Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
  • A61P37/04—Immunostimulants

Definitions

• the present invention relates to combinations of antiviral agents. More specifically it is concerned with combinations of 1 ,3-oxathiolane nucleoside analogues with other antiviral agents, in particular agents effective against HIV.
• HIV Human immunodeficiency virus
• AIDS acquired immune deficiency syndrome
• Nucleosides such as AZT, ddC and ddl inhibit HIV replication in vitro, and appear to exert their antiviral activity on the virus-encoded reverse transcriptase enzyme after metabolism by the cell to their 5'-triphosphate derivatives.
• AZT reduces morbidity and mortality in patients with AIDS.
• HIV infection of cells results in integration of the virus genome into the host chromosome, and so it has been necessary to continue AZT treatment for long periods of time.
• the consequences of long-term AZT therapy are associated bone-marrow toxicity and the appearance of AZT-resistant variants of HIV-1.
• some AIDS patients treated with ddC develop peripheral neuropathy and ddl has been shown to induce pancreatitis and peripheral neuropathy.
• AZT demonstrates synergistic antiviral activity in vitro in combination with agents that act at HIV-1 replicative steps other than reverse transcription, including recombinant soluble CD4 castanospermine and recombinant interferon alpha.
• combinations of compounds can give rise to increased cytotoxicity.
• AZT and recombinant interferon alpha have an increased cytotoxic effect on normal human bone marrow progenitor cells.
• a combination comprising 3TC or a pharmaceutically acceptable derivitive thereof and a non- nucleoside inhibitor of HIV selected from a ⁇ [(benzoxazol-2-yl)methyl]amino ⁇ -5- alkyl-6-alkyl-2-(1 H)-pyridinone or a derivative thereof bearing an unsubstituted or substituted pyridyl or phenyl substituent.
• the invention provides a combination of 3TC and a compound selected from 3- ⁇ [(4,7-dichlorobenzoaxazol-2-yl)methyl]amino)-5-ethyl-6-methyl-2-(1 H)- pyridinone,
• (+)-enantiomer that is to say no more than about 5% w/w of the (+)-enantiomer, preferably no more than about 2%, in particular less than about 1% w/w will be present.
• a pharmaceutically acceptable derivative is meant any pharmaceutically acceptable salt, ester, or salt of such ester, of a parent compound or any other compound which, upon administration to the recipient, is capable of providing (directly or indirectly) the parent compound or an antivirally active metabolite or residue thereof.
• 3TC may be modified to provide pharmaceutically acceptable derivatives thereof at functional groups in both the base moiety and at the hydroxymethyl group of the oxathioiane ring. Modification at all such functional groups are included within the scope of the invention. However of particular interest are pharmaceutically acceptable derivatives obtained by modification of the 2-hydroxymethyl group of the oxathioiane ring.
• Preferred esters of 3TC include the compounds in which the hydrogen of the 2- hydroxymethyl group is replaced by an acyl function R-CO- in which the non- carbonyl moiety R of the ester is selected from hydrogen, straight or branched chain alkyl (e.g. methyl, ethyl, n-propyl, t-butyl, n-butyl), alkoxyalkyl (e.g. methoxymethyl), aralkyl (e.g. benzyl), aryloxyalkyl (e.g. phenoxymethyl), aryl (e.g.
• any alkyl moiety present advantageously contains 1 to 16 carbon atoms, particularly 1 to 4 carbon atoms.
• Any aryl moiety present in such esters advantageously comprises a phenyl group.
• esters may be a C- ⁇ .-j ⁇ alkyl ester, an unsubstituted benzyl ester or a benzyl ester substituted by at least one halogen (bromine, chlorine, fluorine or iodine), C- ⁇ ⁇ alkyl, C-j. ⁇ alkoxy, nitro or trifluoromethyl groups.
• halogen bromine, chlorine, fluorine or iodine
• Pharmaceutically acceptable salts of 3TC include those derived from pharmaceutically acceptable inorganic and organic acids and bases.
• suitable acids include hydrochloric, hydrobromic, sulphuric, nitric, perchloric, fumaric, maleic, phosphoric, glycollic, lactic, salicylic, succinic, toluene-p- sulphonic, tartaric, acetic, citric, methanesulphonic, formic, benzoic, malonic, naphthalene-2-sulphonic and benzenesulphonic acids.
• Other acids such as oxalic, while not in themselves pharmaceutically acceptable, may be useful as intermediates in obtaining the compounds of the invention and their pharmaceutically acceptable acid addition salts.
• Salts derived from appropriate bases include alkali metal (e.g. sodium), alkaline earth metal (e.g. magnesium), ammonium and NR4 + (where R is C-j _4alkyl) salts.
• 3TC is either synergistic with the second component of the combination and/or reduces the cytotoxic effects of the second component.
• 3TC and the non-nucleoside inhibitors of HIV are realised over a wide ratio for example 1 :250 to 250:1 preferably 1 :50 to 50:1 , particularly about 1 :10 to 10:1 by weight.
• each compound will be employed in the combination in an amount at which it exhibits antiviral activity when used alone.
• a method for the treatment of a viral infection in a mammal comprising co-administration of 3TC or a pharmaceutically acceptable derivative thereof and a non-nucleoside inhibitor of HIV replication as defined herein.
• Therapeutic methods comprising administration of a combination of a 3TC and more than one of the non- nucleoside inhibitors of HIV, either together or in a plurality of paired combinations, is also within the scope of the invention.
• 3TC and the second antiviral agent may be administered either simultaneously (either separately or in combination) or sequentially. If administration is sequential, the delay in administering the second of the active ingredients should not be such as to lose the benefit of any synergistic effect of the combination. Preferably administration will be simultaneous.
• a suitable dose will be in the range of from about 1 to about 750mg/kg e.g. from about 10 to about 75 mg/kg of bodyweight per day, such as 3 to about 120mg per kilogram body weight of the recipient per day, preferably in the range of 6 to 90mg/kg/day, most preferably in the range of 15 to 60mg/kg/day of each of the active ingredients of the combination.
• the desired dose may conveniently be presented in a single dose or as divided doses administered at appropriate intervals, for example as two, three, four or more sub-doses per day.
• the combination is conveniently administered in unit dosage form; for example containing 10 to 1500mg, conveniently 20 to 10OOmg, most conveniently 50 to 700mg of each active ingredient per unit dosage form.
• the combinations should be administered to achieve peak plasma concentrations of each of the active compound of about 1 to about 75 ⁇ M, preferably about 2 to 50 ⁇ M, most preferably about 3 to about 30 ⁇ M.
• This may be achieved, for example, by the intravenous injection of a 0.1 to 5% solution of the active ingredients, optionally in saline, or orally administered as a bolus containing about 1 to about 100mg of each active ingredient.
• Desirable blood levels may be maintained by a continuous infusion to provide about 0.01 to about 5.0mg/kg/hour or by intermittent infusions containing about 0.4 to about 15mg/kg of each active ingredient.
• the active ingredients of the combination may be administered as the raw chemical it is preferable to present combinations as a pharmaceutical formulation.
• the invention thus further provides a pharmaceutical formulation comprising 3TC or a pharmaceutically acceptable derivative thereof and a non-nucleoside inhibitor of HIV replication as defined herein together with one or more pharmaceutically acceptable carriers therefor and, optionally, other therapeutic and/or prophylactic ingredients.
• the carrier(s) must be 'acceptable' in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
• compositions include those suitable for oral, rectal, nasal, topical (including buccal and sub-lingual), vaginal or parenteral (including intramuscular, sub-cutaneous and intravenous) administration or in a form suitable for administration by inhalation or insufflation.
• the formulations may, where appropriate, be conveniently presented in discrete dosage units and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing into association the active compound with liquid carriers or finely divided solid carriers or both and then, if necessary, shaping the product into the desired formulation.
• compositions suitable for oral administration may conveniently be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution, a suspension or as an emulsion.
• the active ingredient may also be presented as a bolus, electuary or paste.
• Tablets and capsules for oral administration may contain conventional excipients such as binding agents, fillers, lubricants, disintegrates, or wetting agents.
• the tablets may be coated according to methods well known in the art.
• Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for constitution with water or other suitable vehicle before use.
• Such liquid preparations may contain conventional additives such as suspending agents, emulsifying agents, non-aqueous vehicles (which may include edible oils), or preservatives.
• the compounds according to the invention may also be formulated for parenteral administration (e.g. by injection, for example bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre- filled syringes, small volume infusion or in multi-dose containers with an added preservative.
• the compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents.
• the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilisation from solution, for constitution with a suitable vehicle, e.g. sterile, pyrogen-free water, before use.
• the compounds according to the invention may be formulated as ointments, creams or lotions, or as a transdermal patch.
• Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
• Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilising agents, dispersing agents, suspending agents, thickening agents, or colouring agents.
• Formulations suitable for topical administration in the mouth include lozenges comprising active ingredient in a flavoured base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert base such as gelatin and glycerin or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.
• compositions 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, and the suppositories may be conveniently formed by admixture of the active compound with the softened or melted carrier(s) followed by chilling and shaping in moulds.
• Formulations suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or sprays containing in addition to the active ingredient such carriers as are known in the art to be appropriate.
• the compounds of the invention may be used as a liquid spray or dispersible powder or in the form of drops.
• Drops may be formulated with an aqueous or non-aqueous base also comprising one more dispersing agents, solubilising agents or suspending agents. Liquid sprays are conveniently delivered from pressurised packs.
• the compounds according to the invention are conveniently delivered from an insufflator, nebuliser or a pressurised pack or other convenient means of delivering an aerosol spray.
• Pressurised packs may comprise a suitable propellant such as dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
• the dosage unit may be determined by providing a valve to deliver a metered amount.
• the compounds according to the invention may take the form of a dry powder composition, for example a powder mix of the compound and a suitable powder base such as lactose or starch.
• the powder composition may be presented in unit dosage form in, for example, capsules or cartridges or e.g. gelatin or blister packs from which the powder may be administered with the aid of an inhalator or insufflator.
• compositions according to the invention may also contain other active ingredients such as antimicrobial agents, or preservatives.
• 3TC may be obtained as described in International Patent Application No. W091/17159.
• the non-nucleoside inhibitors of HIV replication may be obtained as described in EP0484071.
• Chequerboard titrations are prepared by mixing 25 ⁇ l aliquots from each compound dilution both alone or in combination (to a final volume of 50 ⁇ l in new 96-well microtitre plates). Aliquots of MT-4 cells (10 6 cells/ml) in RPM1 1640 growth medium are infected with HIV-1 strain RF at a moi of 2 x 10"3 infectious doses/cell. Virus is adsorbed at room temperature for 90 minutes, after which the cells are washed in RPM1 1640 growth medium to remove unadsorbed virus and resuspended at 10 6 cells/ml in RPM1 1640 growth medium.
• 50 ⁇ l of infected cell suspension are inoculated into wells containing compound or growth medium only.
• 50 ⁇ l of mock-infected cell suspension are inoculated into wells not containing compound. The plates are then incubated for 7 days at 37°C in 5% C ⁇ 2/air.
• Dose-response curves are plotted for each compound alone (IC50% values) and for reciprocal titrations of each compound at a fixed concentration of the second compound. Isobolograms of all compound combinations giving IC50% values are plotted.
• the two compounds act additively. If the combination IC50% lie to the left of the line, the compounds are acting synergistically.
• Cytotoxicity is determined by examination of the cells employed in Example 1 following drug treatment and/or by comparing the cvtotoxicities of 3TC and the non-nucleoside HIV inhibitors alone and in combination (at ⁇ g/ml ratios of 1 :1 , 1 :5 and 5:1 ) in uninfected peripheral blood lymphocytes and an established T- lymphocyte cell line; cytotoxicity is measured using a [ 3 H]-thymidine uptake assay.

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• 1992
  • 1992-07-16 GB GB929215176A patent/GB9215176D0/en active Pending
• 1993
  • 1993-07-13 EP EP93915908A patent/EP0650362A1/de not_active Withdrawn
  • 1993-07-13 WO PCT/EP1993/001846 patent/WO1994002154A1/en not_active Application Discontinuation
  • 1993-07-13 AU AU45688/93A patent/AU4568893A/en not_active Abandoned
  • 1993-07-13 JP JP6504123A patent/JPH07508997A/ja active Pending
  • 1993-07-13 CA CA002140237A patent/CA2140237A1/en not_active Abandoned

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