SCH-530348, a thrombin receptor (PAR-1) antagonist for the prevention and treatment of atherothrombosis

被引:0
|
作者
Oestreich, Julie [1 ]
机构
[1] Univ Kentucky, Dept Pharmaceut Sci, Lexington, KY 40536 USA
关键词
PERCUTANEOUS CORONARY INTERVENTION; PROTEASE-ACTIVATED RECEPTORS; HIMBACINE ANALOGS; P2Y(12) RECEPTOR; CLOPIDOGREL; POTENT; DISCOVERY; PRASUGREL; OUTCOMES; ASPIRIN;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
SCH-530348 is a novel antiplatelet agent undergoing development by Schering-Plough Corp for the treatment and prevention of atherothrombosis. The compound is an orally administered himbacine analog that potently antagonizes the platelet thrombin receptor protease-activated receptor 1 (PAR-1), which leaves the procoagulant function of thrombin intact. In preclinical studies, SCH-530348 demonstrated no effect on bleed time or coagulation parameters. In both cynomolgus monkeys and humans, the compound had high bioavailability and inhibited ex vivo TRAP (thrombin receptor-activating peptide)-stimulated platelet aggregation in a potent and long-lasting manner. In a phase II clinical trial of patients undergoing percutaneous coronary intervention, SCH-530348 added to standard therapy with aspirin and clopidogrel did not increase major or minor thrombolysis in myocardial infarction bleeding, and demonstrated a trend toward decreased major adverse cardiovascular events versus placebo. At the time of publication, three phase III trials were underway to assess the efficacy and safety of SCH-530348 for at least 1 year in up to 35,000 patients with acute coronary syndromes or atherosclerosis. The distinct mechanism of action of SCH-530348 allows for cardiovascular protection without the liability of increased bleeding associated with other antiplatelet therapies. Phase III trials in high-risk patients will determine the use of SCH-530348 in cardiological practice.
引用
收藏
页码:988 / 996
页数:9
相关论文
共 50 条
  • [41] Aptamer inhibits degradation of platelet proteolytically activatable receptor, PAR-1, by thrombin
    Boncler, MA
    Koziolkiewicz, M
    Watala, C
    THROMBOSIS RESEARCH, 2001, 104 (03) : 215 - 222
  • [42] Design and synthesis of thrombin receptor (PAR-1) antagonists award address.
    Greenlee, WJ
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 228 : U936 - U936
  • [43] Expression of the thrombin receptor (PAR-1,) during rat skeletal muscle differentiation
    Chevessier, F
    Hantaï, D
    Verdìere-Sahuqué, M
    JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 189 (02) : 152 - 161
  • [44] Design and synthesis of novel himbacine based thrombin receptor (Par-1) antagonists
    Chelliah, Mariappan V.
    Chackalamannil, Samuel
    Xia, Yan
    Eagen, Keith
    Tsai, Hsingan
    Clasby, Martin
    Gao, Xiaobang
    Greenlee, William J.
    Ahn, Ho-Sam
    Boykow, George
    Foster, Carolyn
    Hsieh, Yunsheng
    Agans-Fantuzzi, Jacqueline
    Bryant, Matthew
    Chintala, Madhu
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 231
  • [45] Vascular injury response in thrombin receptor (PAR-1) deficient mice.
    Cheung, WM
    D'Andrea, M
    Andrade-Gordon, P
    Leung, WP
    Damiano, BP
    FASEB JOURNAL, 1998, 12 (04): : A477 - A477
  • [46] Distribution and potential biologic function of the thrombin receptor PAR-1 on human keratinocytes
    Algermissen, B
    Sitzmann, J
    Nürnberg, W
    Laubscher, JC
    Henz, BM
    Bauer, F
    ARCHIVES OF DERMATOLOGICAL RESEARCH, 2000, 292 (10) : 488 - 495
  • [47] Cardiovascular responses mediated by protease-activated receptor-2 (PAR-2) and thrombin receptor (PAR-1) are distinguished in mice deficient in PAR-2 or PAR-1
    Damiano, BP
    Cheung, WM
    Santulli, RJ
    Fung-Leung, WP
    Ngo, K
    Ye, RD
    Darrow, AL
    Derian, CK
    De Garavilla, L
    Andrade-Gordon, P
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 1999, 288 (02): : 671 - 678
  • [48] A new approach to antiplatelet treatment with a PAR-1 antagonist in patients with atherosclerosis
    Shimizu, Kenji
    Ogawa, Masami
    Yamaguchi, Hiroya
    Shibata, Junpei
    Jensen, Peder
    Chintala, Madhu
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2008, 106 : 23P - 23P
  • [49] Exquisite Synthesis of a Designed PAR-1 Antagonist
    Miao, Hua-Ming
    Zhao, Gui-Long
    Zhang, Lin-Shan
    Shao, Hua
    Wang, Jian-Wu
    HELVETICA CHIMICA ACTA, 2011, 94 (11) : 1981 - 1993
  • [50] Vorapaxar, an Oral PAR-1 Receptor Antagonist, Does Not Affect the Pharmacokinetics of Rosiglitazone
    Kosoglou, Teddy
    Kumar, Bharath
    Statkevich, Paul
    Schiller, James E.
    Kantesaria, Bhavna
    Hanson, Mary E.
    Sisk, Christine McCrary
    Cutler, David L.
    CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2015, 4 (01): : 56 - 62