M118 – A rationally engineered low-molecular-weight heparin designed specifically for the treatment of acute coronary syndromes
The initial choice of anticoagulant therapy administered in emergency departments for acute coronary syndromes (ACS) has important consequences for subsequent patient care, as neither unfractionated heparin (UFH) nor low-molecularweight heparin (LMWH) are ideally suited for all potential clinical tr...
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Veröffentlicht in: | Thrombosis and haemostasis 2009-11, Vol.102 (5), p.900-906 |
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creator | Kishimoto, Takashi Kei Qi, Yi Wei Long, Alison Capila, Ishan Sasisekharan, Ram Guerrero, Luis Fier, Ian Roach, James Venkataraman, Ganesh |
description | The initial choice of anticoagulant therapy administered in emergency departments for acute coronary syndromes (ACS) has important consequences for subsequent patient care, as neither unfractionated heparin (UFH) nor low-molecularweight heparin (LMWH) are ideally suited for all potential clinical treatment pathways. UFH remains widely used for surgical interventions because of the ability to rapidly reverse its anticoagulant activity. However, the unpredictable pharmacokinetic profile of UFH presents safety issues, and the low subcutaneous bioavailability limits the utility of UFH for patients who are medically managed. LMWH has superior pharmacokinetic properties, but its anticoagulant activity cannot be effectively monitored or reversed during surgery. There is an unmet medical need for a baseline anticoagulant therapy that addresses these shortcomings while retaining the beneficial properties of both UFH and LMWH. We describe here M118, a novel LMWH designed specifically for use in the treatment of ACS. M118 shows broad anticoagulant activity, including potent activity against both factor Xa (~240 IU/mg) and thrombin (factor IIa; ~170 IU/ mg), low polydispersity, high (78%) subcutaneous bioavailability in rabbits, and predictable subcutaneous and intravenous pharmacokinetics. Additionally, the anticoagulant activity of M118 is monitorable by standard coagulation assays and is reversible with protamine. M118 demonstrates superior activity to conventional LMWH in a rabbit model of abdominal arterial thrombosis without increasing bleeding risk, and is currently being evaluated in a phase II clinical trial evaluating efficacy and safety in patients undergoing percutaneous coronary intervention. |
doi_str_mv | 10.1160/TH09-02-0105 |
format | Article |
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UFH remains widely used for surgical interventions because of the ability to rapidly reverse its anticoagulant activity. However, the unpredictable pharmacokinetic profile of UFH presents safety issues, and the low subcutaneous bioavailability limits the utility of UFH for patients who are medically managed. LMWH has superior pharmacokinetic properties, but its anticoagulant activity cannot be effectively monitored or reversed during surgery. There is an unmet medical need for a baseline anticoagulant therapy that addresses these shortcomings while retaining the beneficial properties of both UFH and LMWH. We describe here M118, a novel LMWH designed specifically for use in the treatment of ACS. M118 shows broad anticoagulant activity, including potent activity against both factor Xa (~240 IU/mg) and thrombin (factor IIa; ~170 IU/ mg), low polydispersity, high (78%) subcutaneous bioavailability in rabbits, and predictable subcutaneous and intravenous pharmacokinetics. Additionally, the anticoagulant activity of M118 is monitorable by standard coagulation assays and is reversible with protamine. M118 demonstrates superior activity to conventional LMWH in a rabbit model of abdominal arterial thrombosis without increasing bleeding risk, and is currently being evaluated in a phase II clinical trial evaluating efficacy and safety in patients undergoing percutaneous coronary intervention.</description><identifier>ISSN: 0340-6245</identifier><identifier>EISSN: 2567-689X</identifier><identifier>DOI: 10.1160/TH09-02-0105</identifier><identifier>PMID: 19888526</identifier><language>eng</language><publisher>Germany: Schattauer Verlag für Medizin und Naturwissenschaften</publisher><subject>Acute Coronary Syndrome - drug therapy ; Acute Myocardial Infarction ; Animals ; Anticoagulants - administration & dosage ; Anticoagulants - chemistry ; Anticoagulants - isolation & purification ; Anticoagulants - pharmacology ; Anticoagulants - therapeutic use ; Anticoagulants - toxicity ; Aorta, Abdominal ; Aortic Diseases - drug therapy ; Arterial Occlusive Diseases - drug therapy ; Arterial thrombosis ; Biological Availability ; coagulation inhibitors ; Disease Models, Animal ; Drug Design ; Drug Evaluation, Preclinical ; Factor Xa Inhibitors ; Hemorrhage - chemically induced ; Heparin, Low-Molecular-Weight - administration & dosage ; Heparin, Low-Molecular-Weight - chemistry ; Heparin, Low-Molecular-Weight - isolation & purification ; Heparin, Low-Molecular-Weight - therapeutic use ; Heparin, Low-Molecular-Weight - toxicity ; heparins ; Injections, Intravenous ; Injections, Subcutaneous ; Intestinal Mucosa - chemistry ; Male ; Rabbits ; Swine ; Theme Issue Article ; thrombin ; Thrombin - antagonists & inhibitors</subject><ispartof>Thrombosis and haemostasis, 2009-11, Vol.102 (5), p.900-906</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c621t-76931dc44edc77a1b07eaaa1c5a7c3cf04f91d24afa7205d6ae6921a78fd1e723</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.schattauer.de/typo3temp/pics/cover-991_102c0739cb.jpg</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH09-02-0105.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><link.rule.ids>314,780,784,3018,27924,27925,54559</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19888526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishimoto, Takashi Kei</creatorcontrib><creatorcontrib>Qi, Yi Wei</creatorcontrib><creatorcontrib>Long, Alison</creatorcontrib><creatorcontrib>Capila, Ishan</creatorcontrib><creatorcontrib>Sasisekharan, Ram</creatorcontrib><creatorcontrib>Guerrero, Luis</creatorcontrib><creatorcontrib>Fier, Ian</creatorcontrib><creatorcontrib>Roach, James</creatorcontrib><creatorcontrib>Venkataraman, Ganesh</creatorcontrib><title>M118 – A rationally engineered low-molecular-weight heparin designed specifically for the treatment of acute coronary syndromes</title><title>Thrombosis and haemostasis</title><addtitle>Thromb Haemost</addtitle><description>The initial choice of anticoagulant therapy administered in emergency departments for acute coronary syndromes (ACS) has important consequences for subsequent patient care, as neither unfractionated heparin (UFH) nor low-molecularweight heparin (LMWH) are ideally suited for all potential clinical treatment pathways. UFH remains widely used for surgical interventions because of the ability to rapidly reverse its anticoagulant activity. However, the unpredictable pharmacokinetic profile of UFH presents safety issues, and the low subcutaneous bioavailability limits the utility of UFH for patients who are medically managed. LMWH has superior pharmacokinetic properties, but its anticoagulant activity cannot be effectively monitored or reversed during surgery. There is an unmet medical need for a baseline anticoagulant therapy that addresses these shortcomings while retaining the beneficial properties of both UFH and LMWH. We describe here M118, a novel LMWH designed specifically for use in the treatment of ACS. M118 shows broad anticoagulant activity, including potent activity against both factor Xa (~240 IU/mg) and thrombin (factor IIa; ~170 IU/ mg), low polydispersity, high (78%) subcutaneous bioavailability in rabbits, and predictable subcutaneous and intravenous pharmacokinetics. Additionally, the anticoagulant activity of M118 is monitorable by standard coagulation assays and is reversible with protamine. M118 demonstrates superior activity to conventional LMWH in a rabbit model of abdominal arterial thrombosis without increasing bleeding risk, and is currently being evaluated in a phase II clinical trial evaluating efficacy and safety in patients undergoing percutaneous coronary intervention.</description><subject>Acute Coronary Syndrome - drug therapy</subject><subject>Acute Myocardial Infarction</subject><subject>Animals</subject><subject>Anticoagulants - administration & dosage</subject><subject>Anticoagulants - chemistry</subject><subject>Anticoagulants - isolation & purification</subject><subject>Anticoagulants - pharmacology</subject><subject>Anticoagulants - therapeutic use</subject><subject>Anticoagulants - toxicity</subject><subject>Aorta, Abdominal</subject><subject>Aortic Diseases - drug therapy</subject><subject>Arterial Occlusive Diseases - drug therapy</subject><subject>Arterial thrombosis</subject><subject>Biological Availability</subject><subject>coagulation inhibitors</subject><subject>Disease Models, Animal</subject><subject>Drug Design</subject><subject>Drug Evaluation, Preclinical</subject><subject>Factor Xa Inhibitors</subject><subject>Hemorrhage - chemically induced</subject><subject>Heparin, Low-Molecular-Weight - administration & dosage</subject><subject>Heparin, Low-Molecular-Weight - chemistry</subject><subject>Heparin, Low-Molecular-Weight - isolation & purification</subject><subject>Heparin, Low-Molecular-Weight - therapeutic use</subject><subject>Heparin, Low-Molecular-Weight - toxicity</subject><subject>heparins</subject><subject>Injections, Intravenous</subject><subject>Injections, Subcutaneous</subject><subject>Intestinal Mucosa - chemistry</subject><subject>Male</subject><subject>Rabbits</subject><subject>Swine</subject><subject>Theme Issue Article</subject><subject>thrombin</subject><subject>Thrombin - antagonists & inhibitors</subject><issn>0340-6245</issn><issn>2567-689X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNq9kMFu1DAURS0EokNhxxp5DwHbSZxkWVWFIhWxKRI76439MvYosUe2w2h28A38IV-Cp1PBClaIlfXk8-61DyHPOXvNuWRvbq_ZUDFRMc7aB2QlWtlVsh8-PyQrVjeskqJpz8iTlLaMcdkM7WNyxoe-71shV-TbB857-uPrd3pBI2QXPEzTgaLfOI8Y0dAp7Ks5TKiXCWK1R7exmVrcQXSeGkxu4wuVdqjd6PTd9hgizRZpjgh5Rp9pGCnoJSPVIZaKeKDp4E0MM6an5NEIU8Jn9-c5-fT26vbyurr5-O795cVNpaXguerkUHOjmwaN7jrga9YhAHDdQqdrPbJmHLgRDYzQCdYaCSgHwaHrR8OxE_U5eXXK1TGkFHFUu-jm8hTFmTqaVEeTigl1NFnwFyd8t6xnNL_he3UFeHkCsnU4o9qGJRZ56U9x_kQnbSFnWDD-isy2iFiH5JICb5QFnEPKcJx18Ln4KxdRW_cFlUtpQXVnGyY1g1-Sjm6XFReiFyrZsFc2z1Mp3P7DwmHgfy8z_-F39U_eJP2s</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Kishimoto, Takashi Kei</creator><creator>Qi, Yi Wei</creator><creator>Long, Alison</creator><creator>Capila, Ishan</creator><creator>Sasisekharan, Ram</creator><creator>Guerrero, Luis</creator><creator>Fier, Ian</creator><creator>Roach, James</creator><creator>Venkataraman, Ganesh</creator><general>Schattauer Verlag für Medizin und Naturwissenschaften</general><general>Schattauer GmbH</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></search><sort><creationdate>20091101</creationdate><title>M118 – A rationally engineered low-molecular-weight heparin designed specifically for the treatment of acute coronary syndromes</title><author>Kishimoto, Takashi Kei ; Qi, Yi Wei ; Long, Alison ; Capila, Ishan ; Sasisekharan, Ram ; Guerrero, Luis ; Fier, Ian ; Roach, James ; Venkataraman, Ganesh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c621t-76931dc44edc77a1b07eaaa1c5a7c3cf04f91d24afa7205d6ae6921a78fd1e723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acute Coronary Syndrome - drug therapy</topic><topic>Acute Myocardial Infarction</topic><topic>Animals</topic><topic>Anticoagulants - administration & dosage</topic><topic>Anticoagulants - chemistry</topic><topic>Anticoagulants - isolation & purification</topic><topic>Anticoagulants - pharmacology</topic><topic>Anticoagulants - therapeutic use</topic><topic>Anticoagulants - toxicity</topic><topic>Aorta, Abdominal</topic><topic>Aortic Diseases - drug therapy</topic><topic>Arterial Occlusive Diseases - drug therapy</topic><topic>Arterial thrombosis</topic><topic>Biological Availability</topic><topic>coagulation inhibitors</topic><topic>Disease Models, Animal</topic><topic>Drug Design</topic><topic>Drug Evaluation, Preclinical</topic><topic>Factor Xa Inhibitors</topic><topic>Hemorrhage - chemically induced</topic><topic>Heparin, Low-Molecular-Weight - administration & dosage</topic><topic>Heparin, Low-Molecular-Weight - chemistry</topic><topic>Heparin, Low-Molecular-Weight - isolation & purification</topic><topic>Heparin, Low-Molecular-Weight - therapeutic use</topic><topic>Heparin, Low-Molecular-Weight - toxicity</topic><topic>heparins</topic><topic>Injections, Intravenous</topic><topic>Injections, Subcutaneous</topic><topic>Intestinal Mucosa - chemistry</topic><topic>Male</topic><topic>Rabbits</topic><topic>Swine</topic><topic>Theme Issue Article</topic><topic>thrombin</topic><topic>Thrombin - antagonists & inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kishimoto, Takashi Kei</creatorcontrib><creatorcontrib>Qi, Yi Wei</creatorcontrib><creatorcontrib>Long, Alison</creatorcontrib><creatorcontrib>Capila, Ishan</creatorcontrib><creatorcontrib>Sasisekharan, Ram</creatorcontrib><creatorcontrib>Guerrero, Luis</creatorcontrib><creatorcontrib>Fier, Ian</creatorcontrib><creatorcontrib>Roach, James</creatorcontrib><creatorcontrib>Venkataraman, Ganesh</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kishimoto, Takashi Kei</au><au>Qi, Yi Wei</au><au>Long, Alison</au><au>Capila, Ishan</au><au>Sasisekharan, Ram</au><au>Guerrero, Luis</au><au>Fier, Ian</au><au>Roach, James</au><au>Venkataraman, Ganesh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>M118 – A rationally engineered low-molecular-weight heparin designed specifically for the treatment of acute coronary syndromes</atitle><jtitle>Thrombosis and haemostasis</jtitle><addtitle>Thromb Haemost</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>102</volume><issue>5</issue><spage>900</spage><epage>906</epage><pages>900-906</pages><issn>0340-6245</issn><eissn>2567-689X</eissn><abstract>The initial choice of anticoagulant therapy administered in emergency departments for acute coronary syndromes (ACS) has important consequences for subsequent patient care, as neither unfractionated heparin (UFH) nor low-molecularweight heparin (LMWH) are ideally suited for all potential clinical treatment pathways. UFH remains widely used for surgical interventions because of the ability to rapidly reverse its anticoagulant activity. However, the unpredictable pharmacokinetic profile of UFH presents safety issues, and the low subcutaneous bioavailability limits the utility of UFH for patients who are medically managed. LMWH has superior pharmacokinetic properties, but its anticoagulant activity cannot be effectively monitored or reversed during surgery. There is an unmet medical need for a baseline anticoagulant therapy that addresses these shortcomings while retaining the beneficial properties of both UFH and LMWH. We describe here M118, a novel LMWH designed specifically for use in the treatment of ACS. M118 shows broad anticoagulant activity, including potent activity against both factor Xa (~240 IU/mg) and thrombin (factor IIa; ~170 IU/ mg), low polydispersity, high (78%) subcutaneous bioavailability in rabbits, and predictable subcutaneous and intravenous pharmacokinetics. Additionally, the anticoagulant activity of M118 is monitorable by standard coagulation assays and is reversible with protamine. M118 demonstrates superior activity to conventional LMWH in a rabbit model of abdominal arterial thrombosis without increasing bleeding risk, and is currently being evaluated in a phase II clinical trial evaluating efficacy and safety in patients undergoing percutaneous coronary intervention.</abstract><cop>Germany</cop><pub>Schattauer Verlag für Medizin und Naturwissenschaften</pub><pmid>19888526</pmid><doi>10.1160/TH09-02-0105</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; Thieme Connect Journals |
subjects | Acute Coronary Syndrome - drug therapy Acute Myocardial Infarction Animals Anticoagulants - administration & dosage Anticoagulants - chemistry Anticoagulants - isolation & purification Anticoagulants - pharmacology Anticoagulants - therapeutic use Anticoagulants - toxicity Aorta, Abdominal Aortic Diseases - drug therapy Arterial Occlusive Diseases - drug therapy Arterial thrombosis Biological Availability coagulation inhibitors Disease Models, Animal Drug Design Drug Evaluation, Preclinical Factor Xa Inhibitors Hemorrhage - chemically induced Heparin, Low-Molecular-Weight - administration & dosage Heparin, Low-Molecular-Weight - chemistry Heparin, Low-Molecular-Weight - isolation & purification Heparin, Low-Molecular-Weight - therapeutic use Heparin, Low-Molecular-Weight - toxicity heparins Injections, Intravenous Injections, Subcutaneous Intestinal Mucosa - chemistry Male Rabbits Swine Theme Issue Article thrombin Thrombin - antagonists & inhibitors |
title | M118 – A rationally engineered low-molecular-weight heparin designed specifically for the treatment of acute coronary syndromes |
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