Technical Field:

The present invention relates to a pharmaceutical composition comprising desloratadine or a pharmaceutically acceptable salt thereof, use of the inventive pharmaceutical composition as well as a process of producing the inventive composition. Background of the invention:

EP 0 152 897 B1 discloses descarbonylethoxyloratadine with the chemical name 8-chloro-6,11- dihydro-11-(4-piperdinylidene)-5H-benzo[5,6]cyclohepta[1 ,2-b]pyridine (further referred to as "desloratadine", or "DCL") as a metabolic derivative of loratadine and a long-acting tricyclic histamine antagonist with selective H1 -receptor histamine antagonist activity. Desloratadine is indicated for the relief of the nasal and non-nasal symptoms of allergic rhinitis (seasonal and perennial) as well as for the symptomatic relief of pruritus, reduction in the number and size of hives, in patients with urticaria.

WO 99/01450 A1 discloses several polymorphic forms of desloratadine, such as polymorph forms 1 and 2. WO 96/20708 A1 discloses methods and compositions for treating allergic rhinitis and other disorders, such as allergic asthma, retinopathy and small vessel disorders associated with diabetes mellitus, cough, cold, cold-like and/or flu symptoms and the discomfort, pain, headache, fever, and general malaise associated therewith in human using as active ingredient desloratadine alone or in combination with non-steroidal anti-inflammatory agents or other non-narcotic analgesics. WO 00/02560, however, describes that during the development of pharmaceutical compositions comprising desloratadine it has been discovered that desloratadine was found to discolor when stored at 75 % relative humidity ("RH") and a temperature of 40 ⁰ C (so called "accelerated storage conditions" according to the International Conference on Harmonization (ICH), which imitate the conditions of long term storage). This color instability in the active ingredient was found to be ap- parently due to a very minute amount of a degradation product of desloratadine, namely N- Formyldesloratadine, caused by the presence of a wide variety of excipients commonly used in solid, especially tablet formulations, which are able to undergo Maillard reaction in presence of desloratadine. Excipients found to be unsuitable include acidic excipients including, but not limited to stearic acid, povidone, crospovidone, and other excipients having a pH in water less than 7, as well as other excipients such as lactose, lactose monohydrate, sodium benzoate and glyceryl behenate. Such discolored pharmaceutical compositions do not fulfill the requirement of stability and accordingly, the following approaches have been undertaken to overcome the drawback of degradation of desloratadine in solid pharmaceutical compositions: WO 00/02560 teaches to combine desloratadine with a carrier medium comprising dibasic calcium phosphate and microcrystalline cellulose - in the absence of prior art excipients such as stearic acid or lactose - to provide stable pharmaceutical compositions.

In contrast thereto, EP 0 969 836 B1 discloses lactose-free, non-hygroscopic and anhydrous pharmaceutical compositions of desloratadine. Lactose-free - in the sense of EP 0 969 836 B1 - means that the amount of reactive excipient(s), if any, should be present in an amount insufficient to interact with desloratadine, i.e., should be less than about 20 wt.-%, preferably less than 10 wt.- % and even more preferably less than 1 wt.-%. In case lactose is present in the pharmaceutical composition, EP 0 969 836 B1 teaches to use alpha-lactose monohydrate. As a second embodiment EP 0 969 836 B1 teaches to use large particles of desloratadine with a particle size distribu- tion, wherein 40 wt.-% of desloratadine have a size of 250 μm or larger.

Other methods to reduce the decomposition of desloratadine in pharmaceutical compositions include adding an anti oxidant, preferably inorganic or organic sulfur (CN 1552324 A), an amino acid (EP 1 728 513 A2) or cyclodextrin (WO 2007/096733 A2) to the pharmaceutical composition or include providing desloratadine in molecular admixture with a pharmaceutically acceptable polymer (WO 2008/138563 A1) or providing desloratadine and a lactose based excipient, wherein the composition is free of a basic salt (US 2008/0118555 A1 ).

The above attempts to overcome the decomposition of desloratadine in solid pharmaceutical compositions show, that although lactose undergoes the decomposition reaction with desloratadine, it is, due to its characteristics, still preferred as filler material in the manufacture of a solid pharma- ceutical composition comprising desloratadine.

WO 2004/066984 A2 discloses improved taste masking pharmaceutical compositions which comprise (a) a core region comprising an API for which taste-masking is desired and at least one pharmaceutically acceptable excipient and (b) a taste masking film coating layer comprising: (i) a film-forming, water-insoluble polymer; and (ii) a pH dependent, water-insoluble polymer which dissolves at a pH level of about 5 or below. To prepare the taste masked pharmaceutical composition according to the teaching of the example of WO 2004/066984 A2 core granules comprising desloratadine and anhydrous lactose are initially prepared, fluidized in heated air in a fluidized bed coater and subsequently sprayed in the fluidized bed coater with bottom spray attachment with an aqueous taste masking coating dispersion comprising ethyl cellulose and Eudragit ^® EPO. The resulting taste masked coated granules are then dried, admixed with suitable pharmaceutical excipients and compressed to provide the tablet dosage form. To achieve the technical purpose of WO 2004/066984 A2, namely taste masking, a multiple step process is suggested, wherein under wet and heated conditions the respective tablets are prepared in the fluidized bed coater. Such a multiple step process, however, is in practice undesirable, as i) the time, machine and thus economic investment is high and ii) the wet and heated coating conditions in particular with the high surface area of the core granules may have a negative impact on physico-chemical properties, e.g. decomposition, of the active ingredient. Accordingly, there is still a need for providing a solid pharmaceutical composition comprising desloratadine and lactose with improved stability, wherein the physico-chemical properties, in particular the amount of impurities after storage, more specific the amount of decomposition products of desloratadine in the presence of lactose is reduced, preferably without adding specific pharmaceutically acceptable excipients and/or adjuvants as set out above and wherein the production process is time and cost effective.

Brief description of the invention:

The problem of the present invention is solved by the subjects of the independent claims. Advantages (preferred embodiments) are set out in the detailed description hereinafter as well as in the dependent claims. Accordingly, a first aspect of the present invention relates to a solid pharmaceutical composition in dosage form of a tablet comprising or consisting of desloratadine or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable excipients and/or adjuvants including lactose, characterized in that a) desloratadine or the pharmaceutically acceptable salt thereof is present in a therapeutically effective amount and that b) the lactose is present as anhydrous lac- tose in an amount of 22 to 78 wt.-% based on the total weight of the solid pharmaceutical composition and that the tablet is obtainable by a process comprising the following steps:

a. providing desloratadine or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable excipients and/or adjuvants including anhydrous lactose, b. blending the components provided in step a),

c. optional compacting the blended components of step b), and

d. compression of the blended components of step b) or compacts of step c) to form the solid pharmaceutical composition in dosage form of a tablet,

with the proviso, that the process steps a) through d) are carried out under dry conditions.

A second aspect of the present invention relates to a process of production of a solid pharmaceutical composition in dosage form of a tablet according to the present invention, characterized in that the process comprises or consists of the following steps:

a. providing desloratadine or a pharmaceutically acceptable salt thereof and one or more phar- maceutically acceptable excipients and/or adjuvants including anhydrous lactose,

b. blending the components provided in step a),

c. optional compacting the blended components of step b), and

d. compression of the blended components of step b) or compacts of step c) to form the solid pharmaceutical composition in dosage form of a tablet,

with the proviso, that the process steps a) through d) are carried out under dry conditions.

A third aspect of the present invention relates to the use of anhydrous lactose in the production of a solid pharmaceutical composition in dosage form of a tablet according to the present invention, wherein the amount of anhydrous lactose is in the range of 22 to 78 wt.-% based on the total weight of the solid pharmaceutical composition.

A fourth aspect of the present invention relates to the use of a solid pharmaceutical composition in dosage form of a tablet according of the present invention, wherein the solid pharmaceutical composition is used in the manufacture of a medicament for the treatment or prophylaxis of histamine- induced disorders.

The aspects of the present invention as set out hereinbefore can also comprise, if reasonable to a person skilled in the art, any possible combination of the preferred embodiments as set out in the dependent claims or disclosed in the following detailed description.

Detailed description of the invention:

It has surprisingly been found by the present inventors, that by using anhydrous lactose in the amount of 22 to 78 wt.-% based on the total weight of the solid pharmaceutical composition in dosage form of a tablet comprising desloratadine and by carrying out the production process under dry conditions, the amount of impurities, in particular of decomposition products of desloratadine, after storage under accelerated storage conditions of 40 ⁰ C and 75 % relative humidity (RH) for 1 to 6 months (accelerated storage conditions, ICH guideline Q 1 A (R2) "Stability Testing of new Drug Substances and Products") is lower than when using lactose monohydrate and, thus, stable solid pharmaceutical compositions can be provided with total impurities of not more than 1.0 wt.-% (see hereinafter in particular Part B of the Examples). Accordingly, the inventive solid pharmaceutical composition can comprise lactose as the preferred filler for compression without the need of further adding specific pharmaceutically acceptable excipients and/or adjuvants to inhibit the decomposition reaction between lactose and desloratadine.

In contrast thereto the present inventors show in Part C of the Examples hereinafter that no im- provement of the stability data occurs, when the production process is carried out under wet conditions and in the comparative composition lactose monohydrate (C2) is exchanged by the same amount of anhydrous lactose (C3) or a 1 :1 mixture of anhydrous lactose and mannitol. Accordingly, it is surprising that when using the inventive production process carried out under dry conditions an improvement in stability of desloratadine can be achieved. A further advantage of the present invention is that by using the inventive production process carried out under dry conditions, e.g. direct compression or dry granulation-compression, a simple as well as time and cost effective production process is provided.

In the context of the present invention the inventive pharmaceutical compositions are present in dosage forms of tablets. To further inhibit degradation of desloratadine, preferably the dosage form of a tablet of the inventive pharmaceutical composition reduces interaction with oxygen and/or moisture in the air, preferably by using a suitable coating. Accordingly, the most preferred dosage forms of the inventive compositions are coated tablets.

In context of the present invention desloratadine can be used as the free base or in form of a pharmaceutically acceptable salt (also commonly referred to as desloratadine), preferably in form of the free base. Furthermore, desloratadine can be used in either polymorphic forms 1 or 2 or as a mixture of polymorphic forms 1 and 2. To further reduce the decomposition of desloratadine, preferably anhydrous or low moisture desloratadine is used in the manufacture of inventive compositions. Furthermore, the particle size distribution of desloratadine in the inventive composition is preferably such, that 60 wt.-% of desloratadine particles have a particle size of less than 250 μm (D ₆₀ < 250 μm), more preferably D ₉₀ < 45 μm and/or D ₁₀₀ < 110 μm. Desloratadine is present in the inventive pharmaceutical composition in a therapeutically effective amount, preferably in the range of 1 to 15 wt.-%, more preferred 3 to 10 wt.-% based on the total weight of the inventive composition in dosage form of a tablet, or - in case the inventive composition is present as a coated tablet - based on the total weight of the uncoated tablet (core of the coated tablet). In a most preferred embodiment of the present invention, the amount of desloratadine in one inventive tablet dosage form is 2.5 mg, 5.0 mg, 7.5 mg or 10.0 mg calculated on the free base.

In the context of the present invention anhydrous lactose is used in the amount of 22 to 78 wt.-%, preferably 22 to 30 wt.-%, 45 to 55 wt.-% or 70 to 78 wt.-%, more preferably 25, 50 or 75 wt.-% based on the total weight of the inventive composition in dosage form of a tablet or - in case the inventive composition is present as a coated tablet - based on the total weight of the uncoated tablet (core of the coated tablet). Anhydrous lactose in the sense of the present invention shall comply with the requirements of the relevant monographs, in particular it shall comprise less than 1.0 %, preferably less than 0.5 wt.-% of water based on the European Pharmacopoeia monograph. In addition or alternatively to the preferred embodiments as set out hereinbefore, the inventive composition can contain in addition to anhydrous lactose one, two, three, four, five or more further pharmaceutically acceptable excipients and/or adjuvants, preferably selected from the group comprising or consisting of binders, disintegrants, flavoring agents, glidants, solubilizers, lubricants, coating polymers and aids and/or encapsulating material. The further pharmaceutically acceptable excipients are suitable for the inventive production process, wherein the direct compression (steps a), b) and d)) or compaction-compression (steps a) through d)) procedure is carried out under dry conditions.

In a preferred embodiment one or more of the following substances, which act as binders and/or disintegrants are used: microcrystalline cellulose, maize starch, povidone, hydroxypropyl cellulose, copovidone, pregelatinized starch, dibasic calcium phosphate, sugar, low substituted hydroxypro- pylcellulose, mannitol, crospovidone, sodium starch glycolate, croscarmellose sodium or mixtures thereof, more preferred are microcrystalline cellulose, low substituted hydroxypropylcellulose, mannitol, the combination of microcrystalline cellulose and low substituted hydroxypropylcellulose, or the combination of microcrystalline cellulose and crospovidone. Still further preferred are inven- tive compositions, wherein

a. microcrystalline cellulose is in the range of 30 to 70 wt.-%, preferably 40 to 66 wt.-%, b. low substituted hydroxypropylcellulose is in the range of 10 to 70 wt.-%, preferably 15 to 66 wt.-%,

c. mannitol is in the range of 40 to 70 wt.-%, preferably 50 to 66 wt.-%,

d. microcrystalline cellulose is in the range of 60 to 65 wt.-%, preferably 63 wt.-% and low substituted hydroxypropyl cellulose is in the range of 1 to 7 wt.-%, preferably 5 wt.-%, or e. microcrystalline cellulose is in the range of 10 to 70 wt.-%, preferably 14 to 65 wt.-% and

crospovidone is in the range of 1 to 5 wt.-%, preferably 2 to 3 wt.-%, respectively based on the total weight of the inventive composition in dosage form of a tablet or - in case the inventive composition is present as a coated tablet - based on the total weight of the uncoated tablet (core of the coated tablet).

In other words, in case microcrystalline cellulose and low substituted hydroxypropylcellulose are selected from the group of substances as further pharmaceutical excipients and/or adjuvants, in particular which act as binders and/or disintegrants, then the weight ratio of microcrystalline cellulose is in the range of 60 to 65 wt.-%, preferably 63 wt.-% and low substituted hydroxypropyl cellulose is in the range of 1 to 7 wt.-%, preferably 5 wt.-% meaning that the weight ratios outside the described range of weight ratios are not preferred.

Explicitly not claimed by the present invention is the formulation prepared according to a production process carried out under wet conditions as described in the Example of WO 2004//066984 A2, namely wherein core granules of the following formulation comprising 5 mg desloratadine, 13 mg anhydrous lactose, 19.50 mg microcrystalline cellulose, 3.25 mg calcium carboxymethyl cellulose, 2.20 mg low substituted hydroxypropyl cellulose, 0.10 mg colloidal silicon dioxide and 0.45 mg magnesium stearate are initially prepared, then spray coated in a fluidized bed coater with bottom spray attachment with an aqueous dispersion of ethyl cellulose and Eudragit ^® EPO, a basic butylated methacrylate copolymer and subsequently dried and compacted to a tablet dosage form.

In addition or alternatively to the preferred embodiments as set out hereinbefore, the inventive composition in dosage form of a tablet comprises or consists of one or more substances, which act as lubricants, preferably fatty acids or fatty acid derivatives, such as alkali and earth alkali salts of stearic, lauric and/or palmitic acid, more preferred calcium stearate, magnesium stearate, sodium stearyl fumarate, sodium lauryl sulfate, talc, hydrogenated vegetable oil, zinc stearate, or mixtures thereof. Most preferably magnesium stearate is comprised in the inventive composition as the or one of the lubricants. In general, the amount of lubricants, preferably magnesium stearate is present in the range of 0 to 5 wt.-%, preferably, 1 to 4 wt.-% and most preferred 1 to 2 wt.-% based on the total weight of the inventive composition in dosage form of a tablet or - in case the inventive composition is present as a coated tablet - based on the total weight of the uncoated tablet (core of the coated tablet).

In addition or alternatively to the preferred embodiments as set out hereinbefore, the inventive solid pharmaceutical composition in dosage form of a tablet additionally comprises or consists of a pharmaceutically acceptable coating. Suitable inert coating agents and methods for coating particles or granules are well known in the art. Typically, inert coating agents comprise an inert film- forming agent dispersed in a suitable solvent, and may further comprise other pharmaceutically acceptable adjuvants, such as colorants and/or plasticizers. Preferably, the coating of the inventive composition comprises or consists of one or more of the following film-forming components se- lected from the list consisting of: hydroxypropyl cellulose, hydroxypropylmethyl cellulose, ethyl cellulose, polyvinyl alcohol, polyethylene glycol-polyvinyl alcohol graftpolymer or mixtures thereof. Preferred are combinations of hydroxypropyl cellulose : hydroxypropylmethyl cellulose or hydroxypropyl cellulose : hydroxypropylmethyl cellulose : ethyl cellulose. The ratio of hydroxypropyl cellu- lose : hydroxypropylmethyl cellulose is preferably in the range from 1 :10 to 10:1 , more preferably 1 :1. The ratio of hydroxypropyl cellulose : hydroxypropylmethyl cellulose : ethyl cellulose is preferably in the range of 5:5:1 to 1 :1 :8. As colorants aluminium lakes, such as indigo carmine aluminium lake, and/or iron oxides, such as red iron oxide, and/or titanium dioxide are preferably used in suitable amounts. Preferably, the coating of an inventive solid composition in dosage form of a tablet does not comprise a pH dependent, water-insoluble polymer which dissolves at a pH level of about 5 or below, more specifically preferably does not comprise a basic butylated methacrylate copolymer, e.g. Eudragit ^® EPO.

In addition or alternatively to the preferred embodiments as set out hereinbefore, the inventive composition in dosage form of a tablet further comprises or consists of a therapeutically effective amount of one or more additional active ingredients. Suitable additional active ingredients include pharmaceutically acceptable salts, solvates, enantiomers or mixtures thereof, preferably selected from the group comprising or consisting of decongestants, preferably sympathomimetic nasal decongestants, e.g., pseudoephedrine, or parasympatholytics, e.g., oxybutynin; expecto- rants/mucolytics, e.g., ambroxol; analgesics, opioid analgesics or non-narcotic analgesics; anti- inflammatory drugs, preferably anti-inflammatory non-steroidal drugs (NSAID) or COX-2 inhibitors; anti-tussives; bronchodilators; corticosteroids, e.g., mometasone; leukotriene receptor antagonists, e.g., montelukast; prostaglandin D ₂ antagonists and/or neurokinin receptor antagonists.

In case the inventive composition in dosage form of a tablet comprises or consists of a therapeutically effective amount of one or more additional active ingredients, the inventive composition is preferably present as a multilayer, preferably bilayer tablet, wherein the therapeutically effective amount of desloratadine is present in a first layer and the or one of the additional active ingredients are present in one or more additional layers, preferably in one additional (second) layer.

In case the inventive composition is present as a coated tablet, the therapeutically effective amount of desloratadine is preferably present in the uncoated core of the tablet and the or one of the addi- tional active ingredients is/are present in the coating of the tablet.

In addition or alternatively to the preferred embodiments as set out hereinbefore, the inventive composition in dosage form of a tablet does not comprise or consist of an anti oxidant, preferably in form of inorganic or organic sulfur (such anti oxidants as disclosed in CN 1552324 A and incorporated herein by reference), an amino acid, preferably arginine, cystein, tyrosine, histidine, lysine and/or tryptophan (such amino acids as disclosed in EP 1 728 513 A2 and incorporated herein by reference), cyclodextrin (such cyclodextrins as disclosed in WO 2007/096733 A2 and incorporated herein by reference), desloratadine in molecular admixture with a pharmaceutically acceptable polymer (such desloratadine - polymer molecular admixture as disclosed in WO 2008/138563 A1 and incorporated herein by reference), triglycerides, wax and/or polyethylene glycol (PEG) (such triglycerides, wax and/or polyethylene glycol as disclosed in WO 2007/140987 A1 and incorporated herein by reference). Furthermore in case water-insoluble starch products (such starch products as disclosed in US 2008/0118555 A1 and incorporated herein by reference) are contained in the inventive composition one or more basic salts are also comprised.

With respect to the second aspect of the present invention, namely the inventive process of pro- duction of a solid pharmaceutical composition in dosage form of a tablet according to the present invention, the process steps are readily known in the art and can be carried out by persons skilled in the art. The process steps a) through d) are to be carried out under dry conditions, which mean in the context of the present invention that no solvent, in particular water shall be added. Preferably, the moisture and humidity conditions are such, that inventive solid pharmaceutical composi- tions are produced by the inventive process, which comprise or consists of an amount of unbound water of less than 5 wt.-%, preferably less than 3.5 wt.-%, more preferably less than 2 wt.-% based on the total weight of the inventive composition, whereby the unbound water is measured by the loss of drying method, wherein the composition is analysed at 105 ⁰ C until a constant value is obtained for 1 to 2 minutes using a Mettler Toledo moisture analyzer. With respect to preferred embodiments of desloratadine, anhydrous lactose and the further pharmaceutically acceptable excipients and/or adjuvants suitable for the inventive production process of the second aspect of the present invention, we refer to the description thereof hereinbefore in connection with the inventive solid pharmaceutical composition of the first aspect of the present invention.

In addition or alternatively to the preferred embodiments as set out hereinbefore, desloratadine and one or more pharmaceutically acceptable excipients and/or adjuvants including anhydrous lactose are preferably provided in process step a) of the inventive process after being sifted, preferably with a sieve showing 0.2 to 1 mm aperture.

In addition or alternatively to the preferred embodiments as set out hereinbefore, the compaction in process step c) of the inventive process is preferably carried out by dry granulation technique readily known to a person skilled in the art. Preferably roller compactors, Fitzpatrick roller compactor mills and tabletting machines can be used. More preferably, the compacts produced in step c) are milled prior to carrying out step d). In a further preferred embodiment the (milled) compacts in step c) are sifted, preferably # 30 mesh (= 0.6 mm), and/or are lubricated with (pre sifted, preferably # 40 mesh (= 0.4 mm)) lubricants, preferably magnesium stearate, prior to compression in step d). In accordance with process step d) of the inventive process the compression can be carried out by methods already known to a person skilled in the art, in particular by any available tablet compression method.

In addition or alternatively to the preferred embodiments as set out hereinbefore, the compressed solid pharmaceutical composition in dosage form of a tablet of step d) is in a subsequent step e) coated with one or more pharmaceutically acceptable excipients and/or adjuvants. Suitable methods are already known in the art and suitable pharmaceutically acceptable excipients and/or adjuvants have been already described with respect to the first aspect of the present invention.

As a result a further aspect of the present invention relates to a solid pharmaceutical composition in dosage form of a tablet comprising or consisting of desloratadine or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable excipients and/or adjuvants including lactose obtainable by the inventive process as described hereinbefore, characterized in that a) desloratadine or a pharmaceutically acceptable salt thereof is present in a therapeutically effective amount and that b) the lactose is present as anhydrous lactose in an amount of 22 to 78 wt.-% based on the total weight of the solid pharmaceutical composition. With respect to the preferred embodiments we refer to the description thereof hereinbefore in connection with the inventive solid pharmaceutical composition of the first aspect of the present invention.

With respect to the third aspect of the present invention preferred embodiments of suitable anhydrous lactose has been described hereinbefore in connection with the first aspect of the present invention.

With respect to the fourth aspect of the present invention the medicament is preferably used in the treatment or prophylaxis of allergic rhinitis, allergic asthma, urticaria, symptomatic dermographism, diabetic retinopathy and other small vessel disorders associated with diabetes mellitus, as well as cough, cold, cold-like and/or flu symptoms and the discomfort, pain, headache, fever, and general malaise associated therewith.

The present invention is explained further with the aid of the following non-limiting examples, illustrating the parameters of and compositions employed within the present invention. Unless stated otherwise, all data, in particular percentages, parts and ratios are by weight. Examples:

Part A: Process of production of pharmaceutical compositions

The following procedure illustrates the production procedures of comparative composition (C1 ) and inventive pharmaceutical compositions (F1 to F13) as (coated) tablet formulations:

Ingredients (in mg/tablet) C1 F1 F2 F3 F4 F5 F6

Stage A

Desloratadine (Matrix Laborato¬

5.0 5.0 5.0 5.0 5.0 5.0 5.0 ries, Secunderabad, India)

Lactose Monohydrate

69.0 - - - - - - (Tablettose ^® 80)

Lactose Anhydrous

- 15.0 15.0 15.0 15.0 15.0 25.0 (SuperTab ^® 21 AN)

Microcrystalline Cellulose

23.0 39.4 39.4 39.4 39.4 - 63.0 (Avicer PH 102)

Low substituted Hydroxypropyl

39.4 5.0 cellulose (L-HPC LH11 )

Mannitol (Pearlitol ^® SD200) . . . . . . .

Crospovidone

(Polyplasdone ^® XL)

Magnesium Stearate

3.0 0.6 0.6 0.6 0.6 0.6 2.0 Synpro ^® Mg stearate VG

Core tablet weight (mg) 100.0 60.0 60.0 60.0 60.0 60.0 100.0

Stage B

Hypromellose/Hyprolose (1 :1 ) ^ _n

2.7 1.8 3.0 3.0 3.0

(Opadry ^® blue 20A50668)

Ethycellulose (Ethocel ^® 4cp) 0.3 1.2 - - - lsopropyl alcohol q.s q.s q.s q.s q.s q.s

Water, purified q.s q.s q.s q.s q.s q.s

Coated tablet weight (mg) 105.0 60.0 63.0 63.0 63.0 63.0 103.0

Ingredients (in mg/tablet) F7 F8 F9 F10 F11 F12 F13

Stage A

Desloratadine (Matrix Laborato¬

5.0 5.0 5.0 5.0 5.0 5.0 5.0 ries, Secunderabad, India)

Lactose Anhydrous

(SuperTab ^® 21 AN) 15.0 15.0 50.0 30.0 50.0 75.5 49.1

Microcrystalline Cellulose

(Avicel ^® PH 102) 37.6 43.0 40.0 14.5

Low substituted Hydroxypropyl _{i n} _

_C eIIuI _OS e (L-HPC LHI I ) - - - - - - ηu.υ

Mannitol (Pearlitol ^® SD 200) - 39.4 - 24.4

Crospovidone , .

(Polyplasdone ^® XL) ^{1 8 " " " 3 0 3 0}

ssffassSvo ^o« ° ^{6 2} -° < ^{« 2o 2o} °- ⁹

Core tablet weight (mg) 60.0 60.0 100.0 60.0 100.0 100.0 65.0

Stage B

Hypromellose/Hyprolose (1 :1 )

3.0 3.0 3.0 3.0 3.0 3.0 3.0 (Opadry ^® blue 20A50668)

Ethycellulose (Ethocel ^® 4cp)

lsopropyl alcohol q.s q.s q.s q.s q.s q.s q.s

Water, purified q.s q.s q.s q.s q.s q.s q.s

Coated tablet weight (mg) 63.0 63.0 103.0 63.0 103.0 103.0 68.0

Procedure I: direct compression (F5 to F8 and F10 to F12):

1. sift all the ingredients of stage A through # 40 mesh (= 0.4 mm),

2. blend the sifted ingredients in a blender (pillar blender, Tapasya Engineering Works Pvt.

Ltd.), and

3. compress the tablets using 5.5 mm biconcave, round punches (Ajas Components Pvt. Ltd.).

Procedure II: dry granulation-compression (F1 to F4, F9 and F13):

1. sift ingredients of stage - A through # 40 mesh (= 0.4 mm),

2. blend all the sifted ingredients in blender (pillar blender, Tapasya Engineering Works Pvt. Ltd.),

3. compact the blend using 16 mm FFBE punch (Ajas Components Pvt. Ltd.) to form slugs,

4. mill the slugs in multi mill using 10 mm screen, knives forward at medium speed (Multimill Lab, Gansons Ltd.),

5. pass the milled slugs through # 30 mesh (= 0.6 mm),

6. mill the retentions in multi mill using 1 mm screen knives forward at high speed (Multimill Lab, Gansons Ltd.),

7. pass the milled granules through # 30 mesh (= 0.6 mm),

8. lubricate the granules with # 40 mesh (= 0.4 mm) pre sifted magnesium stearate, and

9. compress tablets using 5.5 mm s/c tooling (Rotary Tablet Machine CMD3-16, Cadmach Machinery Co. Pvt. Ltd.). Optionally the core tablets produced by I: direct compression or II: dry granulation are coated as follows:

1. disperse coating material in isopropyl alcohol under stirring,

2. add required quantity of water to step 1 ,

3. continue stirring up to 45 min, to get homogeneous solution.

4. pass the solution through # 60 mesh (= 0.25 mm), and

5. coat the tablets in automated perforated coating machine (Ganscoater, Gansons Ltd.).

Part B: Stability of inventive pharmaceutical compositions

The present invention provides solid pharmaceutical compositions in dosage form of a tablet com- prising desloratadine and anhydrous lactose obtainable by the inventive production process carried out under dry conditions, which are improved in their stability compared to compositions comprising desloratadine and lactose monohydrate, whereby the improved stability is shown by reduction of impurities. An inventive solid pharmaceutical composition in form of coated tablets produced according to formulation F13 in Part A above as well as a comparative compositions in form of coated tablets produced according to formulation C1 in Part A above are used to carry out stability tests under conditions of 40 ⁰ C and 75 % relative humidity (RH) for up to 6 months (accelerated storage condi- tions, ICH guideline Q 1 A (R2)).

The amount of loratadine, unknown impurities (unknown imp.) and total amount of impurities (total imp.) in wt.-% based on the total weight of the coated tablets of the inventive composition F13 and the comparative composition C1 are measured (according to European Pharmacopoeia 6.5, section 5.10) initially after production (in the following initially) and when stored in high density polye- thylene containers (in the following HDPE; after storage time of 1 , 2, 3, or 6 months (in the following 1 M, 2M, 3M, or 6M):

Unknown Total

Formulation Condition Loratadine

Imp. Imp.

Initial 0.00 0.02 0.02

40 °C/75%RH,1 M 0.00 0.07 0.13

C1 40 °C/75%RH,2M 0.00 0.12 0.19

40 °C/75%RH,3M 0.00 0.17 0.31

40 °C/75%RH,6M 0.00 0.43 0.79

Initial 0.00 0.03 0.05

40 °C/75%RH,1 M 0.00 0.05 0.09

F13 40 °C/75%RH,2M 0.00 0.06 0.11

40 °C/75%RH,3M 0.00 0.07 0.12

40 °C/75%RH,6M 0.00 0.08 0.12

Accordingly, the total amount of impurities and the amount of impurities relative to the initial amount for coated tablets of the comparative composition C1 after storage for one, two, three or six months is higher than for coated tablets of the inventive composition F13 and, thus, inventive compositions comprising desloratadine and anhydrous lactose show an improved stability over compositions of the state of the art comprising desloratadine and lactose monohydrate (C1 ). Part C: Comparative formulations on basis of US 2008/0118555 A1, Example 2

The following formulations have been prepared according the production process carried out under wet conditions described in the description of US 2008/0118555 A1 , Example 2.

Ingredients (in mg/tablet) C2 C3 C4

I. Dry Mix

Desloratadine 5.00 5.00 5.00

Lactose Monohydrate 55.00

Lactose Anhydrous - 55.00 25.00

Corn Starch 20.55 20.55 20.55

Pregelatinized Starch 2.00 2.00 2.00

Mannitol - - 30.00

II. Binder Solution

Water, purified q.s q.s q.s

III. Lubrication

Corn starch 7.00 7.00 7.00

Magnesium stearate 0.45 0.45 0.45

Tablet weight (mg) 90.00 90.00 90.00

The formulation of C2 consists of the same ingredients and has been produced by the same production process carried out under wet conditions as described for the formulation of Example 2 in US 2008/0118555 A1.

The formulations of C3 and C4 differ from the formulation of C2 in that lactose monohydrate is not comprised, however, in place of lactose monohydrate the same amount of anhydrous lactose or a 1 :1 mixture of anhydrous lactose and mannitol is comprised.

Comparative compositions C2 through C4 have been used to carry out stability tests under conditions of 40 ⁰ C and 75 % relative humidity (RH) for up to 3 months (accelerated storage conditions, ICH guideline Q 1 A (R2)). The amount of unknown impurities (unknown imp.) and total amount of impurities (total imp.) in wt.-% based on the total weight of the tablets of the comparative composi- tions C2, C3 and C4 are measured (according to European Pharmacopoeia 6.5, section 5.10) initially after production (in the following initially) and when stored in high density polyethylene containers (in the following HDPE; after storage time of 1 , 2, or 3 months (in the following 1 M ₁ 2M, or 3M). In addition the stability data provided for the formulation of Example 2 in US 2008/0118555 A1 is incorporated:

2008/0118555

Initial 0.08 0.10

A1

Data provided in

application

40°C/75%RH,1 M 0.06 0.18

40°C/75%RH,2M - 0.06 0.17

40°C/75%RH,3M - 0.05 0.16

C2 Initial ND 0.04 0.04

40°C/75%RH,1 M ND 0.07 0.15

40°C/75%RH,2M ND 0.07 0.16

40°C/75%RH,3M ND 0.08 0.18

C3 Initial ND 0.06 0.06

40°C/75%RH,1 M ND 0.07 0.17

40°C/75%RH,2M ND 0.08 0.19

40°C/75%RH,3M ND 0.10 0.22

C4 Initial ND 0.05 0.05

40°C/75%RH,1 M ND 0.07 0.15

40°C/75%RH,2M ND 0.08 0.18

40°C/75%RH,3M ND 0.10 0.22

In contrast to the finding under Part B, the stability data of comparative compositions C2 through C4 show that no improvement of the stability data occurs, when the production process is carried out under wet conditions and lactose monohydrate of the comparative composition (C2) is ex- changed by the same amount of anhydrous lactose (C3) or a 1 :1 mixture of anhydrous lactose and mannitol. Accordingly, it is surprising that when using the inventive production process carried out under dry conditions an improvement in stability of desloratadine can be achieved.