CA2216634C

CA2216634C - Synergistic combinations of zidovudine, 1592u89 and 3tc or ftc

Info

Publication number: CA2216634C
Application number: CA002216634A
Authority: CA
Inventors: David Walter Barry; Martha Heider St. Clair
Original assignee: Wellcome Foundation Ltd
Current assignee: ViiV Healthcare UK Ltd
Priority date: 1995-03-30
Filing date: 1996-03-28
Publication date: 2004-07-20
Anticipated expiration: 2016-03-28
Also published as: CN1103593C; NO974510D0; EP0817637A1; NL300195I1; TR199701074T1; ES2179193T3; PL322532A1; DK0817637T3; KR19980703420A; DE122005000029I2; IL117727A0; BRPI9607851B8; NO2005014I1; AU715213B2; ATE220551T1; JP2954357B2; KR100542536B1; CN1185110A; EP0817637B1; EA199700203A1

Abstract

The present invention relates to therapeutic combinations of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol (1592U89), 3'-azido-3'-deoxythymidine (zidovudine) and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one (3TC) (or, alternatively to 3TC, (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one (FTC)) which have anti-HIV activity. The present invention is also concerned with pharmaceutical compositions containing said combinations and their use in the treatment of HIV infections including infections with HIV mutants bearing resistance to nucleoside and/or non-nucleoside inhibitors.

Description

SYNERGISTIC COMBINATIONS OF ZIDOVUDINE, 1592089 AND 3TC OR FTC
The present invention relates to therapeutic combinations of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol (1592089), 3'-azido-3'-deoxythymidine (zidovudine) and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one (3TC) (or, alternatively to 3TC, (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1 H)-pyrimidin-2-one (FTC)) which have anti-HIV activity. The present invention is also concerned with pharmaceutical compositions containing said combinations and their use in the treatment of HIV infections including infections with HIV mutants bearing resistance to nucleoside and/or non-nucleoside inhibitors.
Zidovudine is now well established as an important and useful chemotherapeutic agent for the treatment andJor prophylaxis of HIV-infections including related clinical conditions such. as AIDS, AIDS-related complex (ARC), AIDS dementia complex (ADC) and also for the treatment of patients who have an asymptomatic HIV infection or who are-anti-HIV.antibody-positive: Treatment with zidovudine prolongs~the~disease--free interval in asymptomatic patients infected with HIV and delays death in symptomatic patients.
Following the widespread clinical use of zidovudine in the treatment of such infections and conditions, it has been observed that in certain instances following prolonged treatment, the virus may develop a certain level of resistance to zidovudine and therefore a loss of sensitivity to the drug.
The therapeutic agent 1592089 (European Specification EP0434450) is a promising anti-HIV chemotherapeutic candidate (International Conference on Antiviral Research 23rd April 1995) showing potent activity against H1V, low cytotoxicity and excellent penetration into the brain, which is important for tf~e treatment of AIDS and HIV
linked central nervous system conditions such as ADC.

Nucleoside analogues containing an oxathiolane residue in place of the sugar residue, for example, nucleosides described in European Patent Specification No. 382526 particularly 4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one(BCH-189) have been found to have anti-HIV activity. BCH-189 is a racemic mixture and although the enantiomers are equipoter~t against H1V the (-)-enantiomer has considerably lower cytotoxicity than the (+)-enantiomer. The (-)-enantiomer has the chemical name (2R,cis)-4-amino-1-~(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1 H)-pyrimidin-2-one, now known as 3TC (Trade-mark) or laanivudirie:
An alternative oxathiolane~ nucleoside analogue is described in International Specification Number W092/14743 (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3 oxathiolan-5-yl)-(1 H)-pyrimidine-2-one, commonly referred to as FTC or 524W91.
To date the treatment of HIV infection has relied to a large extent upon monotherapy with nucleoside reverse transcriptase inhibitors such as zidovudine, didanosine (ddl), zalcitabine (ddC) and stavudine (D4T). However, these drugs eventually become less effective due either to the emergence of HIV resistant mutants or because of toxicity.
Thus, new therapies are needed.
The combination of zidovudine with either ddC or ddl has shown promising results in HIV infected patients (New Eng. J. Med. 1992, 329(9) 581-587, and Program Abstract 1993 9R International Conference an AIDS, abstract US-B25-1). The combination of zidovudine and 3TC has also been studied and widely reported. However, itahould be noted that these results are surprising because drugs with the same site of action are frequently antagonistic or additive (Rev Infect. Dis 1982, 4, 255-260).
Unexpectedly, it has now been found that by combining 1592U89, zidovudine and a synergistic anti-HIV effect is achieved. The result is surprising since all three drugs act upon the same molecule, HIV Reverse Transcript use. It is a feature of this invention that the use of this drug combinations will provide synergistic antiviral effects, more complete viral suppression, viral suppression aver a longer period, limit ' PB1618 the emergence of drug resistant HIV mutants and allow better management of drug-related toxicities.
As an alternative to 3TC the compound FTC may be used.
Thus, according to one aspect, the present invention provides a combination comprising 1592U89 or a physiologically functional derivative thereof, zidovudine or a physiologically functional derivative thereof and 3TC (or, alternatively to 3TC, FTC) or a physiologically functional derivative thereof.
3TC and 1592U89 will normally be provided substantially free of the corresponding enantiomer, that is to say, no more than about 5% w/w of the corresponding enantiomer, preferably no more than about 2% w/w, in particular less than 1 % w/w will be present.
As used herein, the term "physiologically functional derivative" includes any physiologically acceptable salt, ether, ester, salt of such ester of 1592U89, zidovudine or 3TC; or solvates of any thereof and their physiologically functional derivatives; or any other compound which upon administration to the recipient, is capable of providing (directly or indirectly) such a compound or an antivirally active metabolite or residue thereof.
Preferred esters in accordance with the. invention are independently selected from the following group: (1) carboxylic acid esters in which the non-carbonyl moiety of the carboxylic acid portion of the ester grouping is selected from straight or branched chain alkyl (for example, methyl, n-propyl, t-butyl, or n-butyl), cycloalkyl, alkoxyalkyl (for example, methoxymethyl), aralkyl (for example, benzyl), aryloxyalkyl (for example, phenoxymethyl), aryl (for example, phenyl optionally substituted by, for example, _ halogen, C~ _4 alkyl, or C~ _4 alkoxy), or amino; (2) sulphonate esters, such as alkyl- or , aralkylsulphonyl (for example, methanesulphonyl); (3) amino acid esters (for example, L-valyl or L-isoleucyl); and (4) phosphonate esters. In such esters, unless otherwise specified, any alkyl moiety present advantageously contains from 1 to 18 carbon atoms, particularly from 1 to 6 carbon atoms, more particularly from 1 to 4 carbon atoms. Any cycloalkyl moiety present in such esters advantageously contains from 3 to 6 carbon atoms. Any aryl moiety present in such esters advantageously comprises a phenyl group. Any reference to any of the above compounds also includes a reference to a physiologically acceptable salt thereof.
Particularly preferred esters are the mono-, di-, and tri-phosphate esters of zidovudine, 3TC (which may be optionally blocked) or FTC or any other compound which upon administration to a human subject is capable of providing (directly or indirectly) said mono-, di, or triphosphate ester.
A preferred derivative of 1592089 is the-tai-phosphate ester of (-) carbovir.
Examples of physiologically acceptable salts of 1592089, zidovudine or 3TC and their physiologically acceptable derivatives include salts derived from an appropriate base, such as an alkali metal (for example, sodium), an alkaline earth (for example, magnesium), ammonium and NX4+ (wherein X is C1-4 alkyl). Physiologically acceptable salts of an hydrogen atom or an amino group include salts of organic carboxylic acids such as acetic, lactic, tartaric, malic, isethionic, lactobionic and succinic acids, organic sulphonic acids, such as methanesulphonic, ethanesulphonic, benzenesulphonic and p-toluenesulphonic acids and inorganic acids, such as hydrochloric, sulphuric, phosphoric and sulphamic acids. Physiologically acceptable salts of a compound 'of an hydroxy group include the anion of said compound in combination with a suitable cation such as Na+, NHq.+ and NX4t (wherein X is a C~-4 T
alkyl group).
For therapeutic use, salts of 1592089, zidovudine and 3TC will be physiologically acceptable, i.e. they will be salts derived from a physiologically acceptable acid or base. However, salts of acids or bases which are not physiologically acceptable may also find use, for example, in the preparation or purification of a physiologically acceptable compound. All salts, whether or not derived form a physiologically acceptable acid or base, are within the scope of the present invention.
A preferred salt of 1592089 is the succinate salt.
Combinations of 1592089 or a physiologically functional derivatwe thereof, zidovudine or a physiologically functional derivative thereof and 3TC or a physiologically functional derivative thereof may hereinafter be referred to as combinations according to the invention.
The present invention further provides combinations according to the invention for use in therapy, particularly in the treatment and/or prophylaxis of an HIV
infection including infections with HIV mutants bearing resistance to nucleoside inhibitors, particularly zidovudine, 3TC, FTC, ddl, ddC or D4T or combinations thereof and non-nucleoside inhibitors such as Nevirapine (BI-RG-587), Loviride (oc-APA) and Delavuridine (BHAP). Furthermore, the combinations according.to the invention are especially useful for the treatment of AIDS and related clinical conditions such as AIDS
related complex (ARC), progressive generalised lymphadenopathy (PGL), Kaposi's sarcoma, thrombocytopenic purpura, AIDS-related neurological conditions such as AIDS dementia complex, multiple sclerosis or tropical paraperesis, and also anti-HIV
antibody-positive and HIV-positive conditions, including such conditions in asymptomatic patients.
According to another aspect, the present invention provides a method for the treatment or prevention of the symptoms or effects of an.HIV infection in an infected animal, for example, a mammal including a human, which comprises treating said animal with a therapeutically effective amount of a combination of 1592089, zidovudine and 3TC (or, alterantively to 3TC, FTC) or a physiologically functional derivative of any thereof.

It will be appreciated that the compounds of the combination may be administered simultaneously, either in the same or different pharmaceutical formulation or sequentially. If there is sequential administration, the delay in administering the second and third active ingredient should not be such as to lose the benefit of a synergistic therapeutic effect of the combination of the active ingredients.
It will also be understood that 1592089, zidovudine and 3TC (or, alternatively to 3TC, FTC), or the physiologically functional derivatives of any thereof, whether presented simultaneously or sequentially, may be administered individually or in multiples or in any combination thereof. 1592089, zicJovudine and 3TC (or, alternatively to 3TC, FTC), are preferably administered simultaneously or sequentially in separate pharmaceutical formulations, most preferably simultaneously.
The present invention also provides the use of 1592089 in the manufacture of a medicament for administration simultaneously or sequentially with zidovudine and 3TC (or, alternatively to 3TC, FTC), respectively for the treatment and/or prophylaxis of HIV infections and associated clinical conditions hereinbefore described. It will be appreciated that 1592089, zidovudine or 3TC (or, alternatively to 3TC, FTC), or any combination thereof may be used in the manufacture of the above medicament.
The synergistic effects of the combination of 1592089, zidovudine and 3TC (or, alternatively to 3TC, FTC), or a physiologically functional derivative of any thereof are seen over a ratio, for example, of 1 to 20: 1 to 20: 1 to 10 (by weight), preferably 1 to 10: 1 to 10: 1 to 5 (by weight), particularly 1 to 3: 1 to 3: 1 to 2 (by weight) Conveniently each compound will be employed in the combination in an amount at which it exhibits antiviral activity when used alone.
The amount of a combination of 1592089, zidovudirre and 3TC (or, alternatively to 3TC, FTC), required to be effective as an anti-HIV agent will, of course, vary and is ultimately at the discretion of the medical practitioner. The factors to be considered include the route of administration and nature of the formulation, the animal's body weight, age and general condition and the nature and severity of the disease to be treated. .
In general a suitable dose of 1592U89 for administration to a human for treatment of an HIV infection will be in the range of 0.1 to 100 mg per kilogram body weight of the recipient per day, preferably in the range of 0.5 to 50 mg per kilogram body weight per day and most preferably in the range 7 to 30 mg per kilogram body weight per day.
In general a suitable dose of zidovudine will be in the range of 3 to 120 mg per kilogram body weight of the recipient per day, preferably in the range of 6 to 90 mg per kilogram body weight per day and most preferably in the range 10 to 30 mg per kilogram body weight per day.
For 3TC a suitable daily dose will be in the range of from about 0.1 to about 120 mg per kilogram body weight of the recipient per day, preferably in the range of 0.5 to 75 mg per kilogram body weight per day, most preferably in the range of 1 to 40 mg per kilogram body weight per day, such as 5 to 10 mg per kilogram body weight per day.
For FTC a suitable daily dose will be in the range of from about 0.1 to about 120 mg per kilogram body weight of the recipient per day, preferably in the range of 0.5 to 75 mg per kilogram body weight per day, most preferably in the range of 1 to 40 mg per kilogram body weight per day, such as 5 to 10 mg per kilogram body weight per day.
Unless otherwise indicated all weights of active ingredients are calculated in terms of the drug er se. In the case of a physiologically functional derivative of 1592U89, zidovudine, 3TC (or, alternatively to 3TC, FTC), (or, alternatively to 3TC, FTC), or a solvate of any thereof the figures would be increased proportionately. The desired dose is preferably presented as two, three, four, five, six or more sub-doses administered at appropriate intervals throughout the day. These sub-doses may be administered in unit dosage forms, for example, containing from 1 to 1500 mg, preferably from 5 to 1000 mg, most preferably from i0 to 700 mg of active ingredient per unit dosage form. Alternatively, if the condition of the recipient so requires, the dose may be administered as a continuous infusion.
The components of the combination which may be referred to as active ingredients may be administered for therapy to an animal e.g. a mammal including a human in a conventional manner.
While it is possible for the active ingredients of the combination to be administered as the raw chemical it is preferable to present them as a pharmaceutical formulation.
Pharmaceutical formulations according to the present invention comprise a combination according to the invention together with one or more pharmaceutically acceptable carriers or excipients and optionally other therapeutic agerrts.
The carriers) must be acceptable in the sense of being compatible with the other ingredients of the formula and not deleterious to the recipient thereof. When the individual components of the combinatiori are administered separately they are generally each presented as a pharmaceutical formulation. The references hereinafter to formulations refer unless otherwise stated to formulations containing either the combination or a component thereof.
A combination of 1592U89, zidovudine and 3TC (or, alternatively to 3TC, FTC), or a physiologically functional derivative of any thereof may conveniently be presented as a pharmaceutical formulation in a unitary dosage form. A convenient unitary dosage formulation contains the active ingredients in amounts of from 50 mg to 3g each, for example, 100mg to 2g.
It is also possible to combine any two of the active ingredients in a unitary dosage form for simultaneous or sequential administration with the third.active ingredient, for example, a typical unitary dosage may contain 50mg to 3g each of zidovudine and 3TC, preferably 100mg to 2g each of zidovudine and 3TC or 50mg to 3g each of zidovudine and 159208983, preferably 100mg to 2g each of zidovudine and 159208983.
As a further feature of the present invention presented is a unitary dosage form comprising at least two active ingredients selected from zidovudine, 1592089 and 3TC
(or, alternatively to 3TC, FTC) or physiologically functional derivatives of any thereof and a pharmaceutically acceptable carrier therefore.
It will be appreciated that the administration of two active compounds selected from zidovudine, 159089 and 3TC (or, alternatively to 3TC, FTC), is an essential part of the invention, preferably as a prelude to the remaining third active ingredient being administered. The combinations of 1592089 and zidovudine, 1592089 and 3TC, and 1592089 and FTC are prefered, in particular the combination of 1592089 and zidovudine.
In addition we have found that when the compounds described above are combined a synergistic effect is also found.
As yet a further feature of the present invention presented is a combination comprising two compounds selected from zidovudine, 1592089 and 3TC (or, alternatively to 3TC, FTC) provided that the two compounds are not zidovudine and 3TC. Preferably the combination is administered simultaneously or sequentially with the third remaining compound.
More commonly these days pharmaceutical formulations are prescribed to the patient in "patient packs" containing the whole course of treatment in a single package, usually a blister pack. Patient packs have an advantage over traditional prescriptions, where a pharmacists divides a patients supply of a pharmaceutical from a bulk supply, in that the patient always has access to the package insert contained in the patient pack, normally missing in traditional prescriptions. The inclusion of a package insert has been shown to improve patient compliance with the physicians instructions.

It will be understood that the administration of the combination of the invention by means of a single patient pack, or patients packs of each formulation, within a package insert diverting the patient to the correct use of the invention is a desirable additional feature of this invention.
According to a further aspect of the invention provided is a patient pack comprising of at least one active ingredient 1592089, zidovudine, 3TC or FTC of the combination of the invention and an information insert containing directions on the use of the combination of the invention.
According to another aspect the invention provides a triple pack comprising in association for separate administration 1592089 or a physiologically functional derivative thereof, zidovudine or a physiologically functional derivative thereof and 3TC or a physiologically functional derivative thereof.
Formulations include those suitable for oral, rectal, nasal, topical (including transdermal, buccal and sublingual), vaginal or parenteral (including subcutaneous, intramuscular, intravenous and intradermal) administration. The formulations may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art of pharmacy. Such methods represent a further feature of the present invention and include the step of bringing into association the active ingredients with the carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers or finely divided solid carriers or both, and then if necessary shaping the product.
Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules, caplets, caehets or tablets each containing a predetermined amount of the active ingredients; as a powder or granules; as a solution or a suspension in an aqueous or non-aqueous liquid; or as an oil-in-water R'O 96/30025 PCT/EP96/01352 liquid emulsion or a water-in-oil liquid emulsion. The active ingredient may also be presented as a bolus, electuary or paste.
A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing in a suitable machine the active ingredients in a free-flowing form such as a powder or granules, optionally mixed with a binder (e.g. povidone, gelatin, hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (e.g. sodium starch glycollate, cross-linked povidone, cross-linked sodium carboxymethyl cellulose) surface-active or dispersing agent. Molded tablets may be made by molding a mixture of the powdered compound moistened with an inert liquid diluent in a suitable machine. The tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active ingredients therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile. Tablets may optionally be provided with an enteric coating, to provide release in parts of the gut other than the stomach.
Formulations suitable for topical administration in the mouth include lozenges comprising the active ingredients in a flavored base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert basis such as gelatin and glycerin, or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier. Formulations for rectal administration may be presented as a suppository with a suitable base comprising, for example. cocoa butter or a salicylate.
Topical administration may also be by means of a transdermal iontophoretic device.
Formulations suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or spray formulations containing in addition to the active ingredient such carriers as are known in the art to be appropriate.

Pharmaceutical formulations suitable for rectal administration wherein the carrier is a solid are most preferably presented as unit dose suppositories. Suitable carriers include cocoa butter and other materials commonly used in the art. The suppositories may be conveniently formed by admixture of the active combination with the softened or melted carriers) followed by chilling and shaping in moulds.
Formulations suitable for parenteral administration include aqueous and nonaqueous isotonic sterile injection solutions which may contain anti-oxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents; and liposomes or other microparticulate systems which are designed to target the compound to blood components or one or more organs. The formulations may be presented in unit-dose or multi-dose sealed containers, far example, ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example water for injection, immediately prior to use.
Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.
Preferred unit dosage formulations are those containing a daily dose.or daily subdose of the active ingredients, as hereinbefore recited, or an appropriate fraction thereof.
It should be understood that in addition to the ingredients particularly mentioned above the formulations of this invention may include other agents conventional in the art having regard to the type of formulation in question, for example, those suitable for oral administration may include such further agents as sweeteners, thickeners and flavoring agents.
The compounds of the combination of the present invention may be obtained in a conventional manner. Zidovudine can be prepared, for example, as described in U.S. Patent 4724232, Zicbvudine can ~~ ~ d f~ ~~.ich Chemical Co:, Milwaukee, WI 53233, I3SA:

1592089 may be prepared by the method described in European Specification EP0434450 or PCT application PCT/GB/4500225;
Methods for the preparation of 3TC are described in International Patent Application No. W091/17159 Methods for the preparation of FTC are described in International Patent Application No. W092/14743 The following examples are intended for illustration only and are not intended to limit the scope of the invention in any way. "Active ingredient" denotes 1592089, zidovudine, 3TC (or, alternatively to 3TC, FTC), or multiples thereof or a physiologically functional derivative of any of the aforementioned compounds.
Example 1: Tablet Formulation The following formulations A, B and C are prepared by wet granulation of the ingredients with a solution of povidone, followed by addition of magnesium stearate and compression.
Formulation A
m /_~q tablet Active Ingredient 250 Lactose B.P. 210 Povidone B.P. 15 Sodium Starch Glycollate 20 Magnesium Stearate 5 r__~..~_..~__ n mgJtablet Active Ingredient 250 Lactase B.P. 150 Avicel PH 701 ~ 60 Povidone B.P. 15 Sodium Starch Glycollate 20 Magnesium Stearate 5 L....~..L.i:_- !~
m /-'tablet Active Ingredient 250 Lactose B.P. 200 Starch 50 Povidone 5 Magnesium Stearate 4 The following formulations, D and E, are prepared by direct compression of the admixed ingredients. The lactose in formulation E is of the direct compression type (Dairy Crest - "Zeparox"~ ~a~,~.k~4 c......,.. . ~....:.... n mg/tablet Active Ingredient 250 Pregelatinized Starch NF15 150 r..._.r..~_~:__ r mq/tablet Active Ingredient 250 Lactose B.P. 150 Avicel 100 Formulation F (Controlled Release Formulation) The formulation is prepared by wet granulation of the ingredients with a solution of povidone followed by the addition of magnesium stearate and compression.
mq/tablet Active Ingredient 500 Hydroxypropylmethylcellulose 112 (Methocel K4M Premium) Lactose B.P. 53 Povidone B.P. 2g a Magnesium Stearate 7 R'O 96/30025 PCT/EP96/01352 Drug release takes place over a period of about 6-8 hours and is complete after 12 hours.
Example 2: Capsule Formulations _ __ "
A capsule formulation is prepared by admixing the ingredients of formulation D
in Example 1 above and filling into a two-part hard gelatin capsule. Formulation B
(infra) is prepared in a similar manner.
Cr~..~.....1.,+:..... D
mg/capsule Active ingredient 250 Lactose B.P. i 43 Sodium Starch Glycollate 25 Magnesium Stearate 2 C..-..r..i_i:__ n mq/capsule Active Ingredient 250 Macrogel 4000 B.P. 350 Capsules of formulation C are prepared by melting the Macrogel 4000 B.P., dispersing the active ingredient in the melt and filling the melt into a two-part hard gelatin capsule.
r__~..~_~:__ n mq/capsule Active Ingredient 250 Lecithin 100 Arachis Oil 100 Capsules of formulation D are prepared by dispersing the active ingredient in the lecithin and arachis oil and filling the dispersion into soft, elastic gelatin capsules.
Formulation E (Controlled Release Capsule) The following controlled release capsule -formulation is prepared by -extruding ingredients a, b, and c using an extruder, followed by spheronization of the extrudate and drying. The dried pellets are then coated with release-controlling membrane (d) and filled into a two-piece, hard gelatin capsule.
mg/capsule (a) Active Ingredient 250 (b) Microcrystalfine Cellulose 125 (c) Lactose B.P. 125 (d) Ethyl Cellulose 13 Example 3: Injectable Formulation G"..~" , ~.,+:..., n Active Ingredient 200 Hydrochloric Acid Solution 0.1 M or Sodium Hydroxide Solution 0.1 M q.s. to pH 4.0 to 7.0 Sterile water q.s. to 10 ml The active ingredient is dissolved in most of the water (35°-40°C) and the pH adjusted to between 4.0 and 7.0 with the hydrochloric acid or the sodium hydroxide as appropriate. The batch is then made up to volume with the water and filtered through a sterile micropore filter into a sterile 10 ml amber glass vial (type 1) and sealed with sterile closures and overseals.
formulation B
Active Ingredient 125 mg Sterile, Pyrogen-free, pH 7 Phosphate Buffer, q. s. to 25 ml Example 4: Intramuscular injection Active Ingredient 200 mg 8enzyl Alcohol 0.10 g Glycofurol 75 1.45 g Water for injection q.s. to 3.00 ml The active ingredient is dissolved in the glycofurol. Tf~e benzyl alcohol is then added and dissolved, and water added to 3 ml. The mixture is then filtered through a sterile micropore filter and sealed in sterile 3 ml amber glass vials (type 1).

Example 5: Syrup Active Ingredient 250 mg Sorbitol Solution 1.50 g Glycerol 2.00 g Sodium Benzoate 0.005 g Flavor, Peach 17.42.3169 0.0125 ml Purified Water q.s. to 5.00 ml The active ingredient is dissolved in a mixture of the glycerol and most of the purified water. An aqueous solution of the sodium benzoate is then added to the solution, followed by addition of the sorbital solution and finally the flavor. The volume is made up with purified water and mixed well.
Example 6: Suppository mq/capsule suppository Active Ingredient 250 Hard Fat, B.P. (Witepsol H15 - Dynamit Nobel) 1770 One-fifth of the Witepsol H15 is melted in a steam-jacketed pan at 45°C
maximum.
The active ingredient is sifted through a 200~.r.M sieve and added to the molten base with mixing, using a Silverson fitted with a cutting head, until a smooth dispersion is achieved. Maintaining the mixture at 45°C, the remaining Witepsol H15 is added to the suspension and stirred to ensure a homogenous mix. The entire suspension is passed through a 250p.m stainless steel screen and, with continuous stirring, is allowed to cool to 40°C. At a temperature of 38°C to 40°C, 2.02 g of the mixture is filled into suitable, 2 ml plastic molds. The suppositories are allowed to cool to room tem peratu re.

Example 7: Pessaries mg/pessary Active Ingredient 250 Anhydrate Dextrose 380 Potato Starch 363 Magnesium Stearate 7 The above ingredients are mixed directly and pessaries prepared by direct compression of the resulting mixture.
Biological Test Results Peak and Trough Plasma Levels The peak and trough values in micromolar concentrations used in this study came from clinically determined peak and trough plasma levels. These values were meant to reflect actual peak and trough plasma levels achieved in patients when using therapeutic doses of each drug as a single agent.
Drug Peak Level (uM) Trough Level (uM) zidovudine 5 0.4 3TC 9 0.7 1592089 3.5 0.1 FTC i 0 0.5 WO 96!30025 PCT/EP96/01352 Antiviral Activity Alone or in Combination Anti-HIV assay. The human T-cell lymphotropic virus type 1-transformed cell line MT4 was grown and .infected with HIV-1 strain 3B or strain MN (Advanced Biotechnologies Inc., Columbia, Maryland) at 10 times the amount necessary to cause a 50%
reduction of MT4 cell growth (10 X TCID50, 2 X 104 plaque forming units/cell), unless otherwise indicated. Mock-infected cells were also prepared. Following 1 hour incubation, the cells were pipetted onto 96-well dishes at 1 X 104 cells/well. The wells contained various concentrations of zidovudine, and peak or trough plasma levels of 3TC
(or, alternatively to 3TC, FTC), and 159208983 as indicated in table 1. The infected T-lymphoblastoid cells were incubated for 5 days to allow for HIV-1 mediated growth inhibition. Plates were then treated with 28 ~.I of 5% Nonidet P-40 (Sigma) in phosphate-buffered saline (PBS) and 60 p,! samples were transferred to filter-bottomed, 96-well plates (Idexx Corp.). Plates were placed in an automated assay instrument (Idexx Screen Machine) which added propidium iodide to each well, performed a series of washes. and determined the resulting fluorescence (E).
Fluorescence has been shown to correlate directly with cell number, allowing for the quantitation of HIV-1 mediated cytopathic effect (CPE). Uninfected cells were determined to have Oolo CPE and infected untreated cells were determined to have 100% CPE. Percent inhibition of HIV-1 induced CPE and ICgSs (95% inhibitory concentration) were determined.
Fi ure 1 shows graphically the results of the combination of zidovudine, 3TC
and 1592089 against zidovudine and 3TC alone and in combination.

Claims

1. A combination comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically functional derivative thereof and (2R,cis)-4-amino-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically functional derivative thereof.

2. A combination comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically functional derivative thereof and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically functional derivative thereof.

3. A combination according to claim 1 comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically functional derivative thereof, zidovudine or a physiologically functional derivative thereof, and (2R,cis)-4-amino-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically functional derivative thereof.

4. A combination according to claim 2 comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically functional derivative thereof, zidovudine or a physiologically functional derivative thereof, and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically functional derivative thereof.

5. A combination according to any one of clam 1 to 4, wherein the physiologically functional derivative is a physiologically acceptable salt, ether, ester, salt of such ester, or solvate.

6. A combination according to claim 3 wherein the ratio of (1S,4R)-cis-4-[2-amino-6(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, : zidovudine, or a physiologically functional derivative thereof, : (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, is in the ratio of 1 to 20 : 1 to 20 : 1 to 10, by weight.

7. A combination according to claim 4 wherein the ratio of (1S,4R)-cis-4-[2-amino-6(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, : zidovudine, or a physiologically functional derivative thereof, : (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, is in the ratio of 1 to 20 : 1 to 20 : 1 to 10, by weight.

8. A combination according to any one of claims 1 to 7 for use in medical therapy.

9. A pharmaceutical formulation comprising a combination according to any one of claims 1 to 7 in association with one or more pharmaceutically acceptable carriers therefor.

10. A formulation according to claim 9 in unit dosage form.

11. Use of (1S,4R)-cis-4-[2-amino-6(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, in the manufacture of a medicament for administration either simultaneously or sequentially with zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, for the treatment and/or prophylaxis of an HIV infection.

12. Use of (1S,4R)-cis-4-[2-amino-6(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, in the manufacture of a medicament for administration either simultaneously or sequentially with zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, for the treatment and/or prophylaxis of an HIV infection.

13. Use of zidovudine, or a physiologically functional derivative thereof, in the manufacture of a medicament for administration simultaneously or sequentially with (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, for the treatment and/or prophylaxis of an HIV infection.

14. Use of zidovudine or a physiologically functional derivative thereof, in the manufacture of a medicament for administration simultaneously or sequentially with (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, for the treatment and/or prophylaxis of an HIV infection.

15. Use of (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the manufacture of a medicament for administration simultaneously or sequentially with (1S,4R)-cis-4-[2-amino-6(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and zidovudine, or a physiologically functional derivative thereof, for the treatment and/or prophylaxis of an HIV infection.

16. Use of (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the manufacture of a medicament for administration simultaneously or sequentially with (1S,4R)-cis-4-[2-amino-6(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and zidovudine, or a physiologically functional derivative thereof, for the treatment and/or prophylaxis of an HIV infection.

17. Use of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an HIV infection.

18. Use of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an HIV infection.

19. Use of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an HIV infection.

20. Use of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an HIV
infection.

21. Use as claimed in any one of claims 11 to 20 for the treatment and/or prophylaxis of an HIV infection resistant to nucleoside or non-nucleoside inhibitors.

22. Use as claimed in any one of claims 11 to 20 in the treatment of AIDS.

23. Use as claimed in any one of claims 11 to 20 in the treatment of AIDS
related conditions or AIDS dementia complex.

24. A patient pack comprising of at least one active ingredient selected from (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-, hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, and an information insert containing directions on the use of all three active ingredients together in combination.

25. A patient pack comprising of at least one active ingredient selected from (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, zidovudine, or a 26~~

physiologically functional derivative thereof, and (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, and an information insert containing directions on the use of all three active ingredients together in combination.

26. A product comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, as a combined preparation for simultaneous, separate or sequential use in the treatment and/or prophylaxis of an HIV infection.

27. A product comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyimidin-2-one, or a physiologically functional derivative thereof, as a combined preparation for simultaneous, separate or sequential use in the treatment and/or prophylaxis of an HIV infection.

28. A product as claimed in claim 27 wherein the components are present in the ratio of 1 to 20:1 to 20:1 to 10, by weight, respectively.

29. A product comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, as a preparation for simultaneous, separate or sequential use together with (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the treatment and/or prophylaxis of an HIV infection.

30. A product comprising (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, as a preparation for simultaneous, separate or sequential use together with (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, in the treatment and/or prophylaxis of an HIV infection.

31. A product comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, as a preparation for simultaneous, separate or sequential use together with zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hyroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the treatment and/or prophylaxis of an HIV
infection.

32. A product comprising zidovudine, or a physiologically functional derivative thereof, as a preparation for simultaneous, separate or sequential use together with (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, in the treatment and/or prophylaxis of an HIV infection.

33. A product comprising (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, as a preparation for simultaneous, separate or sequential use together with zidovudine, or a physiologically functional derivative thereof, and (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, in the treatment and/or prophylaxis of an HIV infection.

34. A product comprising zidovudine, or a physiologically functional derivative thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, or (2R,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one, or a physiologically functional derivative thereof, as a preparation for simultaneous, separate or sequential use together with (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, or a physiologically functional derivative thereof, in the treatment and/or prophylaxis of an HIV infection.

35. A combination comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, zidovudine (3'-azido-3'-deoxythymidine) or a physiologically acceptable salt thereof, and (2R,cis)-4-amino-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof.

36. A combination according to claim 35 wherein the ratio of said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or salt thereof, : zidovudine or salt thereof, : (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or salt thereof is a ratio of 1 to 3:1 to 3:1 to 2, by weight.

37. A pharmaceutical formulation comprising a combination according to claims 35 or 36 in association with a pharmaceutically acceptable carrier thereof.

38. A formulation according to claim 37 in unit dosage form.

39. A formulation according to claim 38 wherein said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or salt thereof, said zidovudine or salt, and said (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or salt thereof, are each in an amount of 100 mg to 2 g.

40. A formulation according to claim 37, 38 or 39 comprising said physiologically acceptable salt of said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol; said zidovudine and said (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.

41. A formulation according to claim 40 wherein said salt is a salt of an inorganic acid selected from hydrochloric, sulphuric, phosphoric and sulphamic acids.

42. A formulation according to claim 41 wherein said acid is sulphuric acid.

43. A formulation according to claim 37, 38 or 39, comprising said zidovudine and said (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.

44. A formulation according to any one of claims 37 to 43 for the treatment of AIDS.

45. Use of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, zidovudine (3'-azido-3'-deoxythymidine) or a physiologically acceptable salt thereof and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof, in the manufacture of a medicament for the treatment of AIDS.

46. Use according to claim 45 of a physiologically acceptable salt of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol; zidovudine and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.

47. Use according to claim 46 wherein said salt is a salt of an inorganic acid selected from hydrochloric, sulphuric, phosphoric and sulphamic acids.

48. Use according to claim 47 wherein said acid is sulphuric acid

49. A product comprising as components: (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, zidovudine (3'-azido-3'-deoxythymidine) or a physiologically acceptable salt thereof and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof, as a combined preparation for use in the treatment of AIDS.

50. A product as claimed in claim 49 wherein the components are present in the ratio of 1 to 3:1 to 3:1 to 2 by weight, respectively.

51. A product as claimed in claim 50 wherein each of said components is in an amount of 100 mg to 2 g.

52. A product as claimed in claim 49, 50 or 51 wherein said components comprise said physiologically acceptable salt of said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol.

53. A product as claimed in claim 52 wherein said salt is of an inorganic acid selected from from hydrochloric, sulphuric, phosphoric and sulphamic acids.

54. A product as claimed in claim 53 wherein said acid is sulphuric acid.

55. A product as claimed in any one of claims 49 to 54 wherein said components comprise said zidovudine and said (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.

56. A combination according to claim 1 comprising (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, and (2R,cis)-4-amino-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof.

57. A combination according to claim 56 wherein the ratio of said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof,: said (2R,cis)-4-amino-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof is a ratio of 1 to 3:1 to 2, by weight.

58. A pharmaceutical formulation comprising a combination according to claims 56 or 57 in association with a pharmaceutically acceptable carrier thereof.

59. A formulation according to claim 58 in unit dosage form.

60. A formulation according to claim 59 wherein said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, and (2R,cis)-4-amino-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof, are each in an amount of 100 mg to 2 g.

61. A formulation according to claim 58, 59 or 60 comprising said physiologically acceptable salt of said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol and said (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.

62. A formulation according to claim 61 wherein said salt is a salt of an inorganic acid selected from hydrochloric, sulphuric, phosphoric and sulphamic acids.

63. A formulation according to claim 61 wherein said acid is sulphuric acid.

64. A formulation according to any one of claims 56 to 63 for the treatment of AIDS.

65. Use of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof, in the manufacture of a medicament for the treatment of AIDS.

66. Use according to claim 65 of a physiologically acceptable salt of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.

67. Use according to claim 66 wherein said salt is a salt of an inorganic acid selected from hydrochloric, sulphuric, phosphoric and sulphamic acids.

68. Use according to claim 67 wherein said acid is sulphuric acid.

69. A product comprising as components: (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol or a physiologically acceptable salt thereof, and (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one or a physiologically acceptable salt thereof, as a combined preparation for use in the treatment of AIDS.

70. A product as claimed in claim 69 wherein the components are present in a ratio of 1 to 3:1 to 2, by weight.

71. A product as claimed in claim 70 wherein each of said components is in an amount of 100 mg to 2 g.

72. A product as claimed in claim 69, 70 or 71 wherein said components comprise said physiologically acceptable salt of said (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol.

73. A product as claimed in claim 72 wherein said salt is of an inorganic acid selected from hydrochloric, sulphuric, phosphoric and sulphamic acids.

74. A product as claimed in claim 73 wherein said acid is sulphuric acid.

75. A product as claimed in any one of claims 69 to 74 wherein said components comprise said (2R,cis)-4-amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one.