CA2183764C - Use of certain methanebisphosphonic acid derivatives to prevent prosthesis loosening and prosthesis migration - Google Patents

Abstract

The invention relates to the use of certain methanebisphosphonic acid deriva tives (for the manufacture of a pharmaceutical compositi on) for the prevention and treatment of prosthesis loosening and prosthesis migr ation in mammals including man.

Description

W095/30421 ~ ~ ~ ~ ~ ~ 4 PGTI1895100288 Use of certain methanebisnhosohonic acid derivatives to prevent vrosthesis loosening and prosthesis ieration Arthroplasty, especially of the hip joint, is now a common procedure for the treatment of patients with osteoarthritis, rheumatoid arthritis and osteoporotic fracture.
Approximately 800 000 hip replacements are performed globally each year. This number is rising steadily, younger patients are being treated and patients are living much longer and they all expect to lead a mobile, independent life. Despite the indisputable success of this technique, often complications arise and may eventually require costly surgical revision (3 or 4 revisions being not uncommon for a single patient).
The most common complications are aseptic prosthesis loosening [see for example H.
Malchau et al., Acta Orthop. Scand. 64 (1993) 497-506; R.D. Mulroy Jr. and W.H. Harris, J. Bone Joint Surg. (Br) 72-B (1990) 757-760; M. Winter et al., Clin. Orthop.
Rel.
Research 282 (1992) 73-80] and migration of the prosthesis through bone without overt loosening [see for example B.B. Wroblewski and P.D. Siney, Clin. Orthop. Rel.
Research 285 (1992) 45-47; M. Winter et al., loc. cit.]. These complications result in considerable morbidity, such as pain and reduced mobility. They occur with both cemented and uncemented, prostheses, regardless of design, material or coating.
Previous approaches to prevent these complications have concentrated on alterations to the design of the prosthesis and the selection of different materials for its construction [see for example H. Malchau et al., loc. cit.; R.D. Mulroy Jr. and W.H. Harris, loc.
cit.; M. Winter et al., loc. cit.; B.B. Wroblewski and P.D. Siney, loc. cit.; J. Wilson-MacDonald et al., J.
Bone Joint Surg. (Br) 72-B (1990) 423-430]. Apart from some preliminary research with non-steroidal anti-inflammatory drugs [A. Ohlin and U.H. Lerner, Bone and Mineral 20 (1993) 67-78; J.H. Herman et al., J. Rheumatol. 21 (1994) 338-343], a pharmacological approach to prevent or treat the complications of arthroplasty, especially hip arthroplasty, has not been successful.
Methanebisphosphonic acid derivatives, in particular bisphosphonate compounds (_ bisphosphonates), are used clinically to inhibit excessive bone resorption in a variety of diseases such as tumour-induced osteolysis, Paget's disease and osteoporosis [H. Fleisch, Handbook of Expl. Pharmacol. 83 (1988) 441-465j. Radiolabelled bisphosphonates are also used diagnostically to identify sites of high bone turnover [B.D. Collier et al., J. Nucl.
Med. 34 (1993) 2241-2246; I. Fogelman et al., J. Nucl. Med. 34 (1993) 2247-2252].

In the orthopaedic field in general, there is a strong prejudice against using bisphosphonates. Firstly, attempts to use the commercially available bisphosphonate etidronate in the prevention of heterotopic ossification -which is another complication after arthroplasty but is very different from prosthesis loosening and prosthesis migration - proved either ineffective, or even detrimental due to a rebound effect [see for example D.E. Garland, Clin. Orthop.
Rel. Research 263 (1991) 13-29; B.J. Thomas and H.C. Amstutz, The Hip 1987, 59-69; B.J. Thomas, Orthop.
Clin. North America 23 (1992) 347-358].
Furthermore, there is increasing evidence that some bisphosphonates may inhibit bone formation and mineralization. Kanis, for example, teaches in Lancet 1984, 27-33 that bisphosphonates, as inhibitors of bone resorption, may delay the repair of microfractures by reducing the rate of remodelling. As another example, Reid et al. in Lancet 1988, 143-146 found that bisphosphonate treatment, in this particular case done with disodium pamidronate, caused a reduction in bone formation and a very low rate of bone turnover which raised the possibility of impaired microfracture repair. Adamson et al. [Lancet 342 (1993) 1459-1460) reports that pamidronate may inhibit bone mineralization in Paget's disease.
Surprisingly, it has now been found that certain methanebisphosphonic acid derivatives are useful for the cost-effective prevention or treatment of these complications of joint replacement, especially hip replacement, in mammals including man.

-2a-According to ore aspect of the present invention, there is provided use of 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, in manufacture of a pharmaceutical composition for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.
According to another aspect of the present invention, there is provided use of 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.
According to yet another aspect of the present invention, there is provided 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.
According to still another aspect of the present invention, there is provided a pharmaceutical composition comprising 1-hydroxy-2-(imidazol-1-yl)ethane-l,l-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier, diluent or excipient, for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.
This can be demonstrated by appropriate in vitro and in vivo tests. In particular, in vivo experiments show that the bisphosphonates according to the invention are effective in preventing prosthesis loosening in the treated animals, e.g. sheep. This is demonstrated, for example, by the following test methods: 12 adult female sheep, approx.

-2b-50 kg body weight, are randomly divided into 2 groups of 6 animals and all undergo a unilateral total hip replacement operation with implantation of a titanium prosthesis. Immediately after surgery one group of animals receives an i.v. infusion of bisphosphonate and the other group receives saline. This treatment may be subsequently repeated, for example at 4 and 8 weeks. At regular monthly intervals the hip and femoral region of each animal is subjected to both standard and quantitative digital radiography to assess changes in bone density around the prosthesis as an early indicator of prosthesis loosening.
In addition the animals are walked over a Kistler force plate to measure vertical ground reaction force from both hind limbs to determine limb functionality and, indirectly, pain. At 12 months after the operation, and 2 weeks prior to sacrifice, the animals receive a double injection, days apart, of the fluorescent bone label oxytetracycline to facilitate histomorphometric analysis. At the end of the labelling period the animals are killed and the femurs with the implants are removed for post-mortem analysis. Precision sections, cut and polished from the femurs, are subjected to microradiography to determine bone loss around the implant.
Similar sections are also analyzed by histomorphometry to assess bone resorption and formation at the tissue level. Finally sections of bone containing the implant are subjected to a mechanical "push-out" test on a materials testing machine to measure the strength of bonding between the metal implant and the surrounding bone.
A comparison of the test animals treated with a bisphosphonate according to the invention with the controls clearly shows that bisphosphonate treatment is beneficial to prevent and treat prosthesis loosening.
The invention therefore relates to the use of a methanebisphosphonic acid derivative selected from 3-amino-1-hydroxypropane-1,1-diphosphonic acid (pamidronic acid), e.g.
pamidronate;
3-(N,N-dimethylamino}-1-hydroxypropane-1,1-diphosphonic acid, e.g. dimethyl-APD;

4-amino-1-hydroxybutane-1,1-diphosphonic acid (alendronic acid), e.g.
alendronate;
6-amino-1-hydroxyhexane-1,1-diphosphonic acid, e.g. amino-hexyl-BP; 3-(N-methyl-N-n-pentylamino)-1-hydroxypropane-l,l-diphosphonic acid, e.g. methyl-pentyl-APD (_ BM 21.0955); 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid; 1-hydroxy-2-(3-pyridyl)ethane-1,1-diphosphonic acid (risedronic acid), e.g. risedronate, including N-methyl pyridinium salts thereof, for example N-methyl pyridinium iodides such as NE-10244 or NE-10446; 1-(4-chlorophenylthio)methane-1,1-diphosphonic acid (tiludronic acid), e.g. tiludronate; 3-[N-(2-phenylthioethyl)-N-methylamino]-1-hydroxypropane-1,1-diphosphonic acid; 1-hydroxy-3-(pyrrolidin-1-yl)propane-1,1-diphosphonic acid, e.g.
EB 1053 (Leo); I-(N-phenylaminothiocarbonyl)methane-1,1-diphosphonic acid, e.g. FR
78844 (Fujisawa); 5-benzoyl-3,4-dihydro-2H-pyrazole-3,3-diphosphonic acid tetraethyl ester, e.g. U-81581 (Upjohn); 1-hydroxy-2-(imidazo[1,2-a]pyridin-3-yl)ethane-l,l-diphosphonic acid, e.g. YM 529; and 1,1-dichloromethane-1,1-diphosphonic acid (clodronic acid), e.g. clodronate; or a pharmaceutically acceptable salt thereof, or any hydrate thereof, (for the manufacture of a pharmaceutical composition) for the prevention and treatment of prosthesis loosening and prosthesis migration in mammals including man.
As already mentioned above, prosthesis loosening and prosthesis migration often occurs as a complication after arthoplasty. Arthroplasty means a partial, e.g. hemi, or total ar2hroplasty of any joint, especially hip and knee, and in particular hip.
Pharmaceutically acceptable salts are preferably salts with bases, conveniently metal salts derived from groups Ia, Ib, IIa and IIb of the Periodic Table of the Elements, including alkali metal salts, e.g. potassium and especially sodium salts, or alkaline earth metal salts, preferably calcium or magnesium salts, and also ammonium salts with ammonia or organic amines.
Especially preferred pharmaceutically acceptable salts are those where one, two, three or four, in particular one or two, of the acidic hydrogens of the bisphosphonic acid are replaced by a pharmaceutically acceptable canon, in particular sodium, potassium or ammonium, in first instance sodium.
A very preferred group of pharmaceutically acceptable salts is characterized by having one acidic hydrogen and one pharmaceutically acceptable canon, especially sodium, in each ofthe phosphonic acid groups.
All the methanebisphosphonic acid derivatives mentioned above are well known from the literature. This includes their manufacture (see e.g. EP-A-513 760, pp. 13-48). For example, 3-amino-1-hydroxypropane-1,1-diphosphonic acid is prepared as described e.g.
in US patent 3,962;432 as well as in US patents 4,639,338 and 4,711,880, and 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid is prepared as described e.g. in US patent 4,939,130.
A particular embodiment of the invention is represented by the use of a methane-bisphosphonic acid derivative which is selected from 3-amino-1-hydroxypropane-1,1-diphosphonic acid, 3-(N,N-dimethylamino)-1-hydroxypropane-1,1-diphosphonic acid, 4-amino-1-hydroxybutane-1,1-diphosphonic acid, 6-amino-1-hydroxyhexane-1,1-diphos-phonic acid,3-(N-methyl-N-n-pentylamino)-1-hydroxypropane-1,1-diphosphonic acid, 1-hydroxy-2-{imidazol-1-yl)ethane-1,1-diphosphonic acid; 1-hydroxy-2-(3-pyridyl)ethane-1,1-diphosphonic acid, and N-methyl pyridinium salts thereof; 1-(4-chloro-WO 95/30421 21 ~ 3 7 6 4 -S-phenylthio)methane-1,1-diphosphonic acid, 3-[N-(2-phenylthioethyl)-N-methylamino]-1-hydroxypropane-1,1-diphosphonic acid; 1-hydroxy-3-(pyrrolidin-I-yl)propane-1,1-diphosphonic acid,l-{N-phenylaminothiocarbonyl)methane-1,1-diphosphonic acid, 5-benzoyl-3,4-dihydro-2H-pyrazole-3,3-diphosphonic acid tetraethyl ester, 1-hydroxy-2-(imidazo[1,2-a]pyridin-3-yl)ethane-1,1-diphosphonic acid, a pharmaceutically acceptable salt thereof, and any hydrate thereof.
A preferred embodiment of the invention is represented by the use of a methane-bisphosphonic acid derivative which is selected from 3-amino-1-hydroxypropane-1,1-diphosphonic acid, 3-(N,N-dimethylamino)-1-hydroxypropane-1,1-diphosphonic acid, 4-amino-1-hydroxybutane-1,1-diphosphonic acid,6-amino-1-hydroxyhexane-1,1-diphos-phonic acid, 3-{N-methyl-N-n-pentylamino)-1-hydroxypropane-1,1-diphosphonic acid, 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid; I-hydroxy-2-(3-pyridyl)ethane-1,1-diphosphonic acid, 3-[N-(2-phenylthioethyl)-N-methylamino]-1-hydroxypropane-1,1-diphosphonic acid; 1-hydroxy-3-(pyrrolidin-I-yl)propane-1,1-diphosphonic acid, 1-hydroxy-2-(imidazo[1,2-a]pyridin-3-yl)ethane-1,1-diphosphonic acid, a pharmaceutically acceptable salt thereof, and any hydrate thereof.
A very preferred embodiment of the invention is represented by the use of a methane-bisphosphonic acid derivative which is selected from pamidronic acid, alendronic acid, 3-(N-methyl-N-n-pentylamino)-I-hydroxypropane-1,1-diphosphonic acid, 1-hydroxy-(imidazol-1-yl)ethane-1,1-diphosphonic acid,risedronic acid and tiludronic acid, a pharmaceutically acceptable salt thereof, and any hydrate thereof.
An especially preferred embodiment of the invention is represented by the use of a methanebisphosphonic acid derivative which is selected from I-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid and 3-amino-1-hydroxypropane-1,1-diphosphonic acid,a pharmaceutically acceptable salt thereof, and any hydrate thereof.
Further the invention relates to the use of 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphos-phonic acid or a pharmaceutically acceptable salt thereof or any hydrate thereof.
Further the invention relates to the use of 3-amino-1-hydroxypropane-l, l-diphosphonic acid or a pharmaceutically acceptable salt thereof or any hydrate thereof.
The pharmaceutically useful methanebisphosphonic acid derivatives may be used in the R'O 95130421 PGT/1895/00288 form of a possible isomer or of a mixture of isomers, typically as optical isomers such as enantiomers or diastereoisomers or geometric isomers, typically cis-trans isomers. The optical isomers are obtained in the form of the pure antipodes and/or as racemates.
The pharmaceutically useful methanebisphosphonic acid derivatives can also be used in the form of their hydrates or include other solvents used for their crystallisation.
The methanebisphosphonic acid derivative is preferably used in the form of a pharmaceutical preparation that contains a therapeutically effective amount of the active ingredient optionally together with or in admixture with inorganic or organic, solid or liquid, pharmaceutically acceptable carriers which are suitable for administration.
The pharmaceutical compositions may be, for example, compositions for enteral, such as oral, rectal, aerosol inhalation or nasal administration, compositions for parenteral, such as intravenous or subcutaneous administration, or compositions for transdermal administration (e.g. passive or iontophoretic). Furthermore, direct local administration at the time of operation comes into consideration. What is meant by the latter type of administration is the coating of the exposed bone surface to which the implant is attached, with a bisphosphonate according to the invention, for example by washing the bone surface with a bisphosphonate solution. What is not meant by this type of administration is the coating of the prosthesis with bisphosphonates.
Preferably, the pharmaceutical compositions are adapted to oral or parenteral (especially intravenous or transdermal) administration before, during or after prosthesis implantation, or to local administration during prosthesis implantation. Intravenous and oral, first and foremost intravenous, adminstration is considered to be of particular importance.
The particular mode of administration and the dosage will be selected by the attending physician taking into account the particulars of the patient, especially age, weight, life style, activity level, hormonal status (e.g. post-menopausal), bone mineral density and type of prosthesis to be implanted.
The dosage of the active ingredient may depend on various factors, such as effectiveness and duration of action of the active ingredient, mode of administration, warm-blooded species, andlor sex, age, weight and individual condition of the warm-blooded animal.

-7_ Normally the dosage is such that a single dose of from 0.002 - 3.40 mg/kg, especially 0.01 - 2.40 mg/kg, is administered to a warm-blooded animal weighing approximately 75 kg. If desired, this dose may also be taken in several, optionally equal, partial doses.
"mglkg" means mg drug per kg body weight of the mammal - including man - to be treated.
The dose mentioned above - either administered as a single dose (which is preferred) or in several partial doses - may be repeated, for example once daily, once weekly, once every month, once every three months, once every six months or once a year. In other words, the pharmaceutical compositions may be administered in regimens ranging from continuous daily therapy to intermittent cyclical therapy.
Preferably, the methanebisphosphonic acid derivatives are administered in doses which are in the same order of magnitude as those used in the treatment of the diseases classically treated with methanebisphosphonic acid derivatives, such as Paget's disease, tumour-induced hypercalcaemia or osteoporosis. In other words, preferably the methanebisphosphonic acid derivatives are administered in doses which would likewise be therapeutically effective in the treatment of Paget's disease, tumour-induced hypercalcaemia or osteoporosis, i.e. preferably they are administered in doses which would likewise effectively inhibit bone resorption.
Formulations in single dose unit form contain preferably from about I % to about 90 °lo, and formulations not in single dose unit form contain preferably from about 0.1 °Jo to about 20 gb, of the active ingredient. Single dose unit forms such as capsules, tablets or dragdes contain e.g. from about 1 mg to about 500 mg of the active ingredient.
The invention further relates to the use of a composition for the manufacture of a medicament, e.g. in single dose unit form, for the prevention and treatment of prosthesis loosening and prosthesis migration in mammals including man, wherein the composition contains 0.002 - 3.40 mg/kg, especially 0.01 - 2.40 mglkg, of a methanebisphosphonic acid derivative as defined above per dosage form.
Moreover, the invention relates to the use of a methanebisphosphonic acid derivative as defined above at a dose of 0.002 - 3.40 mglkg, especially 0.01 - 2.40 mg/kg, per dosage form for the manufacture of a medicament for the prevention and treatment of prosthesis WO 9S/30421 ~' ~ ~ ~ ~ ~ PCT11895/00288 _g_ loosening and prosthesis migration in mammals including man.
Pharmaceutical preparations for enteral and parenteral administration are, for example, those in dosage unit forms, such as dragBes> tablets or capsules and also ampoules. They are prepared in a manner known per se, for example by means of conventional mixing, granulating, confectioning> dissolving or lyophilising processes. For example, pharmaceutical preparations for oral administration can be obtained by combining the active ingredient with solid carriers, where appropriate granulating a resulting mixture, and processing the mixture or granulate, if desired or necessary after the addition of suitable adjuncts, into tablets or dragBe cores.
Suitable carriers are especially fillers, such as sugars, for example lactose, saccharose, mannitol or sorbitol, cellulose preparations and/or calcium phosphates, for example tricalcium phosphate or calcium hydrogen phosphate, and also binders, such as starch pastes, using, for example, com, wheat, rice or potato starch, gelatin, tragacanth, methyl-cellulose and/or polyvinylpyrrolidone and, if desired, disintegrators, such as the above-mentioned starches, also carboxymethyl starch, crosslinked polyvinylpyrrolidone, agar or alginic acid or a salt thereof, such as sodium alginate. Adjuncts are especially flow-regulating agents and lubricants, for example silicic acid, talc, stearic acid or salts thereof, such as magnesium or calcium stearate, and/or polyethylene glycol.
Drage cores are provided with suitable coatings that may be resistant to gastric juices, there being used, inter alb-concentrated sugar solutions that optionaliy contain gum arabic, talc, polyvinylpyrrolidone, polyethylene glycol andlor titanium dioxide, or lacquer solutions in suitable organic solvents or solvent mixtures or, to produce coatings that are resistant to gastric juices, solutions of suitable cellulose preparations, such as acetylcellulose phthalate or hydroxypropylmethylcellulose phthalate. Colouring substances or pigments may be added to the tablets or drage coatings, for example for the purpose of identification or to indicate different doses of active ingredient.
Other orally administrable pharmaceutical preparations are dry-filled capsules made of gelatin, and also soft, sealed capsules made of gelatin and a plasticiser, such as glycerol or sorbitol. The dry-filled capsules may contain the active ingredient in the form of a granulate, for example in admixture with fillers, such as lactose, binders, such as starches, and/or glidants, such as talc or magnesium stearate, and, where appropriate, stabilisers. In soft capsules the active ingredient is preferably dissolved or suspended in suitable liquids, such as fatty oils, paraffin oil or liquid polyethylene glycols, it being possible also for w0 95130421 PCTI1895I00288 stabilisers to be added.
Parenteral formulations are especially injectable fluids that are effective in various manners, such as intravenously, intramuscularly, intraperitoneally, intranasally, intradermally or subcutaneously. Such fluids are preferably isotonic aqueous solutions or suspensions which can be prepared before use, for example from lyophilised preparations which contain the active ingredient alone or together with a pharmaceutically acceptable carrier. The pharmaceutical preparations may be sterilised and/or contain adjuncts, For example preservatives, stabilisers, wetting agents and/or emulsifiers, solubilisers, salts for regulating the osmotic pressure and/or buffers.
Suitable formulations for transdermal application include an effective amount of the active ingredient with carrier. Advantageous carriers include absorbable pharmacologically acceptable solvents to assist passage through the skin of the host.
Characteristically, transdermal devices are in the form of a bandage comprising a backing member, a reservoir containing the compound optionally with carriers, optionally a rate controlling barrier to deliver the active ingredient of the skin of the host at a controlled and predetermined rate over a prolonged period of time, and means to secure the device to the skin.
The following Examples illustrate the invention described hereinbefore. The term "active ingredient" is to be understood as being any one of the methanebisphosphonic acid derivatives mentioned above as being useful according to the present invention.
Example 1: Capsules containing coated pellets of, for example, disodium pamidronate pentahydrate, as active ingredient:
Core pellet:
active ingredient{ground) 197.3 mg Microcrystalline cellulose 52.7 mg (Avicel~ PH 105) 250.0 mg + Inner coating:
Cellulose HP-M 603 10.0 mg Polyethylene glycol 2.0 mg ~~~1 ~3~~64 WO 95130421 PCTl1B95ID0188 Talc 8.0 mg 270.0 mg + Gastric juice-resistant outer coating:
Eudragit~ L 30 D-(solid) 90.0 mg Triethyl citrate 21.0 mg Antifoam~ AF 2.0 mg Water Talc 7.0 mg 390.0 mg A mixture of disodium pamidronate with Avicel~ PH 105 is moistened with water and kneaded, extruded and formed into spheres. The dried pellets are then successively coated in the fluidized bed with an inner coating, consisting of cellulose HP-M 603, polyethylene glycol (PEG) 8000 and talc, and the aqueous gastric juice-resistant coat, consisting of Eudragit~ L 30 D, triethyl citrate and Antifoam~ AF. The coated pellets are powdered with talc and Fzlled into capsules (capsule size 0) by means of a commercial capsule filling machine, for example Hbfliger and Karg.
Example 2: Monolith adhesive transdermal system, containing as active ingredient, for example, I-hydroxy-2-(imidazol-1-yl)-ethane-I,1-diphosphonic acid:
Composition:
polyisobutylene (PIB) 300 5.0 g (Oppanol B 1, BASF) PIB 35000 3.0 g (Oppanol B 10, BASF) P1B 1200000 -- 9.0 g (Oppanol B 100, BASF) hydrogenated hydrocarbon resin 43.0 g (Escorez 5320, Exxon) I-dodecylazacycloheptan-2-one 20.0 g (Atone, Nelson Res., Irvine/CA) active ingredient Zp~O Q
Total 100.0 g Preparation:
The above components are together dissolved in 150 g of special boiling point petroleum fraction 100-125 by rolling on a roller gear bed. The solution is applied to a polyester film (Hostaphan, Kalle) by means of a spreading device using a 300 ltm doctor blade, giving a coating of about 75 g/m2. After drying (15 minutes at 60°C), a silicone-treated polyester film (thickness 75 p,m, Iaufenberg) is applied as the peel-off film. The finished systems are punched out in sizes in the wanted form of from 5 to 30 cm2 using a punching tool.
The complete systems are sealed individually in sachets of aluminised paper.
Example 3: Vial containing 1.0 mg dry, lyophilized 1-hydroxy-2-(imidazol-1-yl}-ethane-1,1-diphosphonic acid (mixed sodium salts thereof). After dilution with 1 ml of water, a solution (concentration 1 mg/ml) for i.v. infusion is obtained.
Composition:
active ingredient (free diphosphonic acid) 1.0 mg mannitol 46.0 mg Trisodium citrate x 2 H20 ca. 3.0 mg water 1 ml water for injection 1 ml .
In 1 ml of water, the active ingredient is titrated with trisodium citrate x 2 H20 to pH 6Ø
Then, the mannitol is added and the solution is lyophilized and the lyophilisate filled into a vial.
Example 4: Ampoule containing disodium pamidronate pentahydrate dissolved in water.
The solution (concentration 3 mg/ml) is for i.v. infusion after dilution.
Composition:
active ingredient 18.73 mg 2.1.83:7 6.~
WO 95!30421 PCTlIB95/00288 ( = 15.0 mg of anhydrous active ingredient) mannitol 250 mg water for injection 5 ml .
Example 5: Tablets each containing 50 mg of 3-[N-(2-phenylthioethyl)-N-methylamino]-1-hydroxypropane-1,1-diphosphonic acid can be prepared as follows:
Composition (10,000 tablets) Active ingredient 500.0 g Lactose 500.0 g Potato starch 325.0 g Gelatin 8.0 g Talc 60.0 g Magnesium stearate 10.0 g Silicon dioxide (finely divided)20.0 g Ethanol q.s.

The active ingredient is mixed with the lactose and 292 g of potato starch, and the mixture is moistened with an ethanolic solution of the gelatin and granulated through a sieve. After the granules have dried, the remainder of the potato starch, the magnesium stearate and the silicon dioxide are admixed and the mixture compressed to give tablets each weighing 145.0 mg and containing 50.0 mg of active ingredient, which can, if desired, be provided with breaking grooves to enable the dosage to be more finely adjusted.

Claims (24)

CLAIMS:

1. ~Use of 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, in manufacture of a pharmaceutical composition for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.

2. ~Use according to claim 1, wherein the mammal is a human.

3. ~Use according to claim 1 or 2, wherein the prosthesis is a hip prosthesis.

4. ~Use according to any one of claims 1 to 3, wherein the pharmaceutical composition is in a form adapted for intravenous administration.

5. ~Use according to any one of claims 1 to 3, wherein the pharmaceutical composition is in a form adapted for transdermal administration.

6. ~Use according to any one of claims 1 to 3, wherein the pharmaceutical composition is in a form adapted for oral administration.

7. ~Use of 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.

8. ~Use according to claim 7, wherein the mammal is a human.

9. ~Use according to claim 7 or 8, wherein the prosthesis is a hip prosthesis.

10. Use according to any one of claims 7 to 9, wherein the 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, is in a form adapted for intravenous administration.

11. Use according to any one of claims 7 to 9, wherein the 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, is in a form adapted for transdermal administration.

12. Use according to any one of claims 7 to 9, wherein the 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, is in a form adapted for oral administration.

13. 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.

14. The 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, according to claim 13, wherein the mammal is a human.

15. The 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, according to claim 13 or 14, wherein the prosthesis is a hip prosthesis.

16. The 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, according to any one of claims 13 to 15 in a form adapted for intravenous administration.

17. The 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, according to any one of claims 13 to 15 in a form adapted for transdermal administration.

18. The 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or the salt or hydrate thereof, according to any one of claims 13 to 15 in a form adapted for oral administration.

19. A pharmaceutical composition comprising 1-hydroxy-2-(imidazol-1-yl)ethane-1,1-diphosphonic acid, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier, diluent or excipient, for prevention or treatment of prosthesis loosening or prosthesis migration in a mammal.

20. The pharmaceutical composition according to claim 19, wherein the mammal is a human.

21. The pharmaceutical composition according to claim 19 or 20, wherein the prosthesis is a hip prosthesis.

22. The pharmaceutical composition according to any one of claims 19 to 21, in a form adapted for intravenous administration.

23. The pharmaceutical composition according to any one of claims 19 to 21, in a form adapted for transdermal administration.

24. The pharmaceutical composition according to any one of claims 19 to 21, in a form adapted for oral administration.