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Review

New Antithrombotic Drugs in Acute Coronary Syndrome

by
Bastiaan Zwart
1,2,*,
William A. E. Parker
3,4 and
Robert F. Storey
3,4
1
Department of Cardiology, St. Antonius Hospital, 3435 CM Nieuwegein, The Netherlands
2
Department of Cardiology, Catharina Hospital, 5623 EJ Eindhoven, The Netherlands
3
Cardiovascular Research Unit, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield S10 2RX, UK
4
South Yorkshire Cardiothoracic Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield S5 7AU, UK
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2020, 9(7), 2059; https://doi.org/10.3390/jcm9072059
Submission received: 29 May 2020 / Revised: 25 June 2020 / Accepted: 27 June 2020 / Published: 30 June 2020
(This article belongs to the Special Issue Antithrombotic Treatment of Acute Coronary Syndrome)
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Abstract

:
In recent years, much progress has been made in the field of antithrombotic drugs in acute coronary syndrome (ACS) treatment, as reflected by the introduction of the more potent P2Y12-inhibitors prasugrel and ticagrelor, and novel forms of concomitant anticoagulation, such as fondaparinux and bivalirudin. However, despite substantial improvements in contemporary ACS treatment, there remains residual ischemic risk in this group and hence the need for even more effective antithrombotic drugs, while balancing antithrombotic efficacy against bleeding risk. This review discusses recently introduced and currently developed antiplatelet and anticoagulant drugs in ACS treatment.

1. Introduction

Aspirin is the cornerstone of the antithrombotic management of coronary artery disease and other atherothrombotic diseases. Whereas venous thromboembolism (VTE) has traditionally been treated with heparins and other forms of anticoagulation, it is recognized that arterial thrombi have a different composition, with more platelets and less fibrin, and therefore need a different treatment strategy [1]. In patients with acute coronary syndrome (ACS), a combination of aspirin, heparin, and fibrinolytic agents was previously used. Despite developments in the treatment of ACS, such as improvements in percutaneous coronary interventions (PCI), recurrent ischemic events were frequent. This prompted the development of more potent platelet inhibitors. The use of glycoprotein (GP) IIb/IIIa inhibitors (GPI)—parenteral agents (e.g., abciximab, tirofiban) that reduce platelet aggregation by blocking the GPIIb/IIIa receptor on the platelet surface—was found to reduce early adverse cardiac events, including angioplasty failure and restenosis [2,3]. However, GPI treatment was complicated by high bleeding rates. Another frequent complication of PCI was vessel closure due to stent thrombosis. Ticlopidine was an orally-administered antiplatelet agent that proved to be effective in improving the patency of intracoronary stents and was subsequently shown to act by blocking the platelet P2Y12 receptor, a receptor for adenosine diphosphate (ADP) that plays a central role in amplifying platelet activation [4,5,6]. Ticlopidine was succeeded by clopidogrel, another P2Y12-inhibitor with fewer side-effects that was shown to reduce myocardial infarction, cardiovascular death, and stroke in aspirin-treated ACS patients, including those treated with PCI [7,8]. Nowadays, dual antiplatelet therapy (DAPT) consisting of aspirin with a P2Y12-inhibitor is the gold standard for the treatment of ACS and after PCI, whereas GPI use is mostly limited to bail-out indications in cases of no-reflow or thrombotic complications (class IIa) [9,10,11].
In recent years, much further progress has been made in the field of antithrombotic drugs in ACS, as reflected by the introduction of the more potent P2Y12-inhibitors prasugrel and ticagrelor [12,13]. Novel forms of concomitant anticoagulation, which is now routinely added in ACS [9,10], have been developed, such as fondaparinux, a pentasaccharide with indirect anti-factor (F)Xa activity, and bivalirudin, a direct thrombin inhibitor. However, despite substantial improvements in contemporary ACS treatment, there remains residual ischemic risk in this group and hence the need for even more effective antithrombotic drugs. On the other hand, patients treated with potent antithrombotic drugs are exposed to a substantial bleeding risk. Therefore, the ultimate goal is to develop effective antithrombotic drugs with minimal hemorrhagic complications. This review discusses recently introduced and currently developed antiplatelet and anticoagulant drugs in ACS. The drugs discussed in this review and their mechanisms of action are summarized in Table 1 and Figure 1 and Figure 2.

2. Cangrelor

As described, DAPT is now the cornerstone of ACS treatment. However, currently used oral P2Y12-inhibitors have their limitations. Clopidogrel is a prodrug that needs to be metabolized by hepatic cytochrome P450 (CYP) enzymes into its active form and therefore has a delayed onset of action. The more potent P2Y12-inhibitors prasugrel and ticagrelor, which are used in contemporary ACS treatment, have a faster onset of action as compared to clopidogrel and achieve high levels of platelet inhibition within 1–2 h in stable patients [14,15]. However, none of the currently available oral P2Y12-inhibitors achieve instant antiplatelet inhibition, which is desirable especially when patients undergo PCI. When opioids are administered, which is common in the ST-elevation myocardial infarction (STEMI) setting, absorption of prasugrel or ticagrelor is known to be even more delayed, which exposes these patients to an increased risk of stent thrombosis, a dangerous complication of coronary stenting [16,17,18,19]. Parenteral administration of GPI may be considered as an alternative strategy to mitigate the risk of acute stent thrombosis in these patients [20], but the use of GPI bears a considerable bleeding risk and thus might not be an attractive strategy in all patients [21]. Another limitation of all oral P2Y12-inhibitors is the delayed recovery of platelet reactivity after discontinuation, which is relevant when anticipating urgent surgery. Recovery of platelet function following cessation varies from 3–7 days depending on the type of P2Y12-inhibitor and, in the case of clopidogrel, the level of platelet inhibition achieved during treatment [22,23].
Cangrelor, an intravenous, reversibly-binding platelet P2Y12 receptor antagonist, has the potential to overcome the above-mentioned limitations of the oral P2Y12-inhibitors. It has an ultra-quick onset and offset of action and therefore appears very suitable for PCI in the acute STEMI setting. Due to the intravenous method of administration, cangrelor has high bioavailability and is highly potent, with near-complete inhibition of ADP-induced platelet aggregation within 2 min after bolus injection, following which its therapeutic effects are maintained throughout infusion [24,25]. After discontinuation of cangrelor, platelet reactivity recovers back to normal within 1–2 h, due to a mean plasma half-life of 5–10 min.
Efficacy of cangrelor in clinical practice was assessed in the Cangrelor versus standard therapy to achieve optimal management of platelet inhibition (CHAMPION) trials. The CHAMPION-PCI, CHAMPION-PLATFORM, and CHAMPION-PHOENIX were phase III trials that compared cangrelor to either clopidogrel or placebo [26,27,28]. In an individual patient-level meta-analysis of these three trials containing 24,910 patients, cangrelor was found to be effective in reducing the primary outcome of death, myocardial infarction and ischemia-driven revascularization as well as stent thrombosis [29]. In this same meta-analysis, an increase in GUSTO mild bleeding was observed, but not GUSTO moderate bleeding or transfusion rates.
Current European Society of Cardiology (ESC) guidelines indicate that cangrelor may be used in P2Y12-inhibitor naïve patients undergoing PCI with stable coronary artery disease, non-ST-elevation-ACS (NSTE-ACS), or STEMI [9,10,11]. Of note, the benefit of adding cangrelor to the faster acting P2Y12-inhibitors ticagrelor and prasugrel remains unclear, as no phase III trials compared cangrelor to these agents [30]. A further caveat is that cangrelor blocks the binding of thienopyridine active metabolites to the P2Y12 receptor and so the administration of loading doses of prasugrel or clopidogrel should be deferred until the end of the cangrelor infusion [31].
In conclusion, cangrelor provides fast-onset and rapidly reversible platelet inhibition and is effective and safe to use in PCI compared to clopidogrel or placebo. It is approved in patients undergoing PCI who have not been pre-loaded with a P2Y12-inhibitor and are not being treated with GPI [32]. In clinical practice, indications might include high-risk patients who undergo PCI without proper pre-loading with an oral P2Y12-inhibitor (e.g., patients undergoing ad hoc high-risk PCI or STEMI patients presenting with resuscitated cardiac arrest) or opiate-treated STEMI patients in whom absorption of oral P2Y12 inhibitors is known to be delayed [33]. Furthermore, cangrelor might be used as a ‘bridging’ option in patients with recent PCI who need to undergo surgery after discontinuation of oral platelet therapy [22]. Further clinical studies and registries are needed to investigate the use of cangrelor in conjunction with ticagrelor or prasugrel.

3. Novel Antiplatelet Drugs

Several novel antiplatelet drugs have recently been developed. Some exploit novel targets whilst others seek to refine existing drugs in a class. None have yet reached phase III studies in patients with ACS, but clearly there are signs of potential for future use should they be subject to rigorous clinical testing, including in this population to establish safety and efficacy.

3.1. Selatogrel

Selatogrel is a novel, parenterally-active, reversibly-binding P2Y12 inhibitor formulated for subcutaneous (SC) administration [34,35]. Its molecular structure is derived from incorporating the pyrimidine group of ticagrelor into a family of compounds previously investigated as P2Y12 receptor antagonists [36]. Preclinical studies suggested that selatogrel was potent and selective, but also that it might have a wider therapeutic index when compared to clopidogrel or ticagrelor with regards to increase in bleeding risk whilst maintaining antithrombotic effect [37]. Phase I studies of oral selatogrel or prodrug were hindered by poor absorption and palatability [38]. Subsequently, the SC preparation of selatogrel was tested and its safety and tolerability demonstrated [39]. The drug has rapid onset and a radiolabeled drug study suggested no significant plasma metabolites and that elimination was largely faecal, predicting no significant drug–drug interaction [40]. Phase II studies in both acute and chronic settings of ischemic heart disease have now been reported with promising results. In the largest, 345 patients receiving maintenance antiplatelet therapy for chronic coronary syndromes were randomized to receive SC selatogrel, at one of two doses, or placebo [41]. Selatogrel reliably and potently inhibited platelet reactivity by 30 min for around 8 h, the effect wearing off by 24 h. Importantly, selatogrel’s effect appeared additive even in those already receiving oral P2Y12 inhibitors, and there were no incidences of major bleeding. The drug’s profile of effect was broadly similar when tested in 47 patients with acute MI [42]. The clinical setting(s) in which selatogrel may find a niche remains to be determined but, given it provides potent, rapid, and reversible P2Y12 inhibition without the need for intravenous access nor an infusion, it provides a promising option for early pre-hospital administration by caregivers or even self-administration by patients during a suspected ACS event, circumventing the issue of delayed absorption of oral P2Y12 inhibitors by opioids [16]. Consequently, selatogrel might provide benefits over existing standard care and warrants further study in phase III trials.

3.2. Phosphoinositide 3-Kinase β

The enzyme phosphoinositide 3-kinase (PI3K) plays a central role in many cellular signaling systems through the activation of Akt (also known as protein kinase B), and this includes within platelets [43]. The PI3K-1A subtype, including p110α, p110β or p110δ catalytic subunits, is crucial to cell signaling during platelet activation by collagen. Moreover, the p110β subunit, the presence of which designates the enzyme PI3Kβ, has particularly important roles in, for example, the generation of thromboxane A2 upon ADP stimulation and in sustaining function of glycoprotein (GP) IIb/IIIa (also known as integrin αIIbβ3), responsible for the common final pathway of platelet aggregation [44]. PI3Kβ therefore represents a rational target for antiplatelet therapy, made more attractive by the fact that in animal studies its inhibition appears to insignificantly affect primary hemostatic mechanisms [45].
Several PI3Kβ inhibitors have been developed, but human studies have been limited to date. AZD6482 is a selective, potent, and ATP-competitive inhibitor of PI3Kβ that is the active enantiomer of a previously developed racemic mixture [46]. In a study of 40 male healthy volunteers randomized to receive escalating intravenous doses of AZD6482 or placebo, the drug mildly inhibited platelet aggregation responses assessed using a number of methods and agonists. Whilst bleeding time correlated positively with plasma drug levels, the strength of the effect was judged to be small. PI3Kβ also appears to play an important role in tumor progression and another PI3Kβ inhibitor, orally-active GSK2636771, has been tested in a first-in-man study of 65 patients with advanced solid organ malignancy [47]. However, effects on platelet function were not evaluated.

3.3. GP IIb/IIIa Outside-In Signaling

GP IIb/IIIa is of importance in the final common pathway of platelet aggregation. Once activated by intracellular processes such as vasodilator-stimulated phosphoprotein dephosphorylation and calcium mobilization, surface GP IIb/IIIa forms crosslinks with GP IIb/IIIa on other platelets via fibrinogen or von Willebrand factor (vWF) bridges [48]. This can be prevented by the currently-used GP IIb/IIIa inhibitors such as tirofiban, abciximab, and eptifibatide [49]. However, GP IIb/IIIa not only acts as an effector of platelet aggregation through inside-out signaling but also has a role as a receptor in outside-in signaling via numerous pathways leading to amplification of platelet activation, thus propagating thrombosis [50]. Inhibition of outside-in signaling, whilst maintaining inside-out signaling, has been hypothesized to offer the attractive combination of preserving the integrity of the primary hemostatic response whilst preventing the propagation of platelet aggregation that leads to vessel occlusion during thrombosis [51]. Targeting the interaction of Gα13 and the IIIa subunit may achieve this. A peptide, mP6, incorporating the amino acid ExE motif, has been developed as a putative drug, and in animal studies it inhibited the second wave of platelet activation and the propagation of thrombosis in an arterial injury model, without prolonging bleeding time [51]. No human studies have yet been reported.

3.4. Conformation-Specific Targeting of GP IIb/IIIa

Another strategy that has been explored for more targeted inhibition of GP IIb/IIIa only on activated platelets is based on exploiting the conformational change that occurs upon activation of GP IIb/IIIa, exposing the ligand-binding pocket of the receptor. A single chain antibody that binds to GP IIb/IIIa in its active conformation only has been developed and tested in animal models, in which it inhibited thrombus propagation without significant effect on the bleeding time [52].

3.5. Activated Platelet-Targeted CD39 Therapy

Building on the idea of targeting activated platelets via conformation-dependent binding of a single chain antibody to GP IIb/IIIa, a further strategy has been developed and tested in preclinical studies. This involves linking the single chain antibody to the naturally-occuring ecto-nucleoside triphosphate diphosphohydrolase CD39, which therefore degrades adenosine diphosphate (ADP) in the locality of the cell membrane of the activated platelet, thus preventing ADP from stimulating platelets via P2Y1 and, most importantly, P2Y12 receptors [53]. In human platelet-rich plasma, the antibody–CD39 complex was more effective at inhibiting platelet aggregation in response to ADP stimulation than adding non-targeted CD39 and, in animal models, it prevented occlusive thrombus without prolongation of bleeding time [53].

3.6. Inhibitors of Platelet GP VI

Platelets are exposed to large amounts of collagen during atherothrombotic events, and collagen is a key agonist in the initiation and propagation of thrombosis, including through stimulation of platelet GP VI receptors [54]. Presently, no clinically approved drugs directly target platelet collagen receptors. Recently, however, attention has turned to targeting GP VI. Revacept (soluble dimeric glycoprotein VI-Fc fusion protein) has been developed as an inhibitor. In a phase I study of 30 healthy volunteers who received a single administration of intravenous revacept, the drug dose-dependently inhibited collagen-induced platelet aggregation for up to seven days and appeared safe and well-tolerated [55]. A phase II double-blind randomized controlled trial (dbRCT) of revacept vs. placebo in 158 patients with symptomatic carotid artery stenosis, transient ischemic attacks, amaurosis fugax, or stroke was completed in 2018 (NCT01645306) but the full results have not yet been made available. A second placebo-controlled dbRCT phase II study of 334 patients undergoing elective PCI, Intracoronary Stenting and Antithrombotic Regimen: Lesion Platelet Adhesion as Selective Target of Endovenous Revacept (ISAR-PLASTER), has also recently finished and results are awaited [56].
Similarly, a humanized antigen-binding fragment (Fab) against GP VI, ACT017, has been formulated [57]. This too has now been tested in a phase I study of healthy volunteers, who were randomized to receive varying doses of intravenous ACT017 or placebo. Again, the drug was well-tolerated, appeared safe, and dose-dependently inhibited collagen-induced platelet aggregation [58].

3.7. Inhibition of Protein Disulfide Isomerase

The enzyme protein disulfide isomerase (PDI) has a role in the conformational changes associated with the activation of GP IIb/IIIa [59]. Extracellular PDI also promotes thrombin generation by activation of factor V, thrombin being a potent activator of both cellular and acellular thrombosis. Inhibition of PDI attenuates these processes without significantly affecting bleeding time [60].
Isoquercetin is a flavonoid that inhibits PDI and a phase II study has now been reported in the setting of prevention of cancer-associated thrombosis, with pharmacodynamic effects seen, such as reduction in circulating levels of D-dimer and platelet-dependent thrombin generation [61]. A further small phase II/III study is ongoing in this population (NCT02195232), but the effects of isoquercetin have not been studied in those with atherothrombotic cardiovascular disease.
Another PDI inhibitor, HPW-RX40, a derivative of β-nitrostyrene, has also been shown to reduce thrombus formation in vitro and in animal studies [62].

3.8. Inhibition of Protease-Activated Receptors

Thrombin, generated both by activation of the coagulation cascade and by platelets via surface cell membrane scramblase activity, stimulates platelets via protease-activated receptor (PAR) 1 and, at high levels, PAR4 [63]. Previously, PAR1 inhibitors such as vorapaxar showed great promise as an antiplatelet agent that in preclinical studies provided potent effect without prolonging bleeding time, and the drug was tested in two large double blind randomized controlled trials of patients with atherothrombotic cardiovascular disease [64,65]. Although vorapaxar reduced ischemic events and became licensed for clinical use, there was a disappointing excess of bleeding risk that has limited its widespread adoption. It has been suggested that counterproductive inhibition of PAR1-related endothelial cytoprotective signaling pathways resulting in endothelial injury and potentially loss of vessel wall integrity that might contribute to the increased bleeding risk [66]. A new class of PAR1 inhibitor, the parmodulins, have been developed with the intention of inhibiting selectively PAR1-dependent pathways relevant to thrombosis but avoiding any anti-cytoprotective effects (34). Preclinical studies have been encouraging, but clinical studies would clearly be needed to determine if parmodulins have a less detrimental effect on bleeding risk than vorapaxar.
PAR4 has recently been considered as an alternative target to reduce thrombin-induced platelet activation. A novel PAR4 inhibitor, BMS-986120, demonstrated reduced thrombus formation without prolongation of the bleeding time in monkeys [67]. In a subsequent phase I study of 40 healthy volunteers, a single oral dose of BMS-986120 selectively and reversibly inhibited ex vivo platelet-rich thrombus formation upon stimulation with PAR4 agonist peptide in high-shear-stress conditions [68]. In contrast to aspirin or clopidogrel, BMS-986120 had no effect in ex vivo low-shear-stress conditions, which may be promising for bleeding risk although of course requires in vivo evaluation.

3.9. Caplacizumab

A novel antiplatelet agent has recently been licensed for the treatment of adults with acquired thrombotic thrombocytopenic purpura (aTTP), when used in combination with plasma exchange and immunosuppressive drugs. Caplacizumab is a humanized, bivalent, variable domain immunoglobulin fragment, which targets the A1 domain of von Willebrand factor, inhibiting interaction with the platelet glycoprotein Ib-IX-V receptor, which has an important role in platelet adhesion to damaged sub-endothelium and thus is also a potential target for antiplatelet therapy in atherothrombosis. A single intravenous dose of caplacizumab significantly inhibits platelet adhesion, as measured with ristocetin assays, for at least 24 h, and subsequent maintenance subcutaneous administration continues to exert this effect [69]. Whilst efficacy has been proven for treatment of aTTP in a modestly sized phase III study [70], the drug has not yet been investigated in other thrombotic conditions. Capcizumab led to significantly greater risk of gingival bleeding and epistaxis when compared to placebo.

4. Anticoagulation in ACS

In both STEMI and NSTE-ACS, parenteral anticoagulation is recommended [10,11] in addition to antiplatelet therapy, and should be administered at the time of diagnosis. It reduces the generation and/or action of thrombin and thereby targets another pathway in thrombus generation [71]. Several parenteral options are available, which are usually only used as a short course. In NSTE-ACS, the selective FXa inhibitor fondaparinux is the anticoagulant of choice in patients who do not proceed directly to coronary angiography, based on its favorable efficacy–safety profile [10,72]. In STEMI patients and in NSTE-ACS patients who have not been pretreated with anticoagulation, unfractionated heparin (UFH) is the most common anticoagulant used during PCI.

4.1. Enoxaparin in STEMI

Current ESC guidelines advise that enoxaparin should be considered as an alternative anti-coagulant agent to UFH [9,11]. Enoxaparin is a low-molecular-weight heparin (LMWH) that inhibits FXa and, to a lesser extent, factor IIa (thrombin) [73]. From a mechanistic point of view, enoxaparin might be more effective than UFH by targeting a more proximal part of the coagulation cascade. It provides a more predictable antithrombotic effect compared with UFH and therefore does not require monitoring [74]. Furthermore, it has the ability to provide inhibition of thrombin-induced platelet activation [75]. Evidence of a beneficial effect in STEMI stems primarily from the ATOLL trial [76] in which STEMI patients undergoing primary PCI were randomized to either enoxaparin or UFH. A reduction of the main secondary end point, comprising a composite of death, recurrent ACS, or urgent revascularization, was observed with enoxaparin. However, the results of this study might no longer be applicable to current practice, as this study was performed before the introduction of ticagrelor (almost all patients in the study were treated with clopidogrel) and a high proportion of patients received concomitant GPI therapy. Recently, the PENNY PCI study was published [75], investigating the pharmacodynamic effects of enoxaparin regimen in primary PCI in contemporary practice. Enoxaparin was administered in a dose of 0.75 mg/kg (bolus) followed by infusion of enoxaparin 0.75 mg/kg/6 h. Anti-FXa levels were measured at four time points before, during and after PCI. Enoxaparin was found to result in sustained anti-Xa levels during infusion and no bleeding complications were observed. Therefore, enoxaparin might be an attractive alternative to UFH in primary PCI. In particular, it might be an alternative to cangrelor or GPI for addressing the delayed absorption of oral P2Y12-inhibitors, especially in morphine-treated STEMI patients undergoing PCI [17].

4.2. Non-Vitamin-K-Antagonist Oral Anticoagulants (NOACs)

The combination of DAPT with oral anticoagulation is known to bear a two- to three-fold higher bleeding risk without an apparent benefit in terms of ischemic risk in patients with atrial fibrillation undergoing PCI or with ACS [77,78]. However, the introduction of the safer NOACs raised the question of whether there might yet be a window of benefit of adding NOAC to DAPT in ACS patients without a formal indication for oral anticoagulation. To date, several studies have investigated such a strategy.
Dabigatran on top of DAPT was evaluated in the RE-DEEM study, which was a phase II study that included 1861 NSTE-ACS and STEMI patients. Various doses, from 50 mg b.d. to 150 mg b.d., were evaluated against placebo and a dose-dependent increase in major or clinically-relevant minor bleeding was found in the NOAC groups without significant differences in ischemic outcomes [79]. The APPRAISE-2 trial compared apixaban with placebo in 7392 ACS patients with two additional high-risk features. Patients were treated with either aspirin monotherapy (16.3%) or aspirin and clopidogrel (79%) and were randomized to receive concomitant apixaban in a dose of 5 mg b.d. (or 2.5 mg b.d. in case of a creatinine clearance < 40 mL/min) or placebo [80]. The addition of apixaban did not significantly reduce the composite ischemic end point but led to an excess of Thrombolysis in Myocardial Infarction (TIMI) major bleeding (HR 2.59), including intracranial and fatal bleeding. Consequently, the study was stopped prematurely. Recently, the AUGUSTUS trial, which had a 2 × 2 factorial design comparing NOAC vs. VKA and aspirin vs. placebo in patients with atrial fibrillation and either ACS or undergoing PCI (or both), confirmed that dual therapy with full-dose apixaban and an oral P2Y12 inhibitor (i.e., with the omittance of aspirin) is safer than triple therapy, again showing no significant differences in ischemic outcomes although the study was underpowered for this endpoint [81].
Rivaroxaban, another direct FXa inhibitor, has been studied in this setting in the ATLAS ACS– TIMI phase II trial and subsequently in the ATLAS ACS 2–TIMI 51 phase III trial [82,83]. This large-scale study included 15,526 patients with recent ACS (within seven days after admission). All patients received standard medical treatment and were randomized in a 1:1:1 fashion to a regimen of either 2.5 mg b.d. or 5 mg b.d. of rivaroxaban or placebo. Importantly, in this study, a reduced-dose NOAC was used as compared to the “full dose” rivaroxaban 20 mg o.d. The addition of rivaroxaban reduced the composite endpoint of death from cardiovascular causes, myocardial infarction, or stroke (8.9% vs. 10.7%, p = 0.008), although this benefit was counterbalanced by higher rates of both major bleeding unrelated to coronary-artery bypass grafting (2.1% vs. 0.6%, p < 0.001) and intracranial hemorrhage (0.6% vs. 0.2%, p = 0.009). However, a reduction in rates of death from both cardiovascular causes (2.7% vs. 4.1%, p = 0.002) and from any cause (2.9% vs. 4.5%, p = 0.002) was observed in the rivaroxaban 2.5 mg b.d. group.
Finally, several other emerging NOACs have been investigated in the ACS setting but no positive results were observed in these phase II trials [84,85].
In conclusion, so far only rivaroxaban has been shown to reduce ischemic events and mortality in patients with ACS when a reduced dose of 2.5 mg b.d. was used in conjunction with standard ACS treatment. However, rivaroxaban was not studied in the setting of the more potent P2Y12-inhibitors prasugrel and ticagrelor. Current ESC guidelines indicate that low-dose rivaroxaban 2.5 mg b.d. “may be considered” (IIb) if ischemic risk exceeds bleeding risk in patients treated with aspirin and clopidogrel.

4.3. Development of Factor IX, XI, and XII Inhibitors

Looking to the horizon of anticoagulant therapy, the development of FIX, FXI, and FXII inhibitors seems promising. In the last decade, much research has focused on these specific coagulation factors. FXI is the first protein in the hemostatic pathway of intrinsic blood coagulation. FXI activates FIX, whereas factor XI itself is activated by Factor XII (FXII), a component of the contact system together with the proteins prekalikrein and H-kininogen [86]. Attempts to target these upstream factors arose from the observation that patients deficient in FXI or FXII suffer no increase or only mild increase in bleeding events, respectively [87]. On the other hand, in vivo research showed that FXI- or FXII-deficient animals seem to be protected from thrombotic complications [88,89,90]. Similarly, molecular genetic studies in FIX-deficient mice showed a correlation between in vivo FIXa activity and susceptibility to occlusive venous thrombus formation [91]. In humans, elevated levels of FIX, FXI, or FXII are all associated with prothrombotic phenotypes [92].
Following these observations, the old paradigm that thrombosis and bleeding are two sides of the same coin was challenged [93]. Is it possible to develop an antithrombotic drug without any bleeding complications? Several phase I and phase II trials are currently being conducted [94]. Whereas the first results of FIX inhibitors were not as promising as hoped [90,95], several other trials focus on FXI and FXII. FXI might be the most promising target of the two, as there is more epidemiological evidence for its role in thrombosis. Targets for the newly-developed FXI inhibitors include synthesis of FXI in the liver whereas other drugs bind FXI or FXIa, or block its active site [90,96]. Also, monoclonal antibodies are being developed. Although promising, these drugs are only currently in phase II development. Most studies focus on venous thromboembolism and whether these drugs would be effective in ACS is a further step in the future. In conclusion, FIX, FXII, and FXI have emerged as promising targets for novel anticoagulant drugs, with the potential of reducing thrombus formation with minimal effect on hemostatic pathways (i.e., bleeding). Their application in clinical practice, and in ACS in particular, is yet to be determined and further results of clinical studies are awaited.

5. Conclusions

Much progress has been made in the field of antithrombotic drugs in ACS in recent years. Newly introduced drugs in clinical practice are cangrelor, an intravenous P2Y12-antagonist, and the use of enoxaparin in STEMI and rivaroxaban as an adjunctive in ACS. Other potentially interesting drugs are currently being developed, which include several novel potent antiplatelet drugs targeting alternative pathways. Furthermore, the development of FIX, FXI, and FXII inhibitors seems promising, with the potential of reducing thrombus formation with only minimal effect on bleeding. Hence, there is a glance of several promising new antithrombotic drugs on the horizon. Their efficacy and applicability in the ACS setting needs to be further proven in clinical trials.

Author Contributions

Conceptualization, B.Z., W.A.E.P. and R.F.S.; resources, B.Z., W.A.E.P. and R.F.S.; writing—original draft preparation, B.Z. and W.A.E.P.; writing—review and editing, B.Z. and R.F.S.; visualization, W.A.E.P. and R.F.S.; supervision, R.F.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

B.Z. reports speakers/advisory fees from AstraZeneca and Bayer. R.F.S. reports institutional research grants/support from AstraZeneca, Cytosorbents, GlyCardial Diagnostics and Thromboserin; consultancy fees from Amgen, AstraZeneca, Bayer, Bristol Myers Squibb/Pfizer, Cytosorbents, GlyCardial Diagnostics, Haemonetics, Portola and Thromboserin; and honoraria from AstraZeneca, Bayer, Bristol Myers Squibb/Pfizer and Medscape.

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Figure 1. Mechanisms of action of established antithrombotic drugs in the context of the atherothrombotic response. Modified from Parker & Storey (Thrombotic Response, ESC Textbook of Cardiovascular Medicine 3rd edition, 2018, Oxford University Press). 5HT, 5-hydroxytryptamine (serotonin); AA, arachidonic acid; ADP, adenosine diphosphate; ATIII, antithrombin III; ATP, adenosine triphosphate; Ca2+, calcium; COX1, cyclo-oxygenase 1; GP, glycoprotein; IXa, activated factor IX; P2 × 1, platelet ATP receptor; LMWH, low- molecular weight heparin; P2Y1/P2Y12, platelet ADP receptors; PAR, protease activated receptor; PLA2, phospholipase A2; PSGL1, P-selectin glycoprotein ligand 1; TF, tissue factor; TPα, thromboxane receptor α; TXA2, thromboxane A2; TXA2s, thromboxane A2 synthase; Va, activated factor V; VIIa, activated factor VII; VIIIa, activated factor VIII; VASP, vasodilator-stimulated phosphoprotein; vWF, von Willebrand factor; Xa, activated factor X; XIa, activated factor XI; XIIa, activated factor XII; XIIIa, activated factor XII.
Figure 1. Mechanisms of action of established antithrombotic drugs in the context of the atherothrombotic response. Modified from Parker & Storey (Thrombotic Response, ESC Textbook of Cardiovascular Medicine 3rd edition, 2018, Oxford University Press). 5HT, 5-hydroxytryptamine (serotonin); AA, arachidonic acid; ADP, adenosine diphosphate; ATIII, antithrombin III; ATP, adenosine triphosphate; Ca2+, calcium; COX1, cyclo-oxygenase 1; GP, glycoprotein; IXa, activated factor IX; P2 × 1, platelet ATP receptor; LMWH, low- molecular weight heparin; P2Y1/P2Y12, platelet ADP receptors; PAR, protease activated receptor; PLA2, phospholipase A2; PSGL1, P-selectin glycoprotein ligand 1; TF, tissue factor; TPα, thromboxane receptor α; TXA2, thromboxane A2; TXA2s, thromboxane A2 synthase; Va, activated factor V; VIIa, activated factor VII; VIIIa, activated factor VIII; VASP, vasodilator-stimulated phosphoprotein; vWF, von Willebrand factor; Xa, activated factor X; XIa, activated factor XI; XIIa, activated factor XII; XIIIa, activated factor XII.
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Figure 2. Examples of novel antiplatelet agents and their mechanisms of action. ADP, adenosine diphosphate; AMP, adenosine monophosphate; CD, cluster of differentiation; GP, glycoprotein; P2Y12, platelet ADP receptor; PAR, protease activated receptor; PDI, protein disulphide isomerase; PI3Kbeta, phosphoinositide 3-kinase; TPa, thromboxane receptor a; TxA2, thromboxane A2; vWF, von Willebrand factor.
Figure 2. Examples of novel antiplatelet agents and their mechanisms of action. ADP, adenosine diphosphate; AMP, adenosine monophosphate; CD, cluster of differentiation; GP, glycoprotein; P2Y12, platelet ADP receptor; PAR, protease activated receptor; PDI, protein disulphide isomerase; PI3Kbeta, phosphoinositide 3-kinase; TPa, thromboxane receptor a; TxA2, thromboxane A2; vWF, von Willebrand factor.
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Table
Table 1. Of novel antithrombotic drugs tested in clinical trials.
Table 1. Of novel antithrombotic drugs tested in clinical trials.
Type of DrugsClass of DrugsDrugs Name(s)Route of AdministrationMechanism of ActionMain Study FindingsStage of Development
Anticoagulant drugsLow-molecular-weight heparinEnoxaparinSubcutaneous and intravenousinhibiting factor FXa and FIIaSustained anti-Xa levels during infusion in STEMI patients undergoing PCILaunched
Non-vitamin-K-antagonist oral anticoagulantsRivaroxabanOraldirect FXa inhibitorAddition of low-dose rivaroxaban (2.5 mg b.d.) reduced ischemic events and all-cause mortality with an increase in bleeding. No positive study results of other NOACs tested.Launched
Inhibitors of intrinsic pathway of coagulationn/aIntravenous, subcutaneous, and oralInhibitors of “upstream” anticoagulation factors FIX-, FXI-, and FXII. Various targets of action (e.g., hepatic synthesis, monoclonal antibodies)Various phase I and phase II trials currently ongoing. First study results of FXI- and FXII-inhibitors more promising than FIX-inhibitors.Phase I/II
Antiplatelet drugsP2Y12-receptor antagonistCangrelorIntravenousAdenosine triphosphate analogue blocking P2Y12-receptorPhase III trials show reduced MACE and stent thrombosis versus oral clopidogrel.Launched
P2Y12-receptor antagonistSelatogrelSubcutaneousP2Y12 receptor antagonistPotent platelet P2Y12 inhibition within 30 min, reversible by 24 h. No major bleeding events in the largest clinical study.Phase II
PI3Kβ-inhibitorsAZD6482; GSK2636771Intravenous and oralInhibiting the effect of PI3Kβ which acts through platelet cellular signaling systemsMild effect on platelet activity, minimal effect on bleeding times in healthy volunteers. GSK2636771 has been evaluated in a phase I trial for its effect on tumor progression.Phase I
Platelet GP VI-inhibitorsRevacept; ACT017IntravenousInhibition of collagen-induced platelet aggregationIn phase I studies, drugs appeared to be effective and safe. Two phase II studies completed but results have not been fully disclosed yet.Phase II
Protein disulfide isomerase (PDI) inhibitorsIsoquercetin HPW-RX40OralInhibition of PDI attenuates conformational changes in the activation of GP IIb/IIIa and inhibits the generation of thrombin generationIn the setting of prevention of cancer-associated thrombosis, isoquercetin caused a reduction in circulating levels of D-dimer and platelet-dependent thrombin generation was demonstrated. HPW-RX40 has only been tested in preclinical studies.Phase II
PAR1 signaling modulators Parmodulinsn/aInhibition of PAR1 signaling pathways involved in platelet activation, but not those relevant to endothelial cytoprotective effectsPreclinical studies have demonstrated inhibition of thrombin-induced platelet activation.Preclinical
PAR4-inhibitorsBMS-986120OralInhibition of PAR4 activation by thrombinIn a phase I study of healthy volunteers, BMS-986120 inhibited ex vivo platelet-rich thrombus formation upon stimulation with PAR4 agonist peptide in high-shear-stress conditions.Phase I
Platelet glycoprotein Ib-IX-V receptor inhibitorCaplacizumabIntravenousCaplacizumab is a immunoglobulin fragment, which targets the A1 domain of von Willebrand factor, inhibiting interaction with the platelet glycoprotein Ib-IX-V receptor, which has an important role in platelet adhesion to damaged sub-endothelium.Efficacy has been proven in a modestly sized phase III study for treatment of aTTP with an increase in gingival bleeding and epistaxis. No studies have yet been performed in other thrombotic conditions.Launched (for aTTP)
Confirmation-specific GPIIb/IIIa inhibitorsAnti-activated GPIIb/IIIan/aActivated, but not unactivated GPIIb/IIIa is inhibitedInhibited propagation of thrombosis in an animal model without prolonging bleeding time. Preclinical
Inhibitors of GPIIb/IIIa outside-in signalingmP6n/aDisrupts interaction between Gα13 and IIIa, inhibiting downstream signalingInhibited propagation of thrombosis in an animal model without prolonging bleeding time. Preclinical
Platelet-targeted CD39CD39-anti GPIIb/IIIan/aCD39 breaks down ADP. Linking CD39 to anti-GPIIb/IIIa targets the enzyme to platelets.Preclinical studies have shown greater antiplatelet efficacy of platelet-targeted CD39 compared to untargeted CD39.Preclinical

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Zwart, B.; Parker, W.A.E.; Storey, R.F. New Antithrombotic Drugs in Acute Coronary Syndrome. J. Clin. Med. 2020, 9, 2059. https://doi.org/10.3390/jcm9072059

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Zwart B, Parker WAE, Storey RF. New Antithrombotic Drugs in Acute Coronary Syndrome. Journal of Clinical Medicine. 2020; 9(7):2059. https://doi.org/10.3390/jcm9072059

Chicago/Turabian Style

Zwart, Bastiaan, William A. E. Parker, and Robert F. Storey. 2020. "New Antithrombotic Drugs in Acute Coronary Syndrome" Journal of Clinical Medicine 9, no. 7: 2059. https://doi.org/10.3390/jcm9072059

APA Style

Zwart, B., Parker, W. A. E., & Storey, R. F. (2020). New Antithrombotic Drugs in Acute Coronary Syndrome. Journal of Clinical Medicine, 9(7), 2059. https://doi.org/10.3390/jcm9072059

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