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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Thrombosis and haemostasis 2009-11, Vol.102 (5), p.900-906
Hauptverfasser: Kishimoto, Takashi Kei, Qi, Yi Wei, Long, Alison, Capila, Ishan, Sasisekharan, Ram, Guerrero, Luis, Fier, Ian, Roach, James, Venkataraman, Ganesh
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 906
container_issue 5
container_start_page 900
container_title Thrombosis and haemostasis
container_volume 102
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
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1160_TH09_02_0105</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19888526</sourcerecordid><originalsourceid>FETCH-LOGICAL-c621t-76931dc44edc77a1b07eaaa1c5a7c3cf04f91d24afa7205d6ae6921a78fd1e723</originalsourceid><addsrcrecordid>eNq9kMFu1DAURS0EokNhxxp5DwHbSZxkWVWFIhWxKRI76439MvYosUe2w2h28A38IV-Cp1PBClaIlfXk8-61DyHPOXvNuWRvbq_ZUDFRMc7aB2QlWtlVsh8-PyQrVjeskqJpz8iTlLaMcdkM7WNyxoe-71shV-TbB857-uPrd3pBI2QXPEzTgaLfOI8Y0dAp7Ks5TKiXCWK1R7exmVrcQXSeGkxu4wuVdqjd6PTd9hgizRZpjgh5Rp9pGCnoJSPVIZaKeKDp4E0MM6an5NEIU8Jn9-c5-fT26vbyurr5-O795cVNpaXguerkUHOjmwaN7jrga9YhAHDdQqdrPbJmHLgRDYzQCdYaCSgHwaHrR8OxE_U5eXXK1TGkFHFUu-jm8hTFmTqaVEeTigl1NFnwFyd8t6xnNL_he3UFeHkCsnU4o9qGJRZ56U9x_kQnbSFnWDD-isy2iFiH5JICb5QFnEPKcJx18Ln4KxdRW_cFlUtpQXVnGyY1g1-Sjm6XFReiFyrZsFc2z1Mp3P7DwmHgfy8z_-F39U_eJP2s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>M118 – A rationally engineered low-molecular-weight heparin designed specifically for the treatment of acute coronary syndromes</title><source>MEDLINE</source><source>Thieme Connect Journals</source><creator>Kishimoto, Takashi Kei ; Qi, Yi Wei ; Long, Alison ; Capila, Ishan ; Sasisekharan, Ram ; Guerrero, Luis ; Fier, Ian ; Roach, James ; Venkataraman, Ganesh</creator><creatorcontrib>Kishimoto, Takashi Kei ; Qi, Yi Wei ; Long, Alison ; Capila, Ishan ; Sasisekharan, Ram ; Guerrero, Luis ; Fier, Ian ; Roach, James ; Venkataraman, Ganesh</creatorcontrib><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><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 &amp; dosage ; Anticoagulants - chemistry ; Anticoagulants - isolation &amp; 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 &amp; dosage ; Heparin, Low-Molecular-Weight - chemistry ; Heparin, Low-Molecular-Weight - isolation &amp; 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 &amp; 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 &amp; dosage</subject><subject>Anticoagulants - chemistry</subject><subject>Anticoagulants - isolation &amp; 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 &amp; dosage</subject><subject>Heparin, Low-Molecular-Weight - chemistry</subject><subject>Heparin, Low-Molecular-Weight - isolation &amp; 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 &amp; 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 &amp; dosage</topic><topic>Anticoagulants - chemistry</topic><topic>Anticoagulants - isolation &amp; 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 &amp; dosage</topic><topic>Heparin, Low-Molecular-Weight - chemistry</topic><topic>Heparin, Low-Molecular-Weight - isolation &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0340-6245
ispartof Thrombosis and haemostasis, 2009-11, Vol.102 (5), p.900-906
issn 0340-6245
2567-689X
language eng
recordid cdi_crossref_primary_10_1160_TH09_02_0105
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T09%3A41%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=M118%20%E2%80%93%20A%20rationally%20engineered%20low-molecular-weight%20heparin%20designed%20specifically%20for%20the%20treatment%20of%20acute%20coronary%20syndromes&rft.jtitle=Thrombosis%20and%20haemostasis&rft.au=Kishimoto,%20Takashi%20Kei&rft.date=2009-11-01&rft.volume=102&rft.issue=5&rft.spage=900&rft.epage=906&rft.pages=900-906&rft.issn=0340-6245&rft.eissn=2567-689X&rft_id=info:doi/10.1160/TH09-02-0105&rft_dat=%3Cpubmed_cross%3E19888526%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/19888526&rfr_iscdi=true