AU2002300605B2 - Compositions Comprising Conjugates of Stable, Active, Human OB Protein with Antibody FC Chain and Methods - Google Patents

Description

P/001011 28/5191 Regulation 3.2

AUSTRALIA

Patents Act 1990

ORIGINAL

COMPLETE SPECIFICATION STANDARD PATENT Name of Applicant: Amgen Inc.

Actual Inventors David N BREMS and Donna L FRENCH and Margaret A

SPEED

Address for service is: WRAY ASSOCIATES 239 Adelaide Terrace Perth, WA 6000 Attorney code: WR Invention Title: "Compositions Comprising Conjugates of Stable, Active, Human OB Protein with Antibody FC Chain and Methods" This application is a Divisional Application by virtue of Section 39 of Australian Patent Application 71327/98.

The following statement is a full description of this invention, including the best method of performing it known to me:- 112- COMPOSITIONS COMPRISING CONJUGATES OF STABLE, ACTIVE, HUMAN OB PROTEIN WITH ANTIBODY RC CHAIN AND METHODS Field of the Invention The present invention relates to stable, active human GB protein compositions at high concentrations and at or near physiologic p11. Also provided are related compositions, methods of manufacture and methods of using such compositions.

Backaround Although the molecular basis for obesity is largely unknown, the identification of the "GDB gene" and protein encoded ("1OB protein") has shed some light on mechanisms the body uses to regulate body fat deposition. Zhang et Nature 372: 425-432 (1994); see also, the Correction at Nature 374: 479 (1995).

PCT publication No. Wo 96/05309, published February 22, 1996, entitled, "Modulators of Body Weight, Corresponding Nucleic Acids and Proteins, and Diagnostic and Therapeutic Uses Thereof" fully sets forth GB protein and related compositions and methods, and is herein incorporated by reference. An amino acid sequence for human GB protein is set forth at WO 96/05309 (herein incorporated by reference) SEQ ID NOS. 4 and 6 (at pages 172 and 174 of that publication), and the first amino acid residue of the mature protein is at position 22 and is a valine residue. The mature protein is 146 residues (or 145 if the glutamine at position 49 is absent, SEQ ID NO. 6).

The GB protein is active in vi~vo in both ob/cD mutant mice (mice obese due to a detect in the production of the GB gene product) as well as in normal, wild type mice. The biological activity manifests itself in, among other things, weight loss.

S..e aenerally, Barinaga, "Obese" Protein Slims Mice, -2 Science 269: 475-476 (1995) and Friedmnan, "The Alphabet of Weight Contz'ol," Nature 3B5: 119-120 (1997) It is known, for instance, that in ob/ob mutant mice, administration of OH protein results in a decrease in serum insulin levels, and serum glucose levels. It is also known that administration of OB protein results in a decrease in body fat. This was observed in both ob/cb mutant mice, as well as non-obese normal mice.

Pelleymounter et all, Science 269: 540-543 (1995); Ealaas et al., Science 269: 543-546 (1995). _Se~ also, Camptield et al., Science 269: 546-549 (1995) (Peripheral and central administration of microgram doses of OH protein reduced food intake and body weight of ob/ob and diet-induced obese mice but not in db/db obese mice.) In none of these reports have toxicities been observed, even at the highest doses.

For preparationi of a pharmaceutical composition for injection in humans, it has been observed that the human amino acid sequence is insoluble at physiologic pH at relatively high concentrations, such as above about 2 mg active protein/milliliter of liquid. Dosages in the milligram protein per kilogram body weight range, such as .5 or mg/kg/dIay or below, are desirable for injection of therapeutically effective amounts into larger mammals, such as humans. An increase in protein concentration is necessary to avoid injection of large volumes, which can be uncomfortable or possibly painful to the patient.

With the advances in recombinant DNA te chnology, the availability of recombinant proteins for therapeutic use has engendered advances in protein formulation. A review article describing protein -3modification and fusion proteins is Francis, Focus on Growth Factors-3:4-l0 (1992).

One such modification is the use of the Fc region of immunoglobulins. Antibodies comprise two functionally independent parts, a variable domain known as "Fab", which binds antigen, and a constant domain, known as "Fc" which provides the link to effector functions such as complement or phagocytic cells. The Fc portion of an immunoglobulin has a long plasma halflife, whereas the Fab is short-lived. Capon et al., Nature 3317: 525-531 (1989).

Therapeutic proteins have been constructed using the Fc domain to provide longer half-life or to incorporate functions such as Fc receptor binding, protein A binding, complement fixation and placental transfer which all reside in the Fc proteins of immunoglobulins. Id. For example, the Fc region of an IgGl antibody has been fused to the N-terminal end of a molecule which binds CD30 receptors expressed on Hodgkin's Disease tumor cells, anaplastic lymphoma cells, T-cell leukemia cells and other malignant cell types. See, U.S. Patent No. 5,480,981. IL-10, an antiinflammatory and anti-rejection agent has been fused to murine Fcy2a in order to increase the cytokine's short circulating half-life. Zheng, X. at al., The Journal of Immunology, 1J4: 5590-5600 (1995). Studies have also evaluated the use of tumor necrosis factor receptor linked with the Fc protein of human IgGl to treat patients with septic shock. Fisher, C. at al., N. Engl. J. Med., 334: 1697-1702 (1996); Van Zee, K. et al., The Journal of Immunology, 156: 2221-2230 (1996).

Fc has also been fused with CD4 receptor to produce a therapeutic protein for treatment of AIDS. See, Capon et al., Nature, 337:525-531 (1989). In addition, the 4 N-terminus of interleukin 2 has also been fused to the Fc portion of IgG1 or IgG3 to overcome the short half life of interleukin 2 and its systemic toxicity. See, Harvill et al., Immunotechnology, 1: 95-105 (1995).

For insulin, suspension preparations have been reported. But, those conditions which are applicable to insulin are not predictive of those conditions which may be applicable to any other protein, including OB protein. Insulin is a fairly small protein, having particular physical and chemical characteristics; these characteristics are important to determining conditions for formulation. Brange, Galenics of Insulin, Springer-Verlag 1987 describes insulin suspensions see also, Schlichtkrull et al. Insulin Preparations with Prolonged Effect, pp.

729-777 In: Hassellblatt et al., Handbook of Experimental Pharmacology New Series, Vol. XXXII-1/2 Springer-Verlag Berlin, Heidelburg, New York (1975).

To date, there have been no reports of stable preparations of human OB protein at concentrations of at least about 2 mg/ml at physiologic pH, and further, no reports of stable concentrations of active human OB protein at least about 50 mg/ml or above. Moreover, a frozen or lyophilized form may be used to improve shelf-stability but, are less desirable than the readyto-use suspension forms described here. A frozen form requires storage at a constant frozen temperature which may not be possible due to defrost cycles of consumergrade refrigerators and freezers. Furthermore, a lyophilized form must be diluted and mixed which is inconvenient and may compromise patient compliance.

From a producer's point of view, manufacturing, storing and shipping of frozen liquid is expensive and requires far more supervision than distribution of a ready to use formulation. Also, manufacture or otherwise making available a suitable diluent for a lyophilized formulation is more costly and less efficient than not requiring such diluent. There exists a need for concentrated forms of human pharmaceutical compositions containing active OB protein which can be delivered by injection at low volumes. The present invention f ulfills these requirements.

Summary of the Invention The present invention stems from the observation that certain suspension formulations allow the preparation of stable GB protein in concentrations of at least about 2 mg/mi at physiological pH. As used herein, the term, "physiological pHo refers to a pH of about 6.0 to about 8.0. Use of such compositions allow for delivery of relatively low volumes of OB protein therapeutic. As further disclosed herein, the use of precipitating agents allows f or the preparation of suspensions of human GB protein having the characteristics of: 1. improved stability at physiological pH as compared to the same human GB protein in solution form.

Demonstrated below in the working examples are human GB protein suspensions at concentrations of 10 mg/mi or higher and at pH 7, which, when compared to the same concentration in solution at the highest pH which allows solubility (pH-4 for human GB protein in its native form, which is not even physiologic pH)l have better HPLC (high pressure liquid chromatography) profiles. Also demonstrated below is a Fc-QB fusion protein suspension at a concentration of 5 mg/mi at about pH 7 which shows less degradation products upon -6 storage than a comparable Fc-OB fusion protein solution.

2. Sustained injection time-release profile as compared to the same human OB protein in solution form. The working examples below demonstrate a sustained-release effect using the present highly concentrated human OB protein suspensions. Such sustained release effect is advantageous in that the activity of material is maintained over a relatively longer period of time, and thus there is a relatively higher potency, and the need for fewer injections as compared with human OB protein in solution.

Thus, one object of the present invention is a stable preparation of active human OB protein at physiologic pH, having a concentration of at least about 2 mg protein/ml. For instance, a stable preparation of active human OB protein at a concentration of at least 2.0 mg/ml and a pH of 7.0 is provided. The upper limit of concentration is that suspension form which is available for administration to a human, and, as described below, working examples have provided a concentration of as high as 100 mg/ml at physiologic pH between pH 6.0 and pH In another aspect, the present invention relates to a stable preparation of active human OB protein within the pH range of about 6.0 to about having a concentration of at least about 10 mg/ml.

In still another aspect, the present invention relates to a stable preparation of active human OB protein derivatized by the attachment of an Fc region of an immunoglobulin at a concentration of at least about 0.5 mg/ml and a pH of about 6.0 to about More particularly, stable preparations of active 7- Fc-OB fusion protein at a concentration of 5 mg/mi to mg/mi at about pH 7.5 are provided.

In yet other aspects, the present invention provides formulations for stable, active human protein at a concentration of 2 mg protein/mi or above, at pH 6.5 to pH- 7.5. More particularly, formulations for stable, active human 03 protein at a concentration of 20 mg/mi to 100 mg/mi at pH 7.0 are provided.

In another aspect, the present invention provides formulations for stable, active human Os protein at a concentration of 10 mg/mi or above at a pH of 5.0 to In still another aspect, the present invention provides formulations for stable, active human OS protein derivatized by the attachment of an Fc region of an immunoglobulin at a concentration of mg/mi or above and a pH bf about 6.0 to about More particularly, formulations for stable, active Fc- GE fusion protein at a concentration of 5 mg/mi to mg/mi at about pH 7.5 are provided.

Yet other aspects of the present invention include pharmaceutical compositions of the above, methods for manufacturing such compositions, and methods of-threatment using present compositions, an d methods of manufacturing medicamnents containing the present compositions for such treatment.

FIGURES 1A and lB are dose response curves in mice for (lA) the present human GB suspension of Example 1 and (13) a control human 03 protein solution as described in Example 1.

FIGURE 2 is a graph illustrating 03 serum levels in dogs for the present GB protein suspension 8 and for a control human OB protein solution as described in Example 1.

FIGURE 3 is a reversed phase high pressure liquid chromatography (RP-HPLC) tracing of human OB protein formulations at 37 0 C for seven weeks: the human OB protein zinc suspension of Example 1 is the middle tracing, the human OB protein solution control of Example 1 is the top line and a human OB protein suspension kept at -80 0 C for 56 days is the bottom l.ine.

FIGURE 4 is a RP-HPLC tracing of human OB protein formulations at 19°C for 56 days: human OB solution of Example 1 is the top line, the human OB crystalline suspension of Example 2 is the middle line, and the human OB crystalline suspension of Example 2 at for 56 days is the bottom line.

FIGURES 5A-5C are the DNA sequence (SEQ ID NO: 1) and amino acid sequence (SEQ ID NO: 2) of a human metFc-OB protein.

FIGURES 6A-6C are the DNA sequence (SEQ ID NO: 3) and amino acid sequence (SEQ ID NO: 4) of a human metFc-OB protein variant.

FIGURE 7 is a graph depicting the rate of formation of iso asp at asp 108 (asp 335 using the numbering according to SEQ ID NO: as determined by reverse phase HPLC, for recombinant methionyl human Fc- OB protein.

Detailed Description The present stable, active OB protein compositions are generally classified as suspensions, in that the protein moiety is precipitated and suspended in a liquid moiety. The compositions contain an active.OB protein moiety, a precipitating agent, a -9pH modulating agent, and a liquid carrier. The present OB proteins are' either amorphous or in crystalline form.

Preferably, for use as a therapeutic or cosmetic composition in humans, OB protein with the amino acid sequence of native human 03 protein (see Zhang et al., Nature, supra), optionally with an N-terminal methionyl residue incident to bacterial expression, is used. See, PCT Publication WO 96/05309, herein incorporated by reference, for recombinant DNA means to prepare the present OB proteins which may be used. One may make changes in selected amino acids so long as such changes preserve the overall folding or activity of the protein. Table 1, below sets forth conserved amino acid substitutions which may be used, in terms of particular characteristics (basic, acidic, polar, hydrophobic, aromatic, and size (small)). See, in general, Ford et al., Protgin Expression and Purification 2: 95-107, 1991, which is herein incorporated by reference. Small amino terminal extensions, such as an amino-terminal methionine residue, a small linker peptide of up to about 20-25 residues, or a small extension that facilitates purification, such as a poly-histidine tract, an antigenic epitope or a binding domain, may also be present.

10 Table 1 Conservative Amino Acid Substitutions Basic: arginine lysine histidine Acidic: glutamic acid aspartic acid Polar: glutamine asparagine Hydrophobic: leucine isoleucine valine Aromatic: phenylalanine tryptophan tyrosine Small: glycine alanine serine threonine methionine Generally, human OB proteins which will display increased stability in the present suspensions will be those which, upon exposure to physiologic pH, have an exposed hydrophobic region when in solution.

Additionally, human OB proteins derivatized by the attachment of an Fc region of an immunoglobulin to the OB protein moiety display increased stability in the present suspensions.

Generally, an Fc region of an immunoglobulin may be genetically or chemically fused to a human OB protein. Preferably, the Fc region is fused at the Nterminus of the OB protein. See copending U.S.

application Serial No. 08/770,973, filed December 1996, herein incorporated by reference, for preferred Fc-OB fusion proteins.

Preferably, an Fc region with the amino acid sequence of the human immunoglobulin IgG-1 heavy chain (see Ellison, J.W. et al., Nucleic Acids Res. 10: 4071- 11 4079 (1982)) is used. A preferred Fc region is set forth in SEQ ID NO: 2 (see Figure The recombinant Fc-OB sequence of SEQ ID NO: 2 is a 378 amino acid Fc- OB protein (not counting the methionine residue). The first amino acid residue of the Fc-OB protein in Figure glutamic acid, is referred to as +1 with the methionine at the -1 position. Variants or analogs of the Fc portion may be constructed by, for example, making various substitutions of amino acid residues or base pairs.

Cysteine residues can be deleted or replaced with other amino acids to prevent formation of disulfide crosslinks of the Fc sequences. In particular, amino acid at position 5 of SEQ ID NO: 2 is a cysteine residue. One may remove the cysteine residue at position 5 or substitute it with one or more amino acids. For example, an alanine residue may be substituted for the cysteine residue at position resulting in a variant amino acid sequence. Likewise, the cysteine at position 5 of SEQ ID NO: 2 may be substituted with a serine or other amino acid residue or deleted.

A variant or analog may also be prepared by deletion of the amino acids at positions 1, 2, 3, 4 and 5, resulting in a 373 amino acid Fc-OB protein (not counting the methionine residue). This sequence is set forth in SEQ ID NO:4 (see Figure Substitutions at these positions can also be made and are within the scope of this invention.

Modifications may also be made to introduce four amino acid substitutions to ablate the Fc receptor binding site and the complement (Clq) binding site.

According to the numbering of SEQ ID NO: 4, these variant modifications include leucine at position 12 substituted with glutamic acid, glutamic acid at position 98 substituted with alanine, and lysines at positions 100 and 102 substituted with alanines.

Likewise, one or more tyrosine residues can be replaced by phenylalanine residues as well. As described above, one may make changes in selected amino acids as long as such changes preserve the overall folding or activity of the fusion protein.

Furthermore, the Fc region may be also linked to the human OB protein of the Fc-OB fusion protein by "linker" moieties whether chemical or amino acids of varying lengths. Such chemical linkers are well known in the art. Amino acid linker sequences can include but are not limited to: ala, ala, ala; ala, ala, ala, ala; ala, ala, ala, ala, ala; gly, gly; gly, gly, gly; gly, gly, gly, gly, gly; gly, gly, gly, gly, gly, gly, gly; gly-pro-gly; gly, gly, pro, gly, gly; and any combination of subparts (a) through i).

The present precipitating agents may be a salt having a cationic component, and may be selected from among calcium, magnesium, zinc, sodium, iron, cobalt, manganese, potassium and nickel. Preferably, the salt will be compatible for use in a pharmaceutical composition.

Alternatively precipitating agents may be selected from among agents which are pharmaceutically acceptable yet known to precipitate protein, such as 13 polyethylene glycols, or other water soluble polymers as set forth in-the next paragraphs. A useful precipitating agent will induce precipitation of 03 protein at neutral pH but is reversible or redissolveable up~on dilution with physiologically compatible solvents. Without an appropriate precipitating agent, 03 protein precipitates at neutral pH to a torm that is not reversible by dilution with physiologically compatible solvents.

The pH range is preferably from about pH to about pH 8.0, and more preferably from about 6.5 to about 7.5. The most preferable pH for a pharmaceutical composition is that in which the GB protein used may retain its maxirmum biological activity at the selected protein concentration. At non-physiologic pH, the present 08 protein suspensions may also have advantages. At pH below 5.0, the present 03 protein.

suspensions may be more stable (in terms of shalt-life) than equal concentrations of GB protein in solution at equal pH. For example at pH 4.0, and a concentration of mg/ml, the present suspensions may have greater biological activity upon in vivo administration than would the equivalent solution.

The buffer may be selected from among those which attain the desired pH while not altering the precipitating characteristics of the composition.

Preferably, buffers will be acceptable for a pharmaceutical formulation. Tris, MES, and PIPES are acceptable for both the amorphous and crystalline forms. Phosphate is a preferred buffer for the crystalline forms.

The final suspension will preferably have a concentration of 5 mg/mi to 100 mg/mI for ease of therapeutic administration.

14 Methods of Use Therapeutic. Therapeutic uses include weight modulation, the treatment or prevention of diabetes, blood lipid reduction (and treatment of related conditions), increasing lean body mass and increasing insulin sensitivity. In addition, the present compositions may be used for manufacture of one or more medicaments for treatment or amelioration of the above conditions. Methods of administration will typically be by injection, although other means, such as pulmonary delivery may be used. See PCT WO 96/05309, incorporated by reference at page 83 et s eqg., for example. The present suspensions may be spray-dried into particles having an average size of less than microns, or more preferably, 0.5 to 5 microns.

Weiaht Modulation. The present compositions and methods may be used for weight reduction. Viewed another way, the present compositions may be used for maintenance of a desired weight or level of adiposity.

As has been demonstrated in murine models (see supra) administration of the present OB protein results in weight loss. The body mass lost is primarily of adipose tissue, or fat. Such weight loss can be associated with the treatment of concomitant conditions, such as those below, and therefore constitute a therapeutic application. In addition, cosmetic uses are provided herein if weight modulation is solely for improvement in appearance.

Treatment of Diabetes. The present compositions and methods may be used in the prevention or treatment of Type II diabetes. As Type II diabetes can be correlated with obesity, use of the present invention to reduce weight (or maintain a desired 15 weight, or reduce or maintain an adiposity level) can also alleviate -or prevent the development of diabetes.

Moreover, even in the absence of dosages sufficient to result in weight loss, the present compositions may be used to prevent or ameliorate diabetes.

Blood Lipid Modulation. The present compositions and methods may be used in the modulation of blood lipid levels. Ideally, in situations where solely reduction in blood lipid levels is desired, or where maintenance of blood lipid levels is desired, the dosage will be insufficient to result in weight loss.

Thus, during an initial course of therapy of an obese patient, dosages may be administered whereby weight loss and concomitant blood lipid level lowering is achieved. Once sufficient weight loss is achieved, a dosage sufficient to prevent re-gaining weight, yet sufficient to maintain desired blood lipid levels, or other conditions as set forth herein, for example, may be administered. These dosages can be determined empirically, as the effects of OB protein are reversible. Campfield et al., Science 269: 546- 549 (1995) at 547. Thus, if a dosage resulting in weight loss is observed when weight loss is not desired, one would administer a lower dose in order to achieve the desired blood lipid levels, yet maintain the desired weight. See, eg, PCT Publication WO 97/06816 herein incorporated by reference.

Increasing Lean Mass or Insulin Sensitivity.

Ideally, in situations where solely an increase in lean body mass is desired, the dosage will be insufficient to result in weight loss. Thus, during an initial course of therapy of an obese person, dosages may be administered whereby weight loss and concomitant fat tissue decrease/lean mass increase is achieved. Once 16 sufficient weight loss is achieved, a dosage sufficient to prevent regaining weight, yet sufficient to maintain desired lean mass increase (or prevention of lean mass depletion) may be administered. For increasing an individual's sensitivity to insulin, similar dosage considerations may be taken into account. Lean mass increase without weight loss may be achieved sufficient to decrease the amount of insulin (or, potentially, arnylin, amylin antagonists or agonlists, or thiazolidinediones, or other potential diabetes treating drugs) an individual would be administered or the treatment of diabetes. For increasing overall strength, there may be similar dosage considerations.

Lean mass increase with concomitant increase in overall strength may be achieved with doses insufficient to result in weight loss. Other benefits, such as an increase in red blood cells (and oxygenation in the blood) and a decrease in bone resorption or osteoporosis may also be achieved in the absence of weight loss. 3i PCT Publication No. WO 97/18833 herein incorporated by reference.

Combination Therapies. The present compositions and methods may be used in conjunction with other therapies, such as altered diet and exercise. other medicaments, such as those useful for the treatment of diabetes insulin and possibly arnylin, antagonists or agonists thereof, thiazolidinediones (se, POT Publication No. WO 98/08512 herein incorporated by reference), or other potential diabetes treating drugs) cholesterol and blood pressure lowering medicaments (such as those which reduce blood lipid levels or other cardiovascular medicamnents), activity increasing medicaments amphetamines), diuretics (for liquid elimination), and 17 appetite suppressants (such as agents which act on neuropeptide T receptors or serotonin reuptake inhibitors). Such administration may be simultaneous or may be in seriatim. In addition, the present methods may be used in conjunction with surgical procedures, such 'as cosmetic surgeries designed to alter the overall appearance of a body liposuction or laser surgeries designed to reduce body mass, or implant surgeries designed to increase the appearance of body mass). The health benefits of cardiac surgeries, such as bypass surgeries or other surgeries designed to relieve a deleterious condition caused by blockage of blood vessels by fatty deposits, such as arterial plaque, may be increased with concomitant use of the present compositions and methods. Methods to eliminate gall stones, such as ultrasonic or laser methods, may also be used either prior to, during or after a course of the present therapeutic methods.

Furthermore, the present methods may be used as an adjunct to surgeries or therapies for broken bones, damaged muscle, or other therapies which would be improved by an increase in lean tissue mass.

The following examples are offered to more fully illuttrate the invention, but are not to be construed as limiting the scope thereof. Example 1 sets forth preparation of an amorphous (as opposed to a crystalline, as infra) human GB protein suspension at a concentration of 100 mg/mi at pH 7.0. Example 2 sets forth preparation of a crystalline 03 protein suspension. Example 3 demonstrates an improved dose response for 03 protein suspensions as compared to OB protein solutions. Example 4 demonstrates the delayed time action profile of the present suspensions in a dog model. Example 5 sets forth preparation of an 18 amorphous Fc-OB protein suspension. Examples 5 and 7 demonstrate the-improved stability of the present suspensions.

EXAMPLE 1: Preparation of an amorphous OB protein suspension.

This example illustrates preparation of one of the human OB protein suspensions of the present invention. An amorphous human OB protein suspension was prepared by precipitation with zinc salt. At a final pH of 6.0 to pH 8.0, a concentration of 100 mg protein/mi liquid has been obtained. Also set forth is a control composition, of pH 4.0, for a human OB protein solution.

Composition: Protein moiety: recombinant methionyl human OB protein ("rmetHu-leptin") as set forth in SEQ ID NO. 4 of PCT Publication WO 96/05309, beginning with' amino acid number 22 (Val) and ending with amino acid number 167, having at its N-terminus a methionyl residue: Precipitant: Zinc chloride Buffer: Tris, MES and Pipes Final pH: 6.0-8.0 Preparation protocol: Recombinant methionyl human OB protein ("rmetHu-leptin") solution was concentrated to about 40 mg/ml in water for injection, acidified to pH 3.0, with HC. Zinc chloride was added and the suspension was formed by adjusting the pH to near neutrality (approximately pH 7.0) by adding an appropriate buffer. Tris, MES and PIPES buffer have been successfully used. The final conditions were typically 10 to 15 mM buffer, 20 to 1000 iM Zinc, pH 6.0 to 8.0 and 10 mg/ml rmetHu-leptin. The 19 suspensions have been concentrated by allowing the particles to settle at 4 0 C for several hours and removing the supernatant. This procedure may be repeated several times until the maximum concentration is obtained, and has been used to obtain about 100 mg/mi suspensions.

Control Composition: Recombinant methionyl human 08 protein (as above) solution at 20 rrg/ml pH 4.O containing 10 mM acetate and 5% w/v sorbitol was used as a control composition.

EXAMPLE 2: Preparation of a crystalline GB protein suspension.

This example illustrates the preparation of a crystalline 08 protein suspension of the present invention.

Protein moiety: recombinant methionyl human OB protein as in Example 1, above, was used.

Procedure: rmetHu-leptin at a concentration of 15 mg/nil in 1 mM HCi was mixed in a 1:1 ratio with 4 M4 NaCl, 100 mM Tris, pH 8.5, 2% v/v ethanol, at 4 0

C.

Crystals spontaneously formed by slowly adjusting the temperature over several hours to between 14'C and 250C and maintaining that temperature for at least 2 hours depending on the duration of warming to the final temperature. The "mother liquor" the liquid in which the crystals were grown) was replaced with a more suitable solvent for injection by harvesting the crystals by centrifugation and resuspension. in an appropriate crystal stabilizing solvent. A suitable replacement solvent is 2D-25% polyethylene glycol (having a molecular weight of about 4000 daltons to about 20,000 daJltons, the term "about" meaning that the approximate average of molecular weights for commercial 20 PEG preparations), appropriate neutral pH buffer, preferably about pH 6.0 to about pH 8.0, and preferably mMv phosphate buffer pH 6.0 to pH 7.5, and 2% ethanol v/v. In a typical preparation, some residual salt, usually less than 0.25 M, may remain.

EXAMPLE 3: Improved dose response for 03 protein suspensions as compared to OB protein solutions.

This example demonstrates that the present GB protein suspensions are more efficacious than GB protein in solution. Normal lean mice were given daily injections, for 5 days, of either the present suspension, at 1, 10 and 50 mg of protein per kg of body weight, or OB protein solution at the sane dose.

The mice given the suspension lost more weight per unit of mass of GB protein given than did mice given equal doses of the solution formulation- This is illustrated in FIGURE 1A and FIGURE 12. FIGURE 1A shows the percent weight change when the suspension of Example 1 was given. FIGURE lB shows the percent weight change when the control solution of Examnple 1 was given.

This illustrates that the present suspension at the samte dose is more efficacious than that given in solution Form. While not wishing to be bound by theory, this may be due to slower absorption rate of the suspension as compared to the solution. The suspension must dissolve before it enters the blood, so this sustained release effect results in higher efficacy. on a mass basis, less protein in suspension needs to be administered than solution. Further, in solution there is no difference between the 10 and mg/kg dose at day 5 (the last day of dosing) (See Table 2, below) The suspension gives a more definitive dose response curve than does the solution formulation.

21 TABLE 2 PERCENT WEIGHT CHANGE FROM DAY 0 Day 6 Placebo 1.4 Suspension 1 mg/kg -1.7 Suspension 10 mg/kg -5.9 Suspension 50 mg/kg Solution 1 mg/kg 7 Solution 10 mg/)kg. Solution 50 mg/kg The date is an average for 5 mice per treatment.

Methods: Animals: Normal CD-I mice were used.

Base weight: About 20 grams.

Administration: Animals were injected SC each day in the same location for 5 days.

Handling: Animals were group housed, and fed ad libitum.

Compositions: Solution: The rmetHu-leptin solution of Example I was used, at a concentration of 20 mg/ml.

Suspension: The rmetHu-leptin suspension of Example 1 was used, at pH 7.0, 10 mM MES buffer, 500 mM Zn, 20 mg/ml.

PBS: Phosphate buffered saline was used as a placebo.

(Dose responses for controls using suspension liquid or solution liquid alone, with no protein, were similar to PBS, data not shown).

EXAMPLE 4: OB protein serum levels in dogs.

22 This Example demonstrates the delayed time action profile of the present suspensions.

Methods: Beagle dogs were administered suspension or solution rmetHu-leptin. Serum was drawn, and OB protein levels were measured at the times illustrated in FIGURE 2.

TABLE 3 Time after Serum Serum Serum injection concentratio concentration concentration (hours) n Solution Suspension Suspension (crystal) (zinc) 0 0 0 0 532 9.4 50.5 1 1047 12.9 130.4 2 1706 51 298.5 4 1480 87 323.5 8 742 298 247.7 12 301 426 241.1 16 109 389 209.6 24 5 90 57.7 Compositions used: Solution: The solution according to Example 1 was used, at a dose of 5 mg/kg/day.

Suspension: The suspension according to Example 2 was used. See Table.

Animals: The data presented in Table 3 is for an average of 3 animals. Animals were normal beagle dogs.

Handling: Animals were housed individually, and fed ad libitum. Good animal handling practices were obeyed.

23 Assay: An antibody assay was used as in Hotta et al, J. Biol. Chem 2=1: 255327-25331 (1996).

Results: As can be seen from FIGURE 2, the solution concentration peaks at 1 to 2 hours after administration of protein, whereas the suspension concentration peaks much later, after 10-12 hours.

This demonstrates that the suspension maintains a minimum effective dose for a longer time period.

EXAMPLE 5: Preparation of an amorphous Fc-OB protein suspension.

This example illustrates preparation of one of the human Fc-OB protein suspensions of the present invention. An amorphous human Fc-OB protein suspension was prepared by precipitation with zinc salt. Also set forth is a control composition, of pH 7.5, for a human Fc-OB protein solution.

ComPosition: Protein moiety: recombinant methionyl human Fc-OB protein ("rmetHu-Fc-leptin") as set forth in SEQ ID NO: 4, a 373 amino acid fusion protein, the Fc portion of the protein being amino acids 1-227 and the human OB protein portion of the protein being amino acids 228-373, having at its N-terminus a methionyl residue: Precipitant: Zinc chloride Buffer: 100mM Tris Final pH: Preparation protocol: A rmetHu-Fc-leptin solution was concentrated to about 5 mg/m! in 100 mM Tris buffer, pH 7.5. Zinc chloride was added to form the suspension.

24 Control Com-position: A rmet~u-Fc-leptin solution (as ab-ove) at 5 mg/mi, pH 7.5 containing 100 mM Tris was used as a control composition.

EXAMPLE-6: Stability of the present human OB protein suspensions.

This example demonstrates that both the amorphous and the crystalline forms of the present suspensions are more stable under accelerated stability assay conditions than material in solution.

FIGURE 3 illustrates an RP-HPLC tracing comparing the zinc amorphous form of the present suspension (as in Example 1) with the solution form (also as in Example 1) at 37 0 C for a period of 7 weeks. As can be seen, the present suspension (middle line) has fewer peaks (indicating fewer breakdown products) than the solution form (top line) As a comparison, the bottom line presents the zinc amorphous for-m which had been stored for 7 weeks at FIGURE 4 illustrates an RP-HPLC tracing comparing the crystalline suspension form of Example 2 with the solution form (of Example 1) The materials were stored for 56 days at 19 0 C. (Storage at 37CC was not a relevant condition, as the crystalline form loses its crystalline structure at 37 0 FIGURE 4 shows that there are more peaks, indicating more degradation, for the solution form, (main peak 86%) than for the suspension form (main peak The control at the bottom line was the crystalline form stored for 56 days at -80'C. Similar results were observed for 4 0

C,

although degradation occurred more slowly.

The main degradation product appeared to be the aspartate at amino acid position 108 (according to SEQ ID NO: 4 in PCT WO 96/05309, using the "Val" 25/1 residue as position number One may empirically select a more stable chemical moiety at this position, such as another amino acid, to improve stability of the molecule.

Overall, the suspensions of the present invention are more stable than OB protein in solution.

EXAMPLE 7: Stability of the present human Fc-OB protein suspensions.

This example demonstrates that the amorphous form of the present Fc-OB protein suspensions is more stable under accelerated stability assay conditions than material in solution.

The zinc amorphous form of the present suspension (as in Example 5) and the solution form (also as in Example were put on stability studies by storing both the suspension and solution forms at 4 0 C, 29 0 C and 37 0 C for a period of 2 weeks. AS shown in FIGURE 7, the Fc-leptin suspensions stored at 29 0 C and 37°C show a lower percentage of degradation products related to the aspartate at amino acid position 108 of the OB protein than the Fc-leptin solutions stored at the same temperatures, respectively.

While the present invention has been described in terms of preferred embodiments, it is understood that variations and modifications will occur to those skilled in the art. Therefore, it is intended that the appended claims cover all such equivalent variations which come within the scope of the invention as claimed.

25/2 Throughout the specification, unless the context requires otherwise, the word "comprise" or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.

Claims (17)

1. A human OB protein suspension having a pH of about to 8.0 and a concentration of at least 0.5 mg/ml wherein the OB protein is derivatized by the attachment of an Fc region of an immunoglobulin to the N-terminus of the OB protein moiety; said suspension also containing a precipitating agent.

2. A human OB protein suspension of claim 1 wherein the Fc portion of said human Fc-OB protein is selected from the group consisting of: the Fc amino acid sequences as set forth in SEQ ID NOS: 2 and 4; the amino acid sequence of subpart having a different amino acid substituted or deleted in one or more of the following positions (using the numbering according to SEQ ID NO:2): one or more cysteine residues replaced by an alanine or serine residue; (ii) one or more tyrosine residues replaced by a phenylalanine residue; (iii) the amino acid at position 5 replaced with an alanine; (iv) the amino acid at position 20 replaced with glutamic acid; the amino acid at position 103 replaced with an alanine; (vi) the amino acid at position 105 replaced with an alanine; (vii) the amino acid at position 107 replaced with an alanine; 27 (viii) the amino acids at positions i, 2, 3, 4, and deleted; (ix) one or more residues replaced or deleted to ablate the Fc receptor binding site; one or more residues substituted or deleted to ablate the complement (Clq) binding site; and (xi) a combination of subparts i-x; and the amino acid sequence of subparts or (b) having a methionyl residue at the N-terminus.

3. A human OB protein suspension of claim 1 wherein said concentration is at least 5 mg/ml.

4. A human OB protein suspension of claim 1 wherein said concentration is between 5 mg/ml and 50 mg/ml.

5. A human OB protein suspension of claim 1 wherein said pH is pH

6. A human OB protein suspension of claim 2 wherein said human OB protein is rmetHu-Fc-leptin.

7. A human OB protein suspension of claim 1 wherein the precipitating agent is selected from a salt and a water soluble polymer.

8. A human OB protein suspension of claim 1 wherein the precipitating agent is selected from among calcium, magnesium, zinc, sodium, iron, cobalt, manganese, potassium and nickel.

9. A method of treating an individual for a condition by administering an effective dose of a human OB suspension according to claim 1, said condition selected from among: 28 weight modulation, adiposity modulation, diabetes, blood lipid level modulation, increase in lean mass, and increase in insulin sensitivity.

A method of preparing a human OB protein suspension of any one of claims 1-8 comprising: combining, under suitable conditions, a precipitating agent and a human OB protein in solution, wherein the OB protein is derivatized by the attachment of an Fc region of an immunoglobulin to the N-terminus of the OB protein moiety; allowing said human OB protein to precipitate; collecting said precipitated human OB protein; and resuspending said human OB protein in a diluent.

11. The method of claim 10 wherein said human OB protein is resuspended in a diluent having a pH of between 6.0 and

12. A method of claim 10 wherein said human OB protein is rmetHu-Fc-leptin.

13. A suspension according to any one of claims 1 to 8 for therapeutic administration.

14. Use of a suspension according to any one of claims 1 to 8 for the manufacture of a medicament for treating a condition selected from: weight modulation, adiposity modulation, diabetes, 29 blood lipid level modulation, increase in lean mass, and increase in insulin sensitivity.

A pharmaceutical composition comprising a suspension according to any one of claims 1 to 8.

16. A method of cosmetically treating an individual comprising administering to said individual an effective dose suspension according to any one of claims 1 to 8.

17. A suspension according to claim 1 as herein described with reference to example 5 or 7. Dated this THIRTY FIRST day of MARCH 2005. Amgen Inc. Applicant Wray Associates Perth, Western Australia Patent Attorneys for the Applicant