WO 2008/134310 PCT/US2008/061147 STABILIZATION OF LIQUID SOLUTIONS OF RECOMBINANT PROTEIN FOR FROZEN STORAGE [oo1] This application claims benefit of Provisional Patent application 60/926,698, filed April 26, 2007, the disclosure of which is incorporated by reference. FIELD OF THE INVENTION [002] The invention relates to the freezing and storage of liquid solutions of recombinant protein, preferably bulk solutions. BACKGROUND OF THE INVENTION [003] Production of recombinant proteins in cell culture normally involves a series of purification steps, by which the desired protein product is recovered from recombinant host cells and/or the associated culture media. Many important recombinant proteins are produced on a large commercial scale. In the case of pharmaceutical proteins, for example, it is not uncommon for more than one purification stage to be used to achieve the desired level of product purity. [004] It can be necessary to store a bulk solution of recombinant protein which has been initially purified, but not finally purified, prior to final purification for formulation. For example, a protein-containing product of a recombinant fermentation reaction can be initially purified in an affinity or ion exchange column. After an initial pass through the column, the protein product is only partially purified, and the solution still contains contaminants such as remnants of the cell culture and other proteins. Prior to final formulation into a pharmaceutical product, the bulk solution must be further processed to obtain the protein in a satisfactory purity. [005] Normally the solution, e.g. elution buffer, which is used to recover the protein from a first-pass purification treatment is a high salt solution. In the case of elution from a column, a high salt concentration is needed to release the protein from the column. Accordingly, the "bulk" solution recovered from first pass purification treatment can comprise a solution having a high concentration of monovalent salts, normally sodium chloride but potentially potassium chloride, or other salts.
-2 [006] The storage of a "bulk" solution of recombinant protein poses unique challenges due to the high salt concentration and very low protein concentration of the solution. Ideally, proteins are stored below the glass transition temperature to assure stability, since in the glassy state, protein inactivation and denaturation are extremely slow on a pharmaceutical 5 time scale, On the other hand, the presence of high salt concentration in a solution tends to depress its glass transition temperature, and in solutions with high salt concentration and low protein concentration, very low temperatures are needed to achieve this state. [007] Frozen storage at higher temperature is desirable for bulk solutions in large volume quantities for cost and efficiency reasons, but while preserving the stability and activity of the 10 protein. SUMMARY OF THE INVENTION [008] According to one aspect the present invention provides a method for stabilizing a liquid solution of recombinant protein for frozen storage, which comprises: providing a 15 solution of recombinant protein wherein said solution has a monovalent salt concentration, eg. of NaCI and/or KCI, of at least 100 mM; adding a carbohydrate to said solution in an amount sufficient to provide the solution, upon freezing, with a glass transition temperature of -56C or higher; and freezing said solution for storage. [009] According to another aspect the present invention also provides a liquid solution of 20 recombinant protein which is stabilized for frozen storage, which contains a carbohydrate in an amount sufficient to provide the solution, upon freezing, with a glass transition temperature of -56"C or higher. [009A] According to another aspect the present invention provides a composition for stabilized frozen storage of a recombinant protein in solution, said composition comprising the 25 recombinant protein at a concentration between 0.0001 micromolar and 1 .0 micromolar, an NaC and/or KCI concentration of at least 100 mM, and one or more carbohydrates in an amount of 8-25% by weight, which provides the solution, upon freezing, with a glass transition temperature of -56'C or higher. DESCRIPTION OF THE FIGURES 30 [010] Figure 1 shows the effect on preserving recombinant protein activity of adding carbohydrate, with or without other excipients as described in the text, to a bulk solution of -2A recombinant Factor VIII The four different formnulations are designated F1, F2, F3 and F4. Factor VII activity was assayed after freezing and storage at -30'C, at different time points as shown, for up for 24 weeks. Before addition of carbohydrate, the bulk solution contained approximately 600mM NaCI, 10mM CaCl2 WO 2008/134310 PCT/US2008/061147 20mM imidazole and 0.1% Triton X-100, except F3 which was diluted as described herein. The graph plots time against coagulation potency (IU/mL). tol] Figure 2 shows loss of recombinant FVIlI activity after freezing and storage at -70 *C and -30 *C of the bulk Factor Vill solution used in the experiments illustrated in Figure 1 but without stabilization excipients. The designation "LN 2 to -70*C" indicates that the samples were frozen in liquid nitrogen prior to storage at -70 *C, and "LN 2 to -30OC" indicates that the samples were frozen in liquid nitrogen prior to storage at -30 *C. "EVA to -70"C" indicates that the samples were frozen in polymer storage bags and stored at -70 OC. DESCRIPTION OF PREFERRED EMBODIMENTS [012] The liquid solution of recombinant protein may comprise a solution of any recombinant protein obtained from recombinant cell culture using affinity chromatography, ion-exchange chromatography, or the like. In a preferred embodiment, the solution is a bulk solution, which comprises a solution which has been partially purified. In all embodiments, the liquid solution is a high-salt solution, preferably an aqueous solution. (013] Recombinant proteins include, for example and without limitation, coagulation factors, virus antigens, bacterial antigens, fungal antigens, protozoal antigens, peptide hormones, chemokines, cytokines, growth factors, enzymes, blood proteins such as hemoglobin, a-1-antitrypsin, fibrinogen, human serum albumin, prothrombin/thrombin, antibodies, blood coagulation and/or clotting factors, and biologically active fragments thereof; such as Factor V, Factor VI, Factor VIl, Factor VIll and derivatives thereof such as B-domain deleted FVIII, Factor IX, Factor X, Factor XI, Factor XII, Factor XIll, Fletcher Factor, Fitzgerald Factor, and von Willebrand Factor; milk proteins such as casein, lactoferrin, lysozyme, a-1 anti trypsin, protein factors, immune proteins, and biologically active fragments thereof; and antibodies, including monoclonal antibodies, single chain antibodies, antibody fragments, chimeric antibodies, humanized antibodies, and other antibody variant molecules which can be produced in recombinant cell culture. 3 WO 2008/134310 PCT/US2008/061147 [014] A currently preferred recombinant protein is recombinant Factor VIll. Factor Vill as used herein includes engineered variants of Factor VIll, such as B-domain deleted variants of Factor Vill. [015] A "bulk" solution within the meaning of the present invention comprises a partially but not fully purified liquid solution of recombinant protein, which contains at least 100 mM monovalent salt. The monovalent salt is preferably NaCI which is commonly used to elute recombinant proteins from purification columns. However, the NaCI may be replaced, in whole or in part, with KCl. The bulk solution may also contain varying amounts of other salts, such as divalent salts including calcium chloride. [016] By "partially but not fully purified" is meant the liquid solution has been subjected to at least one purification step, but the liquid solution still contains sufficient residual impurities that at least one further purification step is required prior to final product formulation. For example, a "bulk" solution of recombinant Factor Vill must be further purified prior to final formulation, which in the case of Factor Vill and other proteins may include lyophilization. [017] The liquid solution contains at least 100 mM monovalent salt, preferably 100 mM NaCI, more preferably at least 300 mM NaCl, more preferably at least 500 mM NaCI, more preferably at least 560 mM NaCI and still more preferably at least 600 mM NaCI. It is not uncommon for bulk solutions of recombinant protein to have this high monovalent salt concentration following an initial purification stage. [018] In further embodiments of the invention, the liquid solution contains 100-200 mM NaCI, 100-300 mM NaCI, 200-300mM NaCl, 100-400 mM NaCI, 100-500 mM NaCl, 100-600 mM NaCI, 100-800 mM NaCI, 300-500 mM NaCI, 300-600 mM NaCl, 300-800 mM NaCl, 400-600 mM NaCI, 400-800 mM NaCI, 500-600 mM NaCI, 560 700 mM NaCl and 500-800 mM NaCI. [019] The "bulk" solutions of the invention are further characterized by their very low protein concentration. In embodiments of the invention, the concentration of recombinant protein in the bulk solution can be as low as 0.0001 micromolar, 0.001 micromolar, or 0.01 micromolar. In embodiments of the invention, the concentration of recombinant protein in the bulk solution can be as high as 10 micromolar, 1 micromolar, or 0.1 micromolar. Any concentration of protein falling within any 4 WO 2008/134310 PCT/US2008/061147 combination of these upper and lower limits is an embodiment of a "bulk" solution within the meaning of the invention. [020] The carbohydrate is added to the liquid solution, prior to freezing, in an amount sufficient to provide the solution, upon freezing, with a glass transition temperature of -56 *C or higher, more preferably at least -34 *C, or any temperature expressed by a whole or fractional number therebetween. The normal glass transition temperature of a high salt, low protein bulk solution is substantially less than -56 *C, e.g. -60 to -70 "C. The amount of added carbohydrate needed to elevate the glass transition temperature to -56 "C should take into account, as one factor, the protein concentration. Higher protein concentrations tend to themselves elevate the glass transition temperature of a bulk solution. As other factors, the amount of carbohydrate should not excessively increase the viscosity of the solution, and preferably the viscosity is maintained below about 9.0 cP. The conductance of the solution can be changed by carbohydrate addition, and preferably, should be maintained below about 39 mS/cm. [021] Freezing the solution, in the context of the present invention, means freezing the bulk liquid solution, and is to be distinguished from freeze-drying, which involves different technical considerations. [022] The carbohydrate can be the type of carbohydrate normally used in pharmaceutical formulations, including sugars and di-, oligo- and poly- saccharides. Examples include dextrans, cyclodextrans, chitosans, starches, halyuronic acids, cellulose, raffinose, maltose, lactose, stachyose, and combinations thereof. Preferred examples are carbohydrates which are approved for injection, which includes sucrose, trehalose, hydroxyethylstarch, dextran, or combinations thereof. Pharmaceutical grade carbohydrates are available commercially from a number of suppliers. [023] The precise amount of carbohydrate needed to protect the solution during freezing can be readily determined, for example by differential scanning calorimetry, and depends on the particular protein and the particular carbohydrate. Currently preferred amounts of carbohydrate are 8-25% (wlw) based on weight of liquid solution. 5 WO 2008/134310 PCT/US2008/061147 [024] In specific embodiments of the invention, the amounts of carbohydrate are about 8-15%, 12-20%, 16-20%, 15-25%, and 20-25% (w/w) based on weight of liquid solution. [025] Other components from the initial purification (e.g. elution) may be present in a bulk solution, including a surfactant (e.g. Tween 80 or Triton-X), calcium chloride, or imidazole. Other excipients can be added to the liquid solutions. As shown in the below formulations, additional surfactant may be added as an excipient. As a further excipient, an amino acid (e.g. glycine) may be added. EXAMPLES [026] The invention is illustrated using, as exemplary recombinant protein, recombinant Factor VIII. Recombinant Factor VillI is produced using methods known in the art, for example as described in US Pat. Nos. 5,576,194; 5,804,420; and 5,733,873. In preferred embodiments, recombinant Factor Vill is produced in mammalian cells in large-scale fermentation reactors, in media which can be serum free and/or protein free. Preferably the recombinant Factor Vill is secreted into the media by the recombinant cells. [027] Recombinant Factor VIIl (full length) was expressed from host cells and purified from clarified tissue culture fluid by membrane adsorber chromatography. The membrane adsorber process isolates and concentrates recombinant Factor Vill from the tissue culture fluid by binding and elution (generally as described in Suck et al., J. Biotechnology, 121: 361-367, 2006.) The eluate was divided into four batches and each batch was transferred into a sterile bottle (400 mL in each bottle). In addition to recombinant Factor VIlI and residual impurities which remain, the eluate (bulk solution) contained approximately 600mM NaCI, 10mM CaCl 2 , 20mM imidazole and 0.1% Triton X-100. The concentration of recombinant Factor VIII in the eluate was approximately 0.067 micromolar. [028] A carbohydrate or combination of carbohydrates, along with other excipients as indicated, were then added to each bottle at room temperature in the amounts shown as Formulations I, 2, 3 and 4 in Table 1 below. 6 WO 2008/134310 PCT/US2008/061147 TABLE 1 Formulation 1 Formulation 2 Formulation 3 Formulation 4 8% Sucrose 15% Sucrose 10% Hydroxyethyl 15% Dextran 3% Glycine starch 8% Trehalose 8% Trehalose 80 ppm Tween 80 ppm Tween [029] All components in Table 1 are shown in percent by weight based on weight of solution. Carbohydrates and other excipients were obtained commercially. Each fresh formulated batch was sampled. Samples from Formulations (1), (2), (3) and (4) were assessed for Factor VIII activity using a standard coagulation assay. [030] Formulation 3 was prepared from the same eluate but was diluted with a buffer containing 20 mM imidazole and 10 mM CaCl 2 to decrease the NaCl concentration by half. This dilution was performed to examine the applicability of the process of the invention to solution having a lower, but still relatively high, monovalent salt concentration. [031] The glass transition temperature of each sample was determined using Differential Scanning Calorimetry (DuPont Modulated DSC). The glass transition temperatures exhibited by Formulations I, 2, 3 and 4 were, respectively, -56 *C, 52.1 *C, -34.9 0C and -35.5 0 C. In each case, the glass transition temperature is significantly higher than the glass transition temperature observed in the absence of an added carbohydrate (which for the same bulk solution without carbohydrate was determined to be between -60 and -70 *C). The viscosities of the formulations were: Formulation 1: 1.8428 cP; Formulation 2: 3.1089 cP; Formulation 3: 6.8076 cP; and Formulation 4: 7.2123 cP. The conductivities of the formulations were: Formulation 1: 27.8 mS/cm; Formulation 2: 25.57 mS/cm; Formulation 3: 21,05 mS/cm; and Formulation 4: 32.1 mS/cm. 7 8 (032] All of the formulations were found to be stable after frozen storage at -80, -30 -18 and -140C up to 24 weeks, as determined by coagulation assay for Factor VilI activity at various time points, without significant loss of activity. [033] As shown in Figure 1, all four formulations in accordance with the invention 5 maintained Factor Vill coagulation activity at substantially the initial level after storage at 30*0 for up to 24 weeks, [034] As shown in Figure 2, in the absence of the added excipients, the solution lost substantially all of its Factor VII coagulation activity after only 1 day of storage at -300C, [035] Throughout this specification and the claims which follow, unless the context requires 10 otherwise, the word "comprise", and variations such as 'comprises" or "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. [036] The reference in this specification to any prior publication (or information derived from 1 5 it), or to any matter which is known, is not, and should not be taken as, an acknowledgement or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.