Pharmaceutical formulations for sustained drug delivery

Abstract

Sustained delivery formulations comprising a water-insoluble complex of a peptidic compound (e.g., a peptide, polypeptide, protein, peptidomimetic or the like) and a carrier macromolecule are disclosed. The formulations of the invention allow for loading of high concentrations of peptidic compound in a small volume and for delivery of a pharmaceutically active peptidic compound for prolonged periods, e.g., one month, after administration of the complex. The complexes of the invention can be milled or crushed to a fine powder. In powdered form, the complexes form stable aqueous suspensions and dispersions, suitable for injection. In a preferred embodiment, the peptidic compound of the complex is an LHRH analogue, preferably an LHRH antagonist, and the carrier macromolecule is an anionic polymer, preferably carboxymethylcellulose. Methods of making the complexes of the invention, and methods of using LHRH-analogue-containing complexes to treat conditions treatable with an LHRH analogue, are also disclosed.

Description

BACKGROUND OF THE INVENTION

A variety of diseases and clinical disorders are treated by the administration of a pharmaceutically active peptide. One such example is prostate cancer, which is a sex hormone dependent cancer and which can be treated by administration of a luteinizing hormone releasing hormone (LHRH) analogue that disturbs the production of luteinizing hormone (LH), which regulates the synthesis of male hormones. In particular, to decrease LH production, peptidic analogues of LHRH that act as superagonists of the luteinizing hormone releasing hormone receptor, such as leuprolide and goserelin, have been used.

In many instances, the therapeutic effectiveness of a pharmaceutically active peptide depends upon its continued presence in vivo over prolonged time periods. To achieve continuous delivery of the peptide in vivo, a sustained release or sustained delivery formulation is desirable, to avoid the need for repeated administrations. One approach for sustained drug delivery is by microencapsulation, in which the active ingredient is enclosed within a polymeric membrane to produce microparticles. For example, LHRH superagonists, such as leuprolide and goserelin, typically are encapsulated within a microparticle comprising a poly-lactide/poly-glycolide copolymer to prepare formulations suitable for depot injection that provide sustained delivery of the superagonist over several weeks to months (see e.g., U.S. Pat. Nos. 4,675,189; 4,677,191; 5,480,656 and 4,728,721).

Additional sustained delivery formulations for administering pharmaceutically active peptides in vivo continuously for prolonged time periods are needed.

SUMMARY OF THE INVENTION

The present invention provides pharmaceutical compositions comprising a stable water-insoluble complex composed of a peptidic compound (e.g., a peptide, polypeptide, protein, peptidomimetic and the like), preferably a pharmaceutically active peptidic compound, and a carrier macromolecule that allow for sustained delivery of the peptidic compound in vivo upon administration of the complex. Accordingly, the complex of the invention can permit continuous delivery of a pharmaceutically active peptidic compound to a subject for prolonged periods of time, e.g., one month. Moreover, the association of the peptidic compound and the carrier macromolecule in a tight, stable complex allows for loading of high concentrations of the peptidic compound into the formulation.

The complex of the invention is formed by combining the peptidic compound and the carrier macromolecule under conditions such that a substantially water-insoluble complex is formed, e.g., aqueous solutions of the peptidic compound and carrier macromolecule are mixed until the complex precipitates. The complex may be in the form of a solid (e.g., a paste, granules, a powder or a lyophilizate) or the powdered form of the complex can be pulverized finely enough to form stable liquid suspensions or semi-solid dispersions.

In a preferred embodiment, the peptidic compound of the water-insoluble complex is an LHRH analogue, more preferably an LHRH antagonist, and the carrier macro molecule is an anionic polymer, preferably carboxymethylcellulose. The complex of the invention is suitable for sterilization, such as by gamma irradiation or electron beam irradiation, prior to administration in vivo.

Methods for treating a subject for a condition treat able with an LHRH analogue by administering to the subject an LHRH-analogue-containing composition of the invention are also provided. In a preferred embodiment, the treatment methods of the invention are used in the treatment of prostate cancer.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B show graphs depicting the plasma testosterone levels (in ng/ml; open black boxes) and plasma PPI-149 levels (in ng/ml; closed boxes) in rats (1A) and dogs (1B) over time following intramuscular injection of a complex of PPI-149 and carboxymethylcellulose.

FIG. 2 is a graph depicting the plasma testosterone levels (in ng/ml; open boxes) and plasma PPI-149 levels (in ng/ml; closed boxes) in rats over time following intramuscular injection of a complex of the LHRH antagonist PPI-149 and carboxymethylcellulose on day 0 and injection of the LHRH agonist Lupron™ at day 30, demonstrating suppression of the Lupron™-induced testosterone surge by the PPI-149 pretreatment.

FIGS. 3A-3C are a series of graphs depicting the plasma testosterone levels (in ng/ml) in male Sprague-Dawley rats over time, following intramuscular injection of a PPI-149-CMC (FIG. 3A), PPI-258-CMC (FIG. 3B) or Cetrorelix™-CMC (FIG. 3C).

FIG. 4 is a graph depicting the plasma testosterone levels (in ng/ml; open boxes) and plasma PPI-149 levels (in ng/ml; closed boxes) in dogs over time following subcutaneous injection of PPI-149-CMC at the indicated dosages at 28 day intervals, demonstrating prolonged suppression of plasma testosterone levels.

FIG. 5 is a graph depicting the plasma testosterone levels (in ng/ml; open boxes) and plasma PPI-149 levels (in ng/ml; closed boxes) in dogs over time following intramuscular injection of PPI-149-CMC at the indicated dosages at 28 day intervals, demonstrating prolonged suppression of plasma testosterone levels.

DETAILED DESCRIPTION OF THE INVENTION

This invention pertains to pharmaceutical compositions comprising a stable water-insoluble complex composed of a peptidic compound (e.g., a peptide, polypeptide, protein, peptidomimetic and the like) and a carrier macro molecule, methods of making such compositions and methods of using such compositions. The advantages of the pharmaceutical compositions of the invention include the ability for delivery of a pharmaceutically active peptidic compound, either systemically or locally, for prolonged periods (e.g., several weeks, one month or several months) and the ability to load high concentrations of peptidic compound into the complex.

In order that the invention may be more readily understood, certain terms are first defined.

As used herein, the term “peptidic compound” is intended to refer to compounds composed, at least in part, of amino acid residues linked by amide bonds (i.e., peptide bonds). The term “peptidic compound” is intended to encompass peptides, polypeptide and proteins. Typically, a peptide will be composed of less than about 100 amino acids, more typically less than about 50 amino acid residues and even more typically, less than about 25 amino acid residues. The term “peptidic compound” is further intended to encompass peptide analogues, peptide derivatives and peptidomimetics that mimic the chemical structure of a peptide composed of naturally-occurring amino acids. Examples of peptide analogues include peptides comprising one or more non-natural amino acids. Examples of peptide derivatives include peptides in which an amino acid side chain, the peptide backbone, or the amino- or carboxy-terminus has been derivatized (e.g., peptide compounds with methylated amide linkages). Examples of peptidomimetics include peptidic compounds in which the peptide backbone is substituted with one or more benzodiazepine molecules (see e.g., James, G. L. et al. (1993) Science 260:1937-1942), “inverso” peptides in which all L-amino acids are substituted with the corresponding D-amino acids, “retro-inverso” peptides (see U.S. Pat. No. 4,522,752 by Sisto) in which the sequence of amino acids is reversed (“retro”) and all L-amino acids are replaced with D-amino acids)“inverso”) and other isosteres, such as peptide back-bone (i.e., amide bond) mimetics, including modifications of the amide nitrogen, the α-carbon, amide carbonyl, complete replacement of the amide bond, extensions, deletions or backbone crosslinks. Several peptide backbone modifications are known, including ψ[CH₂S], ψ[CH₂NH], ψ[CSNH₂], ψ[NHCO], ψ[COCH₂], and ψ[(E) or (Z) CH═CH]. In the nomenclature used above, ψ indicates the absence of an amide bond. The structure that replaces the amide group is specified within the brackets. Other possible modifications include an N-alkyl (or aryl) substitution (ψ[CONR]), backbone crosslinking to construct lactams and other cyclic structures, and other derivatives including C-terminal hydroxymethyl derivatives, O-modified derivatives and N-terminally modified derivatives including substituted aramides such as alkylamides and hydrazides.

As used herein, the term “pharmaceutically active peptidic compound” is intended to refer to a peptidic compound that exhibits pharmacologic activity, either in its present form or upon processing in vivo (i.e., pharmaceutically active peptidic compounds include peptidic compounds with constitutive pharmacologic activity and peptidic compounds in a “prodrug” form that have to be metabolized or processed in some way in vivo following administration in order to exhibit pharmacologic activity).

As used herein, the terms “multivalent cationic peptidic compound” and “multivalent anionic peptidic compound” are intended to refer to peptidic compounds comprising a multiplicity of positive or negative charges, respectively. A “bivalent cationic” or “bivalent anionic” peptidic compound is intended to refer to a peptidic compound comprising two positive or negative charges, respectively. A “trivalent cationic” or “trivalent anionic” peptidic compound is intended to refer to a peptidic compound comprising three positive or negative charges, respectively.

As used herein, the term “LHRH analogue” is intended to encompass peptidic compounds that mimic the structure of luteinizing hormone releasing hormone. An LHRH analogue may be an LHRH agonist or an LHRH antagonist.

As used herein, an “LHRH agonist” is intended to refer to a compound which stimulates the luteinizing hormone releasing hormone receptor (LHRH-R) such that release of luteinizing hormone is stimulated, or an “LHRH antagonist”, which refers to a compound that inhibits LHRH-R such that release of luteinizing hormone is inhibited. Examples of LHRH agonists include leuprolide (trade name: Lupron®; Abbott/TAP), goserelin (trade name: Zoladex®; Zeneca), buserelin (Hoechst), triptorelin (also known as Decapeptyl, D-Trp-6-LHRH and Debiopharm®; Ipsen/Beaufour), nafarelin (trade name” Synarel®; Syntex), lutrelin (Wyeth), cystorelin (Hoechst), gonadorelin (Ayerst) and histrelin (Ortho).

As used herein, the term “LHRH antagonist” is intended to refer to a compound that inhibits the luteinizing hormone releasing hormone receptor such that release of luteinizing hormone is inhibited. Examples of LHRH antagonists include Antide, Cetrorelix, compounds described in U.S. Pat. No. 5,470,947 to Folkers et al.; PCT Publication No. WO 89/01944 by Folkers et al.; U.S. Pat. No. 5,413,990 to Haviv; U.S. Pat. No. 5,300,492 to Haviv; U.S. Pat. No. 5,371,070 to Koerber et al.; U.S. Pat. No. 5,296,468 to Hoeger et al.; U.S. Pat. No. 5,171,835 to Janaky et al.; U.S. Pat. No. 5,003,011 to Coy et al.; U.S. Pat. No. 4,431,635 to Coy; U.S. Pat. No. 4,992,421 to De et al.; U.S. Pat. No. 4,851,385 to Roeske; U.S. Pat. No. 4,801,577 to Nestor, Jr. et al.; and U.S. Pat. No. 4,689,396 to Roeske et al. and compounds disclosed in U.S. patent application Ser. No. 08/480,494, entitled “LHRH Antagonist Peptides”, and a corresponding PCT application thereof (PCT Application No. PCT/US96/09852), also entitled “LHRH Antagonist Peptides”, the entire contents of both of which are expressly incorporated herein by reference. An especially preferred LHRH antagonist comprises the structure: Ac-D-Nal¹, 4-Cl-D-Phe², D-Pal³, N-Me-Tyr⁵, D-Asn⁶, Lys(iPr)⁸, D-Ala¹⁰-LHRH, referred to herein as PPI-149.

As used herein, the term “carrier macromolecule” is intended to refer to a macromolecule that can complex with a peptidic compound to form a water-insoluble complex. Prior to complexing with the peptidic compound, the carrier macromolecule typically is water-soluble. Preferably, the macromolecule has a molecular weight of at least 5 kDa, more preferably 10 kDa. The term “anionic carrier macromolecule” is intended to include negatively charged high molecular weight molecules, such as anionic polymers. The term “cationic carrier macromolecule” is intended to includes positively charged high molecular weight molecules, such as cationic polymers.

As used herein, the term “water-insoluble complex” is intended to refer to a physically and chemically stable complex that forms upon appropriate combining of a peptidic compound and carrier macromolecule according to procedures described herein. This complex typically takes the form of a precipitate that is produced upon combining aqueous preparations of the peptidic compound and carrier macromolecule. Although not intending to be limited by mechanism, the formation of preferred water-insoluble complexes of the invention is thought to involve (i.e., be mediated at least in part by) ionic interactions in situations where the peptidic compound is cationic and the carrier molecule is anionic or vice versa. Additionally or alternatively, the formation of a water-insoluble complex of the invention may involve (i.e., be mediated at least in part by) hydrophobic interactions. Still further, formation of a water-insoluble complex of the invention may involve (i.e., be mediated at least in part by) covalent interactions. Description of the complex as being “water-insoluble” is intended to indicate that the complex does not substantially or readily dissolve in water, as indicated by its precipitation from aqueous solution. However, it should be understood that a “water-insoluble” complex of the invention may exhibit limited solubility (i.e., partial solubility) in water either in vitro or in the aqueous physiological environment in vivo.

As used herein, the term “sustained delivery” is intended to refer to continual delivery of a pharmaceutical agent in vivo over a period of time following administration, preferably at least several days, a week or several weeks. Sustained delivery of the agent can be demonstrated by, for example, the continued therapeutic effect of the agent over time (e.g., for an LHRH analogue, sustained delivery of the analogue can be demonstrated by continued suppression of testosterone synthesis over time). Alternatively, sustained delivery of the agent may be demonstrated by detecting the presence of the agent in vivo over time.

As used herein, the term “subject” is intended to include is intended to include warm-blooded animals, preferably mammals, more preferably primates and most preferably humans.

As used herein, the term “administering to a subject” is intended to refer to dispensing, delivering or applying a composition (e.g., pharmaceutical formulation) to a subject by any suitable route for delivery of the composition to the desired location in the subject, including delivery by either the parenteral or oral route, intramuscular injection, subcutaneous/intradermal injection, intravenous injection, buccal administration, transdermal delivery, administration by the rectal, colonic, vaginal, intranasal, respiratory tract, intrathecal, or intracerebral route, administration to cells in ex vivo treatment protocols, topical delivery, and delivery on a surface, e.g., a biocompatible surface, for example on the surface of a surgically implanted device, e.g., a stent, shunt, or catheter.

As used herein, the term “a condition treatable with an LHRH analogue” is intended to include diseases, disorders and other conditions in which administration of an LHRH agonist or LHRH antagonist has a desired effect, e.g., a therapeutically beneficial effect. Examples of conditions treatable with an LHRH analogue include hormone-dependent cancers (including prostate cancer, breast cancer, ovarian cancer, uterine cancer and testicular cancer), benign prostatic hypertrophy, precocious puberty, endometriosis, uterine fibroids, infertility (through in vitro fertilization) and fertility (i.e., contraceptive uses).

One aspect of the present invention pertains to a pharmaceutical composition comprising a water-insoluble complex of a pharmaceutically active peptidic compound and a carrier macromolecule. In a preferred embodiment, formation of the water-insoluble complex is mediated at least in part by ionic interactions between the pharmaceutically active peptidic compound and the carrier macromolecule. In these embodiments, either the pharmaceutically active peptidic compound is cationic and the carrier macromolecule is anionic or the pharmaceutically active peptidic compound is anionic and the carrier macromolecule is cationic. In another embodiment, formation of the water-insoluble complex is mediated at least in part by hydrophobic interactions between the pharmaceutically active peptidic compound and the carrier macromolecule. In a preferred embodiment, the peptidic compound used in the complex is a multivalent cationic peptidic compound, such as a bivalent or trivalent cationic peptidic compound and the carrier macromolecule is an anionic macromolecule.

The pharmaceutical compositions of the invention permit sustained delivery of the peptidic compound to a subject in vivo after administering the composition to the subject, wherein the duration of the sustained delivery can be varied depending upon the concentration of peptidic compound and carrier macromolecule used to form the complex. For example, in one embodiment, a single dose of the water-insoluble complex provides sustained delivery of the peptidic compound to a subject for at least one week after the pharmaceutical composition is administered to the subject. In another embodiment, a single dose of the water-insoluble complex provides sustained delivery of the peptidic compound to a subject for at least two weeks after the pharmaceutical composition is administered to the subject. In yet another one embodiment, a single dose of the water-insoluble complex provides sustained delivery of the peptidic compound to a subject for at least three weeks after the pharmaceutical composition is administered to the subject. In still another embodiment, a single dose of the water-insoluble complex provides sustained delivery of the peptidic compound to a subject for at least four weeks after the pharmaceutical composition is administered to the subject. Formulations that provide sustained delivery for longer or shorter durations are also encompassed by the invention, such as formulations that provide continuous delivery for 1 day, 1-7 days, one month, two months, three months, and the like. Continuous delivery of the peptidic compound for a period of several months can be accomplished, for example, by repeated monthly dosages, each of which provide sustained delivery of the peptidic compound for approximately one month (see, e.g., Example 14).

Any size peptidic compound may be suitable for use in the complex as long as the peptidic compound has the ability to form a water-insoluble noncovalent complex with the carrier macromolecule upon combination of the peptidic compound and carrier macromolecule. However, in certain preferred embodiments, the peptidic compound is a peptide that is about 5 to about 20 amino acids in length, about 8 to about 15 amino acids in length or about 8 to about 12 amino acids in length. A variety of pharmaceutically active peptides may be used in the formulations, non-limiting examples of which include LHRH analogues (discussed further below), bradykinin analogues, parathyroid hormone, adenocorticotrophic hormone (ACTH), calcitonin, and vasopressin analogues (e.g., 1-deamino-8-D-arginine vasopressin (DDAVP)). Other non-limiting examples of pharmaceutically active peptides that can be used in the formulations and methods of the invention include octreotide, endorphin, liprecin, erythropoietin, platelet aggrgation inhibitor (epoprostenol), angiotensin II, antidiuretic hormone, neurotrophic factors, keratinocyte growth factor, leukemia inhibiting factor, monocyte chemoattractant protein-1, endothelial growth factors, thymosin alpha 1, thymosin alpha 1 IIb/IIa inhibitor, thymosin beta 10, thymosin beta 9, thymosin beta 4, alpha-1 antitrypsin, phosphodiesterase (PDE) compounds, VLA-4 (very late antigen-4), VLA-4 inhibitors, bisphosponates, respiratory syncytial virus antibody, cystic fibrosis transmembrane regulator (CFTR) protein, deoxyreibonuclease (Dnase), bactericidal/permeability increasing protein (BPI), anti-CMV antibody, oxytocin, growth hormones, pituitary hormones, somatostatin, asparaginase, chroionic gonadotropin, growth hormone releasing hormone, growth hormone releasing peptide, interferons (e.g., interferons α, β and γ), colony stimulating factor, bone morphogenic proteins (BMP) (e.g., 1, 2, 3, 4, 5, 6, and 7), interleukins (e.g., interleukin-1, -2, -3, -4, -5, -6, -7, -8, -9, -10, -11, -13, -14, -15, -16, -17, -18, -19, -20, -21, -22, -23, -24, -25, -26, -27, -28, -29 and -30), glucocerebrosidase, macrophage activating factor, macrophage peptide, B cell factor, T cell factor, protein A, suppressive factor of allergy, cell necrosis glycoprotein, immunotoxin, lymphotoxin, tumor necrosis factor, tumor inhibitory factor, transforming growth factor, alpha-i antitrypsin, albumin, apolipoprotein-E, apolipoprotein A1, erythropoietin, hyper-glycosylated erythropoietin, factor VII, factor VIII, factor IX, plasminogen activator, urokinase, streptokinase, protein C, protein S, C-reactive protein, renin inhibitor, collagenase inhibitor, superoxide dismutase, leptin, platelet derived growth factor, epidermal growth factor, osteogenic growth factor, osteogenesis stimulating protein, calcitonin, insulin, atriopeptin, cartilage inducing factor, connective tissue activator protein, follicle stimulating hormone, luteinizing hormone, FSH releasing hormone, nerve growth factor, parathyroid hormone, prostoglandin, relaxin, secretin, somatomedin, insulin-like growth factor, thrombolytics, pamiteplase, lanoteplase, and teneteplase; nerve growth factor (NGF), osteoprotegerin, dornase alpha, erythropoiesis stimulating protein (NESP), coagulation factors such as Factor V, Factor VII, Factor VIIa, Factor VIII, Factor IX, Factor X, Factor XII, Factor XIII, von Willebrand factor; ceredase, cerezyme, alpha-glucosidase, collagen, cyclosporin, alpha defensins, beta defensins, exedin-4, thrombopoietin (TPO), heparin, human serum albumin, low molecular weight heparin (LMWH), alpha-1 proteinase inhibitor, elcatonin, fibrinogen, filgrastim (granulocyte colony-stimulating factor), adrenocorticotrophic hormone, glucagon, cholecystokinin, pancreatic polypeptide, gastrin releasing peptide, corticotropin releasing factor, thyroid stimulating hormone, TNF receptor (e.g., TNFR(P75) and TNFR(P55)), IL-1 receptor antagonist (e.g., IL1-Ra), cell surface antigen (e.g., CD2, 3, 4, 5, 7, 11a, 11b, 18, 19, 20, 23, 25, 33, 38, 40, 45 and 69), TNF-α, NF-κB, antimicrobial antifungal and antibacterial analogues, non-limiting examples of which include, ADENOREGULIN, Aureins, Gaegurins, Thanatin, Ranatuerin-2CB, Ranatuerin-2CA, Cecropin A, Cecropin B, Melittin B, Indolicidin, Tritrpticin, Androctonin, Tachystatin A, Dermaseptins, Gomesin, Hepcidin 20, Hepcidin 25, Peptide PGQ, Protegrins, RatNPs Seminalplasmin, Tracheal antimicrobial peptide, Dolabellanin B2, AFP1, AFP2, Dermaseptin BI, Buforin I, Buforin II, Histones, Opistoporins, Ponericins, Penaeidins, Spingerin, Skin peptide tyrosine-tyrosine, Lingual antimicrobial peptide, Tricholongin, Termicin, Holotricins, Penaeidins, Nk-Lysin, Magainin 2, Neutrophil defensins, Cyclic Ddfensin, Alpha-basrubrin, Melanotropin alpha (Alpha-MSH), Brevinin, Pseudins (1, 2, 3, 4), Anti-fungal protein 1 (pafp-s), Misgurin, P-1 8, Pseudo-hevein (Minor hevein), MUC7 20-Mer, Histatins (3, 5, 8), Nigrocin, lactoferrin (Lf), Ranalexin, antiviral analogues, e.g., Antiviral protein Y3, Alloferon 1, Lactoferricin B, hexapeptide, Tricyclic peptide RP, Indolicidin, GNCP-2, GNCP-1, HNP-1 Defensin, HNP-2 Defensin, Defensin, CORTICOSTATIN III (MCP-1), CORTICOSTATIN IV (MCP-2), NP-3A defensin, Protegrin 2, Protegrin 3, Protegrin 3, Protegrin 4, Protegrin 5, RatNP-1, RatNP-2, RatNP-3, RatNP-4, Caerin 1.1, Circulin A (CIRA), Circulin B (CIRB), Cyclopsychotride A (CPT), Ginkbilobin, Alpha-basrubrin. Fragments, analogues, derivatives, e.g., peptidomimetics, as well as recombinant forms of any of the foregoing peptidic compounds may be used in the phramaceutical formulations of the present invention. Monoclonal antibodies, polyclonal antibodies, antibody fragments, and virus-derived vaccine antigens raised against any of the foregoing peptidic compounds are also contemplated for use in the pharmaceutical formulations of the present invention.

Although a variety of carrier macromolecules may be suitable for formation of the water-insoluble complexes of the invention, preferred macromolecules are polymers, preferably water-soluble polymers. In a preferred embodiment, the carrier macromolecule is an anionic polymer, such as an anionic polyacohol derivative, or fragment thereof, and salts thereof (e.g., sodium salts). Anionic moieties with which the polyalcohol can be derivatized include, for example, carboxylate, phosphate or sulfate groups. A particularly preferred anionic polymer is an anionic polysaccharide derivative, or fragment thereof, and salts thereof (e.g., sodium salts). The carrier macromolecule may comprise a single molecular species (e.g., a single type of polymer) or two or more different molecular species (e.g., a mixture of two types of polymers). Examples of specific anionic polymers include carboxymethylcellulose, algin, alginate, anionic acetate polymers, anionic acrylic polymers, xantham gums, sodium starch glycolate, and fragments, derivatives and pharmaceutically acceptable salts thereof, as well as anionic carageenan derivatives, anionic polygalacturonic acid derivatives, and sulfated and sulfonated polystyrene derivatives. A preferred anionic polymer is carboxymethylcellulose sodium salt. Examples of cationic polymers include poly-L-lysine and other polymers of basic amino acids.

In a particularly preferred embodiment of the invention, the peptidic compound of the water-insoluble complex is an LHRH analogue, for example an LHRH agonist or, more preferably, an LHRH antagonist. Such LHRH analogues typically are 10 amino acids in length. Preferred LHRH antagonists include LHRH antagonists that comprise a peptide compound, wherein a residue of the peptide compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises a D-asparagine (D-Asn) structure. As used herein, the term “D-asparagine structure” is intended to include D-Asn and analogues, derivatives and mimetic thereof that retain the functional activity of D-Asn. Other preferred LHRH antagonists include LHRH antagonists that comprise a peptidic compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein

A is pyro-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal

B is His or 4-Cl-D-Phe

C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N—O), or D-Trp

D is Ser

E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile;

F is wherein

R and X are, independently, H or alkyl; and

L comprises a small polar moiety;

G is Leu or Trp;

H is Lys(iPr), Gln, Met, or Arg

I is Pro; and

J is Gly-NH₂ or D-Ala-NH₂; or a pharmaceutically acceptable salt thereof.

The term “small polar moiety” refers to a moiety which has small steric bulk and is relatively polar. Polarity is measured as hydrophilicity by the P scale. The partition coefficient, P, between 1-octanol and water has been used as a reference for measuring the hydrophilicity of a compound. Hydrophilicity can be expressed as log P, the logarithm of the partition coefficient (Hansch, et al., Nature 194:178 (1962); Fujita, et al., J. Am. Chem. Soc. 86:5175 (1964)). Standard tables of hydrophilicity for many molecules, and lipophilicity (hydrophobicity) substituent constants (denoted π) for many functional groups, have been compiled (see, e.g., Hansch and Leo, “Substituent Constants for Correlation Analysis in Chemistry and Biology,” Wiley, New York, N.Y., (1979)). The hydrophilicity of a vast range of candidate hydrophilicity moieties can be quite accurately predicted with the aid of these tables. For example, the measured log P (octanol/water) of naphthalene is 3.45. The substituent constant p for —OH is −0.67. Therefore, the predicted log P for β-naphthol is 3.45+(−0.67)=2.78. This value is in good agreement with the measured log P for β-naphthol, which is 2.84. As used herein, the term “small polar moiety” refers to moieties that have a log P between −1 and +2 and a steric bulk that is less than the steric bulk of Trp.

In certain embodiments, L comprises a small polar moiety with the proviso that F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci. Preferably, F is selected from the group consisting of D-Asn, D-Gln and D-Thr. More preferably, F is D-Asn. Preferably, E is tyrosine (Tyr) or N-methyl-tyrosine (N-Me-Tyr). In a particularly preferred embodiment, the LHRH antagonist has the following structure: Ac-D-Nal¹, 4-Cl-D-Phe², D-Pal³, N-Me-Tyr⁵, D-Asn⁶, Lys(ipr)⁸, D-Ala¹⁰-LHRH (referred to herein as PPI-149). A particularly preferred complex of the invention comprises PPI-149 and carboxymethylcellulose.

In addition to the water-insoluble complex, the pharmaceutical formulations of the invention can comprise additional pharmaceutically acceptable carriers and/or excipients. As used herein, “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible. Preferably, the carrier is suitable for topical, oral, buccal, vaginal, rectal, pulmonary, nasal, transdermal, intravenous, intramuscular, subcutaneous, intrathecal, intracerebral, or parenteral administration (e.g., by injection). Excipients include pharmaceutically acceptable stabilizers and disintegrants. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the peptidic compound, use thereof in the pharmaceutical formulations is contemplated. Supplementary active compounds can also be incorporated into the compositions.

A pharmaceutical composition of the invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, oral, nasal, transdermal (topical), transmucosal, rectal, transvaginal, or buccal administration.

Pharmaceutical formulations suitable for injectable use can include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor ELT (BASF, Parsippany, N.J.) or phosphate buffered saline (PBS). In all cases, the formulation must be sterile and should be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fingi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyetheylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, sodium chloride in the formulation. Solutions or suspensions for parenteral, intradermal, or subcutaneous administration may also include antioxidants such as ascorbic acid or sodium bisulfite, chelating agents such as ethylenediaminetetraacetic acid, buffers such as acetates, citrates or phosphates, and agents for the adjustment of tonicity such as sodium chloride or dextrose. pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral formulation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.

Sterile injectable solutions can be prepared by incorporating the water-insoluble complex in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by an appropriate sterilization method, such as, for example, filter sterilization, gamma-irradiation, and the like. In one embodiment, dispersions are prepared by incorporating the water-insoluble complex of the invention into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the methods of preparation may be vacuum drying and freeze-drying which yields a powder of the the water-insoluble complex of the invention plus any additional desired ingredient from a previously sterile-filtered solution thereof. Other compositions useful for attaining systemic delivery of the water-insoluble complex of the invention include sublingual, buccal and nasal dosage forms. Such compositions typically comprise one or more of soluble filler substances such as sucrose, sorbitol and mannitol; and binders such as acacia, microcrystalline cellulose, carboxymethyl cellulose and hydroxypropyl methyl cellulose. Glidants, lubricants, sweeteners, colorants, antioxidants and flavoring agents disclosed above may also be included.

The compounds of the invention may also be formulated as depot preparations. Such formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the compounds may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example as a sparingly soluble salt.

Peroral pharmaceutical formulations of the water-insoluble complex of the invention include liquid solutions, emulsions, suspensions, and the like. The pharmaceutically acceptable carriers suitable for preparation of such formulations are well known in the art. Typical components of carriers for syrups, elixirs, emulsions and suspensions include ethanol, glycerol, propylene glycol, polyethylene glycol, liquid sucrose, sorbitol and water. For a suspension, typical suspending agents include methyl cellulose, sodium carboxymethyl cellulose, tragacanth, and sodium alginate; typical wetting agents include lecithin and polysorbate 80; and typical preservatives include methyl paraben and sodium benzoate. Peroral liquid formulations may also contain one or more components such as sweeteners, flavoring agents and colorants.

Oral formulations generally include an inert diluent or an edible carrier. They can be enclosed in capsules (e.g., gelatine, cellulosic, or pullulan capsules), or compressed into tablets. For the purpose of oral administration, the water-insoluble complex of the invention can be incorporated with excipients and used in the form of tablets, troches, or capsules. Oral formulations can also be prepared using a fluid carrier for use as a mouthwash, wherein the compound in the fluid carrier is applied orally and swished and expectorated or swallowed. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the formulation. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

In solid dosage forms for oral administration (capsules, tablets, pills, dragees, powders, granules and the like), the water-insoluble complex is mixed with one or more pharmaceutically-acceptable carriers. In the case of capsules, tablets and pills, the pharmaceutical formulations may also comprise buffering agents. Solid formulations of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like.

A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared using binder (for example, gelatin or hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (for example, sodium starch glycolate or cross-linked sodium carboxymethyl cellulose), surface-active or dispersing agent. Molded tablets may be made by molding in a suitable machine a mixture of the water-insoluble complex thereof moistened with an inert liquid diluent. Tablets, and other solid dosage forms, such as dragees, capsules, pills and granules, may optionally be scored or prepared with coatings and shells, such as enteric coatings and other coatings well known in the pharmaceutical-formulating art.

Systemic administration of the water-insoluble complex of the invention can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal, e.g., intranasal, administration can be accomplished through the use of, for example, nasal sprays, nasal drops, or powders.

Transmucosal formulations for rectal or vaginal administration may be presented as a suppository or retention enema, which may be prepared by mixing the water-insoluble complex of the invention with one or more suitable non-irritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate. Such excipients or carriers are generally solid at room temperature, but liquid at body temperature, and therefore, they will melt in the rectum or vaginal cavity and release water-insoluble complex.

The transdermal formulations of this invention can also be administered topically to a subject via percutaneous passage of the formulation into the systemic circulation of the subject., e.g., by the direct laying on or spreading of the formulation on the epidermal or epithelial tissue of the subject. Topical administration can also involve the use of transdermal administration such as transdermal patches or iontophoresis devices. Such compositions include, for example, lotions, creams, solutions, gels and solids. These topical compositions may comprise an effective amount, usually at least about 0.1%, or evan from about 1% to about 5%, of a water-insoluble complex of the invention. Suitable carriers for topical administration typically remain in place on the skin as a continuous film, and resist being removed by perspiration or immersion in water. Generally, the carrier is organic in nature and capable of having dispersed or dissolved therein the water-insoluble complex. The carrier may include pharmaceutically acceptable emolients, emulsifiers, thickening agents, solvents and the like. Other components can be incorporated into the transdermal patches as well. For example, formulations and/or transdermal patches can be formulated with one or more preservatives or bacteriostatic agents including, but not limited to, methyl hydroxybenzoate, propyl hydroxybenzoate, chlorocresol, benzalkonium chloride, and the like.

Dosage forms for topical administration of the water-insoluble complex can include creams, pastes, sprays, lotions, gels, ointments, eye drops, nose drops, ear drops, suppositories, and the like. In such dosage forms, the water-insoluble complex of the invention can be mixed to form white, smooth, homogeneous, opaque cream or lotion with, for example, benzyl alcohol 1% or 2% (wt/wt) as a preservative, emulsifying wax, glycerin, isopropyl palmitate, lactic acid, purified water and sorbitol solution. In addition, the formulations can contain polyethylene glycol 400. They can be mixed to form ointments with, for example, benzyl alcohol 2% (wt/wt) as preservative, white petrolatum, emulsifying wax, and tenox II (butylated hydroxyanisole, propyl gallate, citric acid, propylene glycol). Woven pads or rolls of bandaging material, e.g., gauze, can be impregnated with the compositions in solution, lotion, cream, ointment or other such form can also be used for topical application.

Pharmaceutical formulations are also provided which are suitable for administration as an aerosol, by inhalation. For administration by inhalation, the water-insoluble complex may be delivered in the form of an aerosol spray from pressured container or dispenser which contains a suitable propellant, e.g., a gas such as carbon dioxide, or a nebulizer.

Dry Powder formulations for inhalation may be delivered using any suitable dry powder inhaler (DPI), i.e., an inhaler device that utilizes a subject's inhaled breath as a vehicle to transport the dry powder pharmaceutical formulation to the lungs. Examples of such devices are Inhale Therapeutic Systems' dry powder inhalation devices as described in Patton, J. S., et al., U.S. Pat. No. 5,458,135, Oct. 17, 1995; Smith, A. E., et al., U.S. Pat. No. 5,740,794, Apr. 21, 1998; and in Smith, A. E., et. al., U.S. Pat. No. 5,785,049, Jul. 28, 1998, herein incorporated by reference. When administered using a device of this type, the powdered formulation is contained in a receptacle having a puncturable lid or other access surface, preferably a blister package or cartridge, where the receptacle may contain a single dosage unit or multiple dosage units. Convenient methods for filling large numbers of cavities (i.e., unit dose packages) with metered doses of dry powder formulation are described, e.g., in Parks, D. J., et al., International Patent Publication WO 97/41031, Nov. 6, 1997, incorporated herein by reference.

Other dry powder dispersion devices for pulmonary administration of dry powders include those described, for example, in Newell, R. E., et al, European Patent; No. EP 129985, Sep. 7, 1988); in Hodson, P. D., et al., European Patent No. EP472598, Jul. 3, 1996; in Cocozza, S., et al., European Patent No. EP 467172, Apr. 6, 1994, and in Lloyd, L. J. et al., U.S. Pat. No. 5,522,385, Jun. 4, 1996, incorporated herein by reference. Also suitable for delivering the dry powders of the present invention are inhalation devices such as the Astra-Draco “TURBUHALER”. This type of device is described in detail in Virtanen, R., U.S. Pat. No. 4,668,218, May 26, 1987; in Wetterlin, K., et al., U.S. Pat. No. 4,667,668, May 26, 1987; and in Wetterlin, K., et al., U.S. Pat. No. 4,805,811, Feb. 21, 1989, all of which are incorporated herein by reference. Other suitable devices include dry powder inhalers such as Rotahaler((Glaxo), DiscustD (Glaxo), Spiros_inhaler (Dura Pharmaceuticals), and the Spinhaler (Fisons). Also suitable are devices which; employ the use of a piston to provide air for either entraining powdered formulation, lifting formulation from a carrier screen by passing air through the screen, or mixingair with powder formulation in a mixing chamber with subsequent introduction of the powder to the subject through the mouthpiece of the device, such as described in Mulhauser, P., et al, U.S. Pat. No. 5,388,572, Sep. 30, 1997, incorporated herein by reference.

The water-insoluble complex of the present invention may also be delivered using a pressurized, metered dose inhaler (MDI), e.g., the Ventolin metered dose inhaler, or a nebulizer, containing a solution or suspension of water-insoluble complex in a pharmaceutically inert liquid propellant, e.g. dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, tetrafluoroethane, heptafluoropropane, carbon dioxide or other suitable gas., as described in Laube, et al., U.S. Pat. No. 5,320,094, Jun. 14, 1994, and in Rubsamen, R. M., et al, U.S. Pat. No. 5,672,581 (1994), both incorporated herein by reference. Nebulizers for delivering an aerosolized solution include the AERX_(Aradigm), the Ultravent (Mallinkrodt), the Pari LC Plus_ or the Pari LC Star_(Part GmbH, Germany), the DeVilbiss Pulmo-Aide, and the Acorn II (Marquest Medical Products). In the case of a pressurized aerosol the dosage unit may be determined by providing a valve to deliver a metered amount. Capsules and cartridges of, e.g., gelatin for use in an inhaler or insulator may be formulated containing a powder mix of a water-insoluble complex of the invention and a suitable powder base such as lactose or starch.

According to yet another embodiment, the water-insoluble complex of this invention may be incorporated into compositions for coating an implantable medical device, such as prostheses, artificial valves, vascular grafts, stents and catheters (such as, balloon catheters and indwelling catheters), and/or shunts, including mechanical shunts. Suitable coatings and the general preparation of coated implantable devices are described in U.S. Pat. Nos. 6,099,562; 5,886,026; and 5,304,121, the disclosures of which are incorporated herein by reference. The coatings typically comprise biocompatible polymeric materials such as a hydrogel polymer, polymethyldisiloxane, polycaprolactone, polyethylene glycol, polylactic acid, ethylene vinyl acetate, and mixtures thereof. The implantable medical devices useful in the methods of the present invention can be metallic or plastic, and may comprise a biodegradable coating or porous non-biodegradable coating.

In one embodiment, the water-insoluble complex of the invention is coated on a medical device, e.g., a stent, implanted into a subject during a medical procedure, such as, for example, angioplasty. In one embodiment, the pharmaceutically active compound incorporated into the water-soluble complex and coated on the medical device implanted into a subject prevents restenosis following the placement of the medical device in the subject. In one embodiment, restenosis is inhibited by inhibiting late-stage endothelialization

In another embodiment, the water-insoluble complex of the invention is irreversibly bonded to a medical device, e.g., a stent, implanted into a subject during a medical procedure, such as, for example, angioplasty. Without wishing to be bound by theory, the irreversible bonding of the water-insoluble complex to the medical device may not only reduce restenosis, but may also encourage encapsulation of the carrier macromolecule and the stent into the vessel wall such that the carrier macromolecule is unavailable for release into the bloodsteam and potentially form emboli or accumulate in the liver or spleen as circulating particulate matter. Accordingly, in one embodiment, restenosis is enhanced by promoting early stage re-endothelialization.

Non-limiting examples of pharmaceutically active peptidic compounds that are suitable for incoporation into a water-insoluble complex and coated or irreversibly bound on a medical device and implanted in a subject during a medical procedure, include angiogenesis inhibitors, such as Angiostatin, Endostatin, Interleukin 12, Recombinant human platelet factor 4(rPF4), Thrombospondin, and TNP-470; vascular smooth muscle cell anti-proliferative agents, such as transforming growth factor beta; anti-thrombogenic agents such as urokinase, and PPACK (dextrophenylalanine proline arginine chloromethylketone); angiogenic and anti-angiogenic agents; agents blocking smooth muscle cell proliferation such as angiopeptin and monoclonal antibodies capable of blocking smooth muscle cell proliferation; antineoplastic/antiproliferative/anti-mitotic agents such as endostatin and angiostatin; anesthetic agents such as L-arginine; anti-coagulants such as D-Phe-Pro-Arg chloromethyl ketone, an RGD peptide-containing compound, platelet receptor antagonists, anti-thrombin antibodies, anti-platelet receptor antibodies, vascular cell growth promotors such as growth factors, growth factor receptor antagonists; vascular cell growth inhibitors such as growth factor inhibitors, growth factor receptor antagonists, inhibitory antibodies, antibodies directed against growth factors, bifunctional molecules consisting of a growth factor and a cytotoxin, bifunctional molecules consisting of an antibody and a cytotoxin; survival proteins which protect against cell death, such as anti-apoptotic Bcl-2 family factors and Akt kinase; bone morphogenic proteins (BMP) (e.g., 1, 2, 3, 4, 5, 6, and 7); and combinations thereof.

The pharmaceutical formullation of the invention may also be administered intrathecally into the cerebrospinal fluid (CSF). The intrathecal administration of the water-insoluble complex of the present invention may comprise introducing the pharmaceutical formulaltion into a cerebral ventricle. Alternatively, the intrathecal administration may comprise introducing the pharmaceutical formulaltion into the lumbar area. In yet another alternative, the intrathecal administration comprises introducing the pharmaceutical composition into the cistema magna. Any such administration is-preferably via a bolus injection. In other embodiments, the intrathecal administration is achieved by use of an infusion pump.

The administration of the pharmaceutical formulations of the invention may also be intracerebrally. Administration may be by, for example, direct intracerebral administration, or by, for example, stereotactic microinjection.

Intracerebral administration, may be provided by perfusion via a mechanized delivery system, such as an osmotic pump, or by implantation.

In addition to pharmaceutical formulations of LHRH analogues complexed with a carrier macromolecule, the invention further encompasses packaged formulations containing such complexes and syringes containing such complexes. For example, the invention provides a packaged formulation for treating a subject for a condition treatable with an LHRH analogue, comprising a water-insoluble complex of an LHRH analogue (preferably PPI-149) and a carrier macromolecule (preferably carboxymethylcellulose), packaged with instructions for using the water-insoluble complex for treating a subject for a condition treatable with an LHRH analogue. In another embodiment, the invention provides a syringe having a lumen, wherein a water-insoluble complex of an LHRH analogue (preferably PPI-149) and a carrier macromolecule (preferably, carboxymethyl-cellulose) is included in the lumen.

The complex of the invention is prepared by combining the peptidic compound and the carrier macromolecule under conditions such that a water-insoluble complex of the peptidic compound and the carrier macromolecule forms. Accordingly, another aspect of the invention pertains to methods for preparing pharmaceutical formulations. In one embodiment, the method comprises:

providing a peptidic compound and a carrier macromolecule;

combining the peptidic compound and the carrier macromolecule under conditions such that a water-insoluble complex of the peptidic compound and the carrier macromolecule forms; and

preparing a pharmaceutical formulation comprising the water-insoluble complex. For example, a solution of the peptidic compound and a solution of the carrier macromolecule are combined until a water-insoluble complex of the peptidic compound and the carrier macromolecule precipitates out of solution. In certain embodiments, the solutions of the peptidic compound and the carrier macromolecule are aqueous solutions. Alternatively, if the peptidic compound or the carrier molecule (or both) is not substantially water soluble prior to combination the two, then the peptidic compound and/or carrier macromolecule can be dissolved in a water-miscible solvent, such as an alcohol (e.g., ethanol) prior to combining the two components of the complex. In another embodiment of the method of preparing the water-insoluble complex, the solution of the peptidic compound and the solution of the carrier macromolecule are combined and heated until a water-insoluble complex of the peptidic compound and the carrier macromolecule precipitates out of solution. The amounts of peptidic compound and carrier macromolecule necessary to achieve the water-insoluble complex may vary depending upon the particular peptidic compound and carrier macromolecule used, the particular solvent(s) used and/or the procedure used to achieve the complex. Typically, however, the peptidic compound will be in excess relative to the carrier macromolecule on a molar basis. Often, the peptidic compound also will be in excess on a weight/weight basis, as demonstrated in the Examples. In certain embodiments, the carrier macromolecule, preferably carboxymethylcellulose sodium, and the peptidic compound, preferably PPI-149, are combined at a ratio of 0.2:1 (w/w) of carrier macromolecule:peptidic compound. In various other embodiments, the ratio of carrier macromolecule to peptidic compound (w/w) can be, for example, 0.5:1, 0.4:1, 0.3:1, 0.25:1, 0.15:1 or 0.1:1. Non-limiting examples of conditions and procedures for preparing a water-insoluble complex of the invention are described further in Example 1-5 and 8-9.

Once the peptidic compound/macromolecule complex precipitates out of solution, the precipitate can be removed from the solution by means known in the art, such as filtration (e.g., through a 0.45 micron nylon membrane), centrifugation and the like. The recovered paste then can be dried (e.g., in vacuo or in a 70° C. oven) and the solid can be milled or pulverized to a powder by means known in the art (e.g., hammer or gore milling, or grinding in mortar and pestle). Following milling or pulverizing, the powder can be sieved through a screen (preferably a 90 micron screen) to obtain a uniform distribution of particles. Moreover, the recovered paste can be frozen and lyophilized to dryness. The powder form of the complex can be dispersed in a carrier solution to form a liquid suspension or semi-solid dispersion suitable for injection. Accordingly, in various embodiments, a pharmaceutical formulation of the invention is a dry solid, a liquid suspension or a semi-solid dispersion, as described above. Examples of liquid carriers suitable for use in liquid suspensions include saline solutions, glycerin solutions and lecithin solutions.

In another embodiment, the pharmaceutical formulation of the invention is sterile formulation. For example, following formation of the water-insoluble complex, the complex can be sterilized, optimally by gamma irradiation or electron beam sterilization. Accordingly, the method of the invention for preparing a pharmaceutical formulation described above can further comprise sterilizing the water-insoluble complex by gamma irradiation or electron beam irradiation. Preferably, the formulation is sterilized by gamma irradiation using a gamma irradiation dose of at least 15 KGy. In other embodiments, the formulation is sterilized by gamma irradiation using a gamma irradiation dose of at least 19 KGy or at least 24 KGy. As demonstrated in Example 11, the formulations of the invention remain acceptably stable upon gamma irradiation.

Alternatively, to prepare a sterile pharmaceutical formulation, the water-insoluble complex can be isolated using conventional sterile techniques (e.g., using sterile starting materials and carrying out the production process aseptically). Accordingly, in another embodiment of the method for preparing a pharmaceutical formulation described above, the water-insoluble complex is formed using aseptic procedures.

Methods of forming a water-insoluble complex of the invention are described further in Examples 1-5 and 8-9. Pharmaceutical formulations, including powders, liquid suspensions, semi-solid dispersions, dry solids (e.g., lyophilized solids), and sterilized forms thereof (e.g., by gamma irradiation), prepared according to the methods of the invention, are also encompassed by the invention.

Yet another aspect of the invention pertains to methods of using the pharmaceutical formulations of the invention to treat a subject suffering from a condition treatable by the pharmaceutically active peptidic compound included in the water-insoluble complex. Accordingly, in a preferred embodiment, the invention provides a method for treating a subject for a condition treatable with an LHRH analogue, comprising administering to the subject a pharmaceutical formulation comprising a water-insoluble complex of an LHRH analogue and a carrier macromolecule.

The pharmaceutical formulation can be administered to the subject by any route suitable for achieving the desired therapeutic result(s), although preferred routes of administration are parenteral routes, in particular intramuscular (i.m.) injection and subcutaneous/intradermal (s.c./i.d.) injection. Alternatively, the formulation can be administered to the subject orally. Other suitable parental routes include intravenous injection, buccal administration, transdermal delivery and administration by the rectal, vaginal, intranasal or respiratory tract route. It should be noted that when a formulation that provides sustained delivery for weeks to months by the i.m or s.c./i.d. route is administered by an alternative route, there may not be sustained delivery of the agent for an equivalent length of time due to clearance of the agent by other physiological mechanisms (i.e., the dosage form may be cleared from the site of delivery such that prolonged therapeutic effects are not observed for time periods as long as those observed with i.m or s.c./i.d. injection).

The pharmaceutical formulation contains a therapeutically effective amount of the LHRH analogue. A “therapeutically effective amount” refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired result. A therapeutically effective amount of an LHRH analogue may vary according to factors such as the disease state, age, and weight of the individual, and the ability of the LHRH analogue (alone or in combination with one or more other drugs) to elicit a desired response in the individual. Dosage regimens may be adjusted to provide the optimum therapeutic response. A therapeutically effective amount is also one in which any toxic or detrimental effects of the antagonist are outweighed by the therapeutically beneficial effects. A non-limiting range for a therapeutically effective amount of an LHRH analogue is 0.01 to 10 mg/kg. A preferred dosage of the LHRH analogue PPI-149 for sustained reduction of plasma testosterone levels for 28 days is approximately 0. 1-10 mg/kg, more preferably 0.3-1.2 mg/kg (expressed as free peptide) in a liquid suspension volume of approximately 1 mL or less. It is to be noted that dosage values may vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.

The treatment method of the invention can be applied to the treatment of various conditions, diseases and disorders in which administration of an LHRH analogue has a desired clinical effect. Examples of disease and disorders include hormone-dependent cancers, such as prostate cancer, breast cancer, ovarian cancer, uterine cancer and testicular cancer, benign prostatic hypertrophy, precocious puberty, endometriosis and uterine fibroids. Accordingly, the invention provides methods of treating these diseases and disorders by administering a pharmaceutical formulation of the invention. Additionally, LHRH analogues can be used to alter fertility. Accordingly, the methods of the invention also can be used in vitro fertilization and contraceptive purposes.

In a particularly preferred embodiment, the method is used to treat prostate cancer, the LHRH analogue used in the formulation is an LHRH antagonist, most preferably PPI-149, and the method allows for sustained delivery of the LHRH analogue in vivo for at least four weeks after administration by intramuscular or subcutaneous administration. An LHRH analogue, preferably PPI-149, formulated according to the invention can be used to inhibit growth of prostate cancer cells by administering the LHRH analogue to a subject suffering from prostate cancer. Moreover, an LHRH antagonist, preferably PPI-149, formulated according to the invention, can be used to inhibit the testosterone surge that accompanies the use of an LHRH agonist by preadministering the LHRH antagonist, preferably PPI-149, to a subject suffering from prostate cancer before initiating LHRH agonist therapy. Methods for inhibiting LHRH agonist-induced testosterone surge, and other methods for treating prostate cancer using LHRH antagonist, to which the formulations of the present invention can be applied, are described further in U.S. patent application Ser. No. 08/573,109, entitled “Methods for Treating Prostate Using LHRH Antagonists”, filed Dec. 15, 1995, and a continuation-in-part patent application thereof, Ser. No. 08/755,593, also entitled “Methodsfor Treating Prostate Using LHRH Antagonists”, filed Nov. 25, 1996, the contents of both of which are incorporated into published PCT application WO 97/22357. The entire contents of the U.S. applications and published PCT application are expressly incorporated herein by reference.

Specific processes for complexing a pharmaceutically active peptidic compound with a carrier macromolecule are set forth in Examples 1-5 and 8-9 below. Also described are test results that demonstrate that an LHRH antagonist-containing complex can enable sustained delivery of the pharmaceutically active peptide in vivo (Example 6) and can inhibit LHRH-agonist induced testosterone surge (Example 7). The following examples, which further illustrate the invention, should not be construed as limiting. The contents of all references, patents and published patent applications cited throughout this application are hereby incorporated by reference.

EXAMPLE 1

A 100 ml solution of the LHRH antagonist PPI-149 was prepared by dissolving 6.25 mg/ml of PPI-149 in water. An equal sample (100 ml minimum) of USP carboxymethylcellulose sodium (CMC) (low viscosity grade, Hercules Chemical Co.) was prepared at 0.125% w/v and mixed until dissolved. Equal portions of the PPI-149 and CMC solutions were mixed (giving a CMC:peptide ratio of 0.2:1 (w/w)) and a solid material was obtained. The solid material was stirred overnight and then collected by filtration over a 0.45 micron nylon filter. HPLC evaluation of the solution filtrate indicated at least 95% of the PPI-149 compound was converted to the solid complex. was removed from solution. The recovered white paste was rinsed twice with water and then transferred to a vial and dried in vacuo. Upon drying for 72 hours, 633 mg of a white powder was obtained. The solid material was then powdered in a mortar and pestle. Elemental analysis indicated 57% peptide in the complex.

EXAMPLE 2

25 mg of PPI-149 was dissolved in 1 ml of water. To this was added 1 ml of a 0.5% carboxymethylcellulose solution. The mixture formed a silky white solid upon mixing. The mixture was heated to reflux for five minutes and a flocculent white precipitate was formed. This material was isolated by centrifugation/decantation. The solid was resuspended in water and collected by repeated centrifugation. HPLC evaluation of the solution filtrate indicated at least 90% of the PPI-149 compound was converted to the solid complex. The white precipitate was dried in vacuo and the solid material was comminuted in a mortar and pestle. Elemental analysis indicated 77% peptide in the complex.

EXAMPLE 3

50 mg of PPI-149 was dissolved in 2 mL of 5% mannitol and mixed with 2 mL of 0.5% carboxymethylcellulose (low viscosity, USP, Spectrum Quality Chemicals). The mixture was stirred and immediately yielded a white precipitate. The suspension was frozen and lyophilized to dryness to yield a PPI-149 sustained delivery complex.

EXAMPLE 4

25 mg of PPI-149 was dissolved in 1 mL water. To this was added 1 mL of 0.5% sodium alginate, USP (Spectrum). The mixture immediately formed a white precipitate upon mixing. This material was isolated by centrifugation/decantation. The solid was resuspended in water and collected by repeated centrifugation. The white precipitate was dried in vacuo. Elemental analysis was performed to obtain a peptide content of 66%.

EXAMPLE 5

25 mg of PPI-149 was dissolved in 1 mL water. Ammonia was added to adjust the pH to 11.0. To this was added 1 mL of 0.5% alginic acid, USP (Spectrum). The mixture immediately formed a white precipitate upon mixing. This material was isolated by centrifugation/decantation. The solid was resuspended in water and collected by repeated centrifugation. The white precipitate was dried in vacuo. Elemental analysis was performed to obtain a peptide content of 79%.

EXAMPLE 6

A water-insoluble complex of the LHRH antagonist PPI-149 and carboxymethylcellulose was prepared according to the preceding examples. A suspension of the PPI-149/CMC complex was prepared and a single dose was injected intramuscularly into rats and dogs. The dosage for the rats was 50 μg/kg/day×60 days and the dosage for the dogs was 40 μg/kg/day×28 days. Plasma testosterone levels (in ng/ml) were determined at various time points as a measure of the activity of the LHRH antagonist in the animal. Representative results, shown in the graph of FIG. 1, demonstrate that intramuscular injection of the PPI-149/CMC complex leads to sustained suppression of plasma testosterone levels for at least 42 days in the rats and at least 28 days in the dogs (indicated by the open boxes in FIG. 1), demonstrating sustained delivery of the LHRH antagonist. Plasma levels of PPI-149 (in ng/ml) were also monitored in the animals (indicated by the closed boxes in FIG. 1). An initial spike of PPI-149 was observed for about the first eight days, after which time PPI-149 was essentially undetectable in the plasma. Despite the inability to detect PPI-149 in the plasma beyond about day 8, the testosterone level results demonstrate that PPI-149 was still therapeutically active in vivo over the course of the experiment.

EXAMPLE 7

A water-insoluble complex of the LHRH antagonist PPI-149 and carboxymethylcellulose was prepared according to the preceding examples. A suspension of the PPI-149/CMC complex was prepared and a single dose was injected intramuscularly into rats on day 0. On day 30, the LHRH agonist Lupron™ (leuprolide) was injected into the rats. Plasma testosterone levels (in ng/ml; indicated by the open boxes in FIG. 2) were determined at various time points as a measure of the activity of the LHRH antagonist in the animal. Plasma levels of PPI-149 (in ng/ml) were also monitored in the animals (indicated by the closed boxes in FIG. 2). Representative results, shown in the graph of FIG. 2, demonstrate that pretreatment with the PPI-149/CMC complex rapidly reduces plasma testosterone to castration levels and, moreover, blocks the LHRH agonist-induced testosterone surge. Despite the inability to detect PPI-149 in the plasma beyond about day 8, the testosterone level results demonstrate that PPI-149 was still therapeutically active in vivo over the course of the experiment.

EXAMPLE 8

In this example, an insoluble complex was formed between the LHRH analogue PPI-258 and carboxymethylcellulose (CMC). PPI-258 has the structure: acetyl-D-napthylalanyl-D-4-Cl-phenylalanyl-D-pyridylalanyl-L-seryl-L-tyrosyl-D-asparaginyl-L-leucyl-L-N^e-isopropyl-lysyl-L-propyl-D-alanyl-amide. To prepare a PPI-258/CMC depot, 174.8 mg (148.6 mg net) of PPI-258 was added to 29.72 mL of water and the material was stirred to suspend and dissolve the peptide. To this stirred solution was added 1.85 mL of a 2% sodium CMC solution (Hercules). A solid precipitate was immediately observed. Upon heating to reflux, the suspension became translucent and then appeared as white precipitate. After a 5 minute reflux, the reaction was cooled and the solid was isolated by centrifligation. The solid was rinsed with water, and dried in vacuo overnight. The dried power was powdered in a mortar and pestle and sieved through a 90 micron stainless steel screen. The sieved powder (90 micron sieve) was collected and characterized. Total yields were 198.4 mg of dried solid which yielded 110.8 mg of sized powder after the milling step. Characterization provided the following compositional makeup of the complex: Peptide PPI-258—80%, CMC—18.8%, water—6.6%.

EXAMPLE 9

In this example, an insoluble complex was formed between the LHRH analogue Cetrorelix™ (also known as SB-75) and carboxymethylcellulose (CMC). Cetrorelix™ has the structure: acetyl-D-napthylalanyl-D-4-Cl-phenylalanyl-D-pyridylalanyl-L-seryl-L-tyrosyl-D-citrulyl-L-leucyl-L-arginyl-L-prolyl-D-alanyl-amide. To prepare a Cetrorelix/CMC depot, 102.8 mg (87 mg net) of Cetrorelix™ was added to 17.4 mL of water and the material was stirred to suspend and dissolve the peptide. To this stirred solution was added 1.1 mL of a 2% sodium CMC solution (Hercules). A clumpy white precipitate was immediately observed. The suspension was heated to reflux for 5 minutes and cooled to yield a solid white precipitate. The solid was isolated by centrifugation, was rinsed with water, and dried in vacuo overnight. The dried powder was powdered in a mortar and pestle and sieved through a 90 micron stainless steel screen. The powder was collected and characterized. Total yields were 95 mg of dried solid which yielded 60 mg of sized powder after the milling step. Characterization provided the following compositional makeup of the complex: Peptide Cetrorelix™—75%, CMC—20.7%, water—6.5%

EXAMPLE 10:

In this example, the sustained release of three different LHRH analogues, PPI-149, PPI-258 and Cetrorelix™, prepared as CMC depot formulations as described in three previous examples, was examined in vivo. Three different formulation vehicles were tested, saline, glycerin (15% glycerin/4% dextrose) and lecithin. Sprague-Dawley rats (25 males, weight range 300-325 g) were used and the efficacy of the LHRH analogue was determined based on reduction in plasma testosterone levels.

The dosages and routes of administration were as follows:

		Dose	Dose	Dose		Route
Group	Compound	(mg/kg)	(μg/kg/day)	(mg/rat)	Vehicle	Admin.
A	PPI-149	9	300	2.7	saline	IM
B	PPI-149	9	300	2.7	glycerin	IM
C	PPI-149	9	300	2.7	glycerin	SC
D	PPI-149	9	300	2.7	lecithin	IM
E	PPI-258	9	300	2.7	saline	IM
F	Cetrorelix ™	9	300	2.7	saline	IM

The actual dose of peptide was 300 pg/kg/day for 30 days, which was 2.7 mg/rat given as a single 200 μL intramuscular (IM) or subcutaneous (SC) injection. The total volume required to inject 5 rats/group was 1.3 mL at a concentration of 13.5 mg/mL active peptide. The volume of injection was kept constant and the weight of the powder was adjusted for total peptide content, as follows:

	Vol. Req.	Weight Req.	Weight used	Vol.
Group	mL	mg Powder	mg Powder	used mL
A	1.3	22.5	29.5	1.7	mL saline
B, C	2.6	45	71.1	4.1	mL glycerin/
					dextrose
D	1.3	22.5	35.2	2.03	mL 0.5%
					lecithin/
					mannitol
E	1.3	22.5	31	1.79	mL saline
F	1.3	22.5	20.9	1.21	mL saline

A single 200 μL intramuscular, or subcutaneous injection of test article was made into the upper flank of the left hind limb or under the skin between the scapulae, respectively, on Day 0 under anesthesia.

To test plasma testosterone levels, approximately 0.4 mL of blood was removed from the retro-orbital sinus on Day 1 after dosing and at days 3, 7, 14, 21, 28 and 35. Blood was processed to plasma and frozen on dry ice for determination of testosterone plasma levels by standard methods.

Representative results, shown in FIGS. 3A-3C, demonstrate that plasma testosterone levels in male Sprague-Dawley rats were reduced and maintained at low levels for at least 28 days and as long as 50 days in response to sustained release of the LHRH analogues PPI-149, PPI-258 and Centrolix™ prepared as CMC depot formulations (shown in FIGS. 3A, 3B and 3C, respectively). These results indicate that all three formulations are effective in reducing plasma testosterone levels in vivo and maintaining reduced plasma testosterone levels over time.

EXAMPLE 11

In this example, PPI-149-CMC formulations were exposed to gamma irradiation for purposes of sterilization, followed by evaluation of both physical and chemical properties of the irradiated formulations. Data described below indicate that γ-irradiation is a viable means of sterilization of PPI-149-CMC depot.

Peptide Stability

Approximately 40 mg of each of two separate PPI-149-CMC lots was packed separately (under an air headspace) in to a number of Type 1 Glass vials, sealed with rubber stoppers and aluminum seals. Vials were then subjected to a variety of nominal doses of gamma-irradiation. Two vials were analyzed for peptide purity (expressed as %) at each level of γ-irradiation exposure for each of the two lots. The results indicated that at γ-irradiation doses up to and including 24 KGy, PPI-149-CMC consistently exhibited less than a 2% reduction in peptide purity (as determined by HPLC impurity profile). A second study utilizing higher doses of gamma exposure was performed on an additional laboratory lot of PPI-149-CMC. PPI-149-CMC demonstrated remarkably good chemical stability when exposed to high γ-irradiation doses.

A subsequent preformulation study was implemented to compare the degradation profile obtained following PPI-149-CMC γ-irradiation with that obtained following autoclaving of PPI-149 injectable solution (1 mg/mL). Two samples were prepared: a) PPI-149-CMC exposed to 19 KGy γ-irradiation; b) A PPI-149 Solution (1 mg/mL) subjected to autoclaving (121° C./20 minutes). The HPLC chromatograms of the two samples demonstrated that the degradation profile for the two samples appeared to be qualitatively similar (given similar relative retention times of the major peaks).

Stressed Stability Storage Following Gamma-Irradiation

Stress-storage preformulation studies were also performed on vials post-gamma-irradiation. Sealed vials from two laboratory lots of PPI-149-CMC were exposed to 19 KGy gamma-irradiation and stored at 25° C., 37° C. and 50° C. for up to one month. The chemical stability data in these preformulation studies indicated that γ-irradiation at a dose of 19 KGy followed by stressed-storage stability did not result in major chemical instability even under highly stressed-storage conditions (e.g., 1 week at 50° C.). The data indicate at γ-irradiation doses up to and including 19 KGy, storage of PPI-149-CMC for up to 28 days at or below 50° C., consistently exhibited less than a 2% reduction in peptide purity (as determined by HPLC impurity profile). Despite an apparent difference in initial moisture content between the two lots studied, no significant difference in peptide purity was determined in either initial preformulation stability samples or those stored for up to a month.

PPI-149-CMC Particle Size Analysis

A particle size method using laser light scattering was developed, that is applicable to sizing studies of PPI-149-CMC. To illustrate the utility of the method, a preformulation experiment is presented, which was performed to investigate the effect of gamma-irradiation on the particle size of PPI-149-CMC. This experiment was conceived with the prior understanding that amorphous solid materials may be predisposed to particle consolidation, upon storage. Two samples of a laboratory lot of PPI-149-CMC were packed in type I glass vials, closed with gray butyl rubber stoppers and sealed with aluminum seals. Particle evaluation was performed prior to and following exposure to a gamma irradiation dose of 15.5 KGy. Particle evaluation was performed by laser light scattering (utilizing a Malvern Mastersizer STM equipped with a reverse fourier lens). 20 mg samples for particle size analysis by laser light scattering were dispersed in approximately 0.5 mL deionised water by vigorous shaking, then sonicated in a bath at ambient temperature for 5 minutes. After running a background count, a method qualification experiment was performed. Sample dispersion was added drop-wise to the continuous feed reservoir (approximately 60 mL nominal volume) until approximately 20% obscuration was obtained. The mixer rotation speed was held at 2700 rpm throughout the experiment (plus background check). At this speed no vortex-induced bubbles were generated, but an adequately stable dispersion was maintained. Eight scans were performed, analysis of acquired data indicated a standard deviation of <0.03% as the extreme of any data point taken. When the sample dispersion was held in the reservoir for 15 minutes and then re-run, no significant change resulted, indicating the absence of particle dissolution over the course of the experiment.

Samples were analyzed using the experimental parameters given above. Eight scans were performed and mean particle diameter data was determined. Two distinct size distributions were noted, and all had a clean cut-off at the high-end particle size, indicating the absence of particle aggregation. One lot of PPI-149-CMC had apparently lower mean volume diameter prior to gamma irradiation than the sample post-irradiation. This preformulation study would seem to indicate some particle consolidation occurred during the sterilization process.

EXAMPLE 12

In this example, various preformulation experiments were performed to investigate the effect of both gamma-irradiation and temperature/humidity stress on the solid state form of PPI-149-CMC.

X-Ray Powder Diffraction

In the initial experiment, two 60 mg samples of PPI-149-CMC were packed (under an air headspace) in type I glass vials, closed with gray butyl rubber stoppers and sealed with aluminum seals. One sample was then exposed to a gamma-irradiation dose of 19.0 KGy. The solid state form of the two 60 mg Samples was then studied by X-ray powder diffraction. Diffractograms were compared prior to and following exposure to a gamma irradiation dose of 19.0 Kgy.

In a subsequent study, a 60 mg sample of PPI-149-CMC (post gamma-irradiation) was placed in a type I glass vial and placed in a pre-equilibrated constant humidity incubator at 50° C./75% Relative Humidity for 5 days. Immediately after withdrawal from the incubator, the sample container was closed with a gray butyl rubber stopper and sealed with an aluminum seal. The X-ray powder diffractogram of this stressed sample was then compared to another sample of the same lot that had been held at room temperature in a closed container. The samples were analyzed using a Siemens D500 automated Powder Diffractometer equipped with a graphite monochromator and a Cu(λ=1.54 Å) X-Ray source operated at 50 kV, 40 mA. The two-theta scan range was 4-40° using a step scan window of 0.050/1.2 second step. Beam slits were set at No. (1) 1°, (2) 1°, (3) 1°, (4) 0.15°and (5) 0.15° widths. Two-theta calibration was performed using an NBS mica standard (SRM 675). The samples were analyzed using a zero background sample plate.

The data indicated that prior to gamma irradiation, PPI-149-CMC had no apparent crystalline or pseudo-crystalline structure. In fact, it gave an X-ray powder diffraction pattern characteristic of an amorphous solid (a broad hump between 2-20° 20, with no significant peaks in the diffractogram). The PPI-149-CMC sample post-irradiation generated a very similar diffraction pattern to the non-irradiated sample, indicating that gamma-irradiation processing (at doses up to and including 19 KGy) does not apparently induce a solid-state polymorphic transition within the material. In a similar manner, the temperature/humidity stressed sample of PPI-149-CMC generated a very similar diffraction pattern to both the non-irradiated sample and the irradiated sample, which strongly suggests that PPI-149-CMC is not unduly prone to induction of solid-state polymorphic transitions within the material.

Hygroscopicity

Preformulation studies on PPI-149-CMC (post-irradiation) were performed to determine the equilibrium moisture uptake (measured by weight gain) at constant temperature (25° C.) under various conditions of relative humidity. Analysis of the equilibrium moisture (% water) as a fuinction of relative humidity (% RH) indicated that moisture content gradually increased up to approximately 80% relative humidity. At high relative humidity (95% RH) PPI-149-CMC was capable of significant moisture sorption. At relative humidities at or below 80% RH, significant precautions in terms of protection from moisture are deemed unnecessary; thus certain manufacturing steps may be undertaken under ambient humidity conditions (provided humidity extremes are avoided).

EXAMPLE 13

In this example, dissolution studies on PPI-149-CMC were performed. Experiments were performed utilizing both sink and non-sink conditions. PPI-149-CMC has an approximate solubility of 100 μg/mL (measured and expressed as free peptide) at 25° C. in 0.1 M phosphate buffered saline at pH 7.3. Under sink conditions (defined as <10% of the saturated solubility in the system at a given temperature), even in the absence of stirring, PPI-149-CMC dissolved rapidly (measured and expressed as free peptide). In a similar experiment, the equilibrium solubility of PPI-149-CMC was determined (measured and expressed as free peptide) at 25° C. in 0.1M phosphate buffered saline at pH 7.3, using three samples: PPI-149-CMC alone, PPI-149-CMC in the presence of 10% additional (by weight) PPI-149 (expressed as free peptide, but introduced as PPI-149 with associated acetate) and PPI-149-CMC in the presence of 50% additional (by weight) Carboxymethylcellulose sodium USP. All three samples gave ostensibly a similar peptide equilibrium solubility. As the buffer system selected approximates physiological conditions, the presence of additional free Carboxymethylcellulose or peptide species present in PPI-149-CMC seems unlikely to affect solubility.

EXAMPLE 14

In this example, the pharmacokinetics, pharmacodynamics and safety of repeated subcutaneous (SC) and intramuscular (IM) doses of PPI-149-CMC were characterized in dogs.

In a first study, conducted for three months, forty male beagle dogs were evaluated, using monthly IM or SC injections of PPI-149-CMC at 1.2 mg/kg (Day 1), 0.3 or 0.6 mg/kg (Day 29) and 1.2 mg/kg (Day 57) in a variety of reconstitution vehicles. Eight groups of five dogs were assigned to the study as shown below:

	Route
	Reconstitution Vehiclea, b	Dosec (mg/kg)	of
Group	N	Day 1	Day 29	Day 57	Day 1	Day 29	Day 57	Admin.
Ad	5	Saline	Glycerin	Lecithin	0	0	0	IM
B	5	Glycerin	Glycerin	Lecithin	1.2	0.3	1.2	IM
C	5	Glycerin	Glycerin	Lecithin	1.2	0.6	1.2	IM
D	5	PEG	Glycerin	Lecithin	1.2	0.3	1.2	IM
E	5	PEG	Glycerin	Lecithin	1.2	0.3	1.2	SC
Fd	5	Lecithin	Glycerin	Lecithin	1.2	0.6	1.2	IM
Gd	5	Lecithin	Glycerin	Lecithin	1.2	0.6	1.2	SC
H	5	Glycerin	Glycerin	Lecithin	1.2	0.3	1.2	SC
aReconstitution vehicles are used to reconstitute PPI-149-CMC as a particular suspension. They contain the following (in water):
1. Glycerin = 15% glycerin/5% dextrose
2. PEG = 4% polyethylene glycol-3350/4% mannitol
3. Lecithin = 0.5% lecithin/5% mannitol
bNote: the reconstitution vehicles to be used in clinical studies is 0.9% sodium chloride USP
cAll doses are expressed in terms of peptide (PPI-149) content.
dThree animals were sacrificed at Day 85 for complete anatomical and microscopic histology.

This study was designed such that the efficacy of PPI-149-CMC at an initial dose in different vehicles was assessed during the first month of treatment. During the second month on-study, the dogs received lower doses of PPI-149-CMC in an attempt to determine an efficacious “maintenance” dose. The third month was scheduled to evaluate the long term safety and efficacy characteristics of PPI-149-CMC.

IM or SC doses of PPI-149-CMC formulated in one of the reconstitution vehicles, or IM doses of control article, were administered on each dosing day into the upper flank of the right hind limb (IM) or in the mid-scapular region (SC). Material was drawn into a 1 cc tuberculin syringe with a 23 g short bevel needle. The injection site was wiped with an alcohol swab immediately prior to dosing. The volume injected was based on a specific dose of peptide/kg body weight. It should be noted that all doses refer to the amount of PPI-149 peptide administered.

Each animal was observed at least twice daily during the entire study for overt signs of toxic or pharmacologic effect and changes in general behavior and appearance. All abnormal clinical observations were recorded.

Blood was collected prior to administration of the first dose and at various times following dosing, for complete blood counts (CBC), serum chemistry analysis, and determination of PPI-149 and testosterone concentrations twice weekly by radioimmunoassays.

After three months on-study, nine animals were sacrificed and their tissues collected for gross pathological and histopathological analysis. Animals were selected for sacrifice from the vehicle control group, one of the IM dosing groups and one of the SC dosing groups. The tissues collected for gross pathology and histopathology at the 3 month sacrifice were: administration Site (SC or IM), adrenal glands, aorta, bone, bone marrow, brain, diaphragm, epididymis, esophagus, eyes with optic nerve, heart, kidneys, large intestine (cecum, colon), liver with gall bladder, lungs with bronchi, lymph nodes, pancreas, pituitary gland, prostate gland with urethra, salivary glands, sciatic nerve, skeletal muscle, skin, small intestine (duodenum, jejunum, ileum), spinal cord, spleen, stomach, testes, thymus, thryoid gland with parathyroid, tongue, trachea, urinary bladdr and gross lesions.

There were no significant changes in hematology or blood chemistry from baseline during the study for either treated or control animals. Gross and histological evaluation at the three month sacrifice showed no apparent differences between PPI-149-CMC treated dogs and control (vehicle-treated) animals, with the exception of changes in the testes and prostate, as expected with this LHRH antagonist.

Regarding PPI-149-CMC pharmacokinetics, all dogs treated with 1.2 mg/kg PPI-149-CMC resuspended in a variety of reconstitution vehicles and administered IM or SC showed similar plasma PPI-149 pharmacokinetic profiles, with plasma concentration peaking within the first 2 days and then decreasing slowly in an exponential manner over the following month. PPI-149-CMC gave similar plasma distribution of PPI-149 when suspended in any of the three reconstitution vehicles used in the study.

Regarding PPI-149-CMC endocrine efficacy, castrate levels of testosterone (<0.6 ng/mL) were observed within 24 hours of initiation of PPI-149-CMC dosing in all dogs, and levels generally remained in the castrate range throughout the first month regardless of the route of administration or choice of reconstitution vehicle. Twenty-six (26) of 35 dogs (75%) had castrate levels of testosterone in a blood sample obtained immediately prior to administration of the second dose of PPI-149-CMC on Day 29. These results indicate that an initial dose of 1.2 mg/kg in dogs successfully induces a rapid, long-lasting suppression (>28 days) in plasma testosterone. In the second month of dosing, when the efficacy of a “maintenance” dose (a dose lower than the initial dose) was investigated, the results indicated that administration of 0.3 or 0.6 mg/kg of PPI-149-CMC maintained castrate levels of testosterone for more than 20 days in 30 out of 35 dogs. At the end of the second month of treatment (Day 57), 21 of 35 dogs (60%) remained castrate, while 14 animals had testosterone in the normal range (>0.6% ng/mL). A dose of 1.2 mg/kg was administered in the beginning of the third month. Plasma concentrations of PPI-149 were sustained for the following twenty-eight day period while plasma levels of testosterone were again “castrate.” By the end of the third month (Day 85), plasma levels of testosterone were shown to be in the castrate range in 30 of 35 PPI-149-CMC-treated dogs.

In summary, thirty-five (35) dogs received 1.2 mg/kg PPI-149-CMC on Day 1, 0.3 or 0.6 mg/kg PPI-149-CMC on Day 29 and 1.2 mg/kg PPI-149-CMC on Day 57, using IM or SC dosing with a variety of reconstitution vehicles. Of these 35 dogs, 19 animals (54%) had plasma testosterone levels which remained in the castrate range throughout the entire course of therapy. Thus, administration of PPI-149-CMC at 28 day intervals was able to result in complete suppression of plasma testosterone which is rapid (all animals had castrate levels within 24 hours) and long-lasting (maintained throughout the course of administration).

A similar study to that described above was conducted for six months in dogs to further evaluate the long term safety and efficacy characteristics of PPI-149-CMC. Animals received an initial dose of 1.2 mg/kg PPI-149-CMC either IM or SC and five subsequent doses (at a concentration of either 0.3 mg/kg, 0.6 mg/kg or 1.2 mg/kg) at 28 day intervals. Plasma testosterone and PPI-149 levels were evaluated by radioimmunoassay at regular intervals. Representative results are shown in FIG. 4 (for SC treatment) and FIG. 5 (for IM treatment), which illustrate plasma testosterone levels (open boxes) and PPI-149 levels (closed boxes). The particular dosages used at each administration of PPI-149-CMC are shown on the graphs. The results illustrated in FIGS. 4 and 5 further demonstrate that administration of PPI-149-CMC at 28 day intervals was able to result in complete suppression of plasma testosterone which is rapid and long-lasting, with reduced plasma testosterone levels being maintained for as long as six months.

Equivalents

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.

Claims

1. A pharmaceutical composition comprising a water-insoluble complex of a pharmaceutically active peptidic compound and a carrier macromolecule.

2. The pharmaceutical composition of claim 1, wherein formation of the water-insoluble complex is mediated at least in part by ionic interactions between the pharmaceutically active peptidic compound and the carrier macromolecule.

3. The pharmaceutical composition of claim 2, wherein the pharmaceutically active peptidic compound is cationic and the carrier macromolecule is anionic.

4. The pharmaceutical composition of claim 2, wherein the pharmaceutically active peptidic compound is anionic and the carrier macromolecule is cationic.

5. The pharmaceutical composition of claim 1, wherein formation of the water-insoluble complex is mediated at least in part by hydrophobic interactions between the pharmaceutically active peptidic compound and the carrier macromolecule.

6. The pharmaceutical composition of claim 1, wherein a single dose of the water-insoluble complex provides sustained delivery of the pharmaceutically active peptide to a subject for at least one week after the pharmaceutical composition is administered to the subject.

7. The pharmaceutical composition of claim 1, wherein a single dose of the water-insoluble complex provides sustained delivery of the pharmaceutically active peptide to a subject for at least two weeks after the pharmaceutical composition is administered to the subject.

8. The pharmaceutical composition of claim 1, wherein a single dose of the water-insoluble complex provides sustained delivery of the pharmaceutically active peptide to a subject for at least three weeks after the pharmaceutical composition is administered to the subject.

9. The pharmaceutical composition of claim 1, wherein a single dose of the water-insoluble complex provides sustained delivery of the pharmaceutically active peptide to a subject for at least four weeks after the pharmaceutical composition is administered to the subject.

10. The pharmaceutical composition of claim 1, wherein the pharmaceutically active peptidic compound is a multivalent cationic or anionic peptide.

11. The pharmaceutical composition of claim 1, wherein the peptide is 5 to 20 amino acids in length.

12. The pharmaceutical composition of claim 1, wherein the peptide is 8 to 15 amino acids in length.

13. The pharmaceutical composition of claim 1, wherein the peptide is 8 to 12 amino acids in length.

14. The pharmaceutical composition of claim 1, wherein the carrier macromolecule is an anionic polymer.

15. The pharmaceutical composition of claim 1, wherein the carrier macromolecule is an anionic polyalcohol derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

16. The pharmaceutical composition of claim 1, wherein the carrier macromolecule is an anionic polysaccharide derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

17. The pharmaceutical composition of claim 1, wherein the carrier macromolecule is carboxymethylcellulose, or a pharmaceutically acceptable salt thereof.

18. The pharmaceutical composition of claim 1, wherein the carrier macromolecule is selected from the group consisting of algin, alginate, anionic acetate polymers, anionic acrylic polymers, xantham gums, anionic carageenan derivatives, anionic polygalacturonic acid derivatives, sodium starch glycolate, and fragments, derivatives and pharmaceutically acceptable salts thereof.

19. The pharmaceutical composition of claim 1, which is a dry solid.

20. The pharmaceutical composition of claim 1, which is a liquid suspension or semi-solid dispersion.

21. A pharmaceutical composition comprising a water-insoluble complex, wherein the water-insoluble complex consists essentially of a pharmaceutically active peptidic compound and a carrier macromolecule.

22. A pharmaceutical composition comprising a water-insoluble complex of an LHRH analogue and a carrier macromolecule.

23. The pharmaceutical composition of claim 22, wherein formation of the water-insoluble complex is mediated at least in part by ionic interactions between the LHRH analogue and the carrier macromolecule.

24. The pharmaceutical composition of claim 22, wherein formation of the water-insoluble complex is mediated at least in part by hydrophobic interactions between the LHRH analogue and the carrier macromolecule.

25. The pharmaceutical composition of claim 22, wherein a single dose of the water-insoluble complex provides sustained delivery of the LHRH analogue to a subject for at least one week after the pharmaceutical composition is administered to the subject.

26. The pharmaceutical composition of claim 22, wherein a single dose of the water-insoluble complex provides sustained delivery of the LHRH analogue to a subject for at least two weeks after the pharmaceutical composition is administered to the subject.

27. The pharmaceutical composition of claim 22, wherein a single dose of the water-insoluble complex provides sustained delivery of the LHRH analogue to a subject for at least three weeks after the pharmaceutical composition is administered to the subject.

28. The pharmaceutical composition of claim 22, wherein a single dose of the water-insoluble complex provides sustained delivery of the LHRH analogue to a subject for at least four weeks after the pharmaceutical composition is administered to the subject.

29. The pharmaceutical composition of claim 22 wherein the LHRH analogue is an LHRH antagonist.

30. The pharmaceutical composition of claim 29 wherein the LHRH antagonist comprises a peptidic compound, wherein a residue of the peptidic compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises a D-asparagine structure.

31. The pharmaceutical composition of claim 29 wherein the LHRH antagonist comprises a peptidic compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein A is pyro-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-Cl-D-Phe C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N—O), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile; F is wherein R and X are, independently, H or alkyl; and L comprises a small polar moiety; G is Leu or Trp; H is Lys(iPr), Gln, Met, or Arg I is Pro; and J is Gly-NH2 or D-Ala-NH2; or a pharmaceutically acceptable salt thereof.

32. The pharmaceutical composition of claim 31, wherein F is selected from the group consisting of D-Asn, D-Gln and D-Thr.

33. The pharmaceutical composition of claim 31, wherein F is D-Asn.

34. The pharmaceutical composition of claim 31, wherein E is tyrosine or N-methyl -tyrosine.

35. The pharmaceutical composition of claim 29, wherein the LHRH antagonist has the following structure: Ac-D-Nal1, 4-Cl-D-Phe2, D-Pal3, N-Me-Tyr5, D-Asn6, Lys(iPr)8, D-Ala10-LHRH.

36. The pharmaceutical composition of claim 22, wherein the carrier macromolecule is an anionic polymer.

37. The pharmaceutical composition of claim 22, wherein the carrier macromolecule is an anionic polyalcohol derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

38. The pharmaceutical composition of claim 22, wherein the carrier macromolecule is an anionic polysaccharide derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

39. The pharmaceutical composition of claim 22, wherein the carrier macromolecule is carboxymethylcellulose, or a pharmaceutically acceptable salt thereof.

40. The pharmaceutical composition of claim 22, wherein the carrier macromolecule is selected from the group consisting of algin, alginate, anionic acetate polymers, anionic acrylic polymers, xantham gums, anionic carageenan derivatives, anionic polygalacturonic acid derivatives, sodium starch glycolate, and fragments, derivatives and pharmaceutically acceptable salts thereof.

41. The pharmaceutical composition of claim 22, which is a dry solid.

42. The pharmaceutical composition of claim 22, which is a liquid suspension or semi-solid dispersion.

43. A packaged formulation for treating a subject for a condition treatable with an LHRH analogue, comprising the pharmaceutical composition of claim 22 packaged with instructions for using the composition for treating a subject having a condition treatable with an LHRH analogue.

44. The packaged formulation of claim 43, wherein the LHRH analogue has the following structure: Ac-D-Nal1, 4-Cl-D-Phe2, D-Pal3, N-Me-Tyr5, D-Asn6, Lys(iPr)8, D-Ala10-LHRH, and the carrier macromolecule is carboxymethylcellulose, or a pharmaceutically acceptable salt thereof.

45. In a syringe having a lumen, the improvement comprises, inclusion of the pharmaceutical composition of claim 22 in the lumen.

46. The syringe of claim 45, wherein the LHRH analogue has the following structure: Ac-D-Nal1, 4-Cl-D-Phe2, D-Pal3, N-Me-Tyr5, D-Asn6, Lys(iPr)8, D-Ala10-LHRH, and the carrier macromolecule is carboxymethylcellulose, or a pharmaceutically acceptable salt thereof.

47. A method for preparing a pharmaceutical formulation, comprising: providing a peptidic compound and a carrier macromolecule; combining the peptidic compound and the carrier macromolecule under conditions such that a water-insoluble complex of the peptidic compound and the carrier macromolecule forms; and preparing a pharmaceutical formulation comprising the water insoluble complex.

48. The method of claim 47, wherein a solution of the peptidic compound and a solution of the carrier macromolecule are combined until a water-insoluble complex of the peptidic compound and the carrier macromolecule precipitates.

49. The method of claim 48, wherein the solution of the peptidic compound and the solution of the carrier macromolecule are aqueous solutions.

50. The method of claim 48, wherein the solution of the peptidic compound and the solution of the carrier macromolecule are combined and heated until a water-insoluble complex of the peptidic compound and the carrier macromolecule precipitates.

51. The method of claim 47, further comprising sterilizing the water-insoluble complex by gamma irradiation or electron beam irradiation.

52. The method of claim 47, wherein the water-insoluble complex is formed using aseptic procedures.

53. The method of claim 47, wherein the peptidic compound is cationic and the carrier macromolecule is anionic.

54. The method of claim 47, wherein the peptidic compound is anionic and the carrier macromolecule is cationic.

55. The method of claim 47, wherein the peptidic compound is a multivalent cationic or anionic peptide.

56. The method of claim 47, wherein the peptidic compound is an LHRH analogue

57. The method of claim 56, wherein the LHRH analogue is an LHRH antagonist.

58. The method of claim 57, wherein the LHRH antagonist comprises a peptidic compound, wherein a residue of the peptidic compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises a D-asparagine structure.

59. The method of claim 57, wherein the LHRH antagonist comprises a peptidic compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein A is pyro-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-Cl-D-Phe C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N—O), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile; F is wherein R and X are, independently, H or alkyl; and L comprises a small polar moiety; G is Leu or Trp; H is Lys(iPr), Gln, Met, or Arg I is Pro; and J is Gly-NH2 or D-Ala-NH2; or a pharmaceutically acceptable salt thereof.

60. The method of claim 59, wherein F is selected from the group consisting of D-Asn, D-Gln and D-Thr.

61. The method of claim 59, wherein F is D-Asn.

62. The method of claim 59, wherein E is tyrosine or N-methyl-tyrosine.

63. The method of claim 57, wherein the LHRH antagonist has the following structure: Ac-D-Nal1, 4-Cl-D-Phe2, D-Pal3, N-Me-Tyr5, D-Asn6, Lys(iPr)8, D-Ala10-LHRH.

64. The method of claim 47, wherein the carrier macromolecule is an anionic polymer.

65. The method of claim 47, wherein the carrier macromolecule is an anionic polyalcohol derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

66. The method of claim 47, wherein the carrier macromolecule is an anionic polysaccharide derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

67. The method of claim 47, wherein the carrier macromolecule is carboxymethylcellulose, or a pharmaceutically acceptable salt thereof.

68. The method of claim 47, wherein the carrier macromolecule is selected from the group consisting of algin, alginate, anionic acetate polymers, anionic acrylic polymers, xantham gums, anionic carageenan derivatives, anionic polygalacturonic acid derivatives, sodium starch glycolate, and fragments, derivatives and pharmaceutically acceptable salts thereof.

69. The method of claim 47, wherein the pharmaceutical formulation is a dry solid.

70. The method of claim 47, wherein the pharmaceutical formulation is a liquid suspension or semi-solid dispersion.

71. A pharmaceutical formulation prepared according to the method of claim 47.

72. A method for treating a subject for a condition treatable with an LHRH analogue, comprising administering to the subject a pharmaceutical formulation comprising a water-insoluble complex of an LHRH analogue and a carrier macromolecule.

73. The method of claim 72, wherein a single dose of the water-insoluble complex provides sustained delivery of the LHRH analogue to a subject for at least one week after the pharmaceutical composition is administered to the subject.

74. The method of claim 72, wherein a single dose of the water-insoluble complex provides sustained delivery of the LHRH analogue to a subject for at least two weeks after the pharmaceutical composition is administered to the subject.

75. The method of claim 72, wherein a single dose of the water-insoluble noncovalent complex provides sustained delivery of the LHRH analogue to a subject for at least three weeks after the pharmaceutical composition is administered to the subject.

76. The method of claim 72, wherein a single dose of the water-insoluble noncovalent complex provides sustained delivery of the LHRH analogue to a subject for at least four weeks after the pharmaceutical composition is administered to the subject.

77. The method of claim 72, wherein the LHRH analogue is an LHRH antagonist.

78. The method of claim 77, wherein the LHRH antagonist has the following structure: Ac-D-Nal1, 4-Cl-D-Phe2, D-Pal3, N-Me-Tyr5, D-Asn6, Lys(iPr)8, D-Ala10-LHRH.

79. The method of claim 72, wherein the carrier macromolecule is an anionic polymer.

80. The method of claim 72, wherein the carrier macromolecule is an anionic polyalcohol derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

81. The method of claim 72, wherein the carrier macromolecule is an anionic polysaccharide derivative, or fragment thereof, or a pharmaceutically acceptable salt thereof.

82. The method of claim 72, wherein the carrier macromolecule is carboxymethylcellulose, or a pharmaceutically acceptable salt thereof.

83. The method of claim 72, wherein the carrier macromolecule is selected from the group consisting of algin, alginate, anionic acetate polymers, anionic acrylic polymers, xantham gums, anionic carageenan derivatives, anionic polygalacturonic acid derivatives, sodium starch glycolate, and fragments, derivatives and pharmaceutically acceptable salts thereof.

84. The method of claim 72, wherein the pharmaceutical formulation is administered to the subject by a parenteral route.

85. The method of claim 72, wherein the pharmaceutical formulation is administered to the subject orally.

86. The method of claim 72, wherein the pharmaceutical formulation is administered by intramuscular injection or subcutaneous/intradermal injection.

87. The method of claim 72, wherein the condition treatable with an LHRH analogue is a hormone dependent cancer.

88. The method of claim 87, wherein the hormone dependent cancer is prostate cancer.

89. The method of claim 72, wherein the condition treatable with an LHRH analogue is selected from the group consisting of benign prostatic hypertrophy, precocious puberty, endometriosis and uterine fibroids.

90. The method of claim 72, wherein the LHRH analogue is administered for in vitro fertilization or contraceptive purposes.