AU2016201916A1 - Choline salt of an anti-inflammatory substituted cyclobutenedione compound - Google Patents

Abstract

H:\dar\lntenvoen\NRPortbl\DCC\DAR\9889629_I.docx-24/03/20l6 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide choline, solid pharmaceutical compositions and oral dosage forms that contain said compound, and a method of using such compositions and oral dosage forms to treat people who have inflammatory, obstructive or allergic conditions and diseases.

Description

H:\dar\Interwoven\NRPortbl\DCC\DAR\9889629_l.doc ,,24/03/2016 CHOLINE SALT OF AN ANTI-INFLAMMATORY SUBSTITUTED CYCLOBUTENEDIONE COMPOUND This application is a divisional of Australian Patent Application No. 2012303675, the entire content of which is incorporated herein by reference. Field of the invention The present invention relates to a novel salt of a pharmaceutically active agent, solid pharmaceutical compositions and oral dosage forms for the delivery of said salt to patients in need thereof and the use of such solid pharmaceutical compositions and oral dosage forms. Background Compound 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide and a method of preparing same have been disclosed in international patent application WO 2010/015613 as Example 8. Compound 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide is a pharmaceutically active agent and acts as a CXCR2 receptor antagonist and is useful in the treatment of inflammatory, obstructive or allergic conditions and diseases, for example for the treatment of chronic obstructive pulmonary disease (COPD). Oral delivery of pharmaceutically active agents is generally the delivery route of choice, even when treating respiratory diseases, since it is convenient, relatively easy and generally painless resulting in greater patient compliance relative to other modes of delivery. However, biological, chemical and physical barriers such as poor solubility, varying pH in the gastrointestinal tract, powerful digestive enzymes and impermeable gastrointestinal membranes make oral delivery of some pharmaceutically active agents to mammals problematic or even impossible. Compound 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide of formula I CI 0 0 O OH 3 is a weakly acidic compound and is practically insoluble in aqueous solution at pH 1.0 - 7.0 as a free acid (<0.005 mg/ml). -1 - WO 2013/030803 PCT/IB2012/054502 Accordingly, there is a need to provide novel forms of 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide which show at least some superior characteristics over the free acid form. There is also a need for formulations which provide effective bioavailability of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide in plasma. The present invention provides such a novel salt form of 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide and formulation of same which solve the above problems or at least provide a useful alternative to the known salts and formulations of this compound. Summary of the invention In a first aspect, the present invention relates to the choline salt of 6-chloro-3-[2-(1 ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide of formula II 0 0 0 S O H3H H N- C o o - 3

CH

3 a + C~aO

CH

3 In this salt form 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino] 2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide is surprisingly more soluble in simulated gastric fluid than the free acid disclosed in WO 2010/015613. In a second aspect, the invention relates to a solid pharmaceutical composition comprising a) choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1 enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide; b) an alkalizing agent; c) a precipitation inhibiting agent; and d) an additional pharmaceutically acceptable carrier. 2 WO 2013/030803 PCT/IB2012/054502 As used herein, the term "alkalizing agent" is an agent capable of raising the pH of the micro-environment for 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 enylamino]-2-hyd roxy-N-methoxy-N-methyl-benzenesulfon amide in the hydrated formulation to a pH greater than about its pKa (pKa = 5.4). One skilled in the art will appreciate that acidic agents can also be used to adjust the pH of the alkalizing agent as long as the alkalizing agent as a whole raises the pH of the micro environment in the hydrated formulation to greater than about the pKa of 6-chloro-3 [2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide. Suitable alkalizing agents include but are not limited to organic and inorganic basic compounds of a wide range of aqueous solubilities and molecular weights and mixtures thereof. Examples of inorganic basic salts include ammonium hydroxide, alkali metal salts, alkaline earth metal salts such as magnesium oxide, magnesium hydroxide, calcium hydroxide, sodium hydroxide, potassium hydroxide, aluminium hydroxide, potassium carbonate, sodium bicarbonate and the like and mixtures thereof. In particular, an alkalizing agent is selected from magnesium oxide, calcium carbonate, calcium phosphate and combinations thereof. More particularly, the alkalizing agent is magnesium oxide. As used herein, the term "precipitation inhibiting agent " refers to salts, ions, carbohydrates, surfactants, amino acids, polymers and other compounds which, when present in solution, decrease the precipitation (crystallization) of 6-chloro-3-[2 (1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide. Examples of precipitation inhibitors include but are not limited to polyvinyl pyrrolidone, for example those products known as PVP K30, PVP K29/32 and PVPP XL, and hydroxy propyl methyl cellulose (HPMC), for example those products known as PHARMACOAT® low viscous hypromellose-based water soluble film coating agent. As used herein, the term "additional pharmaceutically acceptable carrier" refers to conventional pharmaceutical carriers, such as disintegrants, diluents, lubricants, glidants and binders which are known to a person skilled in the galenic art, and which are added to the composition in addition to the alkalizing agent(s) and the precipitation inhibiting agent(s). For example, known disintegrants such as croscarmellose sodium, sodium starch glycolate and crospovidone may be used as additional pharmaceutically acceptable carriers\. In particular, an additional pharmaceutically acceptable carrier is selected from disintegrants, diluents, lubricants, glidants and binders. More particularly, the pharmaceutically acceptable 3 WO 2013/030803 PCT/IB2012/054502 carrier is selected from croscarmellose sodium, mannitol, microcrystalline cellulose, magnesium stearate and colloidal silicon dioxide. As used herein, the term "oral dosage form" refers to physically discrete units suitable as unitary dosages for humans and other mammals, each unit containing a predetermined quantity of a therapeutic agent in association with one or more pharmaceutically acceptable carrier. Well-known oral dosage forms are for example tablets, capsules and caplets. Throughout this specification and in the claims that follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", should be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. The entire disclosure of each [United States patent and] international patent application mentioned in this patent specification is fully incorporated by reference herein for all purposes. Description of the drawing Figure 1: A is 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2 hydroxy-N-methoxy-N-methyl-benzenesulfonamide; the concentration [ng/mL] relates to the mean concentrations of A (ng/mL, mean ± standard deviation) in plasma of male beagle dogs after adminstration of 63 mg/animal (calculated as free acid; n=5 dogs per treatment group) of A as capsules according to Example 3 (= Form 1), a solid dispersion formulation (= Form 2) and enteric coated beads (= Form 3). Detailed description of the invention In a first aspect the present invention provides a novel salt of 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide, namely 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut 1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide choline of formula IL 4 WO 2013/030803 PCT/IB2012/054502 C 0 O O C l1 N N1H 0 S N- C H H C 3 0 0 CH-"' C H f~OH

CH

3 It was surprisingly found that the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino) 3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide has superior solubility in simulated gastric fluid. Whereas the solubility of the free acid is 0.001 mg/ml in simulated gastric fluid at pH 1.2, the solubility of the choline salt is 8.018 mg/ml. Furthermore, the solubility of the choline salt in simulated gastric fluid is also significantly improved compared to other salts of 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide such as sodium, calcium, N,N-dimethyl-2 aminoethanol and N-(2-hydroxyethyl)pyrrolidine salts. Furthermore, the hygroscopicity of the choline salt is much reduced compared with the free acid. The amount of water absorbed by the free acid is 2.4% and 2.8% by weight after 1 day at 80% and 92% humidity, respectively, and the amount of water absorbed by the choline salt is 0.7% and 0.6% by weight after 1 day at 80% and 92% humidity, respectively. The choline salt has also a much improved dissolution rate at pH 1 and oral exposure when dosed at 10mg/kg to male SPRAGUE DAWLEY@ rats compared to the free acid form. Although the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1 enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide has good solubility in gastric acidic conditions in the stomach, the choline salt of 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide readily converts in gastric acidic conditions into the free acid form which is poorly soluble. The result of this is poor bioavailability of 6-chloro-3-[2 (1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide. 5 WO 2013/030803 PCT/IB2012/054502 In a second aspect the present invention provides a solid pharmaceutical composition of 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylami no] 2-hydroxy-N-methoxy-N-methyl-benzenesulfona mide choline. The solid pharmaceutical composition comprises a) choline salt of 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide; b) an alkalizing agent; c) a precipitation inhibiting agent; and d) an additional pharmaceutically acceptable carrier. It was surprisingly found that this composition has an improved dissolution rate and an improved bioavailability as measured as AUC, mean Cmax and lower inter-animal variability denoted by the %CV (see Example 7, Table 1, Figure 1). It is particularly surprising that the mean concentration of 6-chloro-3-[2-(1-ethyl propylamino)-3,4-d ioxo-cyclobut-1 -enyla mino]-2-hyd roxy-N-methoxy-N-methyl benzenesulfonamide in plasma of male beagle dogs after oral administration of similar doses is higher when a composition according to the second aspect is used than when special delivery formulations are used such as enteric coated beads formulation or solid dispersion formulation (see Example 7, Table 1, Figure 1). In one embodiment (i) of the second aspect of the present invention, the alkalizing agent is selected from magnesium oxide, calcium carbonate, calcium phosphate and combinations thereof. Particularly, the alkalizing agent is magnesium oxide. In one embodiment (ii) of the second aspect or embodiment (i) of the second aspect, the precipitation inhibiting agent is selected from polyvinylpyrrolidone and hydroxypropyl methyl cellulose. Particularly, the precipitation inhibiting agent is polyvinylpyrrolidone. More particularly, polyvinylpyrrolidone is selected from products known as PVP K30, PVP K29/32 and PVPP XL, even more particularly PVP K30. In one embodiment (iii) of the second aspect or embodiment (i) or (ii) of the second aspect, the amount of alkalizing agent is in the range from about 5% to about 30% by weight of the total weight of solid pharmaceutical composition, particularly the amount of alkalizing agent is in the range from about 10% to about 20% by weight of the total weight of solid pharmaceutical composition, more particularly in the range from about 10% to about 15% by weight. 6 WO 2013/030803 PCT/IB2012/054502 In one embodiment (iv) of the second aspect or embodiments (i) to (iii) of the second aspect, the amount of precipitation inhibiting agent is in the range from about 8% to about 20% by weight of the total weight of solid pharmaceutical composition, particularly in the range from about 10% to about 15% by weight. In one embodiment (v) of the second aspect or embodiments (i) to (iv) of the second aspect, the additional pharmaceutically acceptable carrier is selected from disintegrants, diluents, lubricants, glidants and binders, or a mixture thereof. In one embodiment (vi) of the second aspect or embodiments (i) to (v) of the second aspect, the invention relates to a solid pharmaceutical composition comprising a) choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1 enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide; b) magnesium oxide; c) polyvinylpyrrolidone; and d) a mixture of croscarmellose sodium and mannitol. In one particular embodiment (vii) of embodiment (vi) of the second aspect, the composition further comprises microcrystalline cellulose, magnesium stearate and colloidal silicon dioxide. In a third aspect, the present invention relates to an oral dosage form comprising the composition according to the second aspect or embodiments (i)-(vii) of the second aspect. In an embodiment (i) of the third aspect, the amount of the choline salt of 6-chloro-3 [2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enyla mi no]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide is from about 5 to about 100 mg on a dry basis calculated as the free acid. In an embodiment (ii) of the third aspect, the amount of the choline salt of 6-chloro-3 [2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide is about 75 mg on a dry basis calculated as the free acid. 7 WO 2013/030803 PCT/IB2012/054502 In another embodiment (iii) of the third aspect, the amount of the choline salt of 6 chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide is about 25 mg on a dry basis calculated as the free acid. In another embodiment (iv) of the third aspect, the amount of the choline salt of 6 chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide is about 5 mg on a dry basis calculated as the free acid. In a further embodiment (v) of the third aspect or embodiments (i)-(iv) of the third aspect, the dosage form is selected from a tablet, capsule and caplet, particularly a capsule. Such capsules may be prepared by a conventional blending process, for example in a diffusion blender and using appropriate sieving steps to enable a homogenous distribution of the ingredients. As a person skilled in the galenic art would know, the particle sizes of carriers should not differ too much from the particle size of the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1 enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide to avoid segregation during blending. The final blend can be filled manually or an automated capsule filling machine into hard gelatin, HPMC, starch or pullulan capsules. In a fourth aspect, the present invention relates to a composition or oral dosage form according to the second and third aspect, respectively, for use in medicine, particularly for use in the treatment of conditions and diseases mediated by CXCR2, for example inflammatory, obstructive or allergic conditions and diseases, particularly chronic obstructive pulmonary airways disease (COPD), including chronic bronchitis or dyspnea associated therewith, emphysema, bronchiolitis obliterans syndrome and severe asthma. In a fifth aspect, the present invention relates to a method of treating conditions and diseases mediated by CXCR2, for example inflammatory or allergic conditions and diseases, particularly chronic obstructive pulmonary airways disease (COPD), including chronic bronchitis or dyspnea associated therewith, emphysema, bronchiolitis obliterans syndrome and severe asthma, comprising administering to a person or mammal an effective amount of a composition or an oral dosage form according to the second and third aspect, respectively. 8 WO 2013/030803 PCT/IB2012/054502 Additional embodiments and features are set forth in part in the description that follows, and in part will become apparent to those skilled in the art upon examination of the specification or may be learned by the practice of the invention. This invention is further illustrated by the following examples which should not be construed as limiting. Experimental Example 1: Small scale preparation of choline salt of 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide Methanol (15.6 ml) was added under nitrogen at room temperature to 6-chloro-3-[2 (1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide (4.8 g) to give a yellow suspension. This suspension was heated to 65±30C for 15 minutes at or near reflux. Choline hydroxide (2.78 mg) in methanol was added over 30 minutes. The dark brown solution was filtered and washed with methanol (3.6 ml). Isopropanol (12.3 ml) was added over 30 minutes to the dark brown solution and the whole was then cooled to 550C. Seed crystals of 6 chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N methoxy-N-methyl-benzenesulfonamide choline (3 mg) were added and the solution stirred until start of crystallisation. The solution was then cooled to 00C over two hours and stirred at that temperature for two hours. The yellow suspension was filtered and washed with isopropanol (10 ml). The wet filter cake was dried in a vacuum oven overnight at 85C. Example 2: Preparation of choline salt of 6-chloro-3-[2-(1-ethyl-propylamino) 3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide Methanol (81.3 kg, 103 litres) was added under nitrogen to 6-chloro-3-[2-(1-ethyl propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl benzenesulfonamide (25.0 kg) to give a yellow suspension. This suspension was heated to 65±3'C for 15 minutes. A solution of choline hydroxide (14.5 kg) in methanol (15.6 kg, 20 litres) was added to the suspension over a period of 30 minutes. The suspension was stirred for a further 60 minutes and then filtered and washed with methanol (3.3 kg, 4 litres). Isopropanol (64.1 kg, 82 litres) was then added over 30 minutes and the whole cooled to 55±2'C. Seed crystals of 6-chloro-3 [2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N-methoxy-N 9 WO 2013/030803 PCT/IB2012/054502 methyl-benzenesulfonamide choline (0.016 kg) were added and the suspension stirred at 55±20C before cooling down to 0±2'C over 2 hours. The suspension was stirred for a further 2 hours before being centrifuged, washed with isopropanol (52.1 kg, 67 litres), filtered and the obtained crystals (25.4 kg) dried. Example 3: 63 mg capsule (calculated as free acid) of choline salt of 6-chloro-3 [2-(1-ethyl -propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N methoxy-N -methyl -benzenesul fonami de A pharmaceutical composition was prepared in the manner described in Example 1 from the ingredients listed in the following table and filled into capsules: Ingredient Amount (mg) % Function choline salt of 6- 78.06 22.3 Active ingredient chloro-3-[2-(1 -ethyl propylamino)-3,4 dioxo-cyclobut-1 enylamino]-2 hydroxy-N-methoxy N-methyl benzenesulfonamide PVP K30 42.00 12.0 Precipitation inhibiting agent Magnesium oxide 42.00 12.0 Alkalizing agent Cellulose MK GR 42.3 12.1 Filling agent, diluent Mannitol SD200 110.64 31.6 Diluent Na-CMC XL (AC-DI- 28.00 8.0 Disintegrant SOL) Aerosil@ 200 fumed 1.75 0.5 Glidant silica magnesium stearate 5.25 1.5 Lubricant capsule fill weight 350.00 100 Example 4: 75 mg capsule (calculated as free acid) of choline salt of 6-chloro-3 [2-(1-ethyl -propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N methoxy-N -methyl-benzenesulfonamide 10 WO 2013/030803 PCT/IB2012/054502 A pharmaceutical composition was prepared in the manner described in Example 1 from the ingredients listed in the following table and filled into capsules: Ingredient Amount (mg) % Function choline salt of 6- 92.93 25.1 Active ingredient chloro-3-[2-(1 -ethyl propylamino)-3,4 dioxo-cyclobut-1 enylamino]-2 hydroxy-N-methoxy N-methyl benzenesulfonamide PVP K30 44.40 12.0 Precipitation inhibiting agent magnesium oxide 50.00 13.5 Alkalizing agent Cellulose MK GR 55.09 14.9 Filling agent, diluent Mannitol SD200 105.38 28.5 Diluent Na-CMC XL (AC-DI- 14.80 4.0 Disintegrant SOL) Aerosil@ 200 fumed 1.85 0.5 Glidant silica magnesium stearate 5.55 1.5 Lubricant capsule fill weight 370.00 100 empty capsule shell 96.00 Total capsule weight 466.00 Example 5: 25 mg capsule (calculated as free acid) of choline salt of 6-chloro-3 [2-(1 -ethyl -propylamino)-3,4-dioxo-cycl obut-1 -enylamino]-2-hydroxy-N methoxy-N -methyl -benzenes ulfon ami de A pharmaceutical Amount (mg) % Function composition was prepared in the manner described in Example 1 from the ingredients listed in the following table 11 WO 2013/030803 PCT/IB2012/054502 and filled into capsules:lngredient choline salt of 6- 30.98 8.4 Active ingredient chloro-3-[2-(1 -ethyl propylamino)-3,4 dioxo-cyclobut-1 enylamino]-2 hydroxy-N-methoxy N-methyl benzenesulfonamide PVP K30 44.40 12.0 Precipitation inhibiting agent magnesium oxide 50.00 13.5 Alkalizing agent Cellulose MK GR 72.22 19.5 Filling agent, diluent Mannitol SD200 150.20 40.6 Diluent Na-CMC XL (AC-DI- 14.80 4.0 Disintegrant SO L) Aerosil@ 200 fumed 1.85 0.5 Glidant silica magnesium stearate 5.55 1.5 Lubricant capsule fill weight 370.00 100 empty capsule shell 96.00 Total capsule weight 466.00 Example 6: 5 mg capsule (calculated as free acid) of choline salt of 6-chloro-3 [2-(1 -ethyl -propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2-hydroxy-N meth oxy-N -methyl -benzenes u Ifonami de A pharmaceutical Amount (mg) % Function composition was prepared in the manner described in Example 1 from the ingredients listed in the following table and filled into 12 WO 2013/030803 PCT/IB2012/054502 capsules: Ingredient choline salt of 6- 6.20 1.7 Active ingredient chloro-3-[2-(1 -ethyl propylamino)-3,4 dioxo-cyclobut-1 enylamino]-2 hydroxy-N-methoxy N-methyl benzenesulfonamide PVP K30 44.40 12.0 Precipitation inhibiting agent magnesium oxide 50.00 13.5 Alkalizing agent Cellulose MK GR 64.28 17.4 Filling agent, diluent Mannitol SD200 168.12 45.4 Diluent Na-CMC XL (AC-DI- 29.60 8.0 Disintegrant SOL) Aerosil@ 200 fumed 1.85 0.5 Glidant silica magnesium stearate 5.55 1.5 Lubricant capsule fill weight 370.00 100 empty capsule shell 96.00 Total capsule weight 466.00 Example 7: Pharmacokinetic studies of the choline salt of 6-chloro-3-[2-(1 ethyl-propylamino)-3,4-dioxo-cycl obut-1 -enylamino]-2-hydroxy-N-methoxy-N methyl-benzenesulfonamide Male beagle dogs were administered oral single doses of capsules (63 mg choline salt of 6-chloro-3-[2-(1 -ethyl-propylamino)-3,4-dioxo-cyclobut-1 -enylamino]-2 hydroxy-N-methoxy-N-methyl-benzenesulfonamide per capsule calculated as free acid) according to Example 3 (= Form 1), a solid dispersion formulation (= Form 2) and enteric coated beads (= Form 3). The dogs were pretreated with pentagastrine (6 pg/kg) in order to lower the pH in the stomach and mimic more acidic conditions in humans. Three treatment groups (n=5 dogs per treatment group) were used for each Form of administration and the parameters measured are based on plasma 13 H:\dar\Interwovn\NRPortbl\DCC\DAR\9889629_1.docx-24/03/2016 concentrations. Table 1 summarizes the pharmacokinetic parameters for each of the three treatment groups. Table 1 PK parameter Form 1 Form 2 Form 3 Tmax (h)a 2 [1-2] 2 [1-4] 2 [1-2] Cmax (ng/mL) 7510 ±4490 3300 ±2110 6440 ±3860 Cmax/dose 1030 ±588 454 ±283 842 ±516 ((ng/mL)/(mg/kg)) AUClast (h ng/mL) 25600 ±13200 14900 ±8320 19800 ±12700 AUClast / dose 3480 ±1750 2040 ±1090 2570 ±1650 ((h ng/mL)/(mg/kg)) a: median [range] The mean dose normalized AUClast of Form 1 was 1.7 and 1.3 times higher than the one of Form 2 and 3, respectively, with no impact on the Tmax. The systemic exposure of the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4 dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide in the dogs using Form 1, 2 and 3 was compared with the systemic exposure after intravenous administration (912 ± 126 ng h/mL at 0.3 mg/kg). Oral bioavailabilities of 116% for Form 1, 75% for Form 2 and 85% for Form 3 was calculated. Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates. - 14-

Claims (23)

1. Choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut- 1 enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide of formula 11 C 0 O O O : NNHC3 CHCH O/S\ H N CH CH <7 OH CH 3

2. A solid pharmaceutical composition comprising a) choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2 hydroxy-N-methoxy-N-methyl-benzenesulfonamide; b) an alkalizing agent; c) a precipitation inhibiting agent; and d) an additional pharmaceutically acceptable carrier.

3. The composition according to claim 2, wherein the alkalizing agent is selected from magnesium oxide, calcium carbonate, calcium phosphate and combinations thereof.

4. The composition according to claim 2 or 3, wherein the alkalizing agent is magnesium oxide.

5. The composition according to any one of claims 2 to 4, wherein the precipitation inhibiting agent is selected from polyvinylpyrrolidone and hydroxypropyl methyl cellulose.

6. The composition according to any one of claims 2 to 5, wherein the precipitation inhibiting agent is polyvinylpyrrolidone.

7. The composition according to any one of claims 2 to 6, wherein polyvinylpyrrolidone is selected from PVP K30, PVP K29/32 and PVPP XL, in particular PVP K30. -15- H:\dar\Intenvov en\NRPorbl\DCC\DAR\9889629_I.docx-24/03/2016

8. The composition according to any one of claims 3 to 7, wherein the amount of alkalizing agent is in the range from about 5% to about 30% by weight of the total weight of solid pharmaceutical composition.

9. The composition according to any one of claims 2 to 8, wherein the amount of alkalizing agent is in the range from about 10% to about 20% by weight of the total weight of solid pharmaceutical composition, in particular in the range of about 10% to about 15% by weight.

10. The composition according to any one of claims 2 to 9, wherein the amount of precipitation inhibiting agent is in the range from about 8% to about 20% by weight of the total weight of solid pharmaceutical composition, in particular in the range of about 10% to about 15% by weight.

11. The composition according to any one of claims 2 to 10, wherein the additional pharmaceutically acceptable carrier is selected from disintegrants, diluents, lubricants, glidants and binders.

12. The composition according to any one of claims 2 to 11 comprising a) choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2 hydroxy-N-methoxy-N-methyl-benzenesulfonamide; b) magnesium oxide; c) polyvinylpyrrolidone; and d) a mixture of croscarmellose sodium and mannitol.

13. The composition according to claim 12 further comprising microcrystalline cellulose, magnesium stearate, colloidal silicon dioxide, or a mixture of these.

14. An oral dosage form comprising the composition according to any one of claims 2 to 13 and wherein the amount of the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino) 3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide is from about 5 to about 100 mg on a dry basis calculated as the free acid. -16- H:\darMnlerwovcn\NRPortbl\DCC\DAR\9889629_ 1.docx-24/03/2016

15. An oral dosage form comprising the composition according to claim 14 and wherein the amount of the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide is about 75 mg on a dry basis calculated as the free acid.

16. An oral dosage form comprising the composition according to claim 14 and wherein the amount of the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide is about 25 mg on a dry basis calculated as the free acid.

17. An oral dosage form comprising the composition according to claim 14 and wherein the amount of the choline salt of 6-chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo cyclobut- 1 -enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide is about 5 mg on a dry basis calculated as the free acid.

18. The oral dosage form according to any one of claims 14 to 17, wherein the dosage form is selected from a tablet, a capsule and a caplet.

19. The oral dosage form according to claim 18, wherein the dosage from is a capsule, in particular a hard capsule.

20. The compound according to claim 1, or the composition according to any one of claims 2 to 13, or the oral dosage form according to any one of claims 14 to 19, for use in the treatment of conditions and diseases mediated by CXCR2.

21. The compound, composition or oral dosage form according to claim 20, for use in the treatment of inflammatory, obstructive or allergic conditions and diseases.

22. The compound, composition or oral dosage form according to claim 20, for use in the treatment of chronic obstructive pulmonary airways disease (COPD), including chronic bronchitis or dyspnea associated therewith, emphysema, bronchiolitis obliterans syndrome and severe asthma. -17- H:\dar\Intenovcn\NRPortbI\DCC\DAR\9889629_- docx-24/03/2016

23. A method of treating conditions and diseases mediated by CXCR2, for example inflammatory or allergic conditions and diseases, particularly chronic obstructive pulmonary airways disease (COPD), including chronic bronchitis or dyspnea associated therewith, emphysema, bronchiolitis obliterans syndrome and severe asthma, comprising administering to a person or mammal an effective amount of the compound according to claim 1, or the composition according to any one of claims 2 to 13, or the oral dosage form according to any one of claims 14 to 19. -18-