Title of Invention	PHARMACEUTICAL PREPARAITION COMPRISING AN ANTIBODY AGAINST THE EGF RECEPTOR
Abstract	The invention relates to an aqueous pharmaceutical preparation compris-ing an antibody against endothelial growth factor receptor (EGF receptor). The preparation has increased storage stability, even at elevated tem-peratures, and can be used for the treatment of tumours.

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PCT/EP2004/012044 -1 - Pharmaceutical preparation comprising an antibody against the EGF receptor The present invention relates to a stable pharmaceutical preparation comprising an antibody which is directed against the epidermal growth factor receptor (EGFR), and to the preparation and use thereof. Various in vitro and in vivo studies have shown that blockage of EGFR by antibodies acts against tumours at various levels, for example by inhibiting cancer cell proliferation, reducing tumour-mediated angiogenesis, induct-ing cancer cell apoptosis and increasing the toxic effects of radiotherapy and conventional chemotherapy. MAB c225 (INN: cetuximab) is a clinically proven antibody which binds to the EGF receptor. Cetuximab is a chimeric antibody whose variable regions are of murine origin and whose constant regions are of human ori-gin. Cetuximab was described for the first time by Naramura et al., Cancer Immunol. Immunotherapy 1993, 37: 343-349 and in WO 96/40210 A1. MAB 425 is an originally murine antibody which is directed against EGFR which is overexpressed in tumour cells, in particular A431 carcinoma cells. Its humanised and chimeric forms are disclosed, for example, in EP 0 531 472 A1; Kettleborough etal., Protein Engineering 1991, 4: 773-783; Bier et al., Cancer Chemother. Pharmacol. 2001, 47: 519-524; Bier et al., Cancer Immunol. Immunother. 1998, 46: 167-173. EMD 72000 (h425) is a form of MAB 425 which is in clinical phase l/ll and whose constant region is composed of a K and a human g-1 chain. Human anti-EGFR antibodies can be provided by XenoMouse technology, as described in WO 91/10741 A1, WO 94/02602 A1 and WO 96/33735 A1 A specific antibody which has been produced by this technology and is cur- 5/058365 PCT/EP2004/012044 -2- rently undergoing clinical trials is ABX-EGF (Abgenix, Crit. Rev. Oncol. Hematol. 2001, 38: 17-23; Cancer Research 1999, 59: 1236-43). Further antibodies directed against EGFR are described, for example, in EP 0 586 002 B1 and in J. Natl. Cancer Inst. 1993, 85: 27-33 (MAB 528). Like other antibodies, anti-EGFR antibodies are also applied parenterally as a solution for therapeutic use. A particular problem of solutions com-prising these antibodies is their tendency toward aggregation and the for-mation of protein multimers. In the case of reducible multimers, this can be attributed to unintentional intermolecular disulfide bridge formation through interaction between approaching moieties. Hydrophobic interactions and the consequent formation of non-reducible multimers are also possible. Furthermore, deamidation reactions, which subsequently result in protein degradation reactions, also occur. The denaturing reactions described occur, in particular, on storage at elevated temperature or during shear stresses, as occur, for example, during transport. As a consequence of the said aggregation tendency, product precipitation occurs during storage of antibody solutions, meaning that reproducible withdrawal from the container containing the solution is doubtful. In addi-tion, emboli can occur on parenteral administration of particle-containing solution This has the consequence that the administration of the anti-EGFR antibodies to the patient in the requisite dose in each case is not always guaranteed in a reproducible manner by means of antibody solu-tions, and the administration cannot take place with the requisite reliability Although filtration before injection enables the aggregates to be held back, this method, however, comprises an additional step and is therefore com-plex and not very suitable for clinical practice In addition, the problem of dose reproducibihty remains unsolved, since an unknown fraction of anti- 05/058365 PCT/EP2004/012044 -3- bodies is in each case separated off from the solution, and particle formation after filtration continues to represent a safety risk. A common method for the stabilisation of monoclonal antibodies is freeze-drying of solutions comprising antibodies and auxiliaries. However, lyo-philisation is very time- and energy-consuming and thus expensive. In addition, the lyophilisate must first be reconstituted before administration. EP 0 073 371 describes preparations for intravenous administration which comprise immunoglobulins which have a pH of from 3.5 to 5.0 for stabilisa-tion. However, such low pH values result in undesired incompatibility reac-tions at the injection point. US 6,171,586 B1 discloses the use of an acetate buffer pH 4.48 to 5.5, a surfactant and a polyol in an aqueous formulation of antibodies, with NaCI for isotonicity modification being excluded. Owing to the lack of isotonicity modification, incompatibility reactions at the injection point may likewise occur. As examples of further formulations comprising specific antibodies, refer-ence may be made at this point to EP 0 280 358, EP 0 170 983 and US 5,945,098. Of these, EP 0 280 358 describes the addition of dextran to an antibody solution for stabilisation against certain hormones, where stability was achieved over nine months. EP 0 170 983 describes the stabilisation of a thermolabile monoclonal antibody by heating together with hydrolysed ovalbumin. as a result of which the antibody was still stable after storage for 7 days at 45°C How-ever, the addition of proteins of other species to formulations intended for 2005/058365 PCT/EP2004/012044 parenteral administration is undesired owing to the problems associated therewith, in particular their possible antigeneity. US 5,945,098 discloses the use of glycine, polysorbate 80 and polyethyl-ene glycol for the stabilisation of an aqueous solution of immunoglobulin G. DE 10133394 A1 discloses the use of a phosphate buffer in the range from pH 6 to pH 8 and a polyoxyethylene sorbitan fatty acid ester for the stabili-sation of an aqueous solution of the antibody cetuximab. Although this sig-nificantly reduces the formation of visible aggregates, the chemical stabil-ity, in particular under stress conditions, is significantly impaired. Further-more, the formulation does not exhibit stability to (extreme) thermal stress, for example long-term storage at 40°C. The object of the invention was to find an aqueous formulation specifically for the antibodies directed against EGFR which is suitable for parenteral administration, is well tolerated and is stable on storage at room tempera-ture over at least 24 months. The storage stability should also be retained in the case of shear forces acting during transport and under modified cli-matic conditions, in particular at elevated temperature and atmospheric humidity. Furthermore, the formulation should have a simple structure and should not comprise any auxiliaries which are dubious from a toxicological point of view. Surprisingly, a formulation which meets these requirements has been found in the form of a solution which, in addition to an antibody directed against epidermal growth factor (anti-EGFR antibody), comprises a buffer, an amino acid and a surfactant. The present invention therefore relates to an aqueous pharmaceutical preparation which, in addition to an anti-EGFR antibody, comprises a buffer, an amino acid and a surfactant. 2005/058365 PCT/EP2004/012044 -5- For the purposes of the invention, an aqueous preparation is one in which at least some of the solvent present consists of water. Further solvent con-stituents which may be present are all solvents which are suitable for par-enteral use, in particular alcohols, such as, for example, ethanol, propanol, propanediol or glycerol. The aqueous preparation preferably comprises, as solvent, water or ethanol/water mixtures; the solvent particularly preferably consists of water. The antibody present can be any anti-EGFR antibody, in particular the murine, humanised or chimeric antibodies mentioned at the outset and the human anti-EGFR antibodies which have been and can be prepared by means of the said XenoMouse technology. Preference is given to the anti-EGFR antibody cetuximab or EMD 72000 or one of the murine, humanised or chimeric antibody analogues corresponding thereto. Particular prefer-ence is given to aqueous preparations which comprise cetuximab or EMD 72000 as antibody. The anti-EGFR antibody may be present in the formulation according to the invention in a concentration of from 0.1 mg/ml to 50 mg/ml, preferably from 2 mg/ml to 10 mg/ml, particularly preferably about 5 mg/ml. Buffers which can be employed are basically all physiologically tolerated substances which are suitable for setting the desired pH, such as, for example, citrate salts, acetate salts, histidine salts succinate salts, malate salts, phosphate salts or lactate salts, and/or the respective free acids or bases thereof, as well as mixtures of the various salts and/or acids or bases thereof. The buffer preferably consists of one or more citrate salt(s), acetate salt(s), histidine salt(s), succinate salt(s), malate salt(s), phosphate salt(s) or lactate sa!t(s) and/or the respective free acid(s) or base(s) thereof or a mixture of one or more of the various salts and/or the acid(s) or base(s) thereof. The term mixture here covers both mixtures of different 2005/058365 PCT/EP2004/012044 -6- salts of the same acid, such as, for example, mixtures of different citrate salts, and mixtures of salts of different acids, such as, for example, mix-tures of citrate and acetate salts. The buffer preferably consists of one or more citrate salt(s) and/or the free acid thereof (for example citric acid, cit-ric acid monohydrate, trisodium citrate dihydrate, tripotassium citrate monohydrate), acetate salt(s) and/or the free acid thereof (for example acetic acid, sodium acetate, sodium acetate trihydrate) or L-histidine and/or an acid-addition salt thereof, such as, for example, L-histidine monohydrochloride monohydrate. The preparation according to the inven-tion advantageously comprises the buffer in a concentration of from 10 to 100 mmol/l, preferably from 2 to 20 mmol/l, particularly preferably about 10mmol/l. The pH of the preparation is in the range from 5.0 to 6.0, preferably from 5.2 to 5.8, particularly preferably about 5.5. The preparation according to the invention is physiologically well tolerated, can be prepared easily, can be dispensed precisely and is stable with respect to assay, decomposition products and aggregates over the dura-tion of storage, during repeated freezing and thawing processes and mechanical stress. It is stable on storage over a period of at least 3 months to a period of 4 years at refrigerator temperature (2-8°C). Surprisingly, the preparation according to the invention is also stable on storage over a period of up to 2 years at elevated temperatures and higher atmospheric humidity levels, for example at a temperature of 25°C and 60% relative atmospheric humidity, or over a period of 3 months at a temperature of 40°C and 75% relative atmospheric humidity The amino acid present in the preparation can be basic amino acids, such as. for example, arginine, histidine, ornithine, lysine, or neutral amino acids, such as, for example, glycine, methionme, isoleucme, leucine and 2005/058365 PCT/EP2004/012044 -7- alanine, or aromatic amino acids, such as, for example, phenylalanine, tyrosine or tryptophan. Basic amino acids are preferably employed in the form of their inorganic salts (advantageously in the form of the hydrochloric acid salts, i.e. as amino acid hydrochlorides). The amino acid employed is preferably in each case the L-form. The amino acid present in the prepara-tion according to the invention is particularly preferably L-arginine, glycine or L-methionine. The preparation comprises the amino acid in a concentration of from 2 to 200 mmol/l, preferably from 50 to 150 mmol/l, particularly preferably about 100mmol/l. Surfactants which can be employed are all surfactants usually used in pharmaceutical preparations, preferably polyethylene sorbitan fatty acid esters and polyoxyethylene-polyoxypropylene copolymers. Polyethylene sorbitan fatty acid esters are also known under the trade name Tween. Suitable polyethylene sorbitan fatty acid esters are, in particular, polyoxy-ethylene (20) sorbitan monolaurate, polyoxyethylene (20) sorbitan mono-palmitate and polyoxyethylene (20) sorbitan monostearate. Preference is given to polyoxyethylene (20) sorbitan monolaurate and polyoxyethylene (20) sorbitan monooleate, particular preferewnce being given to polyoxy-ethylene (20) sorbitan monooleate. Polyoxyethylene-polyoxypropylene co-polymers are also known under the trade name Poloxamer. A particularly preferred polyoxyethylene-polyoxypropylene copolymer is Poloxamer 407 (CAS 9003-11-6). The surfactants may be present in the formulation in a concentration of from 0.001 % to 1 0% by weight. If polyoxyethylene sorbitan fatty acid esters are present as surfactants, these are preferably present in an amount of from 0.005 to 0.1% by weight, particularly preferably in an amount of about 0 01% by weight. If polyoxyethylene-polyoxypropylene 2005/058365 PCT/EP2004/012044 copolymers are present, these are preferably present in an amount of from 0.01 to 0.5% by weight, particularly preferably about 0.1% by weight. In order to increase the tolerability on parenteral administration, the osmo-lality is preferably in the isotonic range, i.e. at an osmolality of from about 250 to 350 mOsmol/kg. The preparation can then be administered directly intravenously, intraarterially and also subcutaneously substantially without pain. According to an advantageous embodiment, the preparation according to the invention therefore additionally comprises an isotonicity modifier, pref-erably a physiologically tolerated salt, such as, for example, sodium chlo-ride or potassium chloride, or a physiologically tolerated polyol, such as, for example, glucose or glycerol, in a concentration necessary for isotonic-ity modification. The invention therefore furthermore relates to an aqueous preparation comprising an anti-EGFR antibody, a buffer, an amino acid, a surfactant and an isotonicity modifier in a concentration necessary for iso-tonicity modification. Sodium chloride is particularly preferably present as isotonicity modifier. In addition, the solutions according to the invention may comprise further physiologically tolerated auxiliaries, such as, for example, antioxidants, such as ascorbic acid or glutathione, preservatives, such as phenol, m-cresol, methyl- or propylparaben, chlorobutanol, thiomersal or benz-alkonium chloride, polyethylene glycols (PEG), such as PEG 400, PEG 3000, 3350, 4000 or 6000, disaccharides, such as trehalose or saccha-rose, or cyclodextrins, such as hydroxypropyl-ß-cyclodextrin, sulfobutyl-ethyl-(3-cyclodextrin, a-cyclodextrin or g-cyclodextnn According to a particularly advantageous embodiment of the invention, the aqueous preparation comprises about 5 mg/ml of cetuximab or EMD 2005/058365 PCT/EP2004/012044 -9- 72000, about 10 mmol/l of citrate or histidine buffer having a pH of about 5.5, about 100 mmol/l of glycine, arginine or L-methionine, about 100 mmol/l of sodium chloride and about 0.01% of polyoxyethylene (20) sorbitan monooleate. The aqueous preparation can be prepared by adding the said auxiliaries to a solution comprising the anti-EGFR antibody. To this end, defined vol-umes of stock solutions comprising the said further auxiliaries in defined concentration are advantageously added to a solution having a defined concentration of the anti-EGFR antibody, as obtained from its preparation, and the mixture is, if desired, diluted to the pre-calculated concentration with water or buffer solution. Alternatively, the auxiliaries can also be added as solids to the starting solution comprising the anti-EGFR antibody. If the anti-EGFR antibody is in the form of a solid, for example in the form of a lyophilisate, the preparation according to the invention can be pre-pared by firstly dissolving the respective antibodies in water or an aqueous solution comprising one or more of the further auxiliaries, and subse-quently adding the amounts required in each case of stock solutions com-prising the further auxiliaries, the further auxiliaries in solid form and/or water. The anti-EGFR antibody can advantageously also be dissolved directly in a solution comprising all further auxiliaries. One or more of the auxiliaries present in the preparation according to the invention may advantageously already have been added during or at the end of the process for the preparation of the particular EGFR antibody. This can preferably be carried out by dissolving the anti-EGFR antibody directly in an aqueous solution comprising one, more than one or all of the further auxiliaries in the final step of the purification carried out after its preparation In order to prepare the preparation, the respective further ingredient(s) then need only be added in a smaller amount in each case and/or not added at all It is particularly preferred for the respective mgre- 2005/058365 PCT/EP2004/012044 -10- dient to be dissolved directly in an aqueous solution comprising all further auxiliaries in the final step of the purification carried out after its prepara-tion. If the solution comprising the respective antibody and the auxiliaries does not yet have the desired pH, this is set by addition of an acid or base, pref-erably using the acid or base already present in the buffer system. This is followed by sterile filtration. The aqueous preparation according to the invention can advantageously be employed for the treatment of tumour diseases. The examples explain the invention without being restricted thereto. 2005/058365 PCT/EP2004/012044 -11- Example 1 (Comparative Example 1) Aqueous solution comprising: 2 mg/ml of cetuximab 10 mmol/l of sodium phosphate buffer pH 7.2 145 mmol/l of sodium chloride The preparation is carried out by mixing defined volumes of aqueous solu-tions comprising the respective auxiliaries in defined concentration. The following solutions are used: Solution A (active ingredient solution) comprising: 18 mg/ml of cetuximab 10 mmol/l of sodium phosphate buffer pH 7.2 (consisting of 2.07 g/l of disodium hydrogenphosphate 7-hydrate and 0.31 g/l of sodium dihydrogenphosphate monohydrate) 145 mmol/l of sodium chloride (The solution is obtained by re-buffering the active ingredient against solu-tion B with the aid of tangential flow filtration in the final step of the active-ingredient purification taking place after preparation thereof.) Solution B (buffer/salt solution) Corresponds to solution A, but comprises no active ingredient For the preparation of Comparative Solution 1, 1.11 parts by volume of solution A and 8 89 parts by volume of solution B are combined with one another. PCT/EP2004/012044 -12- The solution prepared is filtered using a sterile filter before transfer and transferred into injection vials. The injection vials are subsequently sealed with stoppers and crimped. Example 2 (Comparative Example 2) Aqueous solution comprising: 2 mg/ml of cetuximab 10 mmol/l of sodium phosphate buffer pH 7.2 145 mmol/l of sodium chloride 0.01% by weight of polyoxyethylene (20) sorbitan monooleate The preparation is carried out by mixing defined volumes of aqueous solu-tions comprising the respective ingredients in defined concentration. Besides solution A, the following solution is used. Solution C (buffer/salt solution comprising polyoxyethylene (20) sorbitan monooleate) Corresponds to solution B, but additionally comprises 0.0125% by weight of polyoxyethylene (20) sorbitan monooleate. For the preparation of comparative solution 2, 1.11 parts by volume of solution A and 8.89 parts by volume of solution C are combined with one another The solution prepared is filtered using a sterile filter before transfer and transferred into injection vials. The injection vials are subsequently sealed with stoppers and crimped 2005/058365 PCT/EP2004/012044 -13- Example 3 (formulation according to the invention) 5 mg/ml of cetuximab 10 mmol/l of citrate buffer pH 5.5 100 mmol/l of glycine 100 mmol/l of sodium chloride 0.01% by weight of polyoxyethylene (20) sorbitan monooleate The preparation is carried out by mixing defined volumes of aqueous solu-tions comprising the respective ingredients in defined concentrations. Solution D (active ingredient solution in a citrate buffer) 16 mg/ml of cetuximab 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.1014 g/l of citric acid monohydrate) (The solution is obtained by re-buffering the active ingredient against solu-tion E with the aid of tangential flow filtration in the final step of the active-ingredient purification taking place after preparation thereof.) Solution E (buffer solution): Corresponds to solution D, but comprises no active ingredient. Solution F (buffer/salt solution): Corresponds to solution E, but comprises 145 5 mmol/i of glycine, 145.5 mmol/l of sodium chloride and 0.015% by weight of polyoxyethylene (20) sorbitan monooleate For the preparation of the formulation according to the invention, 3.125 parts by volume of solution D and 6.875 parts by voiume of solution F are combined with one another iz005/058365 PCT/EP2004/012044 -14- The solution prepared is filtered using a sterile filter before transfer and transferred into injection vials. The injection vials are subsequently sealed with stoppers and crimped. Example 4 The following solutions are prepared analogously to the method of the examples described above: Example 4.1, solution comprising: 5 mg/ml of cetuximab 100 mmol/l of glycine 0.01% by weight of polyoxyethylene (20) sorbitan monooleate 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.9410 g/l of trisodium citrate dihydrate) Example 4.2, solution comprising: 5 mg/ml of cetuximab 100 mmol/l of glycine 100 mmol/l of sodium chloride 0.01% by weight of polyoxyethylene (20) sorbitan monooleate 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.1014 g/l of citric acid monohydrate) Example 4 3, solution comprising. 5 mg/ml of EMD 72000 100 mmol/l of glycine 100 mmol/l of sodium chloride 0.01% by weight of polyoxyethylene (20) sorbitan monooleate J2005/058365 PCT/EP2004/012044 -15- 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.1014 g/l of citric acid monohydrate) Example 4.4, solution comprising: 5 mg/ml of cetuximab 100 mmol/l of L-methionine 0.01% by weight of polyoxyethylene (20) sorbitan monooleate 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.1014 g/l of citric acid monohydrate) Example 4.5, solution comprising: 5 mg/ml of cetuximab 100 mmol/l of glycine 0.01% by weight of polyoxyethylene (20) sorbitan monooleate 10 mmol/l of acetate buffer pH 5.5 (consisting of 1.3608 g/l of sodium acetate trihydrate Example 4.6, solution comprising: 5 mg/ml of cetuximab 100 mmol/l of glycine 0.01% by weight of polyoxyethylene (20) sorbitan monooleate 10 mmol/l of histidine buffer pH 5.5 (consisting of 2 069 g/l of L-histidine monohydrochloride monohydrate) Example 4.7, solution comprising: 5 mg/ml of cetuximab 100 mmol/l of glycine 0.01% by weight of polyoxyethylene (20) sorbitan monolaurate 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.1014 g/l of citric acid monohydrate ^005/058365 PCT/EP2004/012044 -16- Example4.8, solution comprising. 5 mg/ml of cetuximab 100 mmol/l of glycine 0.1 % by weight of polyoxyethylene-polyoxypropylene copolymer 407 (Poloxamer 407) 10 mmol/l of citrate buffer pH 5.5 (consisting of 2.1014 g/l of citric acid monohydrate) Example 5 The stability of the formulation according to the invention was tested in a stress test. To this end, vials containing the solution according to Example 3 and, for comparative purposes, vials containing solution according to Examples 1 and 2 were stored at 25°C and 60% relative atmospheric humidity and 40°C and 75% relative atmospheric humidity. In addition, vials containing solutions according to Examples 1, 2 and 3 were shaken for five days in a shaking apparatus at a shaking frequency of 150 min-1 at room temperature and frozen three times in succession at -20°C and sub-sequently thawed again at +5°C. Before storage and after defined storage times, the vials were assessed visually with direct illumination with a cold-light source, and the absorption of the solutions at 350 nm, which repre-sents a measure of the turbidity, was determined. In order to illustrate the influence of storage or treatment, the relative turbidity was in each case calculated relative to the starting value. Furthermore, the vials were ana-lysed by means of HPLC gel filtration with respect to the content of cetuxi-mab, aggregates and decomposition products 2005/058365 PCT/EP2004/012044 -17- The results of the stability investigations are shown in Table 1. Test Storage Cetuxi- Aggreg- Decom- Turbidity Relative Visual solution [time/ mab ates position atg= turbidity assess- conditions] [%] [%] products 350 nm ag= ment [%] 350 nm Exam-ple 1 0 weeks 99.67 0.12 0.22 0.005 1.00 Small par-ticles, low number, clear Exam-ple 1 8 weeks 25°C/60% R.H. 98.99 0.28 0.73 0.0081 1.62 Large par-ticles, large number, clear Exam-ple 1 8 weeks 40°C/75% R.H. 95.08 3.23 1.69 0.0235 4.70 Large par-ticles, large number, clear Exam-ple 1 Shaking for 5 days at 150 rpm and RT 99.60 0.17 0.24 0.829 165.80 Very large particles, very high particle number, cloudy Exam-ple 1 3 freeze/ thaw cycles between -20°C and +5°C 99.68 0.14 0.18 0.0089 1.78 Large par-ticles, high particle content, slightly cloudy Exam-ple 2 0 weeks 99.62 0.18 0.21 0 0048 1.00 No parti-cles, clear Exam-ple 2 8 weeks 25°C/60% R.H. 99.02 0.28 0.70 0.0071 1.48 Small par- tides, low number. clear Exam-ple 2 8 40°C/75% RH 93.95 4 34 1 72 0 0241 5.02 ' Small par-ticles, iow number, clear 2005/058365 -18- PCT/EP2004/012044 Exam- Shaking 99.51 0.26 0.23 "00075" 1.56 No parti- ple 2 for 5 days cles, clear at 150 rpm andRT Exam- 3 freeze/ 99.61 0.21 0.18 0.0064 1.48 No parti- ple 2 thaw cles, clear cycles between -20°C and +5°C Exam- 0 weeks 99.72 0.15 0.14 10.018 11.00 No parti- ple3 cles, clear Exam- 8 weeks 99.38 0.18 0.44 0.020 1.08 Small par- ple 3 25°C/60% ticles, low R.H. number, clear Exam- 8 weeks 98.15 0.46 1.40 0.030 1.63 Small par- ple 3 40°C/75% ticles, low R.H. number, clear Exam- Shaking 99.15 0.70 0.15 0.019 1.04 No parti- ple 3 for 5 days cles, clear at 150 rpm and RT Exam- 3 freeze/t 99.75 0.14 0.12 0.018 1.00 No parti- ple 3 haw cles, clear cycles between -20°C and +5°C Table 1 Summary of the stability data of the formulation according to the invention (Example 3) and the two comparative solutions (Examples 1 and 2) The results clearly show that the formulation according to the invention has significantly increased stability compared with the comparative solutions of the prior art 2005/058365 PCT/EP2004/012044 -19- Patent claims 1. Aqueous preparation comprising an anti-EGFR antibody, a buffer, an amino acid and a surfactant. 2. Preparation according to Claim 1, characterised in that the antibody is cetuximab or EMD 72000 or one of the corresponding murine, humanised or chimeric antibody analogues. 3. Preparation according to Claim 2, characterised in that the antibody is cetuximab or EMD 72000. 4. Preparation according to one or more of Claims 1 to 3, characterised in that the buffer consists of one or more citrate salt(s), acetate salt(s), his- tidine salt(s), succinate salt(s), malate salt(s), phosphate salt(s) or lactate salt(s) and/or the respective free acid(s) or base(s) thereof or a mixture of one or more of the various salts and/or the acid(s) or base(s) thereof. 5. Preparation according to Claim 4, characterised in that the buffer consists of one or more citrate salt(s) and/or the free acid thereof, acetate salt(s) and/or the free acid thereof or L-histidine and/or an acid-addition salt thereof. 6. Preparation according to one or more of Claims 1 to 5. characterised in that the amino acid is L-arginine, glycine or L-methionine 7. Preparation according to one or more of Claims 1 to 6, characterised in that the surfactant is a polyethylene sorbitan fatty acid ester or a polyoxy- ethylene-polyoxypropylene copolymer. 05/058365 PCT/EP2004/012044 -20- 3. Preparation according to Claim 7, characterised in that the polyoxyethylene sorbitan fatty acid ester surfactant is polyoxyethylene (20) sorbitan mono-oleate or polyoxyethylene (20) sorbitan monolaurate. 9. Preparation according to Claim 7, characterised in that the surfactant is Poloxamer 407. 10. Preparation according to one or more of Claims 1 to 9, characterised in that an isotonicity modifier is furthermore present in a concentration neces- sary for isotonicity modification. 11. Preparation according to Claim 10, characterised in that the isotonicity modifier is sodium chloride. 12. Preparation according to one or more of Claims 1 to 11, characterised in that it has a pH of 5 - 7, preferably from pH 5.2 to pH 6.0. 13. Preparation according to Claim 12, characterised in that it has a pH of about 5.5. 14. Preparation according to one or more of Claims 1 to 13, characterised in that it comprises about 5 mg/ml of cetuximab or EMD 72000, about 10 mmol/l of citrate or histidine buffer, about 100 mmol/l of glycine, L-arginine or L-methionine, about 100 mmol/l of sodium chloride and about 0.01% of polyoxyethylene (20) sorbitan monooleate and has a pH of about 5.5. 15. Process for the preparation of a pharmaceutical preparation according to one or more of Claims 1 to 14. characterised in that an aqueous prepara- tion comprising the anti-EGFR antibody is added to one of the said auxiiia- VO 2005/058365 PCT/EP2004/012044 -21 - nes. 16. Use of the preparation according to one or more of Claims 1 to 14 for the treatment of tumour diseases.

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