Patent Application
20150038414
The present invention relates to liquid pharmaceutical compositions, in particular to depot tot mu/aborts comprising somatostatin analogues and to a process for preparing said depot formulations.
Depot formulations are typically administered parenterally. Somatostatin depot formulation may be administered by injection subcutaneously or intramuscularly through a small gauge needle or placed into accessible tissue sites through a cannula. However parenteral administration may be very painful especially if repeated injections are necessary. Furthermore, there may be difficulties with depot formulations which are administered in liquid form and which form a solid implant in the body after injection. Often the solidifying process starts in the syringe before injection and causes needle clogging. Further, these depot formulations may comprise a polymer or a mixture of polymers that has to be dissolved in an organic solvent, e.g. they may comprise more than 5% of an organic solvent. If the organic solvent remains in the solution for injection it might cause severe tissue irritation or necrosis at the site of implantation.
EP 779 805 provides a pharmaceutical composition consisting of a soluble peptide salt which will form a gel upon contact with a body fluid, and up to 30% by weight of the composition of a pharmaceutically acceptable carrier. The peptides described in EP 779805 are somatostatins or a somatostatin analogs, e.g. lanreotide.
Surprisingly it has now been found that advantageous parenteral somatostatin depot formulations may be obtained with a composition comprising a salt of a somatostatin analogue and water having a pH from 3 to 7 without using a polymer and without using an organic solvent.
The present invention provides in one aspect a pharmaceutical composition for parenteral administration comprising a somatostatin analogue salt of aspartate, e.g. mono- or diasparate, glutamate, e.g. mono- or diglutamate, or succinate, e.g., mono- or disuccinate, lactate, acetate or citrate and water, forming a gelling depot after injection in contact with body fluid. The salt:base ratio of the somatostatin analogue salts may range from 0.1 to 2 and provides the solubility of the somatostatin analogue salt. The pharmaceutical composition has a pH between about 30 and 7.0, preferably from between 4.0 and 6.0 and more preferably horn between about 4.0 and 5.0. Optionally the composition may comprise a pharmaceutically acceptable buffer in an amount to stabilize the pH between about 3.0 and 7.0, preferably between about 4.0 and 6.0, most preferably between 4.0 and 5.0.
In another aspect the present invention provides a pharmaceutical composition for parenteral administration comprising a somatostatin analogue salt of aspartate, e.g. mono- or diaspartate, glutamate, e.g. mono- or diglutemate, lactate, succinate, e.g. mono- or disuccinate, acetate or citrate, and water, having a pH between about 3.0 and 7,0, for ling a gelling depot after injection in contact with body fluid.
The composition having a pH between about 3.0 and 1.0 provides good solubility and therefore the composition of the invention may be stored over an extended period of time without precipitation. The composition is administered to the patient by injection wherein the composition will start to form a gelling depot after and not before interaction with patients body fluid. The gelling depot releases the somatostatin analogue salt of aspartate, lactate, succinate, acetate, glutamate or citrate within the patient over an extended period of time
In another aspect the provides a process for preparing a depot formulation by
In a further aspect the invention provides a process for preparing a depot formulation by
The present invention relates to somatostatin analogue salts of aspartate, e.g. mono- or diaspartate, lactate, succinate, e.g. mono- or disuccinate, acetate, glutamate, e.g. mono- or diglutamate or citrate.
Somatostatin is a tetradecapeptide having the structure
Somatostatin analogues of particular interest have been described e.g. in WO 97/01579 and WO 97/25977. Said somatostatin analogues comprise the amine acid sequence of formula I
—(D/L)Trp-Lys-X1-X2—
wherein X1 is a radical of formula (a) or (b)
wherein R1 is optionally substituted phenyl, wherein the substituent may be halogen, methyl, ethyl, methoxy or ethoxy,
R2 is Z1—CH2—R1, —CH2—CO—O—CH2—r1,
wherein Z1 is O or S, and
X2 is an α-amino acid having en aromatic residue on the Cα side chain, or an amino acid unit selected from Dab, Dpr, Dpm, His,(Bzl)HyPro, thienyl-Ala, cyclohexyl-Ala and t-butyl-Ala, the residue Lys of said sequence corresponding to the residue Lysg of the native somatostatin-14.
By somatostatin analogue as used her is meant a straight-chain or cyclic peptide derived from that of the naturally occurring somatostatin-14, comprising the sequence of formula I and wherein additionally one or more amino add units have been omitted and/or replaced by one or more other amino add radical(s) and/or wherein one or more functional groups have been replaced by one r more other functional groups and/or one or more re group been replaced by one or several other isosteric groups. In general the term covers all modified derivatives of the native somatostatin-14 comprising the above sequence of formula I which have binding affinity in the nM range to at least one somatostatin receptor subtype as defined hereinafter.
Preferably, the somatostatin analogue is a compound in which the residues at positions 8 through 11 of the somatostatin-14 are represented by the sequence of formula I as defined above.
More preferably, the somatostatin analogue is a compound as disclosed above comprising a hexapeptide unit, the residues at positions 3 through 6 of said hexepeptide unit comprising the sequence of formula I. Particularly preferred is a somatostatin hexapeptide wherein the residues at positions 1 and 2 of the hexapeptide unit may be any of those as known in the art, e.g. as disclosed by A. S. Daft in Small Peptides, Vol. 19, 292-35.4, Elsevier, 1993 or as substituents for, Phe6 and/or Pha7 of somatostatin-14.
More particularly the somatostatin analogue is a compound in which the hexapeptide unit is cyclic, e.g. having a direct peptide linkage between the α-carbonyl group of the residue at position 6 and the α-amino group of the residue at position 1.
While Lys, X1 and X2 in the sequence of formula I have the L-configuration, Trp may have the D- or L-configuration. Preferably Trp has the D-configuration.
X1 is preferably a residue of formula (a) or (b), R2 being preferably
When X2 comprises an aromatic residue on the Cα side chain, it may suitably be a natural or unnatural α-amino acid, e.g. Phe, Tyr, Trp, Nal, Pal, benzothienyla-Ala, Tic and thyronin, preferably Phe or Nal, more preferably Phe, X2 is preferably an α-amino acid bearing an aromatic residue on the Cα side chain.
When R1 is substituted phenyl, it may suitably be substituted by halogen, methyl, ethyl, methoxy or ethoxy e.g. in ortho and/or para. More preferably R1 is unsubstituted phenyl Z1 is preferably O.
Representative compounds of the invention are e.g. compounds of formula (II)
wherein X1 and X2 are as defined above, A is a divalent residue selected from Pro,
wherein R3 is NR3R9C2-5-alkylene, guanidino-C2-4-alkylene or C2-6alkylene-COOH, R3a is H, C1-4alkyl or has independently one of the significances given for R3, R3b is H or C1-4alkyl, Ra is OH or NR5R6, Rb is —(CH2)1-3)—, R4 is H or CH3, R4a is optionally ring-substituted benzyl, each of R5 and R6 independently is H, C1-4-alkyl, ω-amino-C1-4alkylene, ∫-hydroxy-C1-4alkylene or acyl, R7 is a direct bond or C1-6alkylene, each of Ra and Rs independently is H, C1-4alkyl, ω-hydroxy-C2-4alkylen, acyl or CH2OH—(CHOH)b—CH2— wherein c is 0, 1, 2, 3 or 4, or R8 and R9 form together with the nitrogen atom to which they are attached a heterocyclic group which may comprise a further heteroatom, and R11 is optionally ring-substituted benzyl,—(C2)1-3—OH, CH3—CH(OH)— or —(CH2)1-5—NR5R6, and ZZa is a natural or unnatural α-amino acid unit.
ZZa may have the D- or L-configuration. When ZZa is a natural or unnatural α-amino acid unit, it may suitably be e.g. Thr, Ser, Ala, Val, Ile, Leu, Nle, His, Arg, Lys, Nal, Pal, Tyr, Trp, optionally ring-substituted Phe or Na-benzyl-Gly. When ZZa is Phe, the benzene ring thereof may be substituted by e.g. NH2, NO2, CH3, OCH3 or halogen, preferably in para position. When ZZa is Phe, the benzene ring thereof is preferably unsubstituted.
When A comprises a Pro amino acid residue, any substituent present on the proline ring, e.g. R3-NH-—CO—O— etc., is preferably in position 4. Such substituted proline residue may exist in the cis form, e.g.
as well as in the trans form Each geometric isomer individually as well as mixtures thereof are compounds of the invention.
When A is
where NR8R8 forms a heterocyclic group, such group may be aromatic or saturated and may comprise one nitrogen or one nitrogen and a second heteroatom selected from nitrogen and oxygen. Preferably the heterocyclic group is e.g. pyridyl or morpholino, C2-8Alkylene in this residue is preferably —CH2-CH2—.
Any acyl as R5, R8, R8 and R9 in A may be e.g. R12CO—, wherein R12 is H, C1-4alkyl, C2-4alkanyl, C3-6 cycloalkyl or benzyl preferably methyl or ethyl. When R4a or R11 in A is ring-substituted benzyl, the benzene ring may be substituted as indicated above for ZZa.
Particularly preferred are compounds of formula III
wherein the configuration at C-2 is (R) or (S) or a mixture thereof, and wherein R is NR10R11-C2-8alkylene or guanidine-C2-4alkylene, and each of R10 and R11 independently is H or C1-4alkyl, in free form in salt form or protected form the synthesis of which may be performed as described e.g. in WO 2002/10192 which is hereby incorporated by reference.
The salts are obtained by the process a described e.g. in WO 2002/10192 which is hereby incorporated by reference.
Preferably R is NR10R11-C2-6alkylene. Preferred compounds of formula II are the compounds wherein R is 2-amino-ethyl, namely cyclo[{4-(NH2-C2H4-CO—O—)Pro}-Phg-DTrp-Lys-Tyr(4BzI)-Phe] (referred herein to as Compound A) and cyclo[{4-(NH2-C2H4-NH—CO—O—) Pro}-DPhg-DTrp-Lys-Tyr(4-BzI)-Phe] in free form, salt form or protected form, Phg means —HN—CH(C6H5)—CO— and BzI means benzyl.
A salt of the invention in protected form corresponds to a somatostatin analogue wherein at least one of the amino groups is protected and which by deprotection leads to a compound of formula II, preferably physiologically removable. Suitable amino protecting groups are e.g. as disclosed in “Protective Groups in Organic Synthesis”, T. W. Greene, J. Wiley & Sons N.Y. (1981), 219-287, the contents of which being incorporated herein by reference. Example of such an amino protecting group is acetyl.
The composition according to the present invention may comprise a buffer. Suitable buffers include but are not limited to acetate buffer, lactate buffer, glycin buffer and tartrate buffer. The concentrations of the buffers may be from about 5 mM to 30 mM, preferably from about 10 mM to 25 mM.
In a further aspect the invention provides a pharmaceutical composition in a viscous liquid form that may be injected with a syringe through a needle ranging from 15 to 25 G, e.g. 2 G. The solution may be placed in a syringe after sterile filtration through a 0.2 μm filter having a viscosity of from 1 to 104 mPa.s or after sterile filtration and solvent removal by evaporation or sublimation having a viscosity of from 102 to 10 mPa.s. The solvent removal may be done after placing the solution in the syringe.
The solution in the syringe may be injected through a needle, e.g. a 20 G needle, into the body subcutaneously, intramuscularly, intradermally or intraperitoneally or pieced into accessible tissue sites through a cannula. Once in piece in contact with the patient's body fluid the gelling depot will be formed. The liquid composition for paranteral administration may be filled in a syringe, preferably a prefilled syringe may be provided together with instructions for use.
In another aspect the invention provides a depot formulation for extended release of the pharmaceutically active agent. The implant formed after injection into the body may release the active agent over extended period of time The release period may range from 1 up to 90 days, e.g. 1 up to 60 days, e.g. between 30 to 60 days.
The compositions of the invention are useful for treatment of the own indications of the particular active agent. Compositions of the invention comprising a somatostatin analogue salt of aspartate, lactate, succinate, acetate, glutamate or citrate may be useful in the following indications:
a) for the prevention or treatment of disorders with an aetiology comprising or associated with excess GH-secretion and/or excess of IFG-1 e.g., in the treatment of acromegaly as well as in the treatment of type I or type II diabetes mellitus, especially complications thereof, e.g. angiopathy, diabetic proliferative retinopathy, diabetic macular edema, nephropathy, neuropathy and dawn phenomenon, and other metabolic disorders related to insulin or glucagon release, e.g. obesity, e.g. morbid obesity or hypothalamic or hyperinsulinemic obesity,
c) for the prevention or treatment of angiogenesis, inflammatory disorders as indicated above including inflammatory eye diseases, macular edema, cystoid macular edema, idiopathic cystoid macular edema, exudative age-related macular degeneration, choroidal neovascularization related disorders and proliferative retinopathy,
d) for preventing or combating graft vessel disease allo- or xenotransplant vasculo-pathies, e.g. graft vessel atherosclerosis, e.g. in transplant of organ, e.g. heart, lung, combined heart-lung, liver, kidney or pancreatic transplants, or for preventing or treating vein graft stenosis, restenosis and/or vascular occlusion following vascular injury, e.g. caused by catherization procedures or vascular scraping procedures such as percuteneous transluminal angioplasty, laser treatment or other invasive procedures which disrupt the integrity of the vascular intima or endothelium,
e) for treating somatostatin receptor expressing accumulating tumors such as pituitary tumors, e.g. Cushing's Disease gastro-enteropancreatic, carcinoids, central nervous system, breast, prostatic (including advanced hormone-refractory prostate cancer), ovarian or colonic tumors, small cell lung cancer, maglinant bowel obstruction, paragangliomas, kidney cancer, skin cancer, neuroblastomas, pheochromocytomas, medullary thyroid carcinomas, myelomas, lymphomas, Hodgkins and non-Hodgkins lymphomas, bone tumours and metastases thereof, as well as autoimmune or inflammatory disorders, e.g. rheumatoid arthritis, Graves disease or other inflammatory eye diseases.
Preferably, the compositions of the invention are useful in the treatment of acromegaly, carcinoids and/or Cushing's Disease.
The activity and the characteristics of the liquid compositions of the invention may be indicated in standard clinical or animal tests.
Appropriate dosage of the composition of the invention will of course vary, e.g., depending on the condition to be treated (for example the disease type of the nature of resistance), the drug used, the effect desired and the mode of administration.
For compositions of the invention comprising the somatostatin salt of aspartate, lactate, succinate, acetate, glutamate or citrate satisfactory results are obtained on administration, e.g. parenteral administration, at dosages in the order of from about 0.1 to about 100 mg, preferably from about 3 to about 60 mg per injection per month or about 0.01 to about 4 mg preferably 0.1 to 1 mg per kg animal body weight per month, administered once or in divided doses. Suitable monthly dosages for patients are thus in the order of about 0.1 mg to about 80 mg of a somatostatin analogue salt of aspartate, lactate, succinate, acetate, glutamate or citrate.
The present invention provides a simple pharmaceutical composition of somatostatin analogue salt of aspartate, e.g. mono- or diaspartate, lactate, succinate e.g. mono- or disuccinate, acetate, glutamate, e.g. mono- or diglutamate, or citrate in a salt:base ratio ranging from 0.1 to 2 and water at a defined pH between 3.0 to 7.0, preferably between about 4.0 to 8.0, more preferably between about 4.0 to 5.0. The salt base ratio ranging from 0.1 to 2 provides the solubility of the somatostatin analogue salt at a given pH and the precipitation and depot formation after contact with body fluids and therefore environmental pH change. The pH may be stabilized by a buffer. The process to prepare the composition is simple by adding water to the somatostatin analogue salt. At a pH between about 4.0 to 6.0 the composition shows good solubility and therefore precipitation, e.g. in a prefilled, syringe or needle clogging is avoided. No organic solvents that might use severe side effects at the place of administration are used.
Following is a description by way of example only of processes and compositions of the invention.
A 2 ml solution of the pharmaceutical composition of the present invention is made by mixing 0.8 g somatostatin diaspartate with 1.36 ml water injection.
Release prone in rabbits of the drug product having the composition given in example 1. The composition has been injected parenterally and blood samples have been taken several times during a period of 2 months to measure the somatostatin diasparate.
The di-succinate for of the pharmaceutical composition of the present invention is made by mixing 0.999 g somatostatin di-succinate with 1.6 ml water for injection.
The di-glutamate form of the pharmaceutical composition of the present invention is made by mixing 0.916 g somatostatin di-glutamate with 1.44 ml water for injection.
Release profile in rabbits of the drug product having the composition given in example 3 and 4. The composition has been injected parentarally and blood samples have been taken several times during a period of 2 months to measure the somatostatin disuccinate and somatostatin diglutamate.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0428151.5 | Dec 2004 | GB | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11721082 | Sep 2009 | US |
| Child | 14265605 | US |
