WO2009022009A1

WO2009022009A1 - Pharmaceutical composition comprising a pyrazole-o-glucoside derivative

Info

Publication number: WO2009022009A1
Application number: PCT/EP2008/060739
Authority: WO
Inventors: Klaus Dugi; Michael Mark; Frank Himmelsbach
Original assignee: Boehringer Ingelheim International Gmbh
Priority date: 2007-08-16
Filing date: 2008-08-15
Publication date: 2009-02-19
Also published as: TW200918078A; CL2008002424A1; UY31290A1; AR068102A1; PE20090987A1

Abstract

The invention relates to a pharmaceutical composition according to claim 1 comprising a pyrazole-O-glucoside derivative in combination with a DPP IV inhibitor which is suitable in the treatment or prevention of one or more conditions selected from type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance and hyperglycemia. In addition the present invention relates to methods for preventing or treating of metabolic disorders and related conditions.

Description

Pharmaceutical composition comprising a pyrazole-O-glucoside derivative

Technical Field of the Invention

The invention relates to a pharmaceutical composition comprising a pyrazole-O-glucoside derivative of the formula (I) as described hereinafter in combination with a DPP IV inhibitor as specified hereinafter which is suitable in the treatment or prevention of one or more conditions selected from type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance, impaired fasting blood glucose and hyperglycemia.

Furthermore the invention relates to methods

- for preventing, slowing progression of, delaying, or treating a metabolic disorder;

- for improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAI c; - for preventing, slowing, delaying or reversing progression from impaired glucose tolerance, impaired fasting blood glucose, insulin resistance and/or from metabolic syndrome to type 2 diabetes mellitus;

- for preventing, slowing progression of, delaying or treating of a condition or disorder selected from the group consisting of complications of diabetes mellitus; - for reducing body weight or preventing an increase in body weight or facilitating a reduction in body weight;

- for preventing or treating the degeneration of pancreatic beta cells and/or for improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin secretion; - for preventing, slowing, delaying or treating diseases or conditions attributed to an abnormal accumulation of liver fat;

- maintaining and/or improving the insulin sensitivity and/or for treating or preventing hyperinsulinemia and/or insulin resistance, in patients in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) as defined hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinafter.

In addition the present invention relates to the use of a pyrazole-O-glucoside derivative of the formula (I) as defined hereinafter for the manufacture of a medicament for use in a method as described hereinbefore and hereinafter. In addition the present invention relates to the use of a DPP IV inhibitor as defined hereinafter for the manufacture of a medicament for use in a method as described hereinbefore and hereinafter.

The invention also relates to a use of a pharmaceutical composition according to this invention for the manufacture of a medicament for use in a method as described hereinbefore and hereinafter.

Background of the Invention

The patent applications EP 1 213 296, EP 1 338 603 A1 , EP 1 354 888, EP 1364 957, EP 1 364 958, EP 1 400 529, EP 1 389 621 , WO 03/020737 and the WO 2007/080170 describe novel pyrazole-O-glycoside derivatives. The pyrazole-O-glycoside derivatives are proposed as inducers of urinary sugar excretion and as medicaments in the treatment of diabetes. The European Patent application EP 1 500 403 A1 describes a combination of an inhibitor of renal glucose reabsorption and a hypoglycemic agent. The international patent application WO 2007/014895 describes pyrazole-O-glycoside derivatives as SGLT2 inhibitors and their use in the treatment of metabolic disorders.

Renal filtration and reuptake of glucose contributes, among other mechanisms, to the steady state plasma glucose concentration and can therefore serve as an antidiabetic target. Reuptake of filtered glucose across epithelial cells of the kidney proceeds via sodium- dependent glucose cotransporters (SGLTs) located in the brush-border membranes in the tubuli along the sodium gradient ⁽¹⁾. There are at least 3 SGLT isoforms that differ in their expression pattern as well as in their physico-chemical properties ⁽²⁾. SGLT2 is exclusively expressed in the kidney ⁽³⁾, whereas SGLT1 is expressed additionally in other tissues like intestine, colon, skeletal and cardiac muscle ^{(4 5)}. SGLT3 has been found to be a glucose sensor in interstitial cells of the intestine without any transport function ⁽⁶⁾. Potentially, other related, but not yet characterized genes, may contribute further to renal glucose reuptake ⁽⁷'⁸' ⁹⁾. Under normoglycemia, glucose is completely reabsorbed by SGLTs in the kidney, whereas the reuptake capacity of the kidney is saturated at glucose concentrations higher than 1OmM, resulting in glucosuria ("diabetes mellitus"). This threshold concentration can be decreased by SGLT2-inhibition. It has been shown in experiments with the SGLT inhibitor phlorizin that SGLT-inhibition will partially inhibit the reuptake of glucose from the glomerular filtrate into the blood leading to a decrease in blood glucose concentrations and to glucosuria ^{(10 11)}.

(1 ) Wright, E.M. (2001 ) Am. J. Renal Physiol. 280, F10-F18; (2) Wright, E. M. et al. (2004) Pflugers Arch. 447(5):510-8;

(3) You, G. et al. (1995) J. Biol. Chem. 270 (49) 29365-29371 ;

(4) Pajor AM, Wright EM (1992) J Biol. Chem. 267(6):3557-3560;

(5) Zhou, L. et al. (2003) J. Cell. Biochem. 90:339-346; (6) Diez-Sampedro, A. et al. (2003) Proc. Natl. Acad. Sci. USA 100(20), 11753-1 1758;

(7) Tabatabai, N. M. (2003) Kidney Int. 64, 1320-1330;

(8) Curtis, R.A.J. (2003) US Patent Appl. 2003/0054453;

(9) Bruss,M. and Bonisch,H. (2001 ) Cloning and functional characterization of a new human sugar transporter in kidney (Genbank Ace. No. AJ305237); (10) Rossetti, L. Et al. (987) J. Clin. Invest. 79, 1510-1515; (1 1 ) Gouvea, W.L (1989) Kidney Int. 35(4): 1041 -1048.

DPP IV inhibitors represent a novel class of agents that are being developed for the treatment or improvement in glycemic control in patients with type 2 diabetes.

Specific DPP IV inhibitors currently in clinical trials for the treatment of type 2 diabetes include, for example, the following:

- Sitagliptin (MK-0431 ) having the structural formula A below is (3R)-3-amino-1-[3- (trifluoromethyl)-5,6,7,8-tetrahydro-5H-[1 ,2,4]triazolo[4,3-a]pyrazin-7-yl]-4-(2,4,5- trifluorophenyl)butan-1-one, also named (2R)-4-oxo-4-[3-(trifluoromethyl)-5,6- dihydro[1 ,2,4]triazolo[4,3-a]pyrazin-7(8/-/)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine,

In one embodiment, sitagliptin is in the form of its dihydrogenphosphate salt, i.e. sitagliptin phosphate. In a further embodiment, sitagliptin phosphate is in the form of a crystalline anhydrate or monohydrate. A class of this embodiment refers to sitagliptin phosphate monohydrate. Sitagliptin free base and pharmaceutically acceptable salts thereof are disclosed in US Patent No. 6,699,871 and in Example 7 of WO 03/004498. Crystalline sitagliptin phosphate monohydrate is disclosed in WO 2005/003135 and in WO 2007/050485. For details, e.g. on a process to manufacture or to formulate this compound or a salt thereof, reference is thus made to these documents. A tablet formulation for sitagliptin is commercially available under the trade name Januvia®.

- Vildagliptin (LAF-237) having the structural formula B below is (2S)-{[(3-hydroxyadamantan- 1-yl)amino]acetyl}pyrrolidine-2-carbonitrile, also named (S)-1-[(3-hydroxy-1- adamantyl)amino]acetyl-2-cyano-pyrrolidine,

Vildagliptin is specifically disclosed in US Patent No. 6,166,063 and in Example 1 of WO 00/34241. Specific salts of vildagliptin are disclosed in WO 2007/019255. A crystalline form of vildagliptin as well as a vildagliptin tablet formulation are disclosed in WO 2006/078593. Vildagliptin can be formulated as described in WO 00/34241 or in WO 2005/067976. A modified release vildagliptin formulation is described in WO 2006/135723. For details, e.g. on a process to manufacture or to formulate this compound or a salt thereof, reference is thus made to these documents. A tablet formulation for vildagliptin is expected to be commercially available under the trade name Galvus®.

- Saxagliptin (BMS-477118) having the structural formula C below is (1 S,3S,5S)-2-{(2S)-2- amino-2-(3-hydroxyadamantan-1-yl)acetyl}-2-azabicyclo[3.1.0]hexane-3-carbonitrile, also named (S)-3-hydroxyadamantylglycine-L-c/s-4,5-methanoprolinenitrile,

(C) Saxagliptin is specifically disclosed in US Patent No. 6,395,767 and in Example 60 of WO 01/68603. In one embodiment, saxagliptin is in the form of its HCI salt or its mono-benzoate salt as disclosed in WO 2004/052850. In a further embodiment, saxagliptin is in the form of the free base. In a yet further embodiment, saxagliptin is in the form of the monohydrate of the free base as disclosed in WO 2004/052850. A process for preparing saxagliptin is also disclosed in WO 2005/10601 1 and WO 2005/115982. Saxagliptin can be formulated in a tablet as described in WO 2005/117841. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

- Denagliptin (GSK-823093) having the structural formula D below is (2S,4S)-1-[(2S)-2- amino-3,3-bis(4-fluorophenyl)propionyl]-4-fluoropyrrolidine-2-carbonitrile, also named (2S,4S)-4-fluoro-1-[4-fluoro-beta-(4-fluorophenyl)-L-phenylalanyl]-2-pyrrolidinecarbonitrile

(D)

Denagliptin is specifically disclosed in US Patent No. 7,132,443 and in WO 03/002531. In one embodiment, denagliptin is in the form of its hydrochloride salt as disclosed in Example 2 of WO 03/002531 or its tosylate salt as disclosed in WO 2005/009956. A class of this embodiment refers to denagliptin tosylate. Crystalline anhydrous denagliptin tosylate is disclosed in WO 2005/009956. For details on a process to manufacture this compound or a salt thereof, reference is thus made to these documents.

- Alogliptin (SYR-322) having the structural formula E below is 2-({6-[(3R)-3-aminopiperidin- 1 -yl]-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1 -yl}methyl)benzonitrile

(E)

Alogliptin is specifically disclosed in US 2005/261271 , EP 1586571 and in WO 2005/095381. In one embodiment, alogliptin is in the form of its benzoate salt, its hydrochloride salt or its tosylate salt each as disclosed in WO 2007/035629. A class of this embodiment refers to alogliptin benzoate. Polymorphs of alogliptin benzoate are disclosed in WO 2007/035372. A process for preparing alogliptin is disclosed in WO 2007/1 12368 and, specifically, in WO 2007/035629. Alogliptin (namely its benzoate salt) can be formulated in a tablet and administered as described in WO 2007/033266. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

- (2S)-1 -{[2-(5-Methyl-2-phenyl-oxazol-4-yl)-ethylamino]-acetyl}-pyrrolidine-2-carbonitrile or a pharmaceutically acceptable salt thereof, preferably the mesylate, or (2S)-1-{[1 ,1 ,-Dimethyl-3-(4-pyridin-3-yl-imidazol-1-yl)-propylamino]-acetyl}-pyrrolidine-2- carbonitrile or a pharmaceutically acceptable salt thereof.

These compounds and methods for their preparation are disclosed in WO 03/037327. The mesylate salt of the former compound as well as crystalline polymorphs thereof are disclosed in WO 2006/100181. The fumarate salt of the latter compound as well as crystalline polymorphs thereof are disclosed in WO 2007/071576. These compounds can be formulated in a pharmaceutical composition as described in WO 2007/017423. For details, e.g. on a process to manufacture, to formulate or to use these compounds or a salt thereof, reference is thus made to these documents.

- (S)-1-((2S,3S,11 bS)-2-Amino-9,10-dimethoxy-1 ,3,4,7,1 1 b-hexahydro-2H-pyrido[2,1- a]isoquinolin-3-yl)-4-fluoromethyl-pyrrolidin-2-one or a pharmaceutically acceptable salt thereof.

This compound and methods for its preparation are disclosed in WO 2005/000848. A process for preparing this compound (specifically its dihydrochloride salt) is also disclosed in WO 2008/031749, WO 2008/031750 and WO 2008/055814. This compound can be formulated in a pharmaceutical composition as described in WO 2007/017423. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

- (3,3-Difluoropyrrolidin-1 -yl)-((2S,4S)-4-(4-(pyrimidin-2-yl)piperazin-1 -yl)pyrrolidin-2- yl)methanone or a pharmaceutically acceptable salt thereof.

This compound and methods for its preparation are disclosed in WO 2005/1 16014 and US 7291618. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

- (1 ((3S,4S)-4-amino-1 -(4-(3,3-difluoropyrrolidin-1 -yl)-1 ,3,5-triazin-2-yl)pyrrolidin-3-yl)-5,5- difluoropiperidin-2-one or a pharmaceutically acceptable salt thereof.

This compound and methods for its preparation are disclosed in WO 2007/148185 and US 20070299076. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

- (2S,4S)-1-{2-[(3S,1 R)-3-(1 H-1 ,2,4-Triazol-1-ylmethyl)cyclopentylamino]-acetyl}-4- fluoropyrrolidine-2-carbonitrile or a pharmaceutically acceptable salt thereof.

This compound and methods for its preparation are disclosed in WO 2006/040625 and WO 2008/001195. Specifically claimed salts include the methanesulfonate and p- toluenesulfonate. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

- (R)-2-[6-(3-Amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-4- fluoro-benzonitrile or a pharmaceutically acceptable salt thereof.

This compound and methods for its preparation and use are disclosed in WO 2005/095381 , US 2007060530, WO 2007/035629, WO 2007/074884, WO 2007/1 12368 and WO 2008/033851. Specifically claimed salts include the succinate, benzoate, benzenesulfonate, p-toluenesulfonate, (R)-mandelate and hydrochloride. For details, e.g. on a process to manufacture, to formulate or to use this compound or a salt thereof, reference is thus made to these documents.

For avoidance of any doubt, the disclosure of each of the foregoing documents cited above in connection with the specified DPP IV inhibitors is specifically incorporated herein by reference in its entirety.

Type 2 diabetes is an increasingly prevalent disease that due to a high frequency of complications leads to a significant reduction of life expectancy. Because of diabetes- associated microvascular complications, type 2 diabetes is currently the most frequent cause of adult-onset loss of vision, renal failure, and amputations in the industrialized world. In addition, the presence of type 2 diabetes is associated with a two to five fold increase in cardiovascular disease risk.

After long duration of disease, most patients with type 2 diabetes will eventually fail on oral therapy and become insulin dependent with the necessity for daily injections and multiple daily glucose measurements. The UKPDS (United Kingdom Prospective Diabetes Study) demonstrated that intensive treatment with metformin, sulfonylureas or insulin resulted in only a limited improvement of glycemic control (difference in HbAIc -0.9%). In addition, even in patients within the intensive treatment arm glycemic control deteriorated significantly over time and this was attributed to deterioration of β-cell function. Importantly, intensive treatment was not associated with a significant reduction in macrovascular complications, i.e. cardiovascular events.

Therefore there is an unmet medical need for methods, medicaments and pharmaceutical compositions with a good efficacy with regard to glycemic control, with regard to disease- modifying properties and with regard to reduction of cardiovascular morbidity and mortality while at the same time showing an improved safety profile.

Aim of the present invention The aim of the present invention is to provide a pharmaceutical composition and method for preventing, slowing progression of, delaying or treating a metabolic disorder, in particular of type 2 diabetes mellitus.

A further aim of the present invention is to provide a pharmaceutical composition and method for improving glycemic control in a patient in need thereof.

Another aim of the present invention is to provide a pharmaceutical composition and method for preventing, slowing or delaying progression from impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), insulin resistance and/or metabolic syndrome to type 2 diabetes mellitus.

Yet another aim of the present invention is to provide a pharmaceutical composition and method for preventing, slowing progression of, delaying or treating of a condition or disorder from the group consisting of complications of diabetes mellitus.

A further aim of the present invention is to provide a pharmaceutical composition and method for reducing the weight or preventing an increase of the weight in a patient in need thereof.

Another aim of the present invention is to provide a new pharmaceutical composition with a high efficacy for the treatment of metabolic disorders, in particular of diabetes mellitus, impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), and/or hyperglycemia, which has good to very good pharmacological and/or pharmacokinetic and/or physicochemical properties.

Further aims of the present invention become apparent to the one skilled in the art by description hereinbefore and in the following and by the examples.

Summary of the Invention

Within the scope of the present invention it has now surprisingly been found that a pharmaceutical composition comprising a pyrazole-O-glucoside derivative of the formula (I) as defined hereinafter can advantageously be used in combination with a DPP IV inhibitor as specified hereinafter for preventing, slowing progression of, delaying or treating a metabolic disorder, in particular in improving glycemic control in patients. This opens up new therapeutic possibilities in the treatment and prevention of type 2 diabetes mellitus, overweight, obesity, complications of diabetes mellitus and of neighboring disease states.

Therefore in a first aspect the present invention provides a pharmaceutical composition comprising a pyrazole-O-glucoside derivative of the formula (I)

wherein

R¹ denotes Ci_-3-alkoxy,

L¹, L² independently of each other denote H or F,

R⁶ denotes H, (Ci_-3-alkyl)carbonyl, (Ci_-6-alkyl)oxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl or benzylcarbonyl,

in combination with a DPP IV inhibitor selected from the group consisting of sitagliptin, vildagliptin, saxagliptin, alogliptin, denagliptin, (2S)-1-{[2-(5-Methyl-2-phenyl-oxazol-4-yl)-ethylamino]-acetyl}-pyrrolidine-2-carbonitrile,

(2S)-1-{[1 ,1 ,-Dimethyl-3-(4-pyridin-3-yl-imidazol-1-yl)-propylamino]-acetyl}-pyrrolidine-2- carbonitrile,

(S)-1-((2S,3S,11 bS)-2-Amino-9,10-dimethoxy-1 ,3,4,7,1 1 b-hexahydro-2H-pyrido[2,1- a]isoquinolin-3-yl)-4-fluoromethyl-pyrrolidin-2-one,

(3,3-Difluoropyrrolidin-1-yl)-((2S,4S)-4-(4-(pyrimidin-2-yl)piperazin-1-yl)pyrrolidin-2- yl)methanone,

(1 ((3S,4S)-4-amino-1 -(4-(3,3-difluoropyrrolidin-1 -yl)-1 ,3,5-triazin-2-yl)pyrrolidin-3-yl)-5,5- difluoropiperidin-2-one, (2S,4S)-1 -{2-[(3S, 1 R)-3-(1 H-1 ,2,4-Tιϊazol-1 -ylmethyl)cyclopentylamino]-acetyl}-4- fluoropyrrolidine-2-carbonitrile, and

(R)-2-[6-(3-Amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-4- fluoro-benzonitrile, or its pharmaceutically acceptable salt thereof.

According to another aspect of the invention there is provided a method for preventing, slowing the progression of, delaying or treating a metabolic disorder selected from the group consisting of type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance

(IGT), impaired fasting blood glucose (IFG), hyperglycemia, postprandial hyperglycemia, overweight, obesity and metabolic syndrome in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

According to another aspect of the invention there is provided a method for improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAI c in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

The pharmaceutical composition according to this invention may also have valuable disease- modifying properties with respect to diseases or conditions related to impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), insulin resistance and/or metabolic syndrome.

According to another aspect of the invention there is provided a method for preventing, slowing, delaying or reversing progression from impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), insulin resistance and/or from metabolic syndrome to type 2 diabetes mellitus in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

As by the use of a pharmaceutical composition according to this invention an improvement of the glycemic control in patients in need thereof is obtainable, also those conditions and/or diseases related to or caused by an increased blood glucose level may be treated.

According to another aspect of the invention there is provided a method for preventing, slowing the progression of, delaying or treating of a condition or disorder selected from the group consisting of complications of diabetes mellitus such as cataracts and micro- and macrovascular diseases, such as nephropathy, retinopathy, neuropathy, tissue ischaemia, arteriosclerosis, myocardial infarction, stroke and peripheral arterial occlusive disease, in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter. The term "tissue ischaemia" particularly comprises diabetic macroangiopathy, diabetic microangiopathy, impaired wound healing and diabetic ulcer.

By the administration of a pharmaceutical composition according to this invention and due to the SGLT2 inhibitory activity of the pyrazole-O-glucoside derivative excessive blood glucose levels are not converted to insoluble storage forms, like fat, but excreted through the urine of the patient. Therefore no gain in weight or even a reduction in body weight is the result.

According to another aspect of the invention there is provided a method for reducing the body weight or preventing an increase in body weight or facilitating a reduction in body weight in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

The pharmacological effect of the pyrazole-O-glucoside derivative in the pharmaceutical composition according to this invention is independent of insulin. Therefore an improvement of the glycemic control is possible without an additional strain on the pancreatic beta cells. By an administration of a pharmaceutical composition according to this invention a beta-cell degeneration and a decline of beta-cell functionality such as for example apoptosis or necrosis of pancreatic beta cells can be delayed or prevented. Furthermore the functionality of pancreatic cells can be improved or restored, and the number and size of pancreatic beta cells increased. It may be shown that the differentiation status and hyperplasia of pancreatic beta-cells disturbed by hyperglycemia can be normalized by treatment with a pharmaceutical composition according to this invention.

According to another aspect of the invention there is provided a method for preventing, slowing, delaying or treating the degeneration of pancreatic beta cells and/or the decline of the functionality of pancreatic beta cells and/or for improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin secretion in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

By the administration of a combination or pharmaceutical composition according to the present invention an abnormal accumulation of fat in the liver may be reduced or inhibited. Therefore according to another aspect of the present invention there is provided a method for preventing, slowing, delaying or treating diseases or conditions attributed to an abnormal accumulation of liver fat in a patient in need thereof characterized in that a pyrazole-O- glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter. Diseases or conditions which are attributed to an abnormal accumulation of liver fat are particularly selected from the group consisting of general fatty liver, non-alcoholic fatty liver (NAFL), nonalcoholic steatohepatitis (NASH), hyperalimentation-induced fatty liver, diabetic fatty liver, alcoholic-induced fatty liver or toxic fatty liver.

As a result thereof another aspect of the invention provides a method for maintaining and/or improving the insulin sensitivity and/or for treating or preventing hyperinsulinemia and/or insulin resistance in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

According to another aspect of the invention there is provided the use of a pyrazole-O- glucoside derivative as defined hereinbefore and hereinafter for the manufacture of a medicament for - preventing, slowing the progression of, delaying or treating a metabolic disorder selected from the group consisting of type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), hyperglycemia, postprandial hyperglycemia, overweight, obesity and metabolic syndrome; or

- improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAIc; or - preventing, slowing, delaying or reversing progression from impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), insulin resistance and/or from metabolic syndrome to type 2 diabetes mellitus; or

- preventing, slowing the progression of, delaying or treating of a condition or disorder selected from the group consisting of complications of diabetes mellitus such as cataracts and micro- and macrovascular diseases, such as nephropathy, retinopathy, neuropathy, tissue ischaemia, arteriosclerosis, myocardial infarction, stroke and peripheral arterial occlusive disease; or

- reducing body weight or preventing an increase in body weight or facilitating a reduction in body weight; or - preventing, slowing, delaying or treating the degeneration of pancreatic beta cells and/or the decline of the functionality of pancreatic beta cells and/or for improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin secretion; or

- preventing, slowing, delaying or treating diseases or conditions attributed to an abnormal accumulation of liver fat; or

- maintaining and/or improving the insulin sensitivity and/or for treating or preventing hyperinsulinemia and/or insulin resistance; in a patient in need thereof characterized in that the pyrazole-O-glucoside derivative is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

According to another aspect of the invention there is provided the use of a DPP IV inhibitor as defined hereinbefore and hereinafter for the manufacture of a medicament for

- preventing, slowing the progression of, delaying or treating a metabolic disorder selected from the group consisting of type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), hyperglycemia, postprandial hyperglycemia, overweight, obesity and metabolic syndrome; or

- improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAIc; or - preventing, slowing, delaying or reversing progression from impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), insulin resistance and/or from metabolic syndrome to type 2 diabetes mellitus; or - preventing, slowing the progression of, delaying or treating of a condition or disorder selected from the group consisting of complications of diabetes mellitus such as cataracts and micro- and macrovascular diseases, such as nephropathy, retinopathy, neuropathy, tissue ischaemia, arteriosclerosis, myocardial infarction, stroke and peripheral arterial occlusive disease; or

- reducing body weight or preventing an increase in body weight or facilitating a reduction in body weight; or

- preventing, slowing, delaying or treating the degeneration of pancreatic beta cells and/or the decline of the functionality of pancreatic beta cells and/or for improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin secretion; or

- maintaining and/or improving the insulin sensitivity and/or for treating or preventing hyperinsulinemia and/or insulin resistance; in a patient in need thereof characterized in that the DPP IV inhibitor is administered in combination or alternation with a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter.

According to another aspect of the invention there is provided the use of a pharmaceutical composition according to the present invention for the manufacture of a medicament for a therapeutic and preventive method as described hereinbefore and hereinafter.

Definitions

The term "active ingredient" of a pharmaceutical composition according to the present invention means the pyrazole-O-glucoside derivative and/or the DPP IV inhibitor according to the present invention.

The term "body mass index" or "BMI" of a human patient is defined as the weight in kilograms divided by the square of the height in meters, such that BMI has units of kg/m².

The term "overweight" is defined as the condition wherein the individual has a BMI greater than or 25 kg/m² and less than 30 kg/m². The terms "overweight" and "pre-obese" are used interchangeably. The term "obesity" is defined as the condition wherein the individual has a BMI equal to or greater than 30 kg/m². According to a WHO definition the term obesity may be categorized as follows: the term "class I obesity" is the condition wherein the BMI is equal to or greater than 30 kg/m² but lower than 35 kg/m²; the term "class Il obesity" is the condition wherein the BMI is equal to or greater than 35 kg/m² but lower than 40 kg/m²; the term "class III obesity" is the condition wherein the BMI is equal to or greater than 40 kg/m².

The term "visceral obesity" is defined as the condition wherein a waist-to-hip ratio of greater than or equal to 1.0 in men and 0.8 in women is measured. It defines the risk for insulin resistance and the development of pre-diabetes.

The term "abdominal obesity" is usually defined as the condition wherein the waist circumference is > 40 inches or 102 cm in men, and is > 35 inches or 94 cm in women. With regard to a Japanese ethnicity or Japanese patients abdominal obesity may be defined as waist circumference ≥ 85 cm in men and ≥ 90 cm in women (see e.g. investigating committee for the diagnosis of metabolic syndrome in Japan).

The term "euglycemia" is defined as the condition in which a subject has a fasting blood glucose concentration within the normal range, greater than 70 mg/dL (3.89 mmol/L) and less than 1 10 mg/dL (6.1 1 mmol/L). The word "fasting" has the usual meaning as a medical term.

The term "hyperglycemia" is defined as the condition in which a subject has a fasting blood glucose concentration above the normal range, greater than 110 mg/dL (6.1 1 mmol/L). The word "fasting" has the usual meaning as a medical term.

The term "hypoglycemia" is defined as the condition in which a subject has a blood glucose concentration below the normal range of 60 to 115 mg/dL (3.3 to 6.3 mmol/L).

The term "postprandial hyperglycemia" is defined as the condition in which a subject has a 2 hour postprandial blood glucose or serum glucose concentration greater than 200 mg/dL (1 1.1 1 mmol/L).

The term "impaired fasting blood glucose" or "IFG" is defined as the condition in which a subject has a fasting blood glucose concentration or fasting serum glucose concentration in a range from 100 to 125 mg/dl (i.e. from 5.6 to 6.9 mmol/l), in particular greater than 1 10 mg/dL and less than 126 mg/dl (7.00 mmol/L). A subject with "normal fasting glucose" has a fasting glucose concentration smaller than 100 mg/dl, i.e. smaller than 5.6 mmol/l.

The term "impaired glucose tolerance" or "IGT" is defined as the condition in which a subject has a 2 hour postprandial blood glucose or serum glucose concentration greater than 140 mg/dl (7.78 mmol/L) and less than 200 mg/dL (1 1.11 mmol/L). The abnormal glucose tolerance, i.e. the 2 hour postprandial blood glucose or serum glucose concentration can be measured as the blood sugar level in mg of glucose per dL of plasma 2 hours after taking 75 g of glucose after a fast. A subject with "normal glucose tolerance" has a 2 hour postprandial blood glucose or serum glucose concentration smaller than 140 mg/dl (7.78 mmol/L).

The term "hyperinsulinemia" is defined as the condition in which a subject with insulin resistance, with or without euglycemia, has fasting or postprandial serum or plasma insulin concentration elevated above that of normal, lean individuals without insulin resistance, having a waist-to-hip ratio < 1.0 (for men) or < 0.8 (for women).

The terms "insulin-sensitizing", "insulin resistance-improving" or "insulin resistance-lowering" are synonymous and used interchangeably.

The term "insulin resistance" is defined as a state in which circulating insulin levels in excess of the normal response to a glucose load are required to maintain the euglycemic state (Ford ES, et al. JAMA. (2002) 287:356-9). A method of determining insulin resistance is the euglycaemic-hyperinsulinaemic clamp test. The ratio of insulin to glucose is determined within the scope of a combined insulin-glucose infusion technique. There is found to be insulin resistance if the glucose absorption is below the 25th percentile of the background population investigated (WHO definition). Rather less laborious than the clamp test are so called minimal models in which, during an intravenous glucose tolerance test, the insulin and glucose concentrations in the blood are measured at fixed time intervals and from these the insulin resistance is calculated. With this method it is not possible to distinguish between hepatic and peripheral insulin resistance.

Furthermore insulin resistance, the response of a patient with insulin resistance to therapy, insulin sensitivity and hyperinsulinemia may be quantified by assessing the "homeostasis model assessment to insulin resistance (HOMA-IR)" score, a reliable indicator of insulin resistance (Katsuki A, et al. Diabetes Care 2001 ; 24: 362-5). Further reference is made to methods for the determination of the HOMA-index for insulin sensitivity (Matthews et al., Diabetologia 1985, 28: 412-19), of the ratio of intact proinsulin to insulin (Forst et al., Diabetes 2003, 52(Suppl.1): A459) and to an euglycemic clamp study. In addition, plasma adiponectin levels can be monitored as a potential surrogate of insulin sensitivity. The estimate of insulin resistance by the homeostasis assessment model (HOMA)-IR score is calculated with the formula (Galvin P, et al. Diabet Med 1992;9:921-8):

HOMA-IR = [fasting serum insulin (μll/mL)] x [fasting plasma glucose(mmol/L)/22.5]

As a rule, other parameters are used in everyday clinical practice to assess insulin resistance. Preferably, the patient's triglyceride concentration is used, for example, as increased triglyceride levels correlate significantly with the presence of insulin resistance.

Patients with a predisposition for the development of IGT or IFG or type 2 diabetes are those having euglycemia with hyperinsulinemia and are by definition, insulin resistant. A typical patient with insulin resistance is usually overweight or obese. If insulin resistance can be detected this is a particularly strong indication of the presence of pre-diabetes. Thus, it may be that in order to maintain glucose homoeostasis a person needs 2-3 times as much insulin as a healthy person, without this resulting in any clinical symptoms.

The methods to investigate the function of pancreatic beta-cells are similar to the above methods with regard to insulin sensitivity, hyperinsulinemia or insulin resistance: An improvement of the beta-cell function can be measured for example by determining a HOMA- index for beta-cell function (Matthews et al., Diabetologia 1985, 28: 412-19), the ratio of intact proinsulin to insulin (Forst et al., Diabetes 2003, 52(Suppl.1): A459), the insulin/C- peptide secretion after an oral glucose tolerance test or a meal tolerance test, or by employing a hyperglycemic clamp study and/or minimal modeling after a frequently sampled intravenous glucose tolerance test (Stumvoll et al., Eur J Clin Invest 2001, 31: 380-81).

The term "pre-diabetes" is the condition wherein an individual is pre-disposed to the development of type 2 diabetes. Pre-diabetes extends the definition of impaired glucose tolerance to include individuals with a fasting blood glucose within the high normal range ≥ 100 mg/dL (J. B. Meigs, et al. Diabetes 2003; 52:1475-1484) and fasting hyperinsulinemia (elevated plasma insulin concentration). The scientific and medical basis for identifying prediabetes as a serious health threat is laid out in a Position Statement entitled "The Prevention or Delay of Type 2 Diabetes" issued jointly by the American Diabetes Association and the National Institute of Diabetes and Digestive and Kidney Diseases (Diabetes Care 2002; 25:742-749). Individuals likely to have insulin resistance are those who have two or more of the following attributes: 1 ) overweight or obese, 2) high blood pressure, 3) hyperlipidemia, 4) one or more 1^st degree relative with a diagnosis of IGT or IFG or type 2 diabetes. Insulin resistance can be confirmed in these individuals by calculating the HOMA-IR score. For the purpose of this invention, insulin resistance is defined as the clinical condition in which an individual has a HOMA-IR score > 4.0 or a HOMA-IR score above the upper limit of normal as defined for the laboratory performing the glucose and insulin assays.

The term "type 2 diabetes" is defined as the condition in which a subject has a fasting blood glucose or serum glucose concentration greater than 125 mg/dL (6.94 mmol/L). The measurement of blood glucose values is a standard procedure in routine medical analysis. If a glucose tolerance test is carried out, the blood sugar level of a diabetic will be in excess of 200 mg of glucose per dl_ (1 1.1 mmol/l) of plasma 2 hours after 75 g of glucose have been taken on an empty stomach. In a glucose tolerance test 75 g of glucose are administered orally to the patient being tested after 10-12 hours of fasting and the blood sugar level is recorded immediately before taking the glucose and 1 and 2 hours after taking it. In a healthy subject the blood sugar level before taking the glucose will be between 60 and 1 10 mg per dl_ of plasma, less than 200 mg per dl_ 1 hour after taking the glucose and less than 140 mg per dl_ after 2 hours. If after 2 hours the value is between 140 and 200 mg this is regarded as abnormal glucose tolerance.

The term "late stage type 2 diabetes mellitus" includes patients with a secondary drug failure, indication for insulin therapy and progression to micro- and macrovascular complications e.g. diabetic nephropathy, or coronary heart disease (CHD).

The term "HbAIc" refers to the product of a non-enzymatic glycation of the haemoglobin B chain. Its determination is well known to one skilled in the art. In monitoring the treatment of diabetes mellitus the HbAIc value is of exceptional importance. As its production depends essentially on the blood sugar level and the life of the erythrocytes, the HbAIc in the sense of a "blood sugar memory" reflects the average blood sugar levels of the preceding 4-6 weeks. Diabetic patients whose HbAIc value is consistently well adjusted by intensive diabetes treatment (i.e. < 6.5 % of the total haemoglobin in the sample), are significantly better protected against diabetic microangiopathy. For example metformin on its own achieves an average improvement in the HbA1 c value in the diabetic of the order of 1.0 - 1.5 %. This reduction of the HbA1 c value is not sufficient in all diabetics to achieve the desired target range of < 6.5 % and preferably < 6 % HbAIc. The "metabolic syndrome", also called "syndrome X" (when used in the context of a metabolic disorder), also called the "dysmetabolic syndrome" is a syndrome complex with the cardinal feature being insulin resistance (Laaksonen DE, et al. Am J Epidemiol 2002;156:1070-7). According to the ATP III/NCEP guidelines (Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on

Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) JAMA: Journal of the American Medical Association (2001 ) 285:2486-2497), diagnosis of the metabolic syndrome is made when three or more of the following risk factors are present: 1. Abdominal obesity, defined as waist circumference > 40 inches or 102 cm in men, and > 35 inches or 94 cm in women; or with regard to a Japanese ethnicity or

Japanese patients defined as waist circumference ≥ 85 cm in men and ≥ 90 cm in women;

2. Triglycerides: ≥ 150 mg/dL 3. HDL-cholesterol < 40 mg/dL in men

4. Blood pressure ≥ 130/85 mm Hg (SBP ≥ 130 or DBP ≥ 85)

5. Fasting blood glucose ≥ 110 mg/dL

The NCEP definitions have been validated (Laaksonen DE, et al. Am J Epidemiol. (2002) 156:1070-7). Triglycerides and HDL cholesterol in the blood can also be determined by standard methods in medical analysis and are described for example in Thomas L (Editor): "Labor und Diagnose", TH-Books Verlagsgesellschaft mbH, Frankfurt/Main, 2000.

According to a commonly used definition hypertension is diagnosed if the systolic blood pressure (SBP) exceeds a value of 140 mm Hg and diastolic blood pressure (DBP) exceeds a value of 90 mm Hg. If a patient is suffering from manifest diabetes it is currently recommended that the systolic blood pressure be reduced to a level below 130 mm Hg and the diastolic blood pressure be lowered to below 80 mm Hg.

The terms "treatment" and "treating" comprise therapeutic treatment of patients having already developed said condition, in particular in manifest form. Therapeutic treatment may be symptomatic treatment in order to relieve the symptoms of the specific indication or causal treatment in order to reverse or partially reverse the conditions of the indication or to stop or slow down progression of the disease. Thus the compositions and methods of the present invention may be used for instance as therapeutic treatment over a period of time as well as for chronic therapy. The terms "prophylactically treating", "preventivally treating" and "preventing" are used interchangeably and comprise a treatment of patients at risk to develop a condition mentioned hereinbefore, thus reducing said risk.

Detailed Description

The aspects according to the present invention, in particular the pharmaceutical compositions, methods and uses, refer to pyrazole-O-glucoside derivatives of the formula (I) as defined hereinbefore and hereinafter.

The substituent R¹ preferably denotes methoxy, ethoxy, n-propoxy or i-propoxy.

Preferably L¹ denotes F and L² denotes H or both L¹ and L² denote H or both L¹ and L² denote F.

Preferably R⁶ is selected from among H, (Ci_-3-alkyl)carbonyl, (Ci_-6-alkyl)oxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl and benzylcarbonyl, in particular H, (Ci_-3- alkyl)carbonyl or (Ci_₄-alkyl)oxycarbonyl. Even more preferably R⁶ is selected from among H, acetyl, methoxycarbonyl and ethoxycarbonyl, in particular H or ethoxycarbonyl. Most preferably R⁶ denotes H.

Preferred pyrazole-O-glucoside derivatives are selected from the group of compounds (1 ) to (14):

(1 ) 4-(2,3-difluoro-4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(2) 4-(2,5-difluoro-4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(3) 4-(2,6-difluoro-4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(4) 4-(3,5-difluoro-4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(5) 4-(3-fluoro-4-ethoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 -yloxy- 1 H-pyrazole;

(6) 4-(3-fluoro-4-isopropoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(7) 4-(2-fluoro-4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(8) 4-(2-fluoro-4-isopropoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole;

(9) 4-(2-fluoro-4-ethoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 -yloxy- 1 H-pyrazole;

(10) 4-(2,3-difluoro-4-isopropoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos- 1 -yloxy-1 H-pyrazole;

(1 1 ) 4-(3-fluoro-4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 - yloxy-1 H-pyrazole.

(12) 4-(4-methoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 -yloxy-1 H- pyrazole;

(13) 4-(4-ethoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 -yloxy-1 H- pyrazole;

(14) 4-(4-isopropoxy-benzyl)-1 -isopropyl-5-methyl-3-β-D-glucopyranos-1 -yloxy-1 H- pyrazole;

and those derivatives of the compounds (1 ) to (14) wherein the H-atom (corresponding to the substituent R⁶) of the HO-group linked to the carbon atom at the 6^th position of the β-D- glucopyranosyl group is replaced by a substituent selected from among (d_-3-alkyl)carbonyl and (Ci_₄-alkyl)oxycarbonyl, even more preferably acetyl, methoxycarbonyl or ethoxycarbonyl, in particular ethoxycarbonyl. A more preferred pyrazole-O-glucoside derivative is the compound (7).

According to this invention it is to be understood that the definitions of the above listed pyrazole-O-glucoside derivatives also comprise their hydrates, solvates and polymorphic forms thereof. With regard to the preferred compound (7) an advantageous crystalline form is described in the international patent applciation WO 2007/080170 which hereby is incorporated herein in its entirety. The crystalline form possesses good solubility properties which enables a good bioavailability of the SGLT2 inhibitor. Furthermore the crystalline form is physico-chemically stable and thus provides a good shelf-life stability.

The aspects according to the present invention, in particular the pharmaceutical compositions, methods and uses, refer to a DPP IV inhibitor as defined hereinbefore and hereinafter, or prodrugs thereof, or pharmaceutically acceptable salts thereof.

Preferred DPP IV inhibitors are selected from the group consisting of sitagliptin, vildagliptin, saxagliptin and alogliptin.

According to this invention it is to be understood that the definitions of the above listed DPP IV inhibitors also comprise their pharmaceutically acceptable salts as well as hydrates, solvates and polymorphic forms thereof. With respect to salts, hydrates and polymorphic forms thereof, particular reference is made to those which are referred to above in paragraph "background of the invention".

The pharmaceutical compositions, methods and uses according to this invention most preferably relate to combinations which are selected from the Table 1.

Table 1

Preferred combinations are described by the No. 25, 26, 27 and 28 of the Table 1.

The combination of a pyrazole-O-glucoside derivative and a DPP IV inhibitor according to this invention significantly improves the glycemic control, in particular in patients as described hereinafter, compared with a monotherapy using either the pyrazole-O-glucoside derivative or the DPP IV inhibitor. The improved glycemic control is determined as an increased lowering of blood glucose and an increased reduction of HbAIc. With monotherapy in a patient, in particular in patients as described hereinafter, the glycemic control can usually not be further improved significantly by an administration of the drug above a certain highest dose. In addition a long term treatment using a highest dose may be unwanted in view of potential side effects. Therefore a full glycemic control cannot be achieved in all patients via a monotherapy using either the pyrazole-O-glucoside derivative or the DPP IV inhibitor. In such patients a progression of the diabetes mellitus may continue and complications associated with diabetes mellitus may occur, such as macrovascular complications. The pharmaceutical composition as well as the methods according to the present invention allow a reduction of the HbAI C value to a desired target range, for example < 7 % and preferably < 6.5 %, for a higher number of patients compared with a corresponding monotherapy.

In addition the combination of a pyrazole-O-glucoside derivative and a DPP IV inhibitor according to this invention allows a reduction in the dose of either the pyrazole-O-glucoside derivative or the DPP IV inhibitor or of both active ingredients. A dose reduction is beneficial for patients which otherwise would potentially suffer from side effects in a monotherapy using a higher dose of either the pyrazole-O-glucoside derivative or the DPP IV inhibitor. Therefore the pharmaceutical composition as well as the methods according to the present invention show less side effects, thereby making the therapy more tolerable and improving the patients compliance with the treatment.

A monotherapy using a DPP IV inhibitor according to the present invention is not independent from the insulin secretory capacity or the insulin sensitivity of a patient. On the other hand a treatment with the administration of a pyrazole-O-glucoside derivative according the present invention does not depend on the insulin secretory capacity or the insulin sensitivity of the patient. Therefore any patient independent of the prevailing insulin levels or insulin resistance and/or hyperinsulinemia may benefit from a therapy using a combination of a pyrazole-O-glucoside derivative and a DPP IV inhibitor according to this invention. Independent of their prevailing insulin levels or their insulin resistance or hyperinsulinemia these patients can still be treated with the DPP IV inhibitor because of the combined or alternate administration of the pyrazole-O-glucoside derivative.

A DPP IV inhibitor according to the present invention is able - via the increases in active GLP-1 levels - to reduce the glucagon secretion in a patient. This will therefore limit the hepatic glucose production. Furthermore, the elevated active GLP-1 levels produced by the

DPP IV inhibitor will have beneficial effects on beta-cell regeneration and neogenesis. All these features of DPP IV inhibitors render a combination with SGLT 2 inhibitors quite useful and therapeutically relevant.

When this invention refers to patients requiring treatment or prevention, it relates primarily to treatment and prevention in humans, but the pharmaceutical composition may also be used accordingly in veterinary medicine on mammals.

As described hereinbefore by the administration of the pharmaceutical composition according to this invention and in particular in view of the high SGLT2 inhibitory activity of the pyrazole-O-glucoside derivative therein, excessive blood glucose is excreted through the urine of the patient, so that no gain in weight or even a reduction in body weight may result. Therefore a treatment or prophylaxis according to this invention is advantageously suitable in those patients in need of such treatment or prophylaxis who are diagnosed of one or more of the conditions selected from the group consisting of overweight, class I obesity, class Il obesity, class III obesity, visceral obesity and abdominal obesity or for those individuals in which a weight increase is contraindicated.

The pharmaceutical composition according to this invention and in particular the pyrazole-O- glucoside derivative therein exhibits a very good efficacy with regard to glycemic control, in particular in view of a reduction of fasting plasma glucose, postprandial plasma glucose and/or glycosylated hemoglobin (HbAI c). By administering a pharmaceutical composition according to this invention, a reduction of HbAIc equal to or greater than preferably 0.5 %, even more preferably equal to or greater than 1.0 % can be achieved and the reduction is particularly in the range from 1.0 % to 1.5 %.

Furthermore the method and/or use according to this invention is advantageously applicable in those patients who show one, two or more of the following conditions: (a) a fasting blood glucose or serum glucose concentration greater than 1 10 mg/dL, in particular greater than 125 mg/dL; (b) a postprandial plasma glucose equal to or greater than 140 mg/dL;

(c) an HbA1 c value equal to or greater than 6.5 %, in particular equal to or greater than 8.0 %.

The present invention also discloses the use of the pharmaceutical composition for improving glycemic control in patients having type 2 diabetes or showing first signs of prediabetes. Thus, the invention also includes diabetes prevention. If therefore a pharmaceutical composition according to this invention is used to improve the glycemic control as soon as one of the above-mentioned signs of pre-diabetes is present, the onset of manifest type 2 diabetes mellitus can be delayed or prevented.

Furthermore the pharmaceutical composition according to this invention is particularly suitable in the treatment of patients with insulin dependency, i.e. in patients who are treated or otherwise would be treated or need treatment with an insulin or a derivative of insulin or a substitute of insulin or a formulation comprising an insulin or a derivative or substitute thereof. These patients include patients with diabetes type 2 and patients with diabetes type 1.

It can be found that by using a pharmaceutical composition according to this invention an improvement of the glycemic control can be achieved even in those patients who have insufficient glycemic control in particular despite treatment with an antidiabetic drug, for example despite maximal tolerated dose of oral monotherapy with either metformin or a SGLT2 inhibitor, in particular a SGLT2 inhibitor according to this invention, or a DPP IV inhibitor, in particular a DPP IV inhibitor according to this invention. A maximal tolerated dose with regard to metformin is for example 850 mg three times a day or any equivalent thereof. A maximal tolerated dose with regard to a SGLT2 inhibitor according to this invention, in particular the compound (7), is for example 400 mg twice a day or any equivalent thereof. A maximal tolerated dose with regard to a DPP IV inhibitor according to this invention is for example Sitagliptin 100 mg once daily or any equivalent thereof. In the scope of the present invention the term "insufficient glycemic control" means a condition wherein patients show HbAI c values above 6.5 %, in particular above 8 %.

Therefore according to a preferred embodiment of the present invention there is provided a method for improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAIc in a patient in need thereof who is diagnosed with impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG) with insulin resistance, with metabolic syndrome and/or with type 2 or type 1 diabetes mellitus characterized in that a pyrazole-O-glucoside derivative as defined hereinbefore and hereinafter is administered in combination or alternation with a DPP IV inhibitor as defined hereinbefore and hereinafter.

The lowering of the blood glucose level by the administration of a pyrazole-O-glucoside derivative according to this invention is insulin-independent. Therefore a pharmaceutical composition according to this invention is particularly suitable in the treatment of patients who are diagnosed having one or more of the following conditions insulin resistance, hyperinsulinemia, pre-diabetes, type 2 diabetes mellitus, particular having a late stage type 2 diabetes mellitus, - type 1 diabetes mellitus.

Furthermore a pharmaceutical composition according to this invention is particularly suitable in the treatment of patients who are diagnosed having one or more of the following conditions (a) obesity (including class I, Il and/or III obesity), visceral obesity and/or abdominal obesity, (b) triglyceride blood level ≥ 150 mg/d L,

(c) HDL-cholesterol blood level < 40 mg/dL in female patients and < 50 mg/dL in male patients,

(d) a systolic blood pressure ≥ 130 mm Hg and a diastolic blood pressure ≥ 85 mm Hg,

(e) a fasting blood glucose level ≥ 1 10 mg/dL.

It is assumed that patients diagnosed with impaired glucose tolerance (IGT), impaired fasting blood glucose (IFG), with insulin resistance and/or with metabolic syndrome suffer from an increased risk of developing a cardiovascular disease, such as for example myocardial infarction, coronary heart disease, heart insufficiency, thromboembolic events. A glycemic control according to this invention may result in a reduction of the cardiovascular risks.

A pharmaceutical composition according to this invention, in particular due to the pyrazole-O- glucoside therein, exhibits a good safety profile. Therefore a treatment or prophylaxis according to this invention is advantageously possible in those patients for which the mono- therapy with another antidiabetic drug, such as for example metformin, is contraindicated and/or who have an intolerance against such drugs at therapeutic doses. In particular a treatment or prophylaxis according to this invention may be advantageously possible in those patients showing or having an increased risk for one or more of the following disorders: renal insufficiency or diseases, cardiac diseases, cardiac failure, hepatic diseases, pulmonal diseases, catabolytic states and/or danger of lactate acidosis, or female patients being pregnant or during lactation.

Furthermore it can be found that the administration of a pharmaceutical composition according to this invention results in no risk or in a low risk of hypoglycemia. Therefore a treatment or prophylaxis according to this invention is also advantageously possible in those patients showing or having an increased risk for hypoglycemia. A pharmaceutical composition according to this invention is particularly suitable in the long term treatment or prophylaxis of the diseases and/or conditions as described hereinbefore and hereinafter, in particular in the long term glycemic control in patients with type 2 diabetes mellitus.

The term "long term" as used hereinbefore and hereinafter indicates a treatment of or administration in a patient within a period of time longer than 12 weeks, preferably longer than 25 weeks, even more preferably longer than 1 year.

Therefore a particularly preferred embodiment of the present invention provides a method for therapy, preferably oral therapy, for improvement, especially long term improvement, of glycemic control in patients with type 2 diabetes mellitus, especially in patients with late stage type 2 diabetes mellitus, in particular in patients additionally diagnosed of overweight, obesity (including class I, class Il and/or class III obesity), visceral obesity and/or abdominal obesity.

The effects mentioned above are observed both when the pyrazole-O-glucoside derivative and the DPP IV inhibitor are administered in combination, for example simultaneously, and when they are administered in alternation, for example successively in separate formulations.

It will be appreciated that the amount of the pharmaceutical composition according to this invention to be administered to the patient and required for use in treatment or prophylaxis according to the present invention will vary with the route of administration, the nature and severity of the condition for which treatment or prophylaxis is required, the age, weight and condition of the patient, concomitant medication and will be ultimately at the discretion of the attendant physician. In general however the pyrazole-O-glucoside derivative according to this invention and the DPP IV inhibitor are included in the pharmaceutical composition or dosage form in an amount sufficient that by their administration in combination or alternation the glycemic control in the patient to be treated is improved.

In the following preferred ranges of the amount of pyrazole-O-glucoside derivative and of the DPP IV inhibitor to be employed in the pharmaceutical composition and the methods and uses according to this invention are described. These ranges refer to the amounts to be administered per day with respect to an adult patient and can be adapted accordingly with regard to an administration 2, 3, 4 or more times daily and with regard to other routes of administration and with regard to the age of the patient. Within the scope of the present invention the pharmaceutical composition is preferably administered orally. Other forms of administration are possible and described hereinafter. Preferably the dosage form comprising the pyrazole-O-glucoside is administered orally. The route of administration of the DPP IV inhibitor is oral or usually well known.

In general the amount of the pyrazol-O-glucoside derivative in the pharmaceutical composition and methods according to this invention is preferably in the range from 1/5 to 1/1 of the amount usually recommended for a monotherapy using said pyrazole-O-glucoside derivative. Advantageously, the combination therapy according to the present invention utilizes lower dosages of the individual pyrazole-O-glucoside derivative or of the individual DPP IV inhibitor used in monotherapy or used in conventional therapeutics, thus avoiding possible toxicity and adverse side effects incurred when those agents are used as monotherapies.

The amount of the pyrazole-O-glucoside is preferably in the range from 50 mg to 1200 mg, even more preferably from 100 to 1000 mg, most preferably from 200 to 800 mg per day for a human being, for example for approximately 70 kg body weight. The oral administration is preferred. Therefore a pharmaceutical composition may comprise the hereinbefore mentioned amounts for once daily administration and from 25 mg to 600 mg, even more preferably from 50 to 500 mg, most preferably from 100 to 400 mg for twice daily administration. Particular dosage strengths (e.g. for tablet or capsule) are for example 200, 300, 400 or 500 mg of the compound (7) given twice daily or 400 or 500 mg once daily.

In general the amount of the DPP IV inhibitor in the pharmaceutical composition and methods according to this invention is preferably in the range from 1/5 to 1/1 of the amount usually recommended for a monotherapy using said DPP IV inhibitor.

The doses of DPP IV inhibitors to be administered to mammals, for example human beings, of, for example, approximately 70 kg body weight, may be generally from about 0.5 mg to about 350 mg, for example from about 10 mg to about 250 mg, preferably 20-200 mg, more preferably 20-100 mg, of the active moiety per person per day, or from about 0.5 mg to about 20 mg, preferably 2.5-10 mg, per person per day, divided preferably into 1 to 4 single doses which may, for example, be of the same size. Single dosage strengths comprise, for example, 10, 25, 40, 50, 75, 100, 150 and 200 mg of the DPP IV inhibitor active moiety.

A dosage strength of the DPP IV inhibitor sitagliptin is usually between 25 and 200 mg of the active moiety. A recommended dose of sitagliptin is 100 mg calculated for the active moiety (free base anhydrate) once daily. Unit dosage strengths of sitagliptin free base anhydrate (active moiety) are 25, 50, 75, 100, 150 and 200 mg. Particular unit dosage strengths of sitagliptin (e.g. per tablet) are 25, 50 and 100 mg. An equivalent amount of sitagliptin phosphate monohydrate to the sitagliptin free base anhydrate is used in the pharmaceutical compositions, namely, 32.13, 64.25, 96.38, 128.5, 192.75, and 257 mg, respectively. Adjusted dosages of 25 and 50 mg sitagliptin are used for patients with renal failure.

A dosage range of the DPP IV inhibitor vildagliptin is usually between 10 and 150 mg daily, in particular between 25 and 150 mg, 25 and 100 mg or 25 and 50 mg or 50 and 100 mg daily. Particular examples of daily oral dosage are 25, 30, 35, 45, 50, 55, 60, 80, 100 or 150 mg. In a more particular aspect, the daily administration of vildagliptin is between 25 and 150 mg or between 50 and 100 mg. In another more particular aspect, the daily administration of vildagliptin is 50 or 100 mg. The application of the active ingredient may occur up to three times a day, preferably one or two times a day. Particular dosage forms (e.g. tablets) comprise 50 mg or 100 mg vildagliptin.

Alogliptin may be administered to a patient at a daily dose of between 5 mg/day and 250 mg/day, optionally between 10 mg and 200 mg, optionally between 10 mg and 150 mg, and optionally between 10 mg and 100 mg of alogliptin (in each instance based on the molecular weight of the free base form of alogliptin). Thus, specific dosage amounts that may be used include, but are not limited to 10 mg, 12.5 mg, 20 mg, 25 mg, 50 mg, 75 mg and 100 mg of alogliptin per day. Alogliptin may be administered in its free base form or as a pharmaceutically acceptable salt.

Saxagliptin may be administered to a patient at a daily dose of between 2.5 mg/day and 100 mg/day, optionally between 2.5 mg and 50 mg. Specific dosage amounts that may be used include, but are not limited to 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 30 mg , 40 mg, 50 mg and 100 mg of saxagliptin per day.

The amount of the pyrazole-O-glucoside and of the DPP IV inhibitor in the pharmaceutical composition according to this invention correspond to the respective dosage ranges as provided hereinbefore. For example a pharmaceutical composition comprises an amount of 100 to 400 mg of the compound (7) and of sitagliptin in an amount of 1 to 100 mg (active moiety). According to another example a pharmaceutical composition comprises an amount of 100 to 400 mg of the compound (7) and of vildagliptin in an amount of 1 to 100 mg (active moiety). According to another example a pharmaceutical composition comprises an amount of 100 to 400 mg of the compound (7) and of alogliptin in an amount of 1 to 100 mg (active moiety). According to another example a pharmaceutical composition comprises an amount of 100 to 400 mg of the compound (7) and of saxagliptin in an amount of 1 to 100 mg (active moiety).

In the methods and uses according to the present invention the pyrazole-O-glucoside derivative and the DPP IV inhibitor are administered in combination or alternation. The term "administration in combination" means that both active ingredients are administered at the same time, i.e. simultaneously, or essentially at the same time. The term "administration in alternation" means that at first a first active ingredient is administered and after a period of time the second active ingredient is administered, i.e. both active ingredients are administered sequentially. The period of time may be in the range from 30 min to 12 hours. The administration which is in combination or in alternation may be once, twice, three times or four times daily.

With regard to the administration of the pyrazole-O-glucoside derivative in combination with the DPP IV inhibitor both active ingredients may be present in a single dosage form, for example in a tablet or capsule, or each active ingredient may be present in a separate dosage form, for example in two different or identical dosage forms.

With regard to their administration in alternation each of the active ingredients is present in a separate dosage form, for example in two different or identical dosage forms.

Therefore the pharmaceutical composition according to this invention may be present as single dosage forms which comprise both the pyrazole-O-glucoside derivative and the DPP IV inhibitor as well as separate dosage forms wherein one dosage form comprises the pyrazole-O-glucoside derivative and the other dosage form comprises the DPP IV inhibitor.

The case may arise in which one active ingredient has to be administered more often, for example twice per day, than the other active ingredient, which for example needs administration once daily. Therefore the term "administration in combination or alternation" also includes an administration scheme in which first both active ingredients are administered in combination or alternation and after a period of time only one active ingredient is administered again or vice versa.

Therefore the present invention also includes pharmaceutical compositions which are present a separate dosage forms wherein one dosage form comprises the pyrazole-O- glucoside derivative and the DPP IV inhibitor and the other dosage form comprises either the pyrazole-O-glucoside derivative or the DPP IV inhibitor.

A pharmaceutical composition which is present as a separate or multiple dosage form, preferably as a kit of parts, is useful in combination therapy to flexibly suit the individual therapeutic needs of the patient.

A preferred kit of parts comprises

(a) a first containment containing a dosage form comprising the pyrazole-O-gluoside and at least one pharmaceutically acceptable carrier, and

(b) a second containment containing a dosage form comprising the DPP IV inhibitor and at least one pharmaceutically acceptable carrier.

A further aspect of the present invention is a manufacture comprising the pharmaceutical composition being present as separate dosage forms according to the present invention and a label or package insert comprising instructions that the separate dosage forms are to be administered in combination or alternation.

A yet further aspect of the present invention is a manufacture comprising a medicament which comprises a pyrazole-O-glucoside derivative according to the present invention and a label or package insert which comprises instructions that the medicament may or is to be administered in combination or alternation with a medicament comprising a DPP IV inhibitor according to the present invention.

Another further aspect of the present invention is a manufacture comprising a medicament which comprises a DPP IV inhibitor according to the present invention and a label or package insert which comprises instructions that the medicament may or is to be administered in combination or alternation with a medicament comprising a pyrazole-O- glucoside derivative according to the present invention.

The desired dose of the pharmaceutical composition according to this invention may conveniently be presented in a once daily or as divided dose administered at appropriate intervals, for example as two, three or more doses per day.

The pharmaceutical composition may be formulated for oral, rectal, nasal, topical (including buccal and sublingual), transdermal, vaginal or parenteral (including intramuscular, subcutaneous and intravenous) administration in liquid or solid form or in a form suitable for administration by inhalation or insufflation. Oral administration is preferred. The formulations may, where appropriate, be conveniently presented in discrete dosage units and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing into association the active ingredient with one or more pharmaceutically acceptable carriers, like liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product into the desired formulation.

The pharmaceutical composition may be formulated in the form of tablets, granules, fine granules, powders, capsules, caplets, soft capsules, pills, oral solutions, syrups, dry syrups, chewable tablets, troches, effervescent tablets, drops, suspension, fast dissolving tablets, oral fast-dispersing tablets, etc..

The pharmaceutical composition and the dosage forms preferably comprises one or more pharmaceutical acceptable carriers which must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.

Pharmaceutical compositions suitable for oral administration may conveniently be presented as discrete units such as capsules, including soft gelatin capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution, a suspension or as an emulsion, for example as syrups, elixirs or self-emulsifying delivery systems (SEDDS). The active ingredients may also be presented as a bolus, electuary or paste. Tablets and capsules for oral administration may contain conventional excipients such as binding agents, fillers, lubricants, disintegrants, or wetting agents. The tablets may be coated according to methods well known in the art. Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, emulsifying agents, non-aqueous vehicles (which may include edible oils), or preservatives.

The pharmaceutical composition according to the invention may also be formulated for parenteral administration (e.g. by injection, for example bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre-filled syringes, small volume infusion or in multi-dose containers with an added preservative. The compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredients may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilisation from solution, for constitution with a suitable vehicle, e.g. sterile, pyrogen-free water, before use.

Pharmaceutical compositions suitable for rectal administration wherein the carrier is a solid are most preferably presented as unit dose suppositories. Suitable carriers include cocoa butter and other materials commonly used in the art, and the suppositories may be conveniently formed by admixture of the active compound(s) with the softened or melted carrier(s) followed by chilling and shaping in moulds.

The pharmaceutical compositions and methods according to this invention show advantageous effects in the treatment and prevention of those diseases and conditions as described hereinbefore compared with pharmaceutical compositions and methods which comprise only one of both active ingredients. Advantageous effects may be seen for example with respect to efficacy, dosage strength, dosage frequency, pharmacodynamic properties, pharmacokinetic properties, fewer adverse effects, etc..

Examples of pharmaceutically acceptable carriers are known to the one skilled in the art.

Methods for the manufacture of pyrazole-O-glucoside derivatives according to this invention and of prodrugs thereof are known to the one skilled in the art. Advantageously the compounds according to this invention can be prepared using synthetic methods as described in the literature, in particular as described in the EP 1 338 603 A1 , EP 1 389 621 A1 , WO 03/020737, WO 04/014932, WO 04/018491 , WO 04/019958, WO 04/031203, WO 04/050122 and WO 2007/014895. Advantageously the compound (7) is prepared as described in the EP 1 338 603 A1 (see example 11 ) or WO 2007/010015 (see example 37) or WO 2007/080170.

The methods of synthesis for the DPP IV inhibitors are described in the scientific literature and/ or in published patent documents, particularly in those cited above in paragraph "background of the invention".

The DPP IV inhibitor may be present in the form of a pharmaceutically acceptable salt. Pharmaceutically acceptable salts include, without being restricted thereto, such as salts of inorganic acid like hydrochloric acid, sulfuric acid and phosphoric acid; salts of organic carboxylic acid like oxalic acid, acetic acid, citric acid, malic acid, benzoic acid, maleic acid, fumaric acid, tartaric acid, succinic acid and glutamic acid and salts of organic sulfonic acid like methanesulfonic acid and p-toluenesulfonic acid. The salts can be formed by combining the compound and an acid in the appropriate amount and ratio in a solvent and decomposer. They can be also obtained by the cation or anion exchange from the form of other salts.

The pyrazole-O-glucoside derivative and/or the DPP IV inhibitor or a pharmaceutically acceptable salt thereof may be present in the form of a solvate such as a hydrate or alcohol adduct.

Any of the above mentioned combinations and methods within the scope of the invention may be tested by animal models known in the art. In the following in vivo experiments are described which are suitable to evaluate pharmacologically relevant properties of pharmaceutical compositions and methods according to this invention:

Pharmaceutical compositions and methods according to this invention can be tested in genetically hyperinsulinemic or diabetic animals like db/db mice, ob/ob mice, Zucker Fatty (fa/fa) rats or Zucker Diabetic Fatty (ZDF) rats. In addition, they can be tested in animals with experimentally induced diabetes like HanWistar or Sprague Dawley rats pretreated with streptozotocin.

The effect on glycemic control of the combinations according to this invention can be tested after single dosing of a pyrazole-O-glucoside derivative and a DPP IV inhibitor alone and in combination in an oral glucose tolerance test in the animal models described hereinbefore. The time course of blood glucose is followed after on oral glucose challenge in overnight fasted animals. The combinations according to the present invention significantly improve glucose excursion compared to each monotherapy as measured by reduction of peak glucose concentrations or reduction of glucose AUC. In addition, after multiple dosing of a pyrazole-O-glucoside derivative and a DPP IV inhibitor alone and in combination in the animal models described hereinbefore, the effect on glycemic control can be determined by measuring the HbAIc value in blood. The combinations according to this invention significantly reduce HbAI c compared to each monotherapy.

The possible dose reduction of either the pyrazole-O-glucoside derivative or the DPP-IV inhibitor or of both active ingredients can be tested by the effect on glycemic control of lower doses of the combinations and monotherapies in the animal models described hereinbefore. The combinations according to this invention at the lower doses significantly improve glycemic control compared to placebo treatment whereas the monotherapies at lower doses do not.

The improved independence from insulin of the treatment according to this invention can be shown after single dosing in oral glucose tolerance tests in the animal models described hereinbefore. The time course of plasma insulin is followed after a glucose challenge in overnight fasted animals. The pyrazole-O-glucoside derivative in combination with the DPP IV inhibitor will exhibit lower insulin peak concentrations or insulin AUC at lower blood glucose excursion than the DPP IV inhibitor alone.

The increase in active GLP-1 levels by treatment according to this invention after single or multiple dosing can be determined by measuring those levels in the plasma of animal models described hereinbefore in either the fasting or postprandial state. Likewise, a reduction in glucagon levels in plasma can be measured under the same conditions. The pyrazole-O- glucoside derivative in combination with the DPP IV inhibitor will exhibit higher active GLP-1 concentrations and lower glucagon concentrations than the pyrazole-O-glucoside derivative alone.

A superior effect of the combination of a pyrazole-O-glucoside derivative and a DPP IV inhibitor according to the present invention than of the pyrazole-O-glucoside derivative alone on beta-cell regeneration and neogenesis can be determined after multiple dosing in the animal models described hereinbefore by measuring the increase in pancreatic insulin content, or by measuring increased beta-cell mass by morphometric analysis after immunhistochemical staining of pancreatic sections, or by measuring increased glucose- stimulated insulin secretion in isolated pancreatic islets.

The Examples that follow are intended to illustrate the present invention without restricting it.

Examples of Formulations

The following examples of formulations, which may be obtained analogously to methods known in the art, serve to illustrate the present invention more fully without restricting it to the contents of these examples. The term "active substance" denotes one or more compounds according to the invention, i.e. denotes a pyrazole-O-glucoside derivative according to this invention or a DPP IV inhibitor according to this invention or a combination of said pyrazole- O-glucoside derivative with said DPP IV inhibitor, for example selected from the combinations 1 to 56 as listed in Table 1. Additional suitable formulations for the DPP IV inhibitor may be those formulations which are available on the market, or formulations described in the patent applications cited above in paragraph "background of the invention", or those described in the in the literature, for example as disclosed in current issues of "Rote Liste^®" (Editio Cantor Verlag Aulendorf, Germany) or of "Physician's Desk Reference".

Example 1 : Dry ampoule containing 75 mg of active substance per 10 ml Composition:

Active substance 75.0 mg

Mannitol 50.0 mg water for injections ad 10.0 ml

Preparation:

Active substance and mannitol are dissolved in water. After packaging the solution is freeze- dried. To produce the solution ready for use, the product is dissolved in water for injections.

Example 2: Dry ampoule containing 35 mg of active substance per 2 ml

Composition:

Active substance 35.0 mg

Mannitol 100.0 mg water for injections ad 2.0 ml

Preparation:

Active substance and mannitol are dissolved in water. After packaging, the solution is freeze- dried.

To produce the solution ready for use, the product is dissolved in water for injections.

Example 3: Tablet containing 50 mg of active substance Composition:

(1 ) Active substance 50.0 mg (2) Lactose 98.0 mg

(3) Maize starch 50.0 mg

(4) Polyvinylpyrrolidone 15.0 mg

(5) Magnesium stearate 2.0 mg

215.0 mg

Preparation: (1 ), (2) and (3) are mixed together and granulated with an aqueous solution of (4). (5) is added to the dried granulated material. From this mixture tablets are pressed, biplanar, faceted on both sides and with a dividing notch on one side. Diameter of the tablets: 9 mm.

Example 4: Tablet containing 350 mg of active substance

Preparation:

(1 ) Active substance 350.0 mg

(2) Lactose 136.0 mg

(3) Maize starch 80.0 mg

(4) Polyvinylpyrrolidone 30.0 mg

(5) Magnesium stearate 4.0 mq

600.0 mg

(1 ), (2) and (3) are mixed together and granulated with an aqueous solution of (4). (5) is added to the dried granulated material. From this mixture tablets are pressed, biplanar, faceted on both sides and with a dividing notch on one side. Diameter of the tablets: 12 mm.

Example 5: Capsules containing 50 mg of active substance Composition:

(1 ) Active substance

(2) Dried maize starch

(3) Powdered lactose (4) Magnesium stearate

Preparation:

(1 ) is triturated with (3). This trituration is added to the mixture of (2) and (4) with vigorous mixing. This powder mixture is packed into size 3 hard gelatin capsules in a capsule filling machine.

Example 6: Capsules containing 350 mg of active substance Composition: (1 ) Active substance 350.0 mg

(2) Dried maize starch 46.0 mg

(3) Powdered lactose 30.0 mg (4) Magnesium stearate 4.0 mg

430.0 mg Preparation:

(1 ) is triturated with (3). This trituration is added to the mixture of (2) and (4) with vigorous mixing. This powder mixture is packed into size 0 hard gelatin capsules in a capsule filling machine.

Claims

Patent Claims:

1. A pharmaceutical composition comprising a pyrazole-O-glucoside derivative of the formula (I)

wherein

R¹ denotes Ci_-3-alkoxy;

L¹, L² independently of each other denote H or F;

R⁶ denotes H, (Ci_-3-alkyl)carbonyl, (Ci_-6-alkyl)oxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl or benzylcarbonyl;

in combination with a DPP IV inhibitor selected from the group consisting of sitagliptin, vildagliptin, saxagliptin, alogliptin, denagliptin,

(2S)-1-{[2-(5-Methyl-2-phenyl-oxazol-4-yl)-ethylamino]-acetyl}-pyrrolidine-2- carbonitrile,

(2S)-1-{[1 ,1 ,-Dimethyl-3-(4-pyridin-3-yl-imidazol-1-yl)-propylamino]-acetyl}-pyrrolidine-

2-carbonitrile,

(1 ((3S,4S)-4-amino-1 -(4-(3,3-difluoropyrrolidin-1 -yl)-1 ,3,5-triazin-2-yl)pyrrolidin-3-yl)-

5,5-difluoropiperidin-2-one,

(2S,4S)-1-{2-[(3S_!1 R)-3-(1 H-1 _!2,4-Triazol-1-ylmethyl)cyclopentylamino]-acetyl}-4- fluoropyrrolidine-2-carbonitrile, and

(R)-2-[6-(3-Amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1- ylmethyl]-4-fluoro-benzonitrile, or its pharmaceutically acceptable salt thereof. The pharmaceutical composition according to claim 1 wherein the pyrazole-O- glucoside derivative is selected from the group of compounds (1 ) to (14):

and those derivatives of the compounds (1 ) to (14) wherein the H-atom of the HO- group linked to the carbon atom at the 6^th position of the β-D-glucopyranosyl group is replaced by a substituent selected from among (d_-3-alkyl)carbonyl and (Ci_-4- alkyl)oxycarbonyl.

3. The pharmaceutical composition according to claim 1 or 2 wherein the DPP IV inhibitor is selected from the group consisting of sitagliptin, vildagliptin, saxagliptin and alogliptin, or its pharmaceutically acceptable salt thereof.

4. The pharmaceutical composition according to one of the previous claims characterized in that the composition is suitable for combined or simultaneous or sequential use of the pyrazole-O-glucoside derivative and the DPP IV inhibitor.

5. The pharmaceutical composition according to one of the previous claims characterized in that the pyrazole-O-glucoside derivative and the DPP IV inhibitor are present in a single dosage form.

6. The pharmaceutical composition according to one of the previous claims characterized in that the pyrazole-O-glucoside derivative and the DPP IV inhibitor are present each in a separate dosage form.

7. Method for preventing, slowing the progression of, delaying or treating a metabolic disorder selected from the group consisting of type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance, impaired fasting blood glucose, hyperglycemia, postprandial hyperglycemia, overweight, obesity and metabolic syndrome in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

8. Method for improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAI c in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

9. Method for preventing, slowing, delaying or reversing progression from impaired glucose tolerance, impaired fasting blood glucose, insulin resistance and/or from metabolic syndrome to type 2 diabetes mellitus in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

10. Method for preventing, slowing the progression of, delaying or treating of a condition or disorder selected from the group consisting of complications of diabetes mellitus such as cataracts and micro- and macrovascular diseases, such as nephropathy, retinopathy, neuropathy, tissue ischaemia, arteriosclerosis, myocardial infarction, stroke and peripheral arterial occlusive disease, in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

1 1. Method for reducing body weight or preventing an increase in body weight or facilitating a reduction in body weight in a patient in need thereof characterized in that a pyrazole- O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

12. Method for preventing, slowing, delaying or treating the degeneration of pancreatic beta cells and/or the decline of the functionality of pancreatic beta cells and/or for improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin secretion in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

13. Method for preventing, slowing, delaying or treating diseases or conditions attributed to an abnormal accumulation of liver fat in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

14. Method for maintaining and/or improving the insulin sensitivity and/or for treating or preventing hyperinsulinemia and/or insulin resistance in a patient in need thereof characterized in that a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 is administered in combination or alternation with a DPP IV inhibitor according to claim 1 or 3.

15. Use of a pyrazole-O-glucoside derivative of formula (I) according to claim 1 or 2 for the manufacture of a medicament for use in a method according to claim 7, 8, 9, 10, 1 1 , 12, 13 or 14.

16. Use of a DPP IV inhibitor according to claim 1 or 3 for the manufacture of a medicament for use in a method according to claim 7, 8, 9, 10, 1 1 , 12, 13 or 14.

17. Use of a pharmaceutical composition according to one of the claims 1 to 6 for the manufacture of a medicament for - preventing, slowing the progression of, delaying or treating a metabolic disorder selected from the group consisting of type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance, impaired fasting blood glucose, hyperglycemia, postprandial hyperglycemia, overweight, obesity and metabolic syndrome; or - improving glycemic control and/or for reducing of fasting plasma glucose, of postprandial plasma glucose and/or of glycosylated hemoglobin HbAIc; or preventing, slowing, delaying or reversing progression from impaired glucose tolerance, insulin resistance and/or from metabolic syndrome to type 2 diabetes mellitus; or - preventing, slowing the progression of, delaying or treating of a condition or disorder selected from the group consisting of complications of diabetes mellitus such as cataracts and micro- and macrovascular diseases, such as nephropathy, retinopathy, neuropathy, tissue ischaemia, arteriosclerosis, myocardial infarction, stroke and peripheral arterial occlusive disease; or - reducing body weight or preventing an increase in body weight or facilitating a reduction in body weight; or preventing, slowing, delaying or treating the degeneration of pancreatic beta cells and/or the decline of the functionality of pancreatic beta cells and/or for improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin secretion; or for preventing, slowing, delaying or treating diseases or conditions attributed to an abnormal accumulation of liver fat; or maintaining and/or improving the insulin sensitivity and/or for treating or preventing hyperinsulinemia and/or insulin resistance; in a patient in need thereof.

18. Method according to one of the claims 7 to 14 or use according to one of the claims 15, 16 or 17 wherein the patient is an individual diagnosed of one or more of the conditions selected from the group consisting of overweight, obesity, visceral obesity and abdominal obesity.

19. Method according to one of the claims 7 to 14 or use according to one of the claims 15, 16 or 17 wherein the patient is an individual who shows one, two or more of the following conditions: (a) a fasting blood glucose or serum glucose concentration greater than 110 mg/dL, in particular greater than 125 mg/dL;

(b) a postprandial plasma glucose equal to or greater than 140 mg/dL;

(c) an HbAIc value equal to or greater than 6.5 %, in particular equal to or greater than 8.0 %.

20. Method according to one of the claims 7 to 14 or use according to one of the claims 15, 16 or 17 wherein the patient is an individual wherein one, two, three or more of the following conditions are present: (a) obesity, visceral obesity and/or abdominal obesity,

(b) triglyceride blood level ≥ 150 mg/dL,

(e) a fasting blood glucose level ≥ 1 10 mg/dL.

21. Method according to one of the claims 7 to 14 or use according to one of the claims 15, 16 or 17 wherein the patient is an individual for whom the monotherapy with metformin is contraindicated and/or who has an intolerance against metformin at therapeutic doses.

22. Method according to one of the claims 7 to 14 or use according to one of the claims 15, 16 or 17 wherein the patient is an individual with insufficient glycemic control despite monotherapy with a SGLT2 inhibitor, in particular a pyrazole-O-glucoside derivative of the formula (I) according to claim 1 or 2.

23. Method according to one of the claims 7 to 14 or use according to one of the claims 15, 16 or 17 wherein the patient is an individual with insufficient glycemic control despite monotherapy with a DPP IV inhibitor, in particular a DPP IV inhibitor according to claim 1 or 3.