Semin Thromb Hemost 2002; 28(4): 393-402
DOI: 10.1055/s-2002-34309
Copyright © 2002 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

The Synthetic Pentasaccharide Fondaparinux: First in the Class of Antithrombotic Agents that Selectively Inhibit Coagulation Factor Xa

Maurice Petitou, Philippe Duchaussoy, Jean-Marc Herbert, Gérald Duc, Mohamed El Hajji, Jean-François Branellec, François Donat, José Necciari, Roger Cariou, Jean Bouthier, Eric Garrigou
  • Sanofi-Synthelabo, Toulouse, France
Further Information

Publication History

Publication Date:
23 September 2002 (online)

ABSTRACT

Fondaparinux (Arixtra®), a synthetic pentasaccharide, is the first in a new class of antithrombotic agents that selectively inhibit coagulation factor Xa. In vitro experiments demonstrated that it is a selective inhibitor of factor Xa. In plasma, fondaparinux selectively binds to antithrombin, catalyzes factor Xa inhibition, and thereby inhibits thrombin generation. Its antithrombotic efficacy has been demonstrated in various animal models mimicking venous and arterial thrombosis. In humans, its pharmacokinetic profile is favorable, with a rapid onset of antithrombotic activity and an elimination half-life allowing a convenient once-daily dosing regimen. In several clinical trials, fondaparinux was more effective than the reference drug, enoxaparin, in preventing venous thromboembolism after hip fracture, major knee, and elective hip replacement surgeries. The overall reduction in the risk of venous thromboembolism ranged between 26.3 and 56.4%, depending on the trial. This superior efficacy was achieved without increasing the risk of clinically relevant bleeding. Fondaparinux also showed promising results in the treatment of patients with venous thromboembolism and acute coronary syndromes. Thus, it is now established that selective factor Xa inhibition is an efficient way to prevent venous thrombosis. The advent of fondaparinux offers an opportunity to improve substantially the management of venous thromboembolism.

REFERENCES

  • 1 Casu B. Structure and biological activity of heparin.  Adv Carbohydr Chem Biochem . 1985;  43 51-134
  • 2 Hirsh J, Warkentin T E, Shaughnessy S G. Heparin and low-molecular-weight heparin. Mechanisms of action, pharmacokinetics, dosing, monitoring, efficacy, and safety.  Chest . 2001;  119 64S-94S
  • 3 This point is best illustrated by the venue of symposia such as Differentiation of LMWHs: Applied and Clinical Considerations Fareed J, Haas S, Sasahara A, Chairpersons. January 29-30, 1999. St Petersburg, Florida. The objective of the meeting was ``To review the available data on the differentiation of LMWHs in clinical and applied sciences with leading experts in the field, and to develop a position paper for clinicians to better understand the feasibility of product substitution: its impact on clinical outcome.''
  • 4 Weitz J I, Hirsh J. New anticoagulant drugs.  Chest . 2001;  119 95S-107S
  • 5 Eriksson B I. New therapeutic options in deep vein thrombosis prophylaxis.  Semin Hematol . 2000;  37 7-9
  • 6 Narayanan S. Multifunctional roles of thrombin.  Ann Clin Lab Sci . 1999;  29 275-280
  • 7 Wessler S, Yin E T. On the antithrombotic action of heparin.  Thromb Diath Haemorrh . 1974;  32 71-78
  • 8 Esmon C T, Owen W G, Jackson C M. The conversion of prothrombin to thrombin. II. Differentiation between thrombin- and factor Xa-catalyzed proteolyses.  J Biol Chem . 1974;  249 606-611
  • 9 Esmon C T, Jackson C M. The conversion of prothrombin to thrombin. III. The factor Xa-catalyzed activation of prothrombin.  J Biol Chem . 1974;  249 7782-7790
  • 10 Turpie A GG, Gallus A S, Hoek J A, for the Pentasaccharide Investigators. A synthetic pentasaccharide for the prevention of deep-vein thrombosis after total hip replacement.  N Engl J Med . 2001;  344 619-625
  • 11 Lassen M R, Bauer K A, Eriksson B I, Turpie A GG. Fondaparinux versus enoxaparin for the prevention of venous thromboembolism in elective hip replacement surgery. A randomized double-blind comparison (in press).  Lancet.
  • 12 Turpie A GG, Bauer K A, Eriksson B I. A randomized double-blind comparison of fondaparinux with enoxaparin for the prevention of venous thromboembolism after elective hip replacement surgery (in press).  Lancet.
  • 13 Eriksson B I, Bauer K A, Lassen M R, Turpie A GG. Fondaparinux compared with enoxaparin for the prevention of venous thromboembolism after hip-fracture surgery.  N Engl J Med . 2001;  345 1298-1304
  • 14 Bauer K A, Eriksson B I, Lassen M R, Turpie A GG. Fondaparinux compared with enoxaparin for the prevention of venous thromboembolism after elective major knee surgery.  N Engl J Med . 2001;  345 1305-1310
  • 15 The Rembrandt Investigators. Treatment of proximal deep vein thrombosis with a novel synthetic compound (SR90107A/ ORG31540) with pure anti-factor Xa activity. A phase II evaluation.  Circulation . 2000;  102 2726-2731
  • 16 Coussement P K, Bassand J P, Convens C. A synthetic factor Xa-inhibitor (ORG31540/SR9017A) as an adjunct to fibrinolysis in acute myocardial infarction.  Eur Heart J . 2001;  22 1716-1724
  • 17 Vuillemenot A, Schiele F, Meneveau N. Efficacy of a synthetic pentasaccharide, a pure factor Xa inhibitor, as an antithrombotic agent. A pilot study in the setting of coronary angioplasty.  Thromb Haemost . 1999;  81 214-220
  • 18 Choay J, Petitou M, Lormeau J-C. Structure-activity relationship in heparin: a synthetic pentasaccharide with high affinity for antithrombin III and eliciting high anti-factor Xa activity.  Biochem Biophys Res Commun . 1983;  116 492-499
  • 19 van Boeckel A A C, Petitou M. The unique antithrombin binding domain of heparin: a lead to new synthetic antithrombotics.  Angew Chem Int Ed Engl . 1993;  32 1671-1690
  • 20 van Boeckel A A C, Beetz T, van Aelst F S. Synthesis of a potent antithrombin activating pentasaccharide: a new heparin-like fragment containing two 3-O-sulphated glucosamines.  Tetrahedron Lett . 1988;  29 803-806
  • 21 Petitou M, Jaurand G, Derrien M, Duchaussoy P, Choay J. A, highly potent, heparin-like pentasaccharide fragment containing a glucose residue instead of a glucosamine. Bioorg Med Chem Lett .  1991;  2 95-98
  • 22 Westerduin P, van Boeckel A A C, Basten A. Feasible synthesis and biological properties of six ``non-glycosamino'' glycan analogues of the antithrombin III binding heparin pentasaccharide.  Bioorg Med Chem . 1994;  2 1267-1280
  • 23 Herbert J M, Hérault J P, Bernat A. Biochemical and pharmacological properties of SanOrg 34006, a potent and long-acting synthetic pentasaccharide.  Blood . 1998;  91 4197-4205
  • 24 Petitou M, Duchaussoy P, Lederman I. Synthesis of heparin fragments: a alpha-methyl pentaoside with high affinity for antithrombin III.  Carbohydr Res . 1987;  167 67-75
  • 25 Jaurand G, Basten J, Lederman I, van Boeckel A A C, Petitou M. Biologically active heparin-like fragments with a ``non-glycosamino''glycan structure. Part 1: A pentasaccharide containing a 3-O-methyl iduronic acid unit.  Bioorg Med Chem Lett . 1992;  2 897-900
  • 26 Basten J, Jaurand G, Olde-Hanter B, Petitou M, van Boeckel A A C. Biologically active heparin-like fragments with a ``non-glycosamino''glycan structure. Part 2: A tetra-O-methylated pentasaccharide with high affinity for antithrombin III.  Bioorg Med Chem Lett . 1992;  2 901-904
  • 27 Basten J, Jaurand G, Olde-Hanter B. Biologically active heparin-like fragments with a ``non-glycosamino''glycan structure. Part 3: O-alkylated-O-sulphated pentasaccharides.  Bioorg Med Chem Lett . 1992;  2 905-910
  • 28 Petitou M, Duchaussoy P, Lederman I, Choay J, Sinay P. Binding of heparin to antithrombin III: a chemical proof of the critical role played by a 3-sulfated 2-amino-2-deoxy-d-glucose residue.  Carbohydr Res . 1988;  179 163-172
  • 29 Petitou M, Lormeau J C, Choay J. Interaction of heparin and antithrombin III. The role of O-sulfate groups.  Eur J Biochem . 1988;  176 637-640
  • 30 Jin J, Abrahams J P, Skinner R. The anticoagulant activation of antithrombin by heparin.  Proc Natl Acad Sci USA . 1997;  94 14683-14688
  • 31 Belzar K J, Dafforn T R, Petitou M, Carrell R W, Huntington J A. The effect of a reducing-end extension on pentasaccharide binding to antithrombin.  J Biol Chem . 2000;  275 8733-6741
  • 32 Herbert J M, Petitou M, Lormeau J C. SR 90107/Org 31540, a novel anti-factor Xa antithrombotic agent.  Cardiovasc Drug Rev . 1997;  15 1-26
  • 33 Walenga J M, Peske W P, Bara L, Samama M M, Fareed J. Biochemical and pharmacologic rationale for the development of a synthetic pentasaccharide.  Thromb Res . 1997;  86 1-36
  • 34 Olson S T, Björk I, Sheffer R. Role of the antithrombin-binding pentasaccharide in heparin acceleration of antithrombin-proteinase reactions. Resolution of the antithrombin conformational change contribution to heparin rate enhancement.  J Biol Chem . 1992;  267 12528-12538
  • 35 Lormeau J C, Herault J P, Herbert JM Antithrombin-mediated inhibition of factor VIIa-tissue factor complex by the synthetic pentasaccharide representing the heparin binding site of antithrombin. Thromb Haemost .  1996;  76 5-8
  • 36 Hérault J P, Gaich C, Bono F. Structural studies on synthetic oligosaccharides in relation to factor IXa inhibition (submitted for publication). 
  • 37 Lormeau J C, Herault J P. Comparative inhibition of extrinsic and intrinsic thrombin generation by standard heparin, a low molecular weight heparin and the synthetic AT-III-binding pentasaccharide.  Thromb Haemost . 1993;  69 152-156
  • 38 Beguin S, Choay J, Hemker H C. The action of a synthetic pentasaccharide on thrombin generation in whole plasma.  Thromb Haemost . 1989;  61 397-401
  • 39 Walenga J M, Petitou M, Lormeau J C. Antithrombotic activity of a synthetic heparin pentasaccharide in a rabbit stasis thrombosis model using different thrombogenic challenges.  Thromb Res . 1987;  46 187-198
  • 40 Amar J, Caranobe C, Sié P, Boneu B. Antithrombotic potencies of heparins in relation to their antifactor Xa and antithrombin activities: an experimental study in two models of thrombosis in the rabbit.  Br J Haematol . 1990;  76 94-100
  • 41 Carrié D, Caranobe C, Saivin S. Pharmacokinetic and antithrombotic properties of two pentasaccharides with high affinity to antithrombin III in the rabbit: comparison with CY216.  Blood . 1994;  84 2571-2577
  • 42 Vogel G MT, van Amsterdam G M R, Kop W J, Meuleman D G. Pentasaccharide and Orgaran® arrest, whereas heparin delays thrombus formation in a rat arteriovenous shunt.  Thromb Haemost . 1993;  69 29-34
  • 43 Cadroy Y, Hanson S R, Harker L A. Antithrombotic effects of synthetic pentasaccharide with high affinity for plasma antithrombin III in non-human primates.  Thromb Haemost . 1993;  70 631-635
  • 44 Hobbelen P MJ, Van Dinther G T, Vogel G MT. Pharmacological profile of the chemically synthesized antithrombin III binding fragment of heparin (pentasaccharide) in rats.  Thromb Haemost . 1990;  63 265-270
  • 45 Walenga J, Petitou M, Samama M, Choay J, Fareed J. Importance of a 3-O-sulfate group in heparin pentasaccharide for antithrombotic activity.  Thromb Res . 1988;  52 553-563
  • 46 Donat F, Duret J P, Santoni R. The pharmacokinetics of fondaparinux sodium in healthy volunteers.  Clin Pharmacokinet . 2002;  41(Suppl 2) 1-9
  • 47 Lieu C, Shi J, Donat F. Fondaparinux sodium is not metabolised in mammalian liver fractions and does not inhibit cytochrome P450-mediated metabolism of concomitant drugs.  Clin Pharmacokinet . 2002;  41(Suppl 2) 19-26
  • 48 Faaij R A, Burggraaf J, Cohen A M. Lack of pharmacokinetic and pharmacodynamic interaction between the first synthetic factor Xa inhibitor and warfarin in human volunteers [abstract]. 42nd Annual Meeting of the American Society of Hematology; December 1-5, 2000; San Francisco
  • 49 Santoni A, Duvauchelle T. Safety and pharmacokinetics of co-administration of the first synthetic factor Xa inhibitor and aspirin in human volunteers [abstract]. 42nd Annual Meeting of the American Society of Hematology; December 1-5, 2000; San Francisco
  • 50 Mant T, Fournié P, Ollier C, Donat F, Necciari J. Absence of interaction of fondaparinux sodium with digoxin in healthy volunteers.  Clin Pharmacokinet . 2002;  41(Suppl 2) 43-49
  • 51 Lagrange F, Vergnes C, Brun J L. Absence of placental transfer of pentasaccharide (Fondaparinux, Arixtra®) in the dually-perfused human cotyledon in vitro.  Thromb Haemost . 2002;  87 831-835
  • 52 Geerts W H, Heit J A, Clagett G P. Sixth ACCP Consensus Conference on antithrombotic therapy. Prevention of venous thromboembolism.  Chest . 2001;  119(Suppl) 132S-175S
  • 53 Nicolaides A N. Prevention of venous thromboembolism. International Consensus Statement. Guidelines compiled in accordance with the scientific evidence.  Int Angiol . 2001;  20 1-37
  • 54 Davidson B L. What are the most reliable detection methods for deep vein thrombosis and pulmonary embolism to be used as endpoints in trials of venous thromboprophylaxis?.  Haemostasis . 1998;  28(Suppl 3) 113-119
  • 55 Kearon C, Julian J A, Math M, Newman T E, Ginsberg J S, for the McMaster Diagnostic Imaging Practice Guidelines Initiative. Noninvasive diagnosis of deep venous thrombosis Ann Intern Med .  1998;  128 663-677
  • 56 Levieux A, Rivera V, Levieux D. Immunochemical control of the species origin of porcine crude heparin and detection of ovine and caprine materials.  J Pharm Biomed Anal . 2002;  27 305-313
  • 57 Jaques L B. Heparins-anionic polyelectrolyte drugs.  Pharmacol Rev . 1979;  31 99-167
  • 58 Conrad H E. Heparin-Binding Proteins.  San Diego, CA: Academic Press; 1998
  • 59 Capila I, Linhardt R J. Heparin-protein interactions.  Angew Chem Int Ed Engl . 2002;  41 390-412
  • 60 Gray E, Cesmeli S, Lormeau J-C, Davies A B, Lane D A. Low affinity heparin is an antithrombotic agent.  Thromb Haemost . 1994;  71 203-207
  • 61 Barzu T, Mohlo P, Tobelem G. Binding of heparin and low molecular weight heparin fragments to human vascular endothelial cells in culture.  Nouv Rev Fr Hematol . 1984;  26 243-247
  • 62 Barzu T, Mohlo P, Tobelem G, Petitou M, Caen J P. Binding and endocytosis of heparin by human endothelial cells in culture.  Biochim Biophys Acta . 1985;  845 196-203
  • 63 Zammit A, Pepper D S, Dawes J. Interaction of immobilised unfractionated and LMW heparins with proteins in whole human plasma.  Thromb Haemost . 1993;  70 951-958
  • 64 Baruch D, Ajzenberg N, Denis C. Binding of heparin fractions to von Willebrand factor: effect of molecular weight and affinity for antithrombin III.  Thromb Haemost . 1994;  71 141-146
  • 65 Boneu B, Caranobe C, Cadroy Y. Pharmacokinetic studies of standard unfractionated heparin, and low molecular weight heparins in the rabbit.  Semin Thromb Hemost . 1998;  14 18-27
  • 66 Paolucci F, Clavies M C, Donat F, Necciari J. Fondaparinux sodium mechanism of action: identification of specific binding to purified and human plasma-derived proteins (in press). 
  • 67 Hoffmann P, Bernat A, Dumas A. The synthetic pentasaccharide SR90107A/ORG 31540 does not release lipase activity into the plasma.  Thromb Res . 1997;  326 325-332
  • 68 Maccarana M, Lindahl U. Mode of interaction between platelet factor 4 and heparin.  Glycobiology . 1993;  3 271-277
  • 69 Elalamy I, Lecrubier C, Potevin F. Absence of in vitro cross-reaction of pentasaccharide with the plasma heparin dependent factor of twenty-five patients with heparin associated thrombocytopenia.  Thromb Haemost . 1995;  74 1384-1385
  • 70 Greinacher A, Alban S, Dummel V, Franz G, Mueller-Eckardt C. Characterization of the structural requirements for a carbohydrate based anticoagulant with a reduced risk of inducing the immunological type of heparin-associated thrombocytopenia.  Thromb Haemost . 1995;  74 886-892
  • 71 Björk I, Olson S T, Shore J D. Molecular mechanisms of the accelerating effect of heparin on the reactions between antithrombin and clotting proteinases. In: Lane DA, Lindahl U, eds. Heparin London: Edward Arnold 1989: 229-255
  • 72 Lormeau J C, Hérault J P. The effect of the synthetic pentasaccharide SR 90107/ORG 31540 on thrombin generation ex vivo is uniquely due to ATIII-mediated neutralization of factor Xa.  Thromb Haemost . 1995;  74 1474-1477
  • 73 Ansell J, Hirsh J, Dalen J. Managing oral anticoagulant therapy.  Chest . 2001;  119 22S-38S
  • 74 Petitou M, van Boeckel A A C. Heparin: from the original ``soup'' to well-designed heparin mimetics.  Pure Appl Chem . 1997;  67 1839-1846
    >