Literature DB >> 9469622

Novastan (brand of argatroban): a small-molecule, direct thrombin inhibitor.

M J Hursting1, K L Alford, J C Becker, R L Brooks, J L Joffrion, G D Knappenberger, P W Kogan, T P Kogan, A A McKinney, R P Schwarz.   

Abstract

Because of the unsatisfactory options available for safe and effective antithrombotic therapy, recent, intense research and development efforts have focused on direct, or site-directed, thrombin inhibitors. Argatroban is a small-molecule, reversible, direct thrombin inhibitor selective for the catalytic site of the thrombin molecule. Argatroban's molecular properties (small molecule; fast, selective, and reversible inhibition of the thrombin catalytic site; and similar in vitro potency for inhibiting both clot-bound and soluble thrombin) offer the potential for significant antithrombotic efficacy with minimal systemic anticoagulant effects. Its clinical pharmacologic properties offer the potential for minimal risk of bleeding, very rapid achievement of therapeutic antithrombotic efficacy, predictable dose response, and rapid restoration of the hemostatic systems to baseline on termination of intravenous infusion. The intravenous agent Novastan (brand of argatroban) is currently approved for clinical use in Japan for the treatment of peripheral arterial occlusive disease. Novastan is in advanced clinical development in North and South America for several indications, including (1) anticoagulant/antithrombotic therapy in heparin-induced thrombocytopenia (HIT) and heparin-induced thrombocytopenia, and thrombosis syndrome (HITTS); and (2) adjunctive therapy to thrombolytic agents in acute myocardial infarction. Results from these trials are projected to be available by early 1997.

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Year:  1997        PMID: 9469622     DOI: 10.1055/s-2007-996128

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  22 in total

Review 1.  Management of patients with heparin-induced thrombocytopenia: focus on recombinant hirudin.

Authors:  N Lubenow; A Greinacher
Journal:  J Thromb Thrombolysis       Date:  2000-11       Impact factor: 2.300

Review 2.  Argatroban.

Authors:  Sekar Kathiresan; Jin Shiomura; Ik-Kyung Jang
Journal:  J Thromb Thrombolysis       Date:  2002-02       Impact factor: 2.300

Review 3.  Direct thrombin inhibitors in cardiovascular disease.

Authors:  Kyle A Arsenault; Jack Hirsh; Richard P Whitlock; John W Eikelboom
Journal:  Nat Rev Cardiol       Date:  2012-05-01       Impact factor: 32.419

Review 4.  Thrombin inhibitors and cardiopulmonary bypass.

Authors:  Alan Merry
Journal:  J Extra Corpor Technol       Date:  2006-03

Review 5.  Parenteral anticoagulants: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines.

Authors:  David A Garcia; Trevor P Baglin; Jeffrey I Weitz; Meyer Michel Samama
Journal:  Chest       Date:  2012-02       Impact factor: 9.410

Review 6.  Argatroban.

Authors:  K McKeage; G L Plosker
Journal:  Drugs       Date:  2001       Impact factor: 9.546

7.  Argatroban in heparin-induced thrombocytopenia: rationale for use and place in therapy.

Authors:  Ramandeep K Bambrah; Dat C Pham; Fauzia Rana
Journal:  Ther Adv Chronic Dis       Date:  2013-11       Impact factor: 5.091

8.  In vitro studies using a global hemostasis assay to examine the anticoagulation effects in plasma by the direct thrombin inhibitors: dabigatran and argatroban.

Authors:  Shu He; Håkan Wallèn; Niklas Bark; Margareta Blombäck
Journal:  J Thromb Thrombolysis       Date:  2013-02       Impact factor: 2.300

9.  Incorporation of noncoded amino acids into the N-terminal domain 1-47 of hirudin yields a highly potent and selective thrombin inhibitor.

Authors:  V De Filippis; I Russo; A Vindigni; E Di Cera; S Salmaso; A Fontana
Journal:  Protein Sci       Date:  1999-10       Impact factor: 6.725

10.  Argatroban as an anticoagulant for both hematologic and chemical tests.

Authors:  T Kumura; M Hino; T Yamane; N Tatsumi
Journal:  J Clin Lab Anal       Date:  2000       Impact factor: 2.352

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