ZA200106360B

ZA200106360B - Treatment of thrombosis by combined use of a factor XA inhibitor and aspirin, tissue plasminogen activator (TPA), a GPIIb/IIIa antagonist, low molecular weight heparin or heparin.

Info

Publication number: ZA200106360B
Application number: ZA200106360A
Authority: ZA
Inventors: Pancras C Wong
Original assignee: Du Pont Pharm Co
Priority date: 1999-03-11
Filing date: 2001-08-02
Publication date: 2002-08-02
Also published as: AU3525400A; EP1161279A1; AU766089B2; CA2361650A1; EA200100966A1; IL144798A0; KR20020005614A; JP2002538226A; CN1346292A; BR0010381A; NZ513217A; WO2000053264A1

Description

Title

Treatment of Thrombosis by Combined Use of a Factor Xa

Inhibitor and Aspirin, Tissue Plasminogen Activator (TPA), a GPIIb/IIIa Antagonist, Low Molecular Weight Heparin or

Heparin.

Field of the Invention

This invention relates to the treatment of thrombosis in mammals and more particularly to such treatment by the administration of a combination of (i) a Factor Xa inhibitor, and (II) a compound selected from the group consisting of aspirin, TPA, GPIIb/IIIa antagonist, low molecular weight heparin and heparin, wherein the dose administered for at least one of (i) and (ii) is a subtherapeutic dose.

Background of the Invention

The selected class of Factor Xa inhibitors and the selected class of aspirin, GPIIb/IIIa antagonist, tissue plasminogen activator (TPA), low-molecular-weight-heparin and heparin are essential as camponent parts of the novel compositions of this invention. Aspirin and GPIIb/IIIa antagonists are known in the art as antiplatelet agents.

Tissue plasminogen activator (TPA) is known as a thrombolytic agent. Low-molecular-weight heparin and heparin are known as anticoagulants.

Factor Xa is a blood coagulation protein. It plays a major role in blood coagulation because of its central position at the convergent point of the intrinsic and extrinsic pathways of coagulation. It is pelieved that inhibition of Factor Xa may eliminate the production of thrombin by either the extrinsic or intrinsic pathways without interfering with a basal level of thrompin § activity necessary for normal hemostasis (Harke LA, Hanson

SR and Kelly AB. Antithrombotic strategies targeting thrombin activities, thrombin receptors and thrombin generation. Thrombosis and Haemostasis 78: 736-741, 1997).

Both peptide and nonpeptide Factor Xa inhibitors are currently available (Kaiser B. Thrombin and factor Xa inhibitors. Drugs of the Future 23: 423-436, 1998).

Examples of peptide Factor Xa inhibitors are antistasin and tick anticoagulant peptide, and nonpeptide Factor Xa inhibitors are described in W098/2326, Thromb Haemost 1994; 71: 314-9, Thromb Haemost 1994; 72:393-6, and Thromb

Haemost 1998; 79: 859-64. The antithrombotic effects of these peptide and nonpeptide Factor Xa inhibitors have been well demonstrated in various experimental models of arterial and venous thrombosis (Kaiser B. Thrombin and factor Xa inhibitors. Drugs of the Future 23: 423-436, 1998).

Summary of the Invention

One object of the present invention is to provide a method of treating thrombosis in a mammal comprising: administering to said mammal a therapeutically effective amount of a combination of (i) a Factor Xa inhibitor, and (ii) a compound selected from the group consisting of aspirin, TPA a GPIIb/IIIa antagonist, low molecular weight heparin and heparin, wherein the dose administered for at least one of (i) and (ii) is a subtherapeutic dose.

: PCT/US00/06451 - . .

Another object of the present invention is to provide a method of treating thrombosis in a mammal wherein the combination of (i) and (ii) above are administered in amounts to provide a synergistic effect.

These and other objects, which will become apparent during the following detailed description, have been achieved by the discovery that the administration of a

Factor Xa inhibitor (i) in combination with one of (11) aspirin, tissue plasminogen activator (TPA), a GPIIb/IIIa antagonist, low molecular weight heparin or heparin, with at least one of (i) and (ii), preferably both, being administered at a dose which would be a subtherapeutic dose when administered alone. 15 .

Brief Description of Drawings ] Fig. 1 is a graph showing carotid blood flow versus time for saline vehicle, aspirin alone, a Factor Xa inhibitor alone, and a combination of aspirin and the same

Factor Xa inhibitor;

Fig. 2 is a graph showing carotid blood flow versus time for saline vehicle, a GPIIb/IIIa antagonist alone, a

Factor Xa inhibitor alone, and a combination of the same

IIb/IIla antagonist and Factor X inhibitor;

Fig. 3 is a graph showing carotid blood flow versus time for saline vehicle, fragmin, a Factor Xa inhibitor, and a combination of fragmin and the same Factor Xa inhibitor;

Fig. 4 is a bar chart showing the duration of

: PCT/US00/06451 - - patency for saline vehicle, a Factor Xa inhibitor alone,

TPA alone, and a combination of the same TPA and Factor Xa inhibitor; and

Fig. 5 is a bar chart showing the antithrombotic effect of a saline vehicle and heparin alone, and a combination of heparin with 3 different doses of a Factor

Xa inhibitor.

Detailed Description of the Invention

The combinations of active compounds (i) and (ii) of this invention are useful in the treatment of thrombotic disorders including atherosclerotic arteria. disease, valvular heart disease, heart failure, cerebrovascular disease such as stroke, atrial fibrillation, coronary artery disease such as myocardial infarction and unstable angina, coronary artery bypass grafts, peripheral vascular disease, thromboembolic complications of prosthetic cardiovascular devices such heart valves and vascular grafts and deep vein thrombosis following major orthopaedic surgery, major fractures and/or abdominal surgery. These combinations are also expected to be useful in combining with endovascular stenting procedures such as percutaneous transluminal coronary angioplasty to prevent subsequent arterial thrombus formation and reocclusion.

Factor Xa inhibitor compounds (i) useful in the present invention are well-known in the prior art.

Preferred Factor Xa inhibitors are described in PCT Pat.

Appln. No. US97/22895, filed December 15, 1997; published

July 2, 1998, as WO98/28269, the disclosure of which is hereby incorporated by reference. Specifically preferred compounds within W098/28269 are:

Compound (1):

FF. /

N

7 0=8=0 0

H p

HN 0 ie oH

Fp

Compound (2):

F

= 2 4 0=S=0

N

H

. HoN F

HCl salt

Compound (3): oy

N— /

N

$00

H 2

HoN 0 i us

Fp

Another Factor Xa inhibitor compound is DX-9065a described in Thromb Haemost 1994; 71:314-9; and Thromb

Haemost 1994; 72:393-6. DX-9065a is (+)=-2S-2{4-[[(38)-1~ acetimideyl-3-pyrrolidinylloxylchenvl!-3-[7-amidino-2- naphthyl] propanoic acid hydrochloride pentahydrate. A still further Factor Xa inhibitor compound is YM~60828 described in Thromb Haemost 1998; 79:859-64. YM-60828 is [N-[4-[(l-acetimidoyl-4-piperidyl)oxy] phenyl]-N-[(7~ amidino-2-naphthyl)methyl]sulfamoyl] acetic acid dihydrochloride. Other Factor Xa inhibitor compounds will be readily known by those skilled in the art.

The compounds (ii) useful in the combination of the present inventicn are either commercially available and/or well-known in the prior art. Aspirin, fragmin (Pharmacia

AB, Stockholm, Sweden), heparin (Upjohn, Kalamazoo,

Michigan), and TPA (Genentech, San Francisco, California) are available commercially. Fragmin is a low molecular weight heparin. It is isclated from standard heparin with a mean molecular weight of 4.5 kDa whereas standard heparin has a molecular weight of 750 to 1000 kDa. Low-molecular- weight heparin such as fragmin differs from heparin in both their pharmacokinetic properties and mechanism of action.

The potency for fragmin is expressed in unit of anti-Factor

Xa activity. Each mg of fragmin has about 150 U of anti-

Factor Xa activity.

Preferred GPIIb/IIIa antagonist compounds useful as component (ii) of the combination are described in published PCT Application W095/14683, published 1 June 1995, as the second embodiment. Preferred compounds described therein have the formula:

RS ey

RI—T—V 31 —0 (Ia) or a pharmaceutically acceptable salt thereof, wherein:

R1 is selected from R2a(R3)N-, R2(R3)N(R2N=)C-,

RZ2a (R3)N(CH2)p'Z-, R2(R3)N(R2N=)C(CH2)p"2-,

RZ (R3)N(R2N=)CN(R2)-, R2(R3)NC(O)-, R2(R50)N (R2N=)C-,

R2 (R3)N(R50N=)C-; )

Rei rr _- (CH3) nZ~— 2

R A), , oh J or

Ju (Gia) x )r g

R*RN

Z is selected from a bond, O, or S:

R2 and R3 are independently selected from: H; C1-C6 alkyl;

C7-C1l1 arylalkyl optionally substituted with 0-3 groups selected from hydroxy, halogen, C1-C6 alkoxy, Cl1-C6 alkyl,

CF3, S(O)mCH3, -N(CH3)2, C1-C4 haloalkyl, methylenedioxydiyl, ethylenedioxydiyl; (C1-C10 alkoxy) carbonyl; aryl (C1-C1l0 alkoxy) carbonyl where the aryl group is optionally substituted with 0-3 groups selected from hydroxy, halogen, C1-C6 alkoxy, Cl-C6 alkyl, CF3,

S{O)mCH3, -N(CH3)2, Cl-C4 haloalkyl, methylenedioxydiyl, ethylenedioxydiyl; or hetercaryl (Cl1-C5}alkyl where the . hetercaryl group is opticnally substituted with C-2 grours selected from hydroxy, halogen, Cl1-C6 alkoxy, Cl-C6 alkyl,

CF3, 5(0)mCH3, -N(CH3)2, Cl1-C4 haloalkyl, methylenedioxydiyl, ethylenedioxydiyl;

R2a is R2 or R2(R3)N(R2N=)C; i0 U is a single bond, \Y is selected from: a single bond; -(C1-C7 alkyl)-, substituted with 0-3 groups independently selected from R6® or RrR7; -(C2-C7 alkenyl)-, substituted with 0-3 groups independently selected from R® or 37; ~{C2-C7 alkynyl)-, substituted with 0-3 groups independently selected from R6 or R7; —- (phenyl) -Q-, said phenyl substituted with 0-2 groups independently selected from R® or RY; - (pyridyl) -Q-, said pyridyl substituted with 0-2 groups independently selected from R® or R7; or —(pyridazinyl)-Q-, said pyridazinyl substituted with 0-2 groups independently selected from R® or R7: 0] is selected from a single bond, -0-, -S(0)m~, -N(R12)-, -(CH2)m-, -C(=0)-, -

N(R32)C(=0)-, -C(=0)N(RS2)~, -CH20-, -OCHp-, -

CH2N (R12) -, -N(R12)CH2-, -CH2C(=0)-, -C(=O0)CH2-, -

CH2S(0O)m~, or —-S(O)mCH2-, provided that when b is a single bond, and R1-U-v- is a substituent on C5 of the central 5-membered ring of

Formula Ic, then Q is not -0-, =-S(O)pm-, -N(R12)-, -

C(=0)N(R5@)-, -CH20-, CH2N(R12)- or -CH2S(0)p-:

Ww is selected from: -(C(R%)2)-C(=0)-N(R53)-, or -C(=0) -N (R33) - (C (RY) 2) =;

X is -C(rR%) (R8)-cHR4a-;

R4 is selected from H, C1-Cjp alkyl, C1-Ci0 . alkylcarbonyl, aryl, arylalkyl, cycloalkyl, or cycloalkylalkyl;

R42 is selected from hydroxy, C1-Ci10 alkoxy, nitro, - .

N(RO)ROa, -N(R12)R13, or -N(R16)R17, + aryl substituted with 0-3 R®, or (C1-Ci0 alkyl) carbonyl;

R4b is selected from H, C1-C¢ alkyl, Cp-Cg alkenyl, C2-Cg alkynyl, hydroxy, C1-C¢ alkoxy, C1-Cg¢ alkylthio, C1-Cg alkylsulfinyl, C1-C¢ alkylsulfonyl, nitro, (C1-Cg¢ alkyl)carbonyl, Cg-C10 aryl, -N(R}2)R13, halo, CF3,

CN, (Ci1-Cg alkoxy)carbonyl, carboxy, piperidinyl, morpholinyl or pyridyl:

RS is selected from H or C1-C10 alkyl substituted with 0-§

R4D;

RO@ is selected from hydrogen, hydroxy, C1 to Cg alkyl,

Cz to Cg alkenyl, C3 toc C11 cycloalkyl, C4 te C11 cycloalkylmethyl, C3-C¢ alkoxy, benzyloxy, Cg to Cio aryl, heteroaryl, heteroarylalkyl, C7 to C11 arylalkyl, or adamantylmethyl, C1-Ci1g alkyl substituted with 0-2 R4b; alternately, RS and R32 can be taken together to be 3- azabicyclononyl, 1,2,3,4-tetrahydro-l-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, l-piperidinyl, 1- morpholinyl, l-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or l-piperazinyl, each being optionally substituted with C1-Cg alkyl, Ce-Ci10 aryl, hetercaryl,

C7-Ci1 arylalkyl, (C1-C¢ alkyl)carbonyl, (C3-C7 cycloalkyl)carbonyl, (C1-Cg alkoxy)carbonyl or (C7-C11 arylalkoxy) carbonyl;

ROP is selected from C1-Cg alkyl, C2-Cg alkenyl, C3-C11 cycloalkyl, C4-C1]1 cycloalkylmethyl, Cg-C10 aryl, C7-

C11 arylalkyl, or C1-C10 alkyl substituted with 0-2

R4Db

Y is selected from hydroxy, C1 to Cig alkyloxy, C3 to

C11 cycloalkyloxy, Cg to Cig aryloxy, C7 to Cii aralkyloxy, C3 to C10 alkylcarbonyloxyalkyloxy, C3 to

C10 alkoxycarbonyloxyalkyloxy, C2 to C10 alkoxycarbonylalkyloxy, C5 to Cig cycloalkylcarbonyloxyalkyloxy, Cs to Cig cycloalkoxycarbonyloxyalkyloxy, C5 to Cig cycloalkoxycarbonylalkyloxy, C7 to C11 aryloxycarbonylalkyloxy, Cg to Ci2 _aryloxycarbonyloxyalkyloxy, Cg to C12 arylcarbonyloxyalkyloxy, Cs to C10 alkoxyalkylcarbonyloxyalkyloxy, Cs to C10 {(5-alkyl- 1, 3~-dioxa-cyclopenten-2-one-yl)methyloxy, or Cig to

C14 (5-aryl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy:;

RS and R7 are each independently selected from H, C1-CiQ alkyl, hydroxy, C3-Cig alkoxy, nitro, (C1-Cio : alkyl)carbonyl , -N(R12)R13, cyano, or halo; ; 15

R12 and R13 are each independently selected from H, C3-Cjio0 alkyl, (C1-Ci10 alkoxy)carbonyl, (C1-Cio alkyl) carbonyl, C31-Cj10 alkylsulfonyl, aryl (Ci1-Cjp alkyl)sulfonyl, arylsulfonyl, heteroarylsulfonyl, heteroarylcarbonyl, heteroarylalkylcarbonyl or aryl, wherein said aryl groups being optionally substituted with 0-3 substituents selected from the group consisting of:

Ci1-C4 alkyl, C1-C4 alkoxy, halo, CF3, and NO2;

R15 is selected from H, C1-Cip alkyl, C2-Cip alkenyl,

C2-Cio alkynyl, C1-Cigo alkoxy, aryl, heteroaryl or (C1-C10 alkoxy)carbonyl, CO2R3 or -C(=0)N(RS)R53;

R16 jis selected from:

-c (=0)~0-Rr18a, -C (=0} ~-r18b, -C(=0)N(R18b),, -S02-R182, or -S02-N (R18b) 5;

R17 is selected from: H or C1-Cs alkyl ;

R182 js selected from:

C1-Cg alkyl substituted with 0-2 R19,

Cz-Cg alkenyl substituted with $-2 R19,

C2-Cg alkynyl substituted with 0-2 R19,

C3-Cg cycloalkyl substituted with 0-2 R19, aryl substituted with 0-4 R19, aryl (C1-Ce alkyl)- substituted with 0-4 R19, a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, triazelyl, imidazolyl, benzofuranyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, isoxazolyl, isoxazolinyl, benzimidazolyl, piperidinyl, tetrahydrofuranyl, pyranyl, pyrimidinyl, 3H-indolyl, pyrrolidinyl, piperidinyl, indolinyl, or morpholinyl, said heterocyclic ring being substituted with 0-4 R19;

Ci-Cg alkyl substituted with a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, isoxazolyl, isoxazolinyl, benzofuranyl, indolyl, indolenyl, quinolinyl, isoquinolinyl, benzimidazolyl,

piperidinyl, tetrahydrofuranyl, pyranyl, pyridinyl, 3H-indolyl, indolyl, pyrrolidinyl, piperidinyl, indolinyl, or morpholinyl, said heterocyclic ring being substituted with 0-4 R19;

R18b is selected from R182 or H;

R19 is selected from H, halogen, CF3, CN, NO2, NR12R13, Ci-

Cg alkyl, C2-Cg¢ alkenyl, C2-Cg alkynyl, C3-Cg alkoxy,

C3-C11 cycloalkyl, C4-C11 cycloalkylalkyl, aryl, heteroaryl, aryl(Ci-Cg¢ alkyl)-, (C1-C4 alkyl)sulfonyl, aryl-sulfonyl, or C1-C4 alkoxycarbonyl: n is 0-4; p° is 1-7; p" is 1-7; . r is 0-3.

More preferred compounds have the formula:

RI—Y;

Ng TE i v

N—0 (1b) or a pharmaceutically acceptable salt thereof, wherein:

Rl is selected from: R2a(R3)N-, R2NH(R2N=)C-,

RPNH (R2N=)CNH-, R22 (R3)N(CH2)p'2-,

R2NH (R2N=)C (CH2) pn2-, R2(R3)NC(0)-, R2(R50)N(R2N=)C-,

R2 (R3) N(RSON=) C-;

> Sh 2a,

EL A). wh J or (Ca) )e ;

RZ2R3N n is 0-1; p' is 4-¢; p" is 2-4;

Z is selected from a bond or O; \Y is a single bond, ~(phenyl)- or -{pyridyl)-:

Ww is selected from: -(C(R4) 2) -C(=0) -N (R93) -, -C(=0)-N (R22) -CHo-;

X is selected from: ~CH2-CH(N (R16)R17)-, or -CH2-CH (NRORS2) -;

Y is selected from: hydroxy;

C1 to C10 alkoxy: methylcarbonyloxymethoxy-;

ethylcarbonyloxymethoxy-; t-butylcarbonyloxymethoxy-; cyclohexylcarbonyloxymethoxy-; 1-(methylcarbonyloxy)ethoxy-; 1-(ethylcarbonyloxy)ethoxy-; 1-(t-butylcarbonyloxy)ethoxy-; 1-(cyclohexylcarbonyloxy)ethoxy-; i-propyloxycarbonyloxymethoxy-; t-butyloxycarbonyloxymethoxy-; 1- (i-propyloxycarbonyloxy)ethoxy-; 1-(cyclohexyloxycarbonyloxy) ethoxy-; 1-(t-butyloxycarbonyloxy)ethoxy-; dimethylaminoethoxy-; diethylaminoethoxy-; (5-methyl-1,3-dioxacyclopenten-2-on-4-yl)methoxy-; (5- (t-butyl) -1,3-dioxacyclopenten-2-on-4-yl)methoxy-; (1,3-dioxa-5-phenyl-cyclopenten-2-on-4-yl)methoxy-; : 1-(2-(2-methoxypropyl) carbonyloxy)ethoxy-; : 20 R16 is selected from: -C(=0)-0-R18a, -C (=0) -r18b, -S(=0)2-rR18a or -S02-N(R18b) 5;

R17 is selected from H or C1-Cs alkyl;

Rl8Ba js selected from:

C1-Cg alkyl substituted with 0-2 R19,

C2-Cg alkenyl substituted with 0-2 R19,

C2-Cg alkynyl substituted with 0-2 R19,

C3-Cg cycloalkyl substituted with 0-2 R1S, aryl substituted witch 0-4 R13, aryl (C1-Ce alkyl) - substituted with (-4 R19, a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, PYZrolyi, pyrazolyl, triazolyl, imidazolyl, benzofuranyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, isoxazolyl, isoxazolinyl, benzimidazolyl, piperidinyl, tetrahydrofuranyl, pyranyl, pyrimidinyl, 3H-indolyl, pyrrolidinyl, piperidinyl, indolinyl, or morpholinyl, said heterocyclic ring being substiti tex with 0-2 =19;

C1-Cg alkyl substituted with a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, isoxazolyl, isoxazolinyl, benzofuranyl, indolyl, indolenyl, gquinclinyl, isoquineclinyl, benzimidazoiyil, piperidinyl, tetrahydrofuranyil, pyranyl, pyridinyl, 3H-indolyl, indolyl, pyrrolidinyl, pPiperidinyl, indolinyl, or morpholinyl, said heterocyclic rinc being substituted with 0-4 R19.

A specifically preferred compound has the formula:

Compound (4): [lo] oO 7a on

H MN?”

IF No

HN. Co J /

N

NH, °

OH

Other salts of this compound are also specifically preferred.

Specific examples of other GPIIb/IIIa antagonist compounds are abciximab, eptifibatide, tirofiban, lamifiban, lefradafiban, sibrafiban (Ro-48-3657), orbofiban and xemilofiban described in the paper of Graul et al. and

Scarborough (Graul A, Martel AM and Castaner J.

Xemilifiban; Drugs of the Future 22: 508-517, 1997;

Scarborough RM; Eptifibatide. Drugs of the Future 23: 585- 590, 1998). Others will be readily apparent to those skilled in the art. "Therapeutically effective amount” is intended to include an amount of a combination of compounds claimed effective to treat thrombosis in a mammal. The combination of compounds is preferably a synergistic combination.

Synergy, as described for example by Chou and Talalay, Adv.

Enzyme Regul. 22:27-55 (1984), occurs when the effect (in this case, an antithrombotic effect) of the compounds when administered in combination is greater than the additive effect of the compounds when administered alone as a single agent. In general, a synergistic effect is most clearly demonstrated at suboptimal concentrations of the compounds.

Synergy can be in terms of antihypertensive effect, antithrombotic effect, or some other non-additive beneficial effect of the combination compared with the individual components.

By "administered in ccmkination", "combination, cox "combined" when referring to component (i) and compcnant {ii) of the present invention, it is meant that the components are administered concurrently to the mammal being treated. When administered in combination each component may be administered at the same time or sequentially in any order or at different points in =ime.

Thus, compecnent (i) and component (ii) may be administered separately but sufficiently closely in time so as to provide the desirec therapeutic effect.

By "subtherapeutic dose" when referring to component (i) and component (ii) of the present invention, it is meant that each component when administered to a mammal alone does not give the desired therapeutic effect for the disease being treated.

The invention can be understocd further by the following examples wherein Compcunds (1) - (4) are as shown above. Saline (0.9 weight % NaCl) is the vehicle in all examples.

Example 1

The combination of aspirin and a Factor Xa inhibitor

Rabbits were anesthetized with ketamine (50 mg/kg i.m.) and xylazine (10 mg/kg i.m.) and then surgically prepared with arterial and venous catheters. An electromagnetic flow probe was placed on a segment of an isolated carotid artery to monitor blood flow. Thrombus formation was induced by electrical stimulation of the : carotid artery for 3 min at 4 mA using an external stainless-steel bipolar electrode. Carotid blood flow was measured continuously over a 90-min period to monitor thrombus occlusion. Test agents were infused intravenously 1 hour prior to the electrical stimulation of the carotid artery and continuously during the 90-min period.

As shown in Fig. 1 following the electrical stimulation, thrombus formation was induced and carotid ~ blood flow was gradually declined in saline vehicle-treated animals. At about 40 min after stimulation, the artery was totally occluded and blood flow was zero. Aspirin at 1 mg/kg/hr i.v. (concentration in saline was 0.167 mg/ml) or

Compound (1) (a Factor Xa inhibitor) at 0.1 mg/kg/hr i.v. (concentration in saline was 0.017 mg/ml) did not prevent the occlusion of the artery; and blood flow in these : animals was decreased to zero at about the same time as those in vehicle-treated animals. Surprisingly, Compound : 20 (1) 0.1 mg/kg/hr i.v. in combination with aspirin at 1 mg/kg/hr i.v. prevented the artery from occlusion and maintained the blood flow for at least 90 min. These results indicate that a combination of Compound (1) and aspirin at their subtherapeutic doses unexpectedly produced a significant antithrombotic effect in a rabbit model of arterial thrombosis.

Example 2

The combination of Compound (4) (a GP-IIb/IIla antagonist) and a Factor Xa inhibitor

Experimental protocol was described as above for

Example 1. As shown in Figure 2, Compound (4) (a GP-

IIb/IIIa antagonist) at 0.03 mg/kg/hr i.v. and Compound ’3) (a Factor Xa inhibitor) at C.I mg/kg/hr i.v. Zid -=o= prevent the occlusion of the artery; and blo>d flow in these animals was decreased to zero at about the same time as those in vehicle-treated animals. Surprisingly,

Compound (3) at 0.1 mg/kg/hr i.v. (concentration in saline was 0.017 mg/ml) in combination with Compound (4) at 0.03 mg/kg/hr i.v. (concentration in saline was 0.005 mg/ml) prevented the artery from occlusion and maintained the blood flow for at least 90 min. These results indicate - that a combination of Compcund (3) and Compound (4) at their subtherapeutic doses unexpectedly produced a significant antithrombotic effect in a rabbit model of arterial thrombosis.

Example 3

The combination of fragmin (low-mclecular-weicht-heparin) and a Factor Xa inhibitor

Experimental protocol was described as above for

Example 1. As shown in Figure 3, fragmin (a low-molecular- weight-heparin) at 60 U/kg/hr i.v. was moderately active.

Compound (3) (a Factor Xa inhibitor) at 0.1 mg/kg/hr i.v. did not prevent the occlusion of the artery; and blood flow in these animals was decreased to zero similar to those in vehicle-treated animals. Surprisingly, Compound (3) at 0.1 mg/kg/hr i.v. (concentration in saline was 0.017 mg/ml) in combination with fragmin at 60 U/kg/hr i.v. (concentration in saline was 0.067 mg/ml or 10 U/ml) prevented the artery from occlusion and maintained the blood flow for at least 90 min. These results indicate that a combination of

Compound (3) at its subtherapeutic dose and fragmin at a medium dose unexpectedly produced a significant antithrombotic effect in a rabbit model of arterial thrombosis.

Example 4

The combination of recombinant tissue-type plasminogen activator (TPA) and a Factor Xa inhibitor

Experiments were conducted in rats. It is similar to that of the rabbit protocol as described above in Example 1 except that Compound (2) and/or TPA were given 5 min after a preformed clot was formed. The measured parameter is its duration of patency. As shown in Figure 4, five minutes after the induction of occlusive thrombosis, neither Compound (2) at 5.6 mg/kg (concentration in saline was 0.23 mg/ml) and 1.4 mg/kg/hr i.v. nor TPA at 1 mg/kg i.v. (concentration in saline was 1 mg/ml) produced a therapeutic effect on the duration of patency. However, a combination of Compound (2) at 5.6 mg/kg and 1.4 mg/kg/hr i.v., and TPA at 1 mg/kg i.v. increased the duration of patency to 70%. This result suggests that a Factor Xa inhibitor such as Campound (2) is a promising useful adjunctive agent, which accelerates thrombolysis induced by

TPA or other thrombolytic agents. Compound (2) enhanced the thrombolysis induced by a subtherapeutic dose of TPA.

The combination of heparin and a Factor Xa inhibitor

Experiments were conducted in male guinea pigs anesthetized with a mixture of ketamine (90 mg/kg i.m.) and rylazine (12 mg/kg i.m.). The arterio-venocus shunt was connected between the carotid zrtery and jugular vein. Ths exposure of flowing blood to a silk thread induced the formation of a significant thrombus. Thirty minutes later, the shunt was disconnected and the silk thread covered with thrombus was weighed. The compounds or saline vehicle were given as continuous i.v. infusion starting 1 hr before blood was circulated in the shunt and continuing throughcut the experiment (i.e., 90 min). As shown in figure 5, heparin at 4 U/kg/hr i.v. (concentration in saline was 0.667 U/ml} did not cause antithrombotic effect. However, heparin at 4 U/kg/hr i.v. potentiated the antithrombotic effects of Compound (3) (a Factor Xa inhibitor) at 0.3, 1 or 3 mg/kg/hr i.v. (concentration in saline for 0.3 dose was 0.05 mg/ml). This result suggests that heparin at a subtherapeutic dose enhances the antithrombotic effect of

Compound (3) in a guinea model of venous thrombosis.

The results presented indicate that a combination therapy comprising a Factor Xa inhibitor and one of aspirin, TPA, a GPIIb/IIIa antagonist, low molecular weight heparin or heparin will be effective in treating thrombosis in patients. The method of the present invention provides important advantages over currently available treatments for thrombosis.

DOSAGE AND FORMULATION

The Factor Xa inhibitor (i) and a compound (ii) of this invention can be administered as treatment for thrombosis by any means that produces contact of the active agent with the agents site of action, i.e., Factor Xa, in the body of a mammal. They can be administered by any conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic agents or in a combination of therapeutic agents. They can be administered alone, but preferably are administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.

The dosage administered will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the age, health and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; and the effect desired. A daily dosage of active ingredient can be expected to be about 0.001 to about 1000 milligrams } per kilogram of body weight, with the preferred dose being about 0.01 to about 30 mg/kg.

Dosage forms of compositions suitable for administration contain from about 1 mg to about 100 mg of active ingredient per unit. In these pharmaceutical compositions the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition. The active ingredient can be administered orally in solid dosage forms, such as capsules, tablets and powders, or in liquid dosage forms, such as elixirs, syrups and suspensions. It can also be administered parenterally, in sterile liquid dosage forms.

Gelatin capsules contain the active ingredient and powdered carriers, such as lactose. starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can ba man:factired a= sustained release products to provide for ccntinuous 5S release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract. Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.

In general, water, a suitable oil, saline, agueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances. Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents. Also used are citric acid and its salts, and sodium EDTA. In addition, parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propyl-paraben and chlorcbutanol. Suitable pharmaceutical carriers are described in Remington's

Pharmaceutical Sciences, 17th ed., Mack Publishing Company,

Easton, PA, 1985, a standard reference text in this field, the disclosure of which is hereby incorporated by reference.

Useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows:

Capsules

A large number of unit capsules can be prepared by filling standard two-piece hard gelatin capsules each with 0.1 to 100 mg of powdered active ingredient, 150 mg of lactose, 50 mg of cellulose, and 6 mg magnesium stearic.

Soft Gelatin Capsules

A mixture of active ingredient in a digestible oil such as soybean oil, cottonseed oil or olive oil can be prepared and injected by means of a positive displacement pump into gelatin to form soft gelatin capsules containing 0.1 to 100 mg of the active ingredient. The capsules should then be washed and dried.

Tablets

A large number of tablets can be prepared by conventional procedures so that the dosage unit is 0.1 to 100 mg of active ingredient, 0.2 mg of colloidal silicon dioxide, 5 milligrams of magnesium stearate, 275 mg of microcrystalline cellulose, 11 mg of starch and 98.8 mg of lactose. Appropriate coatings may be applied to increase palatability or delay absorption.

Suspension

An aqueous suspension can be prepared for oral administration so that each 5 mL contain 0.1 to 100 mg of finely divided active ingredient, 200 mg of sodium carboxymethyl cellulose, 5 mg of sodium benzoate, 1.0 g of sorbitol solution, U.S.P., and 0.025 mg of vanillin.

Injectable

A parenteral composition suitable for administration by injection can be prepared by stirring 0.1 to IC) mg by weight of active ingredient In 12% by volume prcryvlzans glycol and water. The solution is sterilized by commonly

E used techniques.

Combination of components (i) and (ii)

Each therapeutic agent component of this invention can independently be in any dosage form, such as those described above, and can also be administered in various ways, as descriked above. In the following description component (ii) is to be understood to represent on= or more agents as described previously. Thus, 1f components {i and (ii) are to be treated the same or independently, each agent of component (ii) may also be treated the same or independently.

Components (i) and (ii) of the present invention may be formulated together, in a single dosage unit (that is, combined together in one capsule, tablet, powder, or liquid, etc.) as a combination product. When component (i) and (ii) are not formulated together in a single dosage unit, the component (i) may be administered at the same time as component (ii) or in any order; for example component (i) c¢f this invention may be administered first, followed by administration of component (ii), or they may be administered in the reverse order. If component (ii) contains more that one agent, e.g., aspirin and heparin, these agents may be administered together or in any order.

When not administered at the same time, preferably the administration of component (i) and (ii) occurs less than about one hour apart. Preferably, the route of administration of component (i) and (ii) is intravenously (i.v.). The terms oral agent, oral inhibitor, oral compound, or the like, as used herein, denote compounds which may be orally administered. Although it is preferable that component (i) and component (ii) both be administered by the same route (that is, for example, both orally) or dosage form, if desired, they may each be administered by different routes (that is, for example, one component of the combination product may be administered orally, and another component may be administered intravenously) or dosage forms.

As is appreciated by a medical practitioner skilled in the art, the dosage of the combination therapy of the invention may vary depending upon various factors such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration, the age, health and weight of the recipient, the nature and extent of the symptoms, the kind of concurrent treatment, the frequency of treatment, and the effect desired, as described above.

The proper dosage of components (i) and (ii) of the ; present invention will be readily ascertainable by a medical practitioner skilled in the art, based upon the present disclosure. By way of general guidance, typically a daily dosage may be about 0.01 milligram to about 1 gram of each component. If component (ii) represents more than one compound, then typically a daily dosage may be about 0.01 milligram to about 0.1 gram of each agent of component (ii). By way of general guidance, when the compounds of component (i) and component (ii) are administered in combination, the dosage amount of each component may be reduced by about 70-80% relative to the usual dosage of the component when it is administered alone as a single agent for the treatment of thrombosis, in view of the synergistic effect of the combination.

The combination products of this invention may be formulated such that, although the active ingredients are combined in a single dosage unit, the physical ccntact between the active ingrsdients is minimized. Irn cxder *c minimize contact, for example, where the product is crallv administered, one active ingredient may be enteric coated.

By enteric coating one of the active ingredients, it is possible not only to minimize the contact between the combined active ingredients, but also, it is possible to control the release of one of these components in the gastrointestinal tract such that one of these components is not released in the stomach but rather is released in the intestines. Another embodiment of this invention where oral administration is desired provides for a combinaticn product wherein one of the active ingredients is coated with a sustained-release material which effects a sustained-release throughout the gastrointestinal tract and also serves to minimize physical contact between the combined active ingredients. Furthermore, the sustained- released component can be additionally enteric coated such that the release of this component occurs only in the intestine. Still another approach would involve the formulation of a combination product in which the one component is coated with a sustained and/or enteric release polymer, and the other component is also coated with a polymer such as a low viscosity grade of hydroxypropyl methylcellulose or other appropriate materials as known in the art, in order to further separate the active components. The polymer coating serves to form an additional barrier to interaction with the other component.

In each formulation wherein contact is prevented between components (i) and (ii) via a coating or some other material, contact may also be prevented between the individual agents of component (ii).

Dosage forms of the combination products of the present invention wherein one active ingredient is enteric coated can be in the form of tablets such that the enteric coated component and the other active ingredient are blended together and then compressed into a tablet or such that the enteric coated component is compressed into one tablet layer and the other active ingredient is compressed into an additional layer. Optionally, in order to further separate the two layers, one or more placebo layers may be present such that the placebo layer is between the layers of active ingredients. In addition, dosage forms of the present invention can be in the form of capsules wherein one active ingredient is compressed into a tablet or in the form of a plurality of microtablets, particles, granules or non-perils, which are then enteric coated. These enteric coated microtablets, particles, granules or non-perils are then placed into a capsule or compressed into a capsule along with a granulation of the other active ingredient.

These as well as other ways of minimizing contact between the components of combination products of the present invention, whether administered in a single dosage form or administered in separate forms but at the same time or concurrently by the same manner, will be readily aprarent to those skilled in the art, based on the present disclosure.

Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.

Claims

What is claimed is:

1. The use of a combination of (i) a Factor Xa inhibitor, and (ii) a compound selected from the group consisting of aspirin, TPA, a GPIIb/IIIa antagonist, low molecular weight heparin and heparin for the manufacture of a medicament for the treatment of thrombosis in a mammal comprising administering to said mammal a therapeutically effective amount of the combination, wherein the dose administered for at least one of (i) and (ii) is a subtherapeutic dose.

2. The use of Claim 1 wherein the combination of (i) and (ii) provides a synergistic effect.

3. The use of Claim 2 wherein (ii) is aspirin.

4, The use of Claim 2 wherein (ii) is TPA.

5. The use of Claim 2 wherein (ii) is a GPIIb/IIIa antagonist.

6. The use of Claim 2 wherein (ii) is a low molecular weight heparin.

7. The use of Claim 2 wherein (ii) is heparin.

8. The use of a combination of (i) a Factor Xa inhibitor, and (ii) a compound selected from the group consisting of aspirin, TPA, a GPIIb/IIIa antagonist, low molecular weight heparin and heparin for the manufacture of a medicament for the treatment of thrombosis. Amended Sheet 19/06/02