Title of Invention

"PHARMACEUTICAL PREPARATION CONSISTING OF TIOTROPIUM BROMIDE"

Abstract

Pharmaceutical preparation consisting of tiotropium bromide as active substance, in a concentration based on tiotropium of between 0.02g per 100ml of formulation and 0.05g per 100ml of formulation, the tiotropium bromide being present in the pharmaceutical preparation is totally dissolved form. water as the only solvent, acid for adjusting the pH to between 2.7 and 3.1, preferably 2.8 and 3.05, benzalkonium chloride in a concentration of between 8mg/100ml and 12mg/100ml, sodium edentate in an amount of between 8mg/ 100ml of formulation and 12mg/100ml of formulation.

Full Text

Aerosol formulation for inhalation comprising a tiotropium salt The present invention relates to a propellant-free aerosol formulation of a pharmaceutically acceptable salt of tiotropium dissolved in water. The formulation according to the invention is particularly suitable for nebulising the active substance using an atomiser in order to administer the active substance by inhalation. Preferred indications are asthma and/or COPD. Tiotropium, chemically (1a,2p,4p,5a,7p)-7-[(nydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02i4]nonane, is known as tiotropium bromide from European Patent Application EP 418 716 A1. The bromide salt of tiotropium has the following chemical structure: (Figure Removed) The compound has valuable pharmacological properties and is known by the name tiotropium bromide. Tiotropium and its salts are highly effective anticholinergics and can therefore provide therapeutic benefit in the treatment of asthma or COPD (chronic obstructive pulmonary disease). The monohydrate of tiotropium bromide is also pharmacologically valuable. Both compounds are a preferred object of the present invention. The present invention relates to liquid active substance formulations of these compounds which can be administered by inhalation; the liquid formulations according to the invention have to meet high quality standards. To achieve an optimum distribution of active substances in the lung it makes sense to use a liquid formulation without propellant gases administered using suitable inhalers. Those inhalers which are capable of nebulising a small amount of a liquid formulation in the dosage needed for therapeutic purposes within a few seconds into an aerosol suitable for therapeutic inhalation are particularly suitable. Within the scope of the invention, preferred nebulisers are those in which an amount of less than 100 microlitres, preferably less than 50 microlitres, most preferably less than 20 microlitres of active substance solution can be nebulised preferably in one puff or two puffs to form an aerosol having an average particle size of less than 20 microns, preferably less than 10 microns, so that the inhalable part of the aerosol already corresponds to the therapeutically effective quantity. An apparatus of this kind for the propellant-free administration of a metered amount of a liquid pharmaceutical composition for inhalation is described in detail for example in International Patent Application WO 91/14468 "Atomizing Device and Methods" and also in WO 97/12687, cf. Figures 6a and 6b and the accompanying description. In a nebuliserof this kind a pharmaceutical solution is converted by means of a high pressure of up to 500 bar into an aerosol destined for the lungs, which is sprayed. Within the scope of the present specification reference is expressly made to the entire contents of the literature mentioned above. In inhalers of this kind the formulations of solutions are stored in a reservoir. It is essential that the active substance formulations used are sufficiently stable when stored and at the same time are such that they can be administered directly, if possible without any further handling, in accordance with their medical purpose. Moreover, they must not contain any ingredients which might interact with the inhaler in such a way as to damage the inhaler or the pharmaceutical quality of the solution or of the aerosol produced. To nebulise the solution a special nozzle is used as described for example in WO 94/07607 or WO 99/16530, to which reference is expressly made here. WO 98/27959 discloses formulations of solutions for the inhaler described above which contain as additive the disodium salt of editic acid (or disodium ethylenediamine tetraacetate dihydrate or sodium edetate). For aqueous formulations of solutions which are to be converted into inhalable aerosols using the inhaler described above, the specification favours a minimum concentration of sodium edetate of 50 mg/100 ml, in order to reduce the incidence of spray anomalies. Among the Examples disclosed there is a formulation containing tiotropium bromide with a pH of 3.2 or 3.4. In this formulation the active substance is dissolved in water. The proportion of sodium edetate is again 50 mg/100 ml. Surprisingly, it has now been found that aqueous formulations of solutions of tiotropium salts are particularly stable when the pH is below 3.2, preferably below 3.1 It has also been found that formulations of this kind show a reduction in the scattering of the composition delivered, compared with the formulation containing tiotropium bromide known from the prior art, when nebulised with the Respimat® inhaler, if the quantity of sodium edetate is between 5 mg and 20 mg per 100 g of formulation. The spray quality of the formulation according to the invention is very good. An aerosol produced in this way has very good properties for administration by inhalation. In addition, the formulation according to the invention has greater stability and reduces the loading of sodium edetate on the patient. It is therefore an aim of the present invention to provide an aqueous active substance formulation containing a pharmaceutically acceptable tiotropium salt which meets the high standards needed in order to be able to achieve optimum nebulisation of a solution using the inhalers mentioned hereinbefore. The active substance formulations according to the invention must be of sufficiently high pharmaceutical quality, i.e. they should be pharmaceutically stable over a storage time of some years, preferably at least one year, more preferably two years. Another aim is to provide propellant-free formulations of solutions containing tiotropium salts which are nebulised under pressure using an inhaler, the composition delivered by the aerosol produced falling reproducibly within a specified range. A further aim is to provide an inhalable formulation having a tiotropium salt as a liquid formulation with water as solvent, which is stable and reduces the loading of chemical substances on the patient to a minimum. According to the invention, any pharmaceutically acceptable salts of tiotropium may be used for the formulation. When the term tiotropium salt is used within the scope of the present invention, this is to be taken as a reference to tiotropium. A reference to tiotropium corresponds to the free ammonium cation. The tiotropium salt accordingly contains an anion as the counter-ion. Tiotropium salts which may be used within the scope of the present invention are preferably compounds which contain, in addition to tiotropium as counter-ion (anion), chloride, bromide, iodide, methanesulphonate, para-toluenesulphonate and/or methylsulphate. Within the scope of the present invention tiotropium bromide is preferred as the salt. References to tiotropium bromide within the scope of the present invention must always be taken as references to all possible amorphous and crystalline modifications of tiotropium bromide. These may for example contain molecules of solvent in their crystalline structure. Of all the crystalline modifications of tiotropium bromide those which also contain water (hydrates) are preferred according to the invention. It is particularly preferred within the scope of the present invention to use tiotropium bromide monohydrate. The formulation preferably does not contain any other active substance which does not contain tiotropium or is a pharmaceutically acceptable salt thereof. In the formulation according to the invention the tiotropium salt or salts is or are dissolved in water. No other solvent is used. In particular, the formulation is free from propellant gases. According to the invention the formulation preferably contains only a single tiotropium salt, preferably tiotropium bromide or tiotropium bromide monohydrate. However, the formulation may also contain a mixture of different tiotropium salts and solvates. The concentration of the tiotropium salt based on the proportion of tiotropium in the finished pharmaceutical preparation depends on the therapeutic effect sought. For most of the complaints which respond to tiotropium the concentration of tiotropium is between 0.01 g per 100 g of formulation and 0.06 g per 100 g of formulation . As the density of the formulation is 1.00 g/cm3, the 100 g of formulation correspond to a volume of 100 ml. Within the scope of the present specification the expression "per 100 ml" or" /100 ml" in each case means per 100 ml of formulation unless otherwise stated. An amount of 0.015 g /100 ml to 0.055 g /100 ml is preferred, an amount of from 0.02 g /100 ml to 0.05 g /100 ml is more preferred. Most preferred is an amount of from 0.023 + 0.001 g per 100 ml of formulation up to 0.045 + O.OOIg per 100 ml of formulation The pH of the formulation according to the invention is between 2.7 and 3.1, preferably between 28 and 3.05, more preferably between 2.80 and 3.0, and most preferably 2.9. The pH is adjusted by the addition of pharmacologically acceptable acids. Examples of inorganic acids which are preferred for this purpose include: hydrochloric acid, hydrobromic acid, nitric acid, sulphuric acid and/or phosphoric acid. Examples of particularly suitable organic acids are: ascorbic acid, citric acid, malic acid, tartaric acid, maleic acid, succinic acid, fumaric acid, acetic acid, formic acid and/or propionic acid, etc. Preferred inorganic acids are hydrochloric acid and sulphuric acid. It is also possible to use acids which form an acid addition salt with the active substance. Of the organic acids, ascorbic acid, fumaric acid and citric acid are preferred, citric acid being most preferred. If desired, mixtures of the abovementioned acids may also be used, particularly in the case of acids which have other properties in addition to their acidifying properties, e.g. those which act as flavourings or antioxidants, such as for example citric acid or ascorbic acid. Of the acids mentioned above, hydrochloric acid and citric acid are expressly mentioned as being particularly preferred. If desired, pharmacologically acceptable bases may be used to titrate the pH precisely. Suitable bases include for example alkali metal hydroxides and alkali metal carbonates. The preferred alkali ion is sodium. If bases of this kind are used, care must be taken to ensure that the resulting salts, which are then contained in the finished pharmaceutical formulation, are pharmacologically compatible with the abovementioned acid. According to the invention, the formulation contains editic acid (EDTA) or one of the known salts thereof, e.g. sodium EDTA or disodium EDTA dihydrate (sodium edetate), as a stabiliser or complexing agent. Preferably, sodium edetate is used. The content based on sodium edetate is between 5 mg /100 ml of formulation and 20 mg /100 ml of formulation, preferably between 5 mg /100 ml of formulation and 15 mg /100 ml of formulation, more preferably between 8 mg /100 ml of formulation and 12 mg /100 ml of formulation, most preferably 10 mg /100 ml of formulation. If a different salt of editic acid or the acid itself is used, analogous amounts of the complexing agent are used. The remarks made concerning sodium edetate also apply analogously to other possible additives which are comparable , although not preferred to EDTA or the salts thereof, which have complexing properties and can be used instead of them, such as for example nitrilotriacetic acid and the salts thereof. By complexing agents is preferably meant within the scope of the present invention molecules which are capable of entering into complex bonds. Preferably, these compounds should have the effect of complexing cations, most preferably metal cations. Other pharmacologically acceptable adjuvants may be added to the formulation according to the invention. By adjuvants and additives are meant, in this context, any pharmacologically acceptable and therapeutically useful substance which is not an active substance, but can be formulated together with the active substance in the pharmacologically suitable solvent, in order to improve the qualities of the active substance formulation. Preferably, these substances have no pharmacological effects or no appreciable or at least no undesirable pharmacological effects in the context of the desired therapy. The adjuvants and additives include, for example, other stabilisers, complexing agents, antioxidants and/or preservatives which prolong the shelf life of the finished pharmaceutical formulation, flavourings, vitamins and/or other additives known in the art. The additives also include pharmacologically acceptable salts such as sodium chloride, for example. The preferred excipients include antioxidants such as ascorbic acid, for example, provided that it has not already been used to adjust the pH, vitamin A, vitamin E, tocopherols and similar vitamins or provitamins occurring in the human body. Preservatives can be added to protect the formulation from contamination with pathogenic bacteria. Suitable preservatives are those known from the prior art, particularly benzalkonium chloride or benzoic acid or benzoates such as sodium benzoate in the concentration known from the prior art. Preferably, benzalkonium chloride is added to the formulation according to the invention. The amount of benzalkonium chloride is between 5 mg /100 ml of formulation and 20 mg /100 ml of formulation, preferably between 5 mg /100 ml of formulation and 15 mg /100 ml of formulation, more preferably between 8 mg /100 ml of formulation and 12 mg / 100ml of formulation, most preferably 10 mg/100 ml of formulation. Preferred formulations contain only benzalkonium chloride, sodium edetate and the acid needed to adjust the pH, preferably hydrochloric acid, in addition to the solvent water and the tiotropium salt. As already mentioned, tiotropium bromide is described in EP 418 716 A1. Crystalline tiotropium bromide monohydrate may be obtained using a process which is described in more detail below. In order to prepare the crystalline monohydrate according to the present invention, the tiotropium bromide obtained by the method disclosed in EP 418 716 A1, for example, first has to be taken up in water, heated, purified with activated charcoal and, after removal of the activated charcoal, the tiotropium bromide monohydrate is slowly crystallised while cooling slowly. The following procedure is preferably followed: In a reaction vessel of suitable dimensions, the solvent is mixed with tiotropium bromide, which has been obtained by the method disclosed in EP 418 716 A1, for example. For each mol of tiotropium bromide put in, 0.4 to 1.5 kg, preferably 0.6 to 1 kg, most preferably about 0.8 kg of water are used as solvent. The mixture obtained is heated with stirring, preferably to above 50°C, most preferably to above 60°C. The maximum temperature which can be selected is determined by the boiling point of the solvent used (water). Preferably, the mixture is heated to a range from 80-90°C. Activated charcoal, either dry or moistened with water, is added to this solution. Preferably, 10 to 50 g, more preferably 15 to 35 g, most preferably about 25 g of activated charcoal are put in per mol of tiotropium bromide used. If desired the activated charcoal is suspended in water before being added to the solution containing tiotropium bromide. 70 to 200 g, preferably 100 to 160 g, more preferably about 135 g of water are used, per mol of tiotropium bromide put in, in order to suspend the activated charcoal. If the activated charcoal is suspended in water beforehand, before being added to the solution containing tiotropium bromide, it is advisable to rinse again with the same amount of water. After the activated charcoal has been added, stirring is continued at constant temperature for between 5 and 60 minutes, preferably between 10 and 30 minutes, more preferably for about 15 minutes and the mixture obtained is filtered to remove the activated charcoal. The filter is then rinsed with water. 140 to 400 g, preferably 200 to 320 g, most preferably about 270 g of water are used for this, per mol of tiotropium bromide used. The filtrate is then slowly cooled, preferably to a temperature of 20-25°C. The cooling preferably takes place at a cooling rate of 1 to 10°C every 10 to 30 minutes, preferably 2 to 8°C every 10 to 30 minutes, more preferably 3 to 5°C every 10 to 20 minutes, most preferably 3 to 5°C about every 20 minutes. If desired, the cooling to 20 to 25°C may be followed by further cooling to below 20°C, more preferably to 10 to15°C. After cooling is complete, stirring is continued for between 20 minutes and 3 hours, preferably between 40 minutes and 2 hours, more preferably for about one hour to complete the crystallisation. The crystals obtained are then isolated by filtering or suction filtering to remove the solvent. If it should prove necessary to subject the crystals obtained to a further washing step, it is advisable to use water or acetone as the washing solvent. 0.1 to 1 0 L, preferably 0.2 to 0.5 L, more preferably about 0.3 L of solvent may be used per mol of tiotropium bromide put in, in order to wash the tiotropium bromide monohydrate crystals obtained. If necessary the washing step may be repeated. The product obtained is dried in vacua or using circulating heated air until a water content of 2.5-4.0 % is obtained. According to one aspect the present invention therefore also relates to formulations of solutions of the type described above using crystalline tiotropium bromide monohydrate which may be obtained by the procedure described above. The pharmaceutical formulations containing tiotropium salts according to the invention are preferably used in an inhaler of the kind described hereinbefore in order to produce the propellant-free aerosols according to the invention. At this point we should once again expressly mention the patent documents described hereinbefore, to which reference is hereby made. As described at the beginning, a further developed embodiment of the preferred inhaler is disclosed in WO 97/12687 and Figure 6 thereof. This nebuliser (Respimat®) can advantageously be used to produce the inhalable aerosols according to the invention containing a tiotropium salt as active substance. Because of its cylindrical shape and handy size of less than 9 to 15 cm long and 2 to 4 cm wide, the device can be carried anywhere by the patient. The nebuliser sprays a defined volume of the pharmaceutical formulation out through small nozzles at high pressures, so as to produce inhalable aerosols. rThe preferred atomiser essentially consists of an upper housing part, a pump housing, a nozzle, a locking clamp, a spring housing, a spring and a storage container, characterised by - a pump housing fixed in the upper housing part and carrying at one end a nozzle body with the nozzle or nozzle arrangement, - a hollow piston with valve body, - a power take-off flange in which the hollow body is fixed and which is located in the upper housing part, - a locking clamping mechanism located in the upper housing part, - a spring housing with the spring located therein, which is rotatably mounted on the upper housing part by means of a rotary bearing, - a lower housing part which is fitted onto the spring housing in the axial direction. The hollow piston with valve body corresponds to a device disclosed in WO 97/12687. It projects partially into the cylinder of the pump housing and is disposed to be axially movable in the cylinder. Reference is made particularly to Figures 1-4 -especially Figure 3 - and the associated parts of the description. At the moment of release of the spring the hollow piston with valve body exerts, at its high pressure end, a pressure of 5 to 60 Mpa (about 50 to 600 bar), preferably 10 to 60 Mpa (about 100 to 600 bar) on the fluid, the measured amount of active substance solution. Volumes of 10 to 50 microlitres are preferred, volumes of 10 to 20 microlitres are more preferable, whilst a volume of 10 to 15 microlitres per actuation is particularly preferred. The valve body is preferably mounted at the end of the hollow piston which faces the nozzle body The nozzle in the nozzle body is preferably microstructured, i.e. produced by micro-engineering. Microstructured nozzle bodies are disclosed for example in WO-99/16530; reference is hereby made to the contents of this specification, especially Figure 1 and the associated description. The nozzle body consists for example of two sheets of glass and/or silicon securely fixed together, at least one of which has one or more microstructured channels which connect the nozzle inlet end to the nozzle outlet end. At the nozzle outlet end there is at least one round or non-round opening 2 to 10 microns deep and 5 to 15 microns wide, the depth preferably being 4.5 to 6.5 microns and the length being 7 to 9 microns. If there is a plurality of nozzle openings, preferably two, the directions of spraying of the nozzles in the nozzle body may run parallel to each other or may be inclined relative to one another in the direction of the nozzle opening. In the case of a nozzle body having at least two nozzle openings at the outlet end, the directions of spraying may be inclined relative to one another at an angle of 20 degrees to 160 degrees, preferably at an angle of 60 to 150 degrees, most preferably 80 to 100°. The nozzle openings are preferably arranged at a spacing of 10 to 200 microns, more preferably at a spacing of 10 to 100 microns, still more preferably 30 to 70 microns. A spacing of 50 microns is most preferred. The directions of spraying therefore meet in the region of the nozzle openings. As already mentioned, the liquid pharmaceutical preparation hits the nozzle body at an entry pressure of up to 600 bar, preferably 200 to 300 bar and is atomised through the nozzle openings into an inhalable aerosol. The preferred particle sizes of the aerosol are up to 20 microns, preferably 3 to 10 microns. The locking clamping mechanism contains a spring, preferably a cylindrical helical compression spring as a store for the mechanical energy. The spring acts on the power take-off flange as a spring member the movement of which is determined by the position of a locking member. The travel of the power take-off flange is precisely limited by an upper stop and a lower stop. The spring is preferably tensioned via a stepping-up gear, e.g. a helical sliding gear, by an external torque which is generated when the upper housing part is turned relative to the spring housing in the lower housing part. In this case, the upper housing part and the power take-off flange contain a single- or multi-speed spline gear. The locking member with the engaging locking surfaces is arranged in an annular configuration around the power take-off flange. It consists for example of a ring of plastics or metal which is inherently radially elastically deformable. The ring is arranged in a plane perpendicular to the axis of the atomiser. After the locking of the spring, the locking surfaces of the locking member slide into the path of the power take-off flange and prevent the spring from being released. The locking member is actuated by means of a button. The actuating button is connected or coupled to the locking member. In order to actuate the locking clamping mechanism the actuating button is moved parallel to the annular plane, preferably into the atomiser, and the deformable ring is thereby deformed in the annular plane. Details of the construction of the locking clamping mechanism are described in WO 97/20590. The lower housing part is pushed axially over the spring housing and covers the bearing, the drive for the spindle and the storage container for the fluid. When the atomiser is operated, the upper part of the housing is rotated relative to the lower part, the lower part taking the spring housing with it. The spring meanwhile is compressed and biased by means of the helical sliding gear, and the clamping mechanism engages automatically. The angle of rotation is preferably a whole-number fraction of 360 degrees, e.g. 180 degrees. At the same time as the spring is tensioned, the power take-off component in the upper housing part is moved along by a given amount, the hollow piston is pulled back inside the cylinder in the pump housing, as a result of which some of the fluid from the storage container is sucked into the high pressure chamber in front of the nozzle. If desired, a plurality of replaceable storage containers containing the fluid to be atomised can be inserted in the atomiser one after another and then used. The storage container contains the aqueous aerosol preparation according to the invention The atomising process is initiated by gently pressing the actuating button. The clamping mechanism then opens the way for the power take-off component. The biased spring pushes the piston into the cylinder in the pump housing. The fluid emerges from the nozzle of the atomiser in the form of a spray. Further details of the construction are disclosed in PCT applications WO 97/12683 and WO 97/20590, to which reference is hereby made. - The components of the atomiser (nebuliser) are made of a material suitable for their function. The housing of the atomiser and - if the function allows - other parts as well are preferably made of plastics, e.g. by injection moulding. For medical applications, physiologically acceptable materials are used. Figures 1a/b, which are identical to Figures 6 a/b of WO 97/12687, show the Respimat® nebuliser with which the aqueous aerosol preparations according to the invention can advantageously be inhaled. Figure 1 a shows a longitudinal section through the atomiser with the spring under tension, Figure 2 b shows a longitudinal section through the atomiser with the spring released The upper housing part (51) contains the pump housing (52), on the end of which is mounted the holder (53) for the atomiser nozzle. In the holder is the nozzle body (54) and a filter (55). The hollow piston (57) fixed in the power take-off flange (56) of the locking clamping mechanism projects partly into the cylinder of the pump housing. At its end the hollow piston carries the valve body (58). The hollow piston is sealed off by the gasket (59) Inside the upper housing part is the stop (60) on which the power take-off flange rests when the spring is relaxed. Located on the power take-off flange is the stop (61) on which the power take-off flange rests when the spring is under tension. After the tensioning of the spring, the locking member (62) slides between the stop (61) and a support (63) in the upper housing part. The actuating button (64) is connected to the locking member. The upper housing part ends in the mouthpiece (65) and is closed off by the removable protective cap (66). The spring housing (67) with compression spring (68) is rotatably mounted on the upper housing part by means of the snap-fit lugs (69) and rotary bearings. The lower housing part (70) is pushed over the spring housing. Inside the spring housing is the replaceable storage container (71) for the fluid (72) which is to be atomised. The storage container is closed off by the stopper (73), through which the hollow piston projects into the storage container and dips its end into the fluid (supply of active substance solution). 14 |L The spindle (74) for the mechanical counter is mounted on the outside of the spring housing. The drive pinion (75) is located at the end of the spindle facing the upper housing part. On the spindle is the slider (76). The nebuliser described above is suitable for nebulising the aerosol preparations according to the invention to form an aerosol suitable for inhalation. If the formulation according to the invention is nebulised using the method described above (Respimat®), the mass expelled, in at least 97%, preferably at least 98% of all the actuations of the inhaler (puffs), should correspond to a defined quantity with a range of tolerance of not more than 25%, preferably 20% of this quantity. Preferably, between 5 and 30 mg, more preferably between 5 and 20 mg of formulation are delivered as a defined mass per puff. However, the formulation according to the invention can also be nebulised using inhalers other than those described above, for example jet-stream inhalers. Examples I. Example of the synthesis of tiotropium bromide monohydrate 15.0 kg of tiotropium bromide are added to 25.7 kg of water in a suitable reaction vessel. The mixture is heated to 80-90°C and stirred at constant temperature until a clear solution is formed. Activated charcoal (0.8 kg), moistened with water, is suspended in 4.4 kg of water, this mixture is added to the solution containing tiotropium bromide and rinsed with 4.3 kg of water. The mixture thus obtained is stirred for at least 15 min. at 80-90°C and then filtered through a heated filter into an apparatus which has been preheated to an outer temperature of 70°C. The filter is rinsed with 8.6 kg of water. The contents of the apparatus are cooled to a temperature of 20-25°C at a rate of 3-5°C every 20 minutes. Using cold water the apparatus is cooled further to 10-15°C and crystallisation is completed by stirring for at least another hour. The crystals are isolated using a suction filter drier, the crystal slurry isolated is washed with 9 L of cold water (10-15°C) and cold acetone (10-15°C). The crystals obtained are dried at 25°C for 2 hours in a nitrogen current. Yield: 13.4 kg of tiotropium bromide monohydrate (86 % of theory). 15 II. Examples of formulations 100 ml of pharmaceutical preparation contain: Example Amount of tiotropium bromide, based on tiotropium Amount of tiotropium bromide monohydrate Amount of benzalkonium chloride Amount of sodium edetate PH, adjusted with HCI (1N) 1 0.045 g — 10 mg 10 mg 2.9 2 0.057 10 mg 10 mg 2.9 3 0.023 g — 10 mg 10 mg 2.9 4 0.028 10 mg 10 mg 2.9 5 0.045 g — 10 mg 10 mg 2.8 6 0.057 10 mg 10 mg 2.8 7 0.023 g — 10 mg 10 mg 2.8 8 0.028 10 mg 10 mg 2.8 9 0.045 g — 10 mg 10 mg 3.0 10 0.057 10 mg 10 mg 3.0 11 hO.O~23 g — 10 mg 10 mg 3.0 12 0.028 10 mg 10 mg 3.0 The remainder is purified water or water for injections at a density of 1.00 g/cmJ at a temperature of 15°C to 31 °C. Further Examples 13 to 24: Analogous to Examples 1 to 12, but with 9 mg of sodium edetate. Further Examples 25 to 36: Analogous to Examples 1 to 12, but with 11 mg of sodium edetate. Further Examples 37 to 48: Analogous to Examples 1 to 12, but with 9 mg of benzalkonium chloride. Further Examples 49 to 60: Analogous to Examples 1 to 12, but with 11 mg of benzalkonium chloride. 16 *ln other examples, the amount of benzalkonium chloride is 8 or 12 mg. In other examples, the amount of sodium edetate is 8 or 12 mg. Of the Examples, Examples 1 to 4 are most preferred. WE CLAIM 1. Pharmaceutical preparation consisting of • tiotropium bromide as active substance, in a concentration based on tiotropium of between 0.02g per 100ml of formulation and 0.05g per 100ml of formulation, the tiotropium bromide being present in the pharmaceutical preparation is totally dissolved form. • water as the only solvent, • acid for adjusting the pH to between 2.7 and 3.1, preferably 2.8 and 3.05, • benzalkonium chloride in a concentration of between 8mg/ 100ml and 12mg/100ml, • sodium edentate in an amount of between 8mg/100ml of formulation and 12mg/100ml of formulation. 2. Pharmaceutical preparation as claimed in claim 1, wherein the pH is between 2.8 and 3.0, preferably 2.9. 3. Pharmaceutical preparation as claimed in any one of claims 1 to 2, wherein the pH is adjusted with an inorganic acid, preferably hydrochloric acid. 4. Pharmaceutical preparation as claimed in any one of claims 1 to 3, wherein 100ml of the formulation are prepared by dissolving 0.057g of tiotropium bromide monohydrate, l0mg of anhydrous benzalkonium chloride, l0mg of sodium edetate in water ad 100ml and 1N hydrochloric acid for adjusting the pH to 2.9. 5. Pharmaceutical preparation as claimed in any one of claims 1 to 3, wherein 100ml of the formulation are prepared by dissolving 0.028g of tiotropium bromide monohydrate, l0mg of anhydrous benzalkonium chloride, lOmg of sodium edetate in water ad 100ml and 1N hydrochloric acid for adjusting the pH to 2.9.

Documents:

2420-DELNP-2004-Abstract-(20-02-2009).pdf

2420-delnp-2004-abstract.pdf

2420-DELNP-2004-Claims-(20-02-2009).pdf

2420-delnp-2004-claims.pdf

2420-DELNP-2004-Correspondence-Others-(20-02-2009).pdf

2420-DELNP-2004-Correspondence-Others-(26-03-2010).pdf

2420-delnp-2004-correspondence-others.pdf

2420-delnp-2004-description (complete).pdf

2420-DELNP-2004-Drawings-(20-02-2009).pdf

2420-delnp-2004-drawings.pdf

2420-DELNP-2004-Form-1-(20-02-2009).pdf

2420-delnp-2004-form-1.pdf

2420-delnp-2004-form-13-(20-02-2009).pdf

2420-delnp-2004-form-18.pdf

2420-DELNP-2004-Form-2-(20-02-2009).pdf

2420-delnp-2004-form-2.pdf

2420-DELNP-2004-Form-26-(26-03-2010).pdf

2420-delnp-2004-form-3.pdf

2420-delnp-2004-form-5.pdf

2420-DELNP-2004-GPA-(20-02-2009).pdf

2420-delnp-2004-gpa.pdf

2420-delnp-2004-pct-210.pdf

2420-delnp-2004-pct-304.pdf

2420-delnp-2004-pct-308.pdf

2420-delnp-2004-pct-332.pdf

2420-delnp-2004-pct-409.pdf