalloproteinase activities and vascular endothelial growth fa...
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Veröffentlicht in: | Anti-cancer drugs 2003-02, Vol.14 (2), p.91-96 |
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creator | Gingras, Denis Boivin, Dominique Deckers, Christophe Gendron, Sébastien Barthomeuf, Chantal Béliveau, Richard |
description | Neovastat (Æ-941) is an antiangiogenic drug isolated from marine cartilage. It interferes with several steps associated with the development of angiogenesis through its ability to induce endothelial cell apoptosis, and to inhibit matrix metalloproteinase activities and vascular endothelial growth factor-mediated signaling pathways, suggesting that Neovastat behaves as a multifunctional antiangiogenic drug. Neovastat is orally bioavailable, and shows significant antitumor and antimetastatic properties in animal models. An excellent safety profile with few side effects has been monitored in more than 800 patients who have been exposed to Neovastat, some of whom for more than 4 years. This indicates that Neovastat is suitable for long-term use, either alone or in combination with other anticancer therapies. Accordingly, Neovastat is currently under evaluation in three pivotal clinical studies with two phase III clinical trials in patients with lung and renal carcinoma, and a phase II clinical trial in patients with multiple myeloma is ongoing. |
doi_str_mv | 10.1097/00001813-200302000-00001 |
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It interferes with several steps associated with the development of angiogenesis through its ability to induce endothelial cell apoptosis, and to inhibit matrix metalloproteinase activities and vascular endothelial growth factor-mediated signaling pathways, suggesting that Neovastat behaves as a multifunctional antiangiogenic drug. Neovastat is orally bioavailable, and shows significant antitumor and antimetastatic properties in animal models. An excellent safety profile with few side effects has been monitored in more than 800 patients who have been exposed to Neovastat, some of whom for more than 4 years. This indicates that Neovastat is suitable for long-term use, either alone or in combination with other anticancer therapies. Accordingly, Neovastat is currently under evaluation in three pivotal clinical studies with two phase III clinical trials in patients with lung and renal carcinoma, and a phase II clinical trial in patients with multiple myeloma is ongoing.</description><identifier>ISSN: 0959-4973</identifier><identifier>EISSN: 1473-5741</identifier><identifier>DOI: 10.1097/00001813-200302000-00001</identifier><identifier>PMID: 12569294</identifier><language>eng</language><publisher>England: Lippincott Williams & Wilkins, Inc</publisher><subject>Angiogenesis Inhibitors - therapeutic use ; Animals ; Cartilage ; Clinical Trials as Topic ; Humans ; Neoplasms - blood supply ; Neoplasms - drug therapy ; Neovascularization, Pathologic - drug therapy ; Tissue Extracts - therapeutic use</subject><ispartof>Anti-cancer drugs, 2003-02, Vol.14 (2), p.91-96</ispartof><rights>2003 Lippincott Williams & Wilkins, Inc.</rights><rights>Copyright 2003 Lippincott Williams & Wilkins</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3021-55b0047af9d9c44010a4a1d6c07db0ca66cb700c06451c462bf5c449acce624f3</citedby><cites>FETCH-LOGICAL-c3021-55b0047af9d9c44010a4a1d6c07db0ca66cb700c06451c462bf5c449acce624f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12569294$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gingras, Denis</creatorcontrib><creatorcontrib>Boivin, Dominique</creatorcontrib><creatorcontrib>Deckers, Christophe</creatorcontrib><creatorcontrib>Gendron, Sébastien</creatorcontrib><creatorcontrib>Barthomeuf, Chantal</creatorcontrib><creatorcontrib>Béliveau, Richard</creatorcontrib><title>Neovastat—a novel antiangiogenic drug for cancer therapy</title><title>Anti-cancer drugs</title><addtitle>Anticancer Drugs</addtitle><description>Neovastat (Æ-941) is an antiangiogenic drug isolated from marine cartilage. It interferes with several steps associated with the development of angiogenesis through its ability to induce endothelial cell apoptosis, and to inhibit matrix metalloproteinase activities and vascular endothelial growth factor-mediated signaling pathways, suggesting that Neovastat behaves as a multifunctional antiangiogenic drug. Neovastat is orally bioavailable, and shows significant antitumor and antimetastatic properties in animal models. An excellent safety profile with few side effects has been monitored in more than 800 patients who have been exposed to Neovastat, some of whom for more than 4 years. This indicates that Neovastat is suitable for long-term use, either alone or in combination with other anticancer therapies. Accordingly, Neovastat is currently under evaluation in three pivotal clinical studies with two phase III clinical trials in patients with lung and renal carcinoma, and a phase II clinical trial in patients with multiple myeloma is ongoing.</description><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>Animals</subject><subject>Cartilage</subject><subject>Clinical Trials as Topic</subject><subject>Humans</subject><subject>Neoplasms - blood supply</subject><subject>Neoplasms - drug therapy</subject><subject>Neovascularization, Pathologic - drug therapy</subject><subject>Tissue Extracts - therapeutic use</subject><issn>0959-4973</issn><issn>1473-5741</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtOwzAQhi0EoqVwBZQVu8A4ceyaHap4SRVsYG1NHKcNpHGxk1bdcQhOyEkwpMAKMYsZ6dc3D_1DSEThlIIUZxCCjmkaJwAphATxl7RDhpSJNM4Eo7tkCDKTMZMiHZAD758CEfR0nwxoknGZSDYk53fGrtC32L6_vmHU2JWpI2zaCptZZWemqXRUuG4WldZFGhttXNTOjcPl5pDslVh7c7StI_J4dfkwuYmn99e3k4tprMNpNM6yHIAJLGUhNWNAARnSgmsQRQ4aOde5ANDAWUY140leZoGTqLXhCSvTETnp5y6dfemMb9Wi8trUNTbGdl6JRMoxZ_JfkI6FYIInARz3oHbWe2dKtXTVAt1GUVCfBqtvg9WPwb0UWo-3O7p8YYrfxq2jAWA9sLZ1a5x_rru1cWpusG7n6q_HpR-fJoVg</recordid><startdate>200302</startdate><enddate>200302</enddate><creator>Gingras, Denis</creator><creator>Boivin, Dominique</creator><creator>Deckers, Christophe</creator><creator>Gendron, Sébastien</creator><creator>Barthomeuf, Chantal</creator><creator>Béliveau, Richard</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200302</creationdate><title>Neovastat—a novel antiangiogenic drug for cancer therapy</title><author>Gingras, Denis ; Boivin, Dominique ; Deckers, Christophe ; Gendron, Sébastien ; Barthomeuf, Chantal ; Béliveau, Richard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3021-55b0047af9d9c44010a4a1d6c07db0ca66cb700c06451c462bf5c449acce624f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Angiogenesis Inhibitors - therapeutic use</topic><topic>Animals</topic><topic>Cartilage</topic><topic>Clinical Trials as Topic</topic><topic>Humans</topic><topic>Neoplasms - blood supply</topic><topic>Neoplasms - drug therapy</topic><topic>Neovascularization, Pathologic - drug therapy</topic><topic>Tissue Extracts - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gingras, Denis</creatorcontrib><creatorcontrib>Boivin, Dominique</creatorcontrib><creatorcontrib>Deckers, Christophe</creatorcontrib><creatorcontrib>Gendron, Sébastien</creatorcontrib><creatorcontrib>Barthomeuf, Chantal</creatorcontrib><creatorcontrib>Béliveau, Richard</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Anti-cancer drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gingras, Denis</au><au>Boivin, Dominique</au><au>Deckers, Christophe</au><au>Gendron, Sébastien</au><au>Barthomeuf, Chantal</au><au>Béliveau, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neovastat—a novel antiangiogenic drug for cancer therapy</atitle><jtitle>Anti-cancer drugs</jtitle><addtitle>Anticancer Drugs</addtitle><date>2003-02</date><risdate>2003</risdate><volume>14</volume><issue>2</issue><spage>91</spage><epage>96</epage><pages>91-96</pages><issn>0959-4973</issn><eissn>1473-5741</eissn><abstract>Neovastat (Æ-941) is an antiangiogenic drug isolated from marine cartilage. It interferes with several steps associated with the development of angiogenesis through its ability to induce endothelial cell apoptosis, and to inhibit matrix metalloproteinase activities and vascular endothelial growth factor-mediated signaling pathways, suggesting that Neovastat behaves as a multifunctional antiangiogenic drug. Neovastat is orally bioavailable, and shows significant antitumor and antimetastatic properties in animal models. An excellent safety profile with few side effects has been monitored in more than 800 patients who have been exposed to Neovastat, some of whom for more than 4 years. This indicates that Neovastat is suitable for long-term use, either alone or in combination with other anticancer therapies. Accordingly, Neovastat is currently under evaluation in three pivotal clinical studies with two phase III clinical trials in patients with lung and renal carcinoma, and a phase II clinical trial in patients with multiple myeloma is ongoing.</abstract><cop>England</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>12569294</pmid><doi>10.1097/00001813-200302000-00001</doi><tpages>6</tpages></addata></record> |
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subjects | Angiogenesis Inhibitors - therapeutic use Animals Cartilage Clinical Trials as Topic Humans Neoplasms - blood supply Neoplasms - drug therapy Neovascularization, Pathologic - drug therapy Tissue Extracts - therapeutic use |
title | Neovastat—a novel antiangiogenic drug for cancer therapy |
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