AU764413B2 - A pharmaceutical composition comprising cyclosporin in a lipid carrier - Google Patents

Description

WO 00/32219 PCT/SE99/02259 A PHARMACEUTICAL COMPOSITION COMPRISING CYCLOSPORIN IN A LIPID CARRIER The present invention refers to a new formulation of a cyclosporin for oral administration giving an improved uptake.

Background of the invention Cyclosporins are a group of biologically active metabolites produced by different species of funghi imperfecti.

The major components, cyclosporins A and C are non-polar cyclic oligopeptides with immunosuppressive, antifungal and antiphlogistic activity. Today a number of minor metabolites have been identified, all being highly hydrophobic oligopeptides. The major use of cyclosporins is to prevent organ rejection after transplantation.

Cyclosporin A, cyclosporine or ciclosporin, is a cyclic oligopeptide consisting of 11 amino acids. The exact mechanism of action of cyclosporine is not known, but it is believed that the effect is due to a specific and reversible inhibition of immunocompetent lymphocytes. Cyclosporine is commercially available under the registered trade marks Sandimmun Neoral®, Neoral" or Sandimmune®, as soft gelatin cpsules, an oral solution or as a concentrate for injection.

Said formulations all contain more than 10 ethanol. The absorption of cyclosporine, administered as Sandimmun Neoral®, Neoral® or Sandimmune®, from the gastro-intestinal tract is, however, incomplete and variable and it is recommended that transplant patients taking the soft gelatin capsules or the oral solution over a period of time are monitored.at repeated intervals for cyclosporine blood levels to avoid toxicity due to high levels, and possible organ rejection due to low absorption, respectively.

Prior art US 4,388,307 refers to a pharmaceutical composition comprising a pharmacologically effective amount of a cyclosporin and a carrier, wherein the carrier comprises a) a transesterification product of a natural vegetable oil, b) a vegetable oil, and c) ethanol. Said composition could be WO 00/32219 PCT/SE99/02259 2 formulated as a drink solution or as capsules for oral administration. The use of ethanol is, however, not desirable and may also cause difficulties when the composition is presented in soft gelatin encapsulated form.

In GB 2 228 198 B it is proposed to use a carrier medium for a cyclosporin which comprises b) a fatty acid triglyceride, c) a glycerol fatty acid partial ester or propylene glycol or sorbitol complete or partial ester, and d) a tenside having a hydrophilic-lipophilic balance (HLB) of at least 10. By this it would be possible to obtain oil-based compositions of a cyclosporin which do not require the presence of solvents or solubilizers such as ethanol. The tensides used in the examples are different ethoxylated reaction products, such as Cremophor RH 40, Tween, and Pluronic. The compositions obtained are said to provide a reduced variability in cyclosporine blood levels. It is, however, a well known fact that ethoxylated surfactants might be the cause of allergenic reactions, partly because of oxidation when exposed to air, and thus should be avoided in medical treatment.

Lipophilic carrier systems have also been described, WO 95/20945 for instance discloses a lipophilic carrier preparation having a continuou lipid phase comprising a polar ipid material in combination with a non-polar lipid. The polar lipid material should be a galactolipid material consisting of at least 50 digalactosyldiacylglycerols and a remainder of other polar lipids. In Example 2 of said publication a preparation of a lipophilic carrier containing 5 cyclosporin A, in combination with a galactolipid material and evening primrose oil is disclosed. Said galactolipid material had been obtained by an industrially applicable process for preparing glycosylglycerides from plants, preferably cereals, by means of extraction and chromatographic separations.

WO 92/05771 describes a lipid particle forming matrix of at least two lipid components; one is non-polar and another is amphiphatic and polar. This particle forming matrix, which can contain bioactive materials, spontaneously forms discrete lipid particles when interacting with aqueous systems. The amphiphatic and polar lipid components are said to be bilayer 3 forming and are chosen from phospholipids such as phosphatidylcholine; the non-polar lipids are mono-, di-or triglycerides.

Description of the invention It has now surprisingly been found that a formulation of a cyclosporin in a lipid carrier consisting of a fractionated vegetable oil in combination with monoglycerides and nonpolar lipids will give an uptake of the cyclosporin in blood which is bioequivalent to the uptake of cyclosporin from a commercial drug containing in addition to cyclosporin and additives also toxic emulsifiers and ethanol.

According to FDA a standard bioequivalence can be defined as a range of 80% to 120% of the product averages for a broad range of drugs (USP 24 NF 19,2058).

The present invention refers to a new pharmaceutical composition comprising a cyclosporin as an active substance in a lipid carrier, which carrier comprises membrane lipids in combination with monoglycerides and optionally non-polar lipids, which is characterized in being liquid at room temperature and containing the following in by weight of the total composition cyclosporin 0.5-25 membrane lipids 10-45 monoglycerides 10-55 non-polar lipids 0-45 Thus, according to an embodiment of the invention, there is provided a pharmaceutical composition comprising a cyclosporin as an active substance in a lipid carrier, which carrier comprises membrane lipids in combination with monoglycerides and optionally non-polar lipids, which is characterized in being liquid at room temperature and containing the following in by weight of the total composition cyclosporin 0.5-25 membrane lipids selected from phospholipids, glycolipids and sphingolipids 10-45 monoglycerides 10-55 non-polar lipids 0-45 The invention especially refers to a pharmaceutical composition wherein the lipid carrier contains 15-20 membrane lipids, 25-50 monoglycerides and 5-30 nonpolar lipids.

i According to another aspect of the invention the lipid carrier of the Spharmaceutical composition contains 15-45 membrane lipids and 25-50 35 monoglycerides.

i Membrane lipids, preferably natural membrane lipids for the sake of biocompatibility and safety, which are all polar lipids, can broadly be defined as belonging to any of the categories phospholipids, glycolipids and sphingolipids.

A558314speci 3a According to another embodiment of the invention, there is provided a method of treatment or prophylaxis of a condition in a patient indicating administration of cyclosporin, said method comprising administering to said patient an effective amount of a composition according to the invention. Typically, said condition comprises rejection s of a transplanted organ.

According to a related aspect of this embodiment, there is also provided the u se of: cyclosporin; membrane lipids selected from phospholipids, glycolipids and sphingolipids; monoglycerides; and non-polar lipids; for the manufacture of a medicament for the prevention of rejection of transplanted organs, said medicament o0 comprising the following in by weight of the total: cyclosporin 0.5-25 membrane lipids 10-45 monoglycerides 10-55 and non-polar lipids 0-45 According to another related aspect of this embodiment of the invention, there is provided a composition according to the invention, when used for preventing rejection of a transplanted organ.

Phospholipids, mainly soy or egg lecithin derived from soybeans and egg respectively, or made by synthetic routes *o A558314spcci WO 00/32219 PCT/SE99/02259 4 contain different phospholipid classes, which can be zwitterionic, such as phosphatidylcholine and phosphatidylethanolamine classes, or negatively charged, such as phosphatidylinositol or phosphatidylglycerol classes.

Glycolipids from plants contain glycolipids which have carbohydrate units, mainly of galactose, linked to glycerol.

Glycosylglycerides are a type of glycolipids which are wellknown constituents of plant cell membranes. The most important classes of these contain one to four sugars linked glycosidically to diacylglycerol. The two most abundant classes contain one and two galactose units, respectively, and are commonly known as mono- and digalactosyldiacylglycerol, MGDG and DGDG representing up to 40 of the dry weight of the thylakoid membranes. Galactolipids, primarily DGDG and DGDG-rich materials, have been investigated and found to be a surface active material of interest in industrial application such as food, cosmetics, and pharmaceutical applications.

Synthetic diglycosyldiacylglycerols based on galactose or any other monosaccharide unit, such as glucose, and natural glycosylglycerides, isolated from any source, based on other carbohydrate units than galactose, such as glucose, can be used in accordance with the invention.

An intrinsic beneficial feature of the galactolipids is the galactose units comprising the polar head group in each lipid molecule, which may sterically stabilise the emulsion droplets in an emulsion. The galactose groups may also interact strongly with water and other polar substances, such as a water-soluble drug or an excipient, added to the emulsion. In investigating the interaction of the glycosylglycerides with non-polar or slightly polar lipids, such as mono-, di- and triglycerides, fatty alcohols and acids, sterols and sterol esters, optionally combined with other polar lipids such as phospholipids and sphingolipids, without water, or with only small amounts of water, it has been found a behaviour which makes such preparations suitable as lipophilic carriers.

According to a preferred aspect of the invention the membrane lipids of the pharmaceutical composition contain WO 00/32219 PCT/SE99/02259 phospholipids and galactolipids. Especially the membrane lipids of the pharmaceutical composition contain DGDG in admixture with phosphatidylcholine.

Galactolipids can be prepared from almost any kind of plant material, for instance according to WO 95/20945 by extraction of the lipids with ethanol and a subsequent purification on a chromatographic column. Preferred plant materials are seeds and kernels from grains and cereals, for instance wheat, rye, oats, and barley. Oat groats as well as wheat gluten have a high lipid concentration and are therefore of advantage to use in the preparation process. A galactolipid material consisting of 50-70 digalactosyldiacylglycerols and 30-50 other polar lipids is manufactured by Scotia LipidTeknik AB, Stockholm, as CPL®- Galactolipid (registered trade mark owned by Scotia Holdings PLC). The other polar lipids being part of said galactolipid material are a mixture of different glyco- and phospholipids, such as MGDG and phosphatidylcholines.

WO 97/11141 describes a method for producing a fractionated vegetable oil which is characterised in containing 10-90 by weight of polar lipids, preferably 20-75 and a remainder of non-polar lipids. Said fractionated vegetable oil contains galactolipids and can also be used for -rovidng the membrane lipids of the invention. The fractionated vegetable oil preferably contains more than 5 by weight, preferably more than 20 glycolipids and preferably more than 3 by weight, preferably more than 15 DGDG. According to a preferred embodiment of the invention the fractionated oil is oat oil consisting of 40-60 polar lipids and a remainder -of non-polar lipids. The composition depends on the starting material and process used for the manufacture of the galactolipids. A fractionated oat oil of this composition consisting of a wide range of polar and amphiphilic lipids in a continuous triglyceride phase is manufactured by Scotia LipidTeknik AB, Stockholm, as Galactolec'", and is also referred to as galactolecithin.

Sphingolipids can be obtained from milk raw materials by extraction and purification, for instance by chromatography, and contain for example sphingomyelin in combination with WO 00/32219 PCT/SE99/02259 6 phosphatidylcholine, mono- and dihexocylceramides and triglycerides. Sphingolipids are a family of lipids based on sphingosine in contrast to the ones previously described which are based on glycerol. Examples of sphingolipids are sphingomyelin, mono- and dihexosylceramides, and gangliosides.

According to a preferred aspect of the invention the membrane lipids should contain DGDG in an amount of 0.1 by weight based on the membrane lipids, preferably 10 Monoglycerides or monoacylglycerols are slightly polar in nature and possess certain surface active properties. They can be obtained by fractionation of vegetable or animal oils.

Preferred monoglycerides of the invention are of a medium chain length, that is having a fatty acid chain of 8-12 carbon atoms, especially 8-10 carbon atoms, and can be obtained from coconut and palm kernel oil.

Monoglycerides in combination with the membrane lipids facilitate the formation of lipid particles of the pharmaceutical composition in the gastro-intestinal tract.

Non-polar lipids are for example natural or synthetic di- or triacylglycerols, such as, or derived.from, vegetable oils, animal oils, synthetic alynerides, fatty acids fatty alcohols, sterols, such as cholesterol, and their esters with fatty acids. The chain length and the degree of saturation of the glycerides should be chosen to give a liquid composition.

Preferably the non-polar lipids of the pharmaceutical composition comprises mainly triacylglycerols.

The invention especially refers to a pharmaceutical composition of cyclosporine in a lipid carrier comprising a mixture of a fractionated vegetable oil and monoglycerides.

A preferred composition of the invention comprises, in by weight of the total composition, 8-12 cyclosporin, 40-50 galactolecithin, and 40-50 MCM, that is C8-C10 monoacylglycerols.

A pharmaceutical composition of the invention preferably comprises cyclosporin A, that is cyclosporine.

Generally a pharmaceutical composition of the invention can be prepared by mixing, optionally after melting in an WO 00/32219 PCT/SE99/02259 7 open water bath at a temperature range of 40-70 0 C, non-polar lipids, such as triglycerides, and the monoglycerides with a cyclosporin and the membrane lipids in a vial. The mixture is then dispersed with a high shear mixer at approximately 1000 rpm and at a temperature range of 40-70°C for 2-4 min. The mixture can optionally contain increasing contents of water or aqueous solution which can lead to the formation of reverse vesicles, reverse micelles or a water-in-oil emulsion. If the lipid mixture is hard to melt or if the content of cyclosporin is high it might be necessary first to dissolve the mixture in ethanol, which is subsequently evaporated.

The pharmaceutical composition is mainly intended for oral administration, but can also be used for enteral, rectal, vaginal, topical, ocular, nasal or aural administration to animals, especially mammals, including humans.

In addition to the essential ingredients the pharmaceutical composition of the invention can also contain conventional additives and excipients, such as antiseptic agents, preservatives, thickening agents, pigments, flavouring and the like, in combinations as needed.

Oral unit dosage forms, such as soft or hard gelatin capsules, can comprise from 5 to 29n mg, preferably from to 100 mg of active substance, that is a cyclosporin, for administration 1-5 times a day.

Examples of cyclosporine formulations The membrane lipid material used in the following examples was a galactolipid material, Galactolec M (from Scotia LipidTeknik AB, Sweden), manufactured from oats in accordance with the process described in WO 97/11141 and referred to as galactolecithin. Said galactolecithin is composed by about 60 non-polar lipids and about 40 polar lipids. DGDG constitutes about 20 by weight of the total mixture.

The cyclosporin used in the formulations below was cyclosporine, that is cyclosporin A (USP XXIII, Medial AG, Switzerland).

WO 00/32219 PCT/SE99/02259 8 ExampleL Ingredient by weight Galactolecithin 67.5 Akoline MCM Cyclosporine 12.5 33.751 g of galactolecithin was weighed into a 100 ml beaker together with 10.007 g of Akoline MCM, that is a mixture of C8-C10 mono- di- and tri- acylglycerols (from Karlshamns AB, Sweden), and 6.245 g of cyclosporine.

The mixture was homogenized by means of a magnetic stirrer for approximately 36 hours. A yellow/brown, cloudy, highly viscous liquid was obtained.

Example_2 Ingredient by weight Galactolecithin MCM Cyclosporine 3.00 g galactolecithin was weighed into a 250 ml roundbottomed flask together with 18.01 g MCM, that is C8-C10 monoacylglycerols (having a purity of 99 fractionated from Akoline MCM by Scotia LipidTeknik AB), and 9.00 g of cyclosporine. The mixture was homogenized by means of a spatula and heated to 60 0 C under magnetic stirring until the active substance and the lipids had been dissolved. The final product obtained was a yellow brown transparent solution.

Example-3 Ingerdient %byweight Galactolecithin 87.5 Cyclosporine 12.5 Using the same procedure as in Example 2 and mixing the galactolecithin with 3.01 g cyclosporine, a final product was obtained having the same appearance as the final product of Example 2.

WO 00/32219 PCT/SE99/02259 9 Example A Ingredint by weight Galactolecithin Akoline MCM Cyclosporine By using the same procedure as in Example 2 and mixing 13.50 g galactolecithin, 13.00 g Akoline MCM, and 3.01 g cyclosporine a final product was obtained having the same appearance as the final product of Example 2.

Example Ingredient by weight Galactolecithin MCM Cyclosporine By using the same procedure as in Example 2 and mixing 13.50 g galactolecithin, 13.51 g MCM and 3.00 g cyclosporine a final product was obtained having the same appearance as the final product of Example 2.

Examplep6 Ingredient by weight Galactolecithin Akoline MCM Cyclosporine By using the same procedure as in Example 2 and mixing 9.01 g galactolecithin, 18.01 g Akoline MCM and 3.00 g cyclosporine a final product was obtained having the same appearance as the final .product of Example 2.

-Coomparat ive Examp 1.

A formulation in accordance with WO 95/20945 was prepared by mixing the following ingredients Ingredient I-y__weight GL 20.0 EPO 67.5 AP 0.02 Cyclosporine 12.50 WO 00/32219 PCT/SE99/02259 GL refers to a galactolipid material, CPL®-Galactolipid (from Scotia LipidTeknik AB, Sweden), containing about 60 DGDG, manufactured from oats in accordance with the process described in WO 95/20945. EPO stands for evening primrose oil (from Scotia Pharmaceuticals Ltd, UK), and AP stands for ascorbyl palmitate.

Additional formulations of cyclosporine were prepared having the composition as stated in the following Table 1, wherein CS cyclosporine G-lec galactolecithin, Galactolec

T

GL galactolipid material, CPL®-Galactolipid h-GL hydrogenated galactolipid material SL sphingolipid material h-PE hydrogenated phosphatidylethanolamine MCT medium chain triacylglycerol, from Karlshamns AB A MCM Akoline MCM Palm palm oil, from Karlshamns AB Soy soybean oil CH cholesterol, from Apoteksbolaget

AB

PC phosphatidylcholine, from Lucas Meyer SL, h-GL and h-PE were obtained from Scotia LipidTeknik An Soy bean oil is a long-chain C16-C20 triglyceride, CPL®- Soybean oil from Scotia LipidTeknik

AB.

The formulations according to Examples 7-9, 11, 13 and 14 were prepared using ethanol as described in the following procedure referring to the formulation of Example 13.

13.123 g of hydrogenated galactolipid was weighed up in a 250 ml round-bottomed flask together with 2.627 g Akoline MCM, 10.513 g of CPL®-Soybean oil and 3.753 g of cyclosporine. 40 ml of 95 ethanol was then added to the flask. The flask was put in a Rotavapor (Bichi, Switzerland) and was heated to 70 0 C and stirred for ten minutes until the substance and the lipid had been dissolved. Then the product was evaporated to complete dryness at a temperature of for a drying time of 80 minutes. 30.02 g of a final product was obtained.

WO 00/32219 PCT/SE99/02259 11 Table 1. Cyclosporine formulations Example No. Ingredients appearance 7 12.5 CS yellow, solid 43.8 GL 8.8 A MCM Palm 8 12.5 CS brown, liquid 43.8 GL 8.8 A MCM

MCT

9 30 CS brown, GL liquid, 7 A MCM cloudy 28 MCT 12.5 CS white, yellow

SL

CH cream G-lec 27.5 MCT 11 12.5 CS yellow, 21.9 SL 43.4 G-lec sol 4.4 A MCM suspension 17.5 Soy 12 12.5 CS yellow, clear

PC

A MCM liquid 52.5 MCT 13 12.5 CS white, solid 43.8 h-GL 8.8 A MCM Soy 14 12.5 CS brown, solid 17.5 h-PE 48.1 G-lec 4.4 A MCM 17.5 Soy Biological test of cyclosporine formulations Absorption tests were performed to study the effect of oral administration of different formulations of cyclosporine WO 00/32219 PCT/SE99/02259 12 in a soft gelatin capsule in comparison to the commercial drug Sandimmun Neoral® (known in most countries as Neoral®), soft gelatin capsules containing 100 mg cyclosporin A, that is cyclosporine, in ethanol as a reference composition. The composition of Sandimmun Neoral® per capsule was in addition to 100 mg cyclosporine and 100 mg ethanol, DL-a-tokoferol, propylene glykol, corn oil, Polyoxyl 40 Hydrogenated Castor Oil (Cremophor RH 40), and colours.

The biological absorption studies were performed in healthy male volunteers. The exclusion criteria were known intolerance to cyclosporine, deviations of clinical relevance, blood donor in the last two months, medical treatment which might interfere with the tests, smoking. The studies were of an open, cross-over design where the majority of the subjects received two treatments after one reference treatment, that is each subject was its own control. Each formulation was tested on three subjects and there were also three subjects who only received the reference composition on all occasions in order to estimate the intraindividual variation. The amount of cyclosporine was the same in all treatments. The intraindividual variation of Sandimmun Neoral® based on 3 subjects at 3 different observations was The interindividual variation, that is the variation in uptake of Sandimmun Neoral® after administration once only to 18 different subjects was 21 During the first visit informed consent and medical history were obtained from the subjects. Haematology and clinical chemistry analyses were performed. At the following three visits the subjects arrived at 7.00 in the morning, fasting since 22.00 the previous evening. The drug was taken about 7.30 together with approximately 150 ml of tap water.

For obtaining blood samples an intravenous indwelling catheter in an arm vein was used. A series of blood samples for analysis of cyclosporine were obtained according to the following schedule: Predose, 30, 60 and 90 minutes after dose, then 2, 2.5, 3, 3.5, 4, 5.5, 7.5, 10, 12, 24, 30 and 48 hours after dose. Lunch was served 4 hours after the drug intake and the subjects were allowed to drink tea, coffee and water. The total amount of blood drawn during the study was WO 00/32219 PCT/SE99/02259 less than 400 ml.

The concentration of the active substance cyclosporine in blood was assessed by a specific method at the Clinical Chemistry laboratory, University Hospital, Lund. Cyclosporine analysis was performed on a Hitachi 917, using an EMIT- (Enzyme Multiple Immunoassay Technique) kit from DADE Behring.

The formulations of Example 1 (in duplicate) and Example 3 according to the invention were tested, as well as the formulation of Comparative Example 1 and the formulations of Examples 7-14.

The following relative absorption values relative to the Sandimmun Neoral®, reflecting the area under curve, AUC, were obtained.

Table 2. Relative absorption of cyclosporine, AUCt, t 12h Example No. Subject 1 'Subject 2 Subject 3 Comp. Ex. 1 0.45 0.53 0.67 Ex. 1 0.66 0.92 1.09 Ex. 1 0.43 0.86 0.89 Ex. 10 0.01 0.02 0.02 Ex. 12 0.12 0.12 0.98* Ex. 3 0.50 0.62 0.70 Ex. 7 0.25 0.28 0.45 Ex. 8 0.36 0.38 0.64 Ex. 9 0.09 0.15 0.21 Ex. 11 0.42 0.47 0.61 Ex. 13 0.32 0.34 0.42 Ex. 14 0.46 0.49 0.52 Subject 3 is considered an outlier These results show that by varying the amounts of the lipid components of the carrier pharmaceutical compositions can be obtained having different, and sometimes a WO 00/32219 PCT/SE99/02259 14 surprisingly improved uptake.

The absorption test described was repeated in order to test the compositions according to Examples 2, and 4-6 as to uptake in comparison to Sandimmun Neoral®.

The average value of the uptake and the standard deviation of all tested compositions, reflecting also the interindividual variation, are given in the following Table 3.

Table e Averaged relative absorption of cvclosnirinp nrT Example Uptake* Uptake No. standard deviation 1 81 24 2 50 4 3 61 4 98 27 80 6 69 22 7 33 11 8 46 16 9 15 6 2 11 50 12 12 13 36 14 49 3 Comp. Ex.1 55 11 I~ s l Average of 3 subjects in comparison to the uptake of Sandimmun Neoral® WO 00/32219 PCT/SE99/02259 Conclusion From the above tests can be concluded that the compositions of Examples 1, 4 and 5 can be considered to be bioequivalent to the commercial drug Sandimmun Neoral®, as having a relative uptake 80 It should be noted that said compositions according to the invention do not contain any harmful additives, but only non-toxic lipids.

It seems to be of importance that the final pharmaceutical composition is liquid at room temperature; cf Examples 7, 11, 13 and 14 which are all solid at room temperature. It can be concluded that the physical state of the pharmaceutical composition matters for the uptake of the active substance in the gastro-intestinal tract.

Too high contents of cyclosporin will also affect the uptake; this is obvious from Example 9.

Monoglycerides are of importance for the uptake. From Examples 3, 8, 10 and also 9, having a monoglyceride content below 10 can be concluded that too low a content of monoglycerides will negatively affect the uptake. This is also true if the content of monoglycerides is too high; Example 2 has a monoglyceride content of 60 bringing about a high viscosity and a poor uptake.

From the results can also be concluded that the content of non-polar lipids must not be too high. Example 12 and Comparative Example 1 both contain too much triglycerides to give an adequate uptake.

The improved variation of the composition of Example compared to the composition of Example 4 is believed to derive from the defined monoglyceride fraction used in Example 5, alternatively on the low content of diglycerides.

The number of tests is, however, not sufficient for a statistical confirmation thereof.

Claims (9)

1. A pharmaceutical composition comprising a cyclosporin as an active substance in a lipid carrier, which carrier comprises membrane lipids in combination with monoglycerides and optionally non-polar lipids, which is characterized in being liquid at room temperature and containing the following in by weight of the total composition cyclosporin 0.5-25 membrane lipids selected from phospholipids, glycolipids and sphingolipids 10-45 monoglycerides 10-55 non-polar lipids 0-45

2. A pharmaceutical composition according to claim 1, wherein the lipid carrier contains 15-20 membrane lipids, 25-50 monoglycerides and 5-30 non- polar lipids in by weight of the total composition.

3. A pharmaceutical composition according to claim 1, wherein the lipid carrier contains 15-45 membrane lipids and 25-50 monoglycerides.

4. A pharmaceutical composition according to any of claims 1-3, wherein the membrane lipids contain digalactosyldiacylglycerol in an amount of 0.1-90 by weight, preferably 10-70 A pharmaceutical composition according to any of claims 14, wherein-the membrane lipids contain phospholipids and galactolipids.

6. A pharmaceutical composition according to any of claims 1-5, wherein the membrane lipids contain digalactosyldiacylglycerol in admixture with phosphatidylcholine.

7. A pharmaceutical composition according to any of claims 1,2,4 and 25 wherein the non-polar lipids mainly comprises triacylglycerols.

8. A pharmaceutical composition according to any of claims 1,2,4-7, wherein the lipid carrier comprises a mixture of a fractionated vegetable oil and monoglycerides.

9. A pharmaceutical composition according to claim 8, comprising in by weight of the total composition cyclosporin 8-12 galactolecithin 40-50 *mixed C8-C10 mono- di- and tri- acylglycerols

40-50 A pharmaceutical composition according to any of claims 1-9, wherein the cyclosporin is cyclosporin A. 11. A pharmaceutical composition as defined in Claim 1 and substantially as hereinbefore described with reference to any one of the examples. A558314speci 17 12. A process for preparing a pharmaceutical composition as defined in Claim 1, said process being substantially as hereinbefore described with reference to any one of the examples. 13. A pharmaceutical composition prepared by a process according to Claim 12. 14. A method of treatment or prophylaxis of a condition in a patient indicating administration of cyclosporin, said method comprising administering to said patient an effective amount of a composition according to any one of Claims 1 to 11 or 13. The method of claim 14, wherein said condition comprises rejection of a transplanted organ. 16. Use of: cyclosporin; membrane lipids selected from phospholipids, glycolipids and sphingolipids; monoglycerides; and non-polar lipids; for the manufacture of a medicament for the prevention of rejection of transplanted organs, said medicament comprising the following in by weight of the total: cyclosporin 0.5-25 membrane lipids 10-45 monoglycerides 10-55 and non-polar lipids 0-45 17. A composition according to any one of claims 1 to 11 or 13, when used for preventing rejection of a transplanted organ. Dated 10 February, 2003 Lipocore Holding AB Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON A558314speci