WO2005102390A2 - Combinaisons comprenant des ligands alpha-2-delta et des antagonistes des recepteurs de nmda - Google Patents

Combinaisons comprenant des ligands alpha-2-delta et des antagonistes des recepteurs de nmda Download PDF

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WO2005102390A2
WO2005102390A2 PCT/IB2005/000988 IB2005000988W WO2005102390A2 WO 2005102390 A2 WO2005102390 A2 WO 2005102390A2 IB 2005000988 W IB2005000988 W IB 2005000988W WO 2005102390 A2 WO2005102390 A2 WO 2005102390A2
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disorders
disorder
pharmaceutically acceptable
ester
solvate
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PCT/IB2005/000988
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WO2005102390A3 (fr
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Masanori Hizue
Aki Imai
Katsuo Toide
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Pfizer Japan, Inc.
Pfizer Inc.
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Definitions

  • This invention relates to a synergistic combination of an alpha-2-delta ligand and an NMDA receptor antagonist (NMDA antagonist), suitably having affinity for the NR2B- subtype (NR2B antagonist), useful for the treatment of pain. It also relates to a method for treating pain through the use of effective amounts of synergistic combinations of an alphas- delta ligand and an NMDA antagonist.
  • NMDA antagonist NMDA receptor antagonist
  • An alpha-2-delta receptor ligand is any molecule which binds to any sub-type of the human calcium channel alpha-2-delta sub-unit.
  • the calcium channel alpha-2-delta sub-unit comprises a number of receptor sub-types which have been described in the literature: e.g. N. S. Gee, J. P. Brown, V. U. Dissanayake, J. Offord, R. Thurlow, and G. N. Woodruff, J-Biol-Chem 111 (10):5768-76, 1996, (type 1); Gong, J. Hang, W. Kohler, Z. Li, and T-Z. Su, J.Membr.Biol.
  • Alpha-2-delta ligands have been described for a number of indications.
  • a second alpha-2-delta ligand, pregabalin, (S)-(+)-4-amino-3-(2- methylpropyl)butanoic acid is described in European patent application publication number EP0641330 as an anti-convulsant treatment useful in the treatment of epilepsy and in EP0934061 for the treatment of pain.
  • n is an integer of from 1 to 4, where there are stereocentres, each center may be independently R or S, preferred compounds being those of Formulae I- IN above in which n is an integer of from 2 to 4.
  • WO 02/85839 describes alpha-2-delta ligands for use in the treatment of a number of indications, including pain, together with combinations with NMDA receptor antagonists, e.g. dextromethorphan ((+)-3-hydroxy-N-methylmorphinan) and its metabolite dextrorphan ((+)-3-hydroxy-N- methylmorphinan), ketamine, memantine, pyrroloquinoline quinone and cis-4- (phosphonomethyl)-2-piperidinecarboxylic acid and their pharmaceutically acceptable salt, ester or solvate.
  • NMDA receptor antagonists e.g. dextromethorphan ((+)-3-hydroxy-N-methylmorphinan) and its metabolite dextrorphan ((+)-3-hydroxy-N- methylmorphinan), ketamine, memantine, pyrroloquinoline quinone and cis-4- (phosphonomethyl)-2-piperidinecarboxylic acid
  • Monoamine neurotransmitters include, for example, serotonin (5-HT), norepinephrine (noradrenaline), and dopamine. These neurotransmitters travel from the terminal of a neuron across a small gap (i.e., the synaptic cleft) and bind to receptor molecules on the surface of a second neuron. This binding elicits intracellular changes that initiate or activate a response or change in the postsynaptic neuron. Inactivation occurs primarily by transport (i.e., reuptake) of the neurotransmitter back into the presynaptic neuron.
  • transport i.e., reuptake
  • Glutamic acid plays a dual role in the central nervous system (CNS) as essential amino acid and the principal excitatory neurotransmitters.
  • CNS central nervous system
  • Ionotropic receptors are classified into three major subclasses, N-methyl-D-aspartate (NMDA), 2-amino-3-(methyl-3-hydroxyisoxazol-4-yl)propionic acid (AMP A) and kainate.
  • NMDA N-methyl-D-aspartate
  • AMP A 2-amino-3-(methyl-3-hydroxyisoxazol-4-yl)propionic acid
  • kainate There is considerable preclinical evidence that hyperalgesia and allodynia following peripheral tissue or nerve injury is not only due to an increase in the sensitivity of primary afferent nociceptors at the site of injury but also depends on NMDA receptor-mediated central changes in synaptic excitability.
  • NMDA receptor antagonists have also been found to decrease both pain perception and sensitization. Also, overactivation of the NMDA receptor is a key event for triggering neuronal cell death under pathological conditions of acute and chronic forms of neurodegeneration.
  • NMDA receptor inhibition has therapeutic utility in the treatment of pain and neurodegenerative diseases, there are significant liabilities to many available NMDA receptor antagonists that can cause potentially serious side effects.
  • NMDA subunits are differentially distributed in the CNS.
  • NR2B is believed to be restricted to the forebrain and laminas I and II of the dorsal horn. The more discrete distribution of NR2B subunit in the CNS may support a reduced side-effect profile of agents that act selectively at this site.
  • NMDA NR2B selective antagonists may have clinical utility for the treatment of neuropathic and other pain conditions in human with a reduced side-effect profile than existing NMDA antagonists (S. Boyce, et al., Neuropharmacology, 38, pp.611-623 (1999)).
  • NMDA antagonists include memantine, ketamine and dextromethorphan, whilst NR2B antagonists include ifenprodil and traxoprodil.
  • WO 9807447 describes combinations of anti-epileptic compounds, including gabapentin, with NMDA receptor antagonists.
  • WO 9912537 and WO 0053225 describe combinations of NMDA antagonists and GABA analogs, including gabapentin and pregabalin.
  • WO 02100434 describes the use of NMDA antagonists in the treatment of central neuropathic pain.
  • WO 03061656 describes a composition for treating disorders of the central nervous system comprising a GABA analog, such as gabapentin or pregabalin, with an NMDA receptor antagonist such as dexfromethomorphan or d-methadone, optionally in combination with another pharmaceutically active substance.
  • a GABA analog such as gabapentin or pregabalin
  • an NMDA receptor antagonist such as dexfromethomorphan or d-methadone
  • WO 9912537 and WO 0053225 describe combinations of anti-epileptic compounds, including gabapentin and pregabalin, in combination with NMDA antagonists as analgesics.
  • WO 03091241 describes NR2B antagonists for a number of indications, together with alpha-2-delta ligands, e.g. gabapentin and pregabalin.
  • combination therapy with an alpha-2-delta ligand and an NMDA antagonist results in improvement in the treatment of pain.
  • an NMDA antagonist suitably an NR2B antagonist
  • the alpha- 2-delta ligand and NMDA antagonist may interact in a synergistic manner to control pain. This synergy allows a reduction in the dose required of each compound, leading to a reduction in the side effects and enhancement of the clinical utility of the compounds.
  • the invention provides, as a first aspect, a synergistic combination product comprising an alpha-2-delta ligand or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • NMDA suitably NR2B, antagonist
  • a pharmaceutically acceptable salt, ester or solvate thereof an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • Useful cyclic alpha-2-delta ligands of the present invention are illustrated by the following formula (I):
  • X is a carboxylic acid or carboxylic acid bioisostere; n is 0, 1 or 2; and
  • R 1 , R la , R 2 , R 2a , R 3 , R 3a , R 4 and R 4a are independently selected from H and C C 6 alkyl, or
  • R 1 and R 2 or R 2 and R 3 are taken together to form a C -C 7 cycloalkyl ring, which is optionally substituted with one or two substituents selected from C ⁇ -C 6 alkyl, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • R 1 , R ,a , R 2a , R 3a , R 4 and R 4a are H and R 2 and R 3 are independently selected from H and methyl, or R la , R 2a , R 3a and R 4a are H and R 1 and R 2 or R 2 and R 3 are taken together to form a C 3 -C 7 cycloalkyl ring, which is optionally substituted with one or two methyl substituents.
  • a suitable carboxylic acid bioisostere is selected from tefrazolyl and oxadiazolonyl.
  • X is preferably a carboxylic acid.
  • R 1 , R la , R 2a , R 3a , R 4 and R 4a are H and R 2 and R 3 are independently selected from H and methyl, or R la , R 2a , R 3a and R 4a are H and R 1 and R 2 or R 2 and R 3 are taken together to form a C 4 -C 5 cycloalkyl ring, or, when n is 0, R 1 , R la , R 2a , R 3a , R 4 and R 4a are H and R 2 and R 3 form a cyclopentyl ring, or, when n is 1, R 1 , R la , R 2a , R 3 , R 4 and R 4a are H and R 2 and R 3 are both methyl or R 1 , R la , R 2a , R 3a , R 4 and R 4a are H and R 2 and R 3 form a cyclobutyl ring, or, when n is 2, R 1 , R la ,
  • n is 0 or 1, R . 1 i :s- h.y.dJrogen or C- ⁇ -C- 6 a _ ⁇ l ⁇ k leisurey. ⁇ l.; ⁇ R>2 i ⁇ s T h..y-dJrogen or ⁇ C ⁇ - rC ⁇ 6 a personallyl.k.nostiy.l..; r R> 3 is hydrogen or C ⁇ -C 6 alkyl; R 4 is hydrogen or -C, alkyl; R 5 is hydrogen or C ⁇ -C 6 alkyl and R 2 is hydrogen or C ⁇ -C 6 alkyl, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • R 1 is C ⁇ -C 6 alkyl
  • R 2 is methyl
  • R 3 - R 6 are hydrogen and n is 0 or 1.
  • R is methyl, ethyl, n-propyl or n-butyl
  • R is methyl
  • R 3 - R 6 are hydrogen and n is 0 or 1.
  • R 1 is suitably ethyl, n-propyl or n-butyl.
  • R is suitably methyl or n-propyl.
  • Compounds of formula (II) are suitably in the 3S, 5R configuration.
  • alpha-2-delta ligands for use with the present invention are those compounds generally or specifically disclosed in US4024175, particularly gabapentin, EP0641330, particularly pregabalin, 3-methylgabapentin, US5563175, WO 9733858, WO 9733859, WO 9908670, WO 9908671, WO 9931057, WO 9931074, WO 9729101, WO 0053225, WO 02085839, particularly [(lR,5R,6S)-6-(aminomethyl)bicyclo[3.2.0]hept- 6-yl] acetic acid, WO 9931075, particularly 3-(l-aminomethyl-cyclohexylmethyl)-4H- [ 1 ,2,4]oxadiazol-5-one and C-[ 1 -(lH-tetrazol-5-ylmethyl)-cycloheptyl]-methylamine, WO 9921824, particularly (3S,4S)-(l-a
  • Preferred alpha-2-delta ligands of the present invention include: gabapentin, pregabalin, 3-methylgabapentin, [(lR,5R,6S)-6-(aminomethyl)bicyclo[3.2.0]hept-6-yl]acetic acid, 3-(l-aminomethyl-cyclohexylmethyl)-4H-[l,2,4]oxadiazol-5-one, C-[l-(lH-tetrazol-5- ylmethyl)-cycloheptyl]-methylamine, (3S,4S)-(l-aminomethyl-3,4-dimethyl-cyclopentyl)- acetic acid, (l ⁇ ,3 ⁇ ,5 ⁇ )(3-amino-methyl-bicyclo[3.2.0]hept-3-yl)-acetic acid, (3S,5R)- 3-aminomethyl-5-methyl-octanoic acid, (3S,5R)-3-amino-5-methyl-hepta
  • alpha-2-delta ligands of the present invention are selected from gabapentin, pregabalin, 3-methylgabapentin and (l ⁇ ,3 ⁇ ,5 ⁇ )(3-amino-methyl- bicyclo[3.2.0]hept-3-yl)-acetic acid, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NMDA antagonists for use in the present invention are the compounds generically and specifically disclosed in: WO 9427591, WO 2002015922, WO 9901416, EP427518 and WO 9640097, or pharmaceutically acceptable salts, esters or solvates thereof.
  • Examples o f N R2B a ntagonists for u se i n t he p resent i nvention a re t he c ompounds generically and specifically disclosed in: EP1251128; WO 2002050070; WO 2001094321; WO 2001092239; WO 2001092204; WO 2001081295; WO 9723458; WO 9723214; WO 9723215; WO 9723216, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in WO 2003091241; EP768086; WO 9710240; WO 9707098; WO 9637226; US5594007; US5455250; US5654302; US5696126; WO 9609295; WO 9608485; WO 9520587; and US5436255, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in WO 03/084931; WO 02/080928; WO 02/068409; WO 02/00629; WO 01/98262; WO 01/32171; WO 01/32174; WO 01/32177; WO 01/32179; WO 01/32615; WO 01/32634; WO 01/30330; WO 00/67751; WO 00/67755; WO 99/30330; WO 99/44640, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in WO 03/010159 and WO 02/34718, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in: WO 03/097637; WO 03/040128; WO 02/060877; WO 02/16321; WO 01/81303; WO 01/81309; EP 0 846 683; EP 1 090 917; EP 1 088 818; EP 1 070 708; WO 00/75109; EP 0 982 026; EP 0 937 458; US 5,889,026; EP 0 846 683; WO 97/32581; EP 0 787 493; EP 0 606 661; and WO 95/32205, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in: EP 0 709 384; WO 98/18793, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in: WO 97/33582; WO 97/24123; and EP 0 351 282, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NR2B antagonists for use in the present invention are the compounds generically and specifically disclosed in WO 03/035641, or pharmaceutically acceptable salts, esters or solvates thereof.
  • NMDA antagonists for use in the present invention include memantine, ketamine, dextromethorphan, CHF-3381, (referred to in Journal of Pharmacology and Experimental Therapeutics 2003,306:2(804-814)), YKP-509 and AZD-4282, whilst NR2B antagonists include ifenprodil, traxoprodil, RGH-896 (Gedeon Richer) and (-)-(R)-6- ⁇ 2-[4-(3- fluorophenyl)-4-hydroxy- 1 -piperidinyl] - 1 -hydroxyethyl-3 ,4-dihydro-2( 1 H)-quinolinone.
  • a combination comprising gabapentin, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA antagonist selected from memantine, ketamine, dextromethorphan, CHF-3381, YKP-509 and AZD-4282, or an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy-l-piperidinyl]-l- hydroxyethyl-3,4-dihydro-2(lH)-quinolinone, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • an NMDA antagonist selected from memantine, ketamine, dextromethorphan, CHF-3381, YKP-509 and AZD-4282
  • an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and
  • a combination comprising pregabalin, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA antagonist selected from memantine, ketamine and dextromethorphan, or an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and (-)-(R)-6- ⁇ 2-[4- (3 -fluorophenyl)-4-hydroxy- 1 -piperidinyl] - 1 -hydroxyethyl-3 ,4-dihydro-2( 1 H)-quinolinone, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • an NMDA antagonist selected from memantine, ketamine and dextromethorphan
  • an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and (-)-(R)-6- ⁇ 2-[4- (3 -fluorophenyl)-4-hydroxy- 1 -piperidinyl]
  • a combination comprising 3-methylgabapentin, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA antagonist selected from memantine, ketamine, dextromethorphan, CHF-3381, YKP-509 and AZD-4282, or an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and(-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy-l- piperidinyl]-l-hydroxyethyl-3,4-dihydro-2(lH)-quinolinone, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • an NMDA antagonist selected from memantine, ketamine, dextromethorphan, CHF-3381, YKP-509 and AZD-4282
  • an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896
  • a combination c omprising ( l ⁇ ,3 ⁇ ,5 )(3-amino-methyl-bicyclo[3.2.0]hept-3-yl)-acetic acid, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA, suitably an NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • a combination comprising (l ⁇ ,3 ⁇ ,5 ⁇ )(3-amino-methyl-bicyclo[3.2.0]hept-3-yl)- acetic acid, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA antagonist selected from memantine, ketamine and dextromethorphan, or an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4- hydroxy-l-piperidinyl]-l-hydroxyethyl-3,4-dihydro-2(lH)-quinolinone, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • a combination comprising (2S,4S)-4-(3-fluorobenzyl)proline, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA, suitably an NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • a combination comprising (2S,4S)-4-(3-fluorobenzyl)proline, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA antagonist selected from memantine, ketamine and dextromethorphan, or an NR2B antagonist selected from ifenprodil, traxoprodil, RGH- 896 and (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy-l-piperidinyl]-l-hydroxyethyl-3,4- dihydro-2(lH)-quinolinone, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • a combination comprising (2S,4S)-4-(3-chlorophenoxy)proline, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA, suitably an NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • a combination comprising (2S,4S)-4-(3-chlorophenoxy)proline, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA antagonist selected from memantine, ketamine and dextromethorphan, or an NR2B antagonist selected from ifenprodil, traxoprodil, RGH-896 and (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy-l-piperidinyl]-l-hydroxyethyl- 3,4-dihydro-2(lH)-quinolinone, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • the combination is selected from: gabapentin and ifenprodil; gabapentin and traxoprodil; gabapentin and RGH-896; gabapentin and (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy- 1 -piperidinyl]- 1 - hydroxyethyl-3, 4-dihydro-2(lH)-quinolinone; pregabalin and ifenprodil; pregabalin and traxoprodil; pregabalin and RGH-896; pregabalin and (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy- 1 -piperidinyl]- 1 - hydroxyethyl-3, 4-dihydro-2(lH)-quinolinone; 3-methylgabapentin and ifenprodil; 3-methylgabapentin and ifenprodil; 3-methyl
  • the combination of the present invention in a single dosage form is suitable for administration to any mammalian subject, preferably human.
  • Administration may b e once (o.d.), twice (b.i.d.) or three times (t.i.d.) daily, suitably b.i.d. or t.i.d., more suitably b.i.d, most suitably o.d..
  • an alpha-2-delta ligand and an NMDA suitably an NR2B, antagonist in the manufacture of a once, twice or thrice, suitably twice or thrice, more suitably twice, most suitably once daily administration medicament for the curative, prophylactic or palliative treatment of pain.
  • a method for the curative, prophylactic or palliative treatment of pain in a mammalian subject comprising once, twice or thrice, suitably twice or thrice, more suitably twice, most suitably once daily administration of an effective, particularly synergistic, c ombination of an alpha-2-delta ligand and an NMDA, suitably an NR2B, antagonist.
  • the optimum range for the effect and absolute dose ranges of each component for the effect may be definitively measured by administration of the c omponents over different w/w ratio ranges and doses to patients in need of treatment.
  • the complexity and cost of carrying out clinical studies on patients renders impractical the use of this form of testing as a primary model for synergy.
  • synergy in one species can be predictive of the effect in other species and animal models exist, as described herein, to measure a synergistic effect and the results of such studies can also be used to predict effective dose and plasma concentration ratio ranges and the absolute doses and plasma concentrations required in other species by the application of pharmacokinetic(PK)/pharmacodynamic(PD) methods.
  • PK pharmacokinetic
  • PD pharmacodynamic
  • a synergistic combination for human administration comprising an alpha-2-delta ligand and an NMDA antagonist, or pharmaceutically acceptable salt, ester or solvate or solvates thereof, in a w/w combination range which corresponds to the absolute ranges observed in a non-human animal model, preferably a rat model, primarily used to identify a synergistic interaction.
  • the ratio range in humans corresponds to a non-human range selected from between 1 :50 to 50:1 parts by weight, 1:50 to 20:1, 1:50 to 10:1, 1:50 to 1 :1, 1:20 to 50:1, 1:20 to 20:1, 1:20 to 10:1, 1 :20 to 1 :1, 1:10 to 50:1, 1:10 to 20:1, 1:10 to 10:1, 1:10 to 1:1, 1:1 to 50:1, 1.1 to 20:1 and 1:1 to 10:1.
  • the human range corresponds to a non-human range of 5:1 to 50:1 parts by weight.
  • the human range corresponds to a synergistic non-human range of the order of 7:1 to 45:1, especially 10:1 to 30:1, parts by weight.
  • a suitable alpha-2-delta ligand: NMDA antagonist ratio range is selected from between 1:50 to 50:1 parts by weight, 1 :50 to 20:1, 1 :50 to 10:1, 1:50 to 1 :1, 1 :20 to 50:1, 1:20 to 20:1, 1 :20 to 10:1, 1:20 to 1:1, 1:10 to 50:1, 1 :10 to 20:1, 1 :10 to 10:1, 1 :10 to 1 :1, 1:1 to 50:1, 1.1 to 20:1 and 1 :1 to 10:1, more suitably 5:1 to 50:1, preferably 7:1 to 45:1, and more preferably 10:1 to 30:1.
  • Optimal doses of each component for synergy can be determined according to published procedures in animal models. However, in man (even in experimental models of pain) the cost can be very high for studies to determine the entire exposure-response relationship at all therapeutically relevant doses of each component of a combination. It may be necessary, at least initially, to estimate whether effects can be observed that are consistent with synergy at doses that have been extrapolated from those that give optimal synergy in animals.
  • a synergistic combination for administration to humans comprising an alpha-2-delta ligand and an NMDA antagonist, or pharmaceutically acceptable salt, ester or solvate thereof, where the dose range of each component corresponds to the absolute ranges observed in a non-human animal model, preferably the rat model, primarily used to identify a synergistic interaction.
  • the dose of alpha-2-delta ligand for use in a human is in a range selected from l-1200mg, l-500mg, 1-lOOmg, l-50mg, l-25mg, 500-1200mg, 100-1200mg, 100- 500mg, 50-1200mg, 50-500mg, or 50-100mg, suitably 50-100mg, b.i.d.
  • NMDA antagonist is in a range selected from l-200mg, l-lOOmg, 1- 50mg, l-25mg, 10-lOOmg, 10-50mg or 10-25 mg, suitably 10-lOOmg, b.i.d or t.i.d, suitably t.i.d.
  • the plasma concentration ranges of the alpha-2-delta ligand and NMDA antagonist combinations of the present invention required to provide a therapeutic effect depend on the species to be treated, and components used.
  • the C max values range from 0.520 ⁇ g/ml to 10.5 ⁇ g/ml.
  • a synergistic combination for administration to humans comprising an alpha-2-delta ligand and an NMDA antagonist, where the plasma concentration range of each component corresponds to the absolute ranges observed in a non-human animal model, preferably the rat model, primarily used to identify a synergistic interaction.
  • the plasma concentration range in the human corresponds to a range of 0.05 ⁇ g/ml to 10.5 ⁇ g/ml for an alpha-2-delta ligand in the rat model.
  • Particularly preferred combinations of the invention include those in which each variable of the combination is selected from the suitable parameters for each variable. Even more preferable combinations of the invention include those where each variable of the combination i s s elected from t he m ore s Amble, most s Amble, p referred or m ore p referred parameters for each variable.
  • Figure 1 Effects of fixed dose ratios of (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4-hydroxy-l- piperidinyl]-l -hydroxyethyl-3, 4-dihydro-2(lH)-quinolinone (Compound A) and 3 -methyl gabapentin (3M-GBP) on the partial sciatic nerve ligation (PSL) induced static allodynia in mice 1 hr after administration. All data are expressed at the 1 h time point postdrug administration.
  • PSL partial sciatic nerve ligation
  • Figure 2 Effects of fixed dose ratios of Compound A and 3M-GBP on the PSL- induced static allodynia in mice 2 hr after administration. All data are expressed at the 2 hr time point postdrug administration.
  • A Dose- response data for Compound A and 3M-GBP alone. Fixed dose ratios of 1 :8 (B), 1 :25 (C), and 1 :42
  • D Compound A and 3M-GBP combinations. Theoretical additive lines were calculated from dose-response data. All compounds were administered p.o., and PWTs to von Frey hairs were examined 2 hr postdrug administration. Results are expressed as median evaluator size required to induce the paw withdrawal in eight animals per group.
  • the compounds of the present combination invention are prepared by methods well known to those skilled in the art. Specifically, the patents, patent applications and publications, mentioned hereinabove, each of which is hereby incorporated herein by reference, exemplify compounds which can be used in the combinations, pharmaceutical compositions, methods and kits in accord with the present invention, and refer to methods of preparing those compounds.
  • the compounds of the present combination invention can exist in unsolvated forms as well as solvated forms, including hydrated forms.
  • the solvated forms, including hydrated forms which may contain isotopic substitutions (e.g. D 2 O, d 6 -acetone, d 6 -DMSO), are equivalent to unsolvated forms and are encompassed within the scope of the present invention.
  • Certain of the compounds of the present combination invention possess one or more chiral centers and each center may exist in the R or S configuration.
  • the present invention includes all enantiomeric and epimeric forms as well as the appropriate mixtures thereof. Separation of diastereoisomers or cis and trans isomers may be achieved by conventional techniques, e.g. by fractional crystallisation, chromatography or H.P.L.C. of a stereoisomeric mixture of a compound of the invention or a suitable salt or derivative thereof.
  • a number of the alpha-2-delta ligands of the present invention are amino acids. Since amino acids are amphoteric, pharmacologically compatible salts can be salts of appropriate non-toxic i norganic o r o rganic a cids or b ases.
  • Suitable base salts are formed from bases which form non-toxic salts and examples are the sodium, potassium, aluminium, calcium, magnesium, zinc, choline, diolamine, olamine, arginine, glycine, tromethamine, benzathine, lysine, meglumine and diethylamine salts. Salts with quaternary ammonium ions can also be prepared with, for example, the tetramethylammonium ion.
  • the compounds of the invention may also be formed as a zwitterion.
  • a suitable salt for amino acid compounds of the present combination invention is the hydrochloride salt.
  • suitable salts see Stahl and Wermuth, Handbook of Pharmaceutical Salts: Properties, Selection, and Use, Wiley- VCH, Weinheim, Germany (2002).
  • the alpha-2-delta ligands and NMDA antagonists of the present invention may contain a carboxylic acid group, and may therefore form esters.
  • esters means a protecting group which can be cleaved in vivo by a biological method such as hydrolysis and forms a free acid or salt thereof. Whether a compound is such a derivative or not can be determined by administering it by intravenous injection to an experimental animal, such as a rat or mouse, and then studying the body fluids of the animal to determine whether or not the compound or a pharmaceutically acceptable salt thereof can be detected.
  • groups for an ester of a carboxyl group or a hydroxy group include: (1) aliphatic alkanoyl groups, for example: alkanoyl groups such as the formyl, acetyl, propionyl, butyryl, isobutyryl, pentanoyl, pivaloyl, valeryl, isovaleryl, octanoyl, nonanoyl, decanoyl, 3-methylnonanoyl, 8-methylnonanoyl, 3-ethyloctanoyl, 3,7- dimethyloctanoyl, undecanoyl, dodecanoyl, tridecanoyl, tetradecanoyl, pentadecanoyl, hexadecanoyl, 1-methylpentadecanoyl, 14-methylpentadecanoyl, 13,13- dimethyltetradecanoyl, heptadecanoyl, 15-
  • clathrates drug-host inclusion complexes wherein, in contrast to the aforementioned solvates, the drug and host are present in non- stoichiometric amounts.
  • references to compounds of the combination invention include references to salts thereof and to solvates and clathrates of compounds of the combination invention and salts thereof.
  • Prodrugs of the above compounds of the combination invention are included in the scope of the instant invention.
  • the chemically modified drug, or prodrug should have a different pharmacokinetic profile to the parent, enabling easier abso ⁇ tion across the mucosal epithelium, better salt formulation and/or solubility, improved systemic stability (for an increase in plasma half-life, for example).
  • Ester or amide derivatives which may be cleaved by, for example, esterases or lipases.
  • ester derivatives the ester is derived from the carboxylic acid moiety of the drug molecule by known means.
  • amide derivatives the amide may be derived from the carboxylic acid moiety or the amine moiety of the drug molecule by known means.
  • a peptide which may be recognized by specific or nonspecific proteinases.
  • a peptide may be coupled to the drug molecule via amide bond formation with the amine or carboxylic acid moiety of the drug molecule by known means.
  • Aminoacyl-glycolic and -lactic esters are known as prodrugs of amino acids (Wermuth C.G., Chemistry and Industry, 1980:433-435).
  • the carbonyl group of the amino acids can be esterified by known means.
  • Prodrugs and soft drugs are known in the art (Palomino E., Drugs of the Future, 1990;15(4):361-368). The last two citations are hereby inco ⁇ orated by reference.
  • the combination of the present invention is useful for the general treatment of pain, particularly neuropathic pain.
  • Physiological pain is an important protective mechanism designed to warn of danger from potentially injurious stimuli from the external environment.
  • the system operates through a specific set of primary sensory neurones and is exclusively activated by noxious stimuli via peripheral transducing mechanisms (Millan 1999 Prog. Neurobio. 57: 1-164 for an integrative Review).
  • These sensory fibres are known as nociceptors and are characterised by small diameter axons with slow conduction velocities. Nociceptors encode the intensity, duration and quality of noxious stimulus and by virtue of their topographically organised projection to the spinal cord, the location of the stimulus.
  • nociceptive nerve fibres of which there are two main types, A-delta fibres (myelinated) and C fibres (non-myelinated).
  • A-delta fibres myelinated
  • C fibres non-myelinated.
  • the activity generated by nociceptor input is transferred after complex processing in the dorsal horn, either directly or via brain stem relay nuclei to the ventrobasal thalamus and then on to the cortex, where the sensation of pain is generated.
  • Intense acute pain and chronic pain may involve the same pathways driven by pathophysiological processes and as such cease to provide a protective mechanism and instead contribute to debilitating symptoms associated with a wide range of disease states. Pain is a feature of many trauma and disease states. When a substantial injury, via disease or trauma, to body tissue occurs the characteristics of nociceptor activation are altered. There is sensitisation in the periphery, locally around the injury and centrally where the nociceptors terminate. This leads to hypersensitivity at the site of damage and in nearby normal tissue. In acute pain these mechanisms can be useful and allow for the repair processes to take place and the hypersensitivity returns to normal once the injury has healed. However, in many chronic pain states, the hypersensitivity far outlasts the healing process and is normally due to nervous system injury.
  • pain can be divided into a number of different areas because of differing pathophysiology, these include nociceptive, inflammatory, neuropathic pain etc. It should be noted that some types of pain have multiple aetiologies and thus can be classified in more than one area, e.g. Back pain, Cancer pain have both nociceptive and neuropathic components.
  • Nociceptive pain is induced by tissue injury or by intense stimuli with the potential to cause injury. Pain afferents are activated by fransduction of stimuli by nociceptors at the site of injury and sensitise the spinal cord at the level of their termination. This is then relayed up the spinal tracts to the brain where pain is perceived (Meyer et al., 1994 Textbook of Pain 13- 44).
  • the activation of nociceptors activates two types of afferent nerve fibres. Myelinated A- delta fibres transmitted rapidly and are responsible for the sha ⁇ and stabbing pain sensations, whilst unmyelinated C fibres transmit at a slower rate and convey the dull or aching pain.
  • Moderate to severe acute nociceptive pain is a prominent feature of, but is not limited to pain from strains/sprains, post-operative pain (pain following any type of surgical procedure), posttraumatic pain, burns, myocardial infarction, acute pancreatitis, and renal colic. Also cancer related acute pain syndromes commonly due to therapeutic interactions such as chemotherapy toxicity, immunotherapy, hormonal therapy and radiotherapy.
  • Moderate to severe acute nociceptive pain is a prominent feature of, but is not limited to, cancer pain which may be tumour related pain, (e.g. bone pain, headache and facial pain, viscera pain) or associated with cancer therapy (e.g.
  • postchemotherapy syndromes chronic postsurgical pain syndromes, post radiation syndromes
  • back pain which may be due to herniated or ruptured intervertabral discs or abnormalities of the lumber facet joints, sacroiliac joints, paraspinal muscles or the posterior longitudinal ligament
  • Neuropathic pain is defined as pain initiated or caused by a primary lesion or dysfunction in the nervous system (IASP definition). Nerve damage can be caused by trauma and disease and thus the term 'neuropathic pain' encompasses many disorders with diverse aetiologies. These include but are not limited to, Diabetic neuropathy, Post he ⁇ etic neuralgia, Back pain, Cancer neuropathy, HIV neuropathy, Phantom limb pain, Ca ⁇ al Tunnel Syndrome, chronic alcoholism, hypothyroidism, trigeminal neuralgia, uremia, or vitamin deficiencies. Neuropathic pain is pathological as it has no protective role.
  • neuropathic pain are difficult to treat, as they are often heterogeneous even between patients with the same disease (Woolf & Decosterd 1999 Pain Supp. 6: S141-S147; Woolf and Mannion 1999 Lancet 353: 1959-1964). They include spontaneous pain, which can be continuous, or paroxysmal and abnormal evoked pain, such as hyperalgesia (increased sensitivity to a noxious stimulus) and allodynia (sensitivity to a normally innocuous stimulus).
  • the inflammatory process is a complex series of biochemical and cellular events activated in response to tissue injury or the presence of foreign substances, which result in swelling and pain (Levine and Taiwo 1994: Textbook of Pain 45-56).
  • Arthritic pain makes up the majority of the inflammatory pain population.
  • Rheumatoid disease is one of the commonest chronic inflammatory conditions in developed countries and rheumatoid arthritis (RA) is a common cause of disability.
  • RA rheumatoid arthritis
  • the exact aetiology of RA is unknown, but current hypotheses suggest that both genetic and microbiological factors may be important (Grennan & Jayson 1994 Textbook of Pain 397-407).
  • -Musculo-skeletal disorders including but not limited to myalgia, fibromyalgia, spondylitis, sero-negative (non-rheumatoid) arthropathies, non-articular rheumatism, dystrophinopathy, Glycogenolysis, polymyositis, pyomyositis.
  • -Central pain or ' thalamic pain' as defined by pain caused by lesion or dysfunction of the nervous system including but not limited to central post-stroke pain, multiple sclerosis, spinal cord injury, Parkinson's disease and epilepsy.
  • GI gastrointestinal
  • BFD functional bowel disorders
  • IBD inflammatory bowel diseases
  • GI disorders include a wide range of disease states that are currently only moderately controlled, including - for FBD, gastro-esophageal reflux, dyspepsia, the irritable bowel syndrome (IBS) and functional abdominal pain syndrome (FAPS), and - for IBD, Crohn's disease, ileitis, and ulcerative colitis, which all regularly produce visceral pain.
  • Other types of visceral pain include the pain associated with dysmenorrhea, pelvic pain, cystitis and pancreatitis.
  • -Head pain including but not limited to migraine, migraine with aura, migraine without aura cluster headache, tension-type headache.
  • -Oro facial pain including but not limited to dental pain, temporomandibular myofascial pain.
  • the invention provides the use of a synergistic effective amount of an alpha-2-delta ligand, or a pharmaceutically acceptable salt, ester or solvate thereof, in the manufacture of a medicament in combination with an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof, for the curative, prophylactic or palliative treatment of pain, particularly neuropathic pain.
  • the invention provides the use of a synergistic effective amount of an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof, in the manufacture of a medicament in combination with an alpha-2 -delta ligand, or a pharmaceutically acceptable salt, ester or solvate thereof, for the curative, prophylactic or palliative treatment of pain, particularly neuropathic pain.
  • a method for the curative, prophylactic or palliative treatment of pain, particularly neuropathic pain comprising simultaneous, sequential or separate administration of a therapeutically synergistic amount of an alphas- delta ligand, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof, to a mammal in need of said treatment.
  • the combination of the present invention is also useful in the treatment of disorders or conditions selected from the group consisting of single episodic or recurrent major depressive disorders, dysthymic disorders, depressive neurosis and neurotic depression, melancholic depression including anorexia, weight loss, insomnia, early morning waking or psychomotor retardation; atypical depression (or reactive depression) including increased appetite, hypersomnia, psychomotor agitation or irritability, seasonal affective disorder and pediatric depression; bipolar disorders or manic depression, for example, bipolar I disorder, bipolar II disorder and cyclothymic disorder; conduct disorder; disruptive behavior disorder; attention deficit hyperactivity disorder (ADHD); behavioral disturbances associated with mental retardation, autistic disorder, and conduct disorder; anxiety disorders such as panic disorder with or without agoraphobia, agoraphobia without history of panic disorder, specific phobias, for example, specific animal phobias, social anxiety, social phobia, obsessive-compulsive disorder, stress disorders including post-traumatic stress disorder and acute stress disorder, and generalized
  • the invention provides the use of a synergistic effective amount of an alpha-2-delta ligand, or a pharmaceutically acceptable salt, ester or solvate thereof, in the manufacture of a medicament in combination with an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof, for the curative, prophylactic or palliative treatment of a disorder or condition selected from the group consisting of single episodic or recurrent major depressive disorders, dysthymic disorders, depressive neurosis and neurotic depression, melancholic depression including anorexia, weight loss, insomnia, early morning waking or psychomotor retardation; atypical depression (or reactive depression) including increased appetite, hypersomnia, psychomotor agitation or irritability, seasonal affective disorder and pediatric depression; bipolar disorders or manic depression, for example, bipolar I disorder, bipolar II disorder and cyclothymic disorder; conduct disorder; disruptive behavior disorder; attention deficit hyperactivity disorder (ADHD); behavioral disturbance
  • ADHD attention deficit hyper
  • the invention provides the use of a synergistic effective amount of an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof, in the manufacture of a medicament in combination with an alpha-2-delta ligand, or a pharmaceutically acceptable salt, ester or solvate thereof, for the curative, prophylactic or palliative treatment of a disorder or condition selected from the group consisting of single episodic or recurrent major depressive disorders, dysthymic disorders, depressive neurosis and neurotic depression, melancholic depression including anorexia, weight loss, insomnia, early morning waking or psychomotor retardation; atypical depression (or reactive depression) including increased appetite, hypersomnia, psychomotor agitation or irritability, seasonal affective disorder and pediatric depression; bipolar disorders or manic depression, for example, bipolar I disorder, bipolar II disorder and cyclothymic disorder; conduct disorder; disruptive behavior disorder; attention deficit hyperactivity disorder (ADHD); behavioral disturbances
  • the biological activity of the alpha-2-delta ligands of the invention may be measured in a radioligand binding assay using [ ⁇ H gabapentin and the c ⁇ subunit derived from porcine brain tissue (Gee N.S., Brown J.P., Dissanayake V.U.K., Offord J., Thurlow R., Woodruff G.N., J. Biol. Chem., 1996;271:5879-5776). Results may be expressed in terms of ⁇ M or nM ⁇ 2 ⁇ binding affinity.
  • NR2B antagonists The ability of compounds of the combination invention to act as NR2B antagonists is determined by their ability to inhibit the binding of NR2B subunit at its receptor sites employing radioactive ligands.
  • the NR2B antagonist activity of the compounds is evaluated by using the standard assay procedure described in, for example, J. Pharmacol., 331, ppl 17- 126, 1997.
  • a human NR2B cell functional assay may be carried out as described in WO 03091241.
  • the elements of the combination of the instant invention may be administered separately, simultaneously or sequentially for the treatment of pain.
  • the combination may also optionally be administered with one or more other pharmacologically active agents.
  • Suitable optional agents include:
  • opioid analgesics e.g. mo ⁇ hine, heroin, hydromo ⁇ hone, oxymo ⁇ hone, levo ⁇ hanol, levallo ⁇ han, methadone, meperidine, fentanyl, ***e, codeine, dihydrocodeine, oxycodone, hydrocodone, propoxyphene, nalmefene, nalo ⁇ hine, naloxone, naltrexone, bupreno ⁇ hine, buto ⁇ hanol, nalbuphine and pentazocine; (ii) nonsteroidal antiinflammatory drugs (NSAIDs), e.g.
  • NSAIDs nonsteroidal antiinflammatory drugs
  • barbiturate sedatives e.g. amobarbital, aprobarbital, butabarbital, butabital, mephobarbital, metharbital, methohexital, pentobarbital, phenobartital, secobarbital, talbutal, theamylal, thiopental and their pharmaceutically acceptable salts, esters or solvates;
  • benzodiazepines having a sedative action, e.g. chlordiazepoxide, clorazepate, diazepam, flurazepam, lorazepam, oxazepam, temazepam, triazolam and their pharmaceutically acceptable salts, esters, or solvates,
  • Hi antagonists having a sedative action e.g. diphenhydramine, pyrilamine, promethazine, chlo ⁇ heniramine, chlorcyclizine and their pharmaceutically acceptable salts, esters or solvates;
  • miscellaneous sedatives such as glutethimide, meprobamate, methaqualone, dichloralphenazone and their pharmaceutically acceptable salts, esters or solvates;
  • skeletal muscle relaxants e.g. baclofen, carisoprodol, chlorzoxazone, cyclobenzaprine, methocarbamol, o ⁇ hrenadine and their pharmaceutically acceptable salts, esters or solvates,
  • alpha-adrenergic active compounds e.g. doxazosin, tamsulosin, clonidine and 4- amino-6,7-dimethoxy-2-(5-methanesulfonamido-l,2,3,4-tetrahydroisoquinol-2-yl)-5- (2 -pyridyl) quinazoline;
  • tricyclic antidepressants e.g. desipramine, imipramine, amytriptiline and nortriptiline;
  • anticonvulsants e.g. carbamazepine and valproate
  • Tachykinin (NK) antagonists particularly NK-3, NK-2 and NK-1 e.g. antagonists, ( ⁇ R,9R)-7-[3,5-bis(trifluoromethyl)benzyl]-8,9,10,l l-tetrahydro-9- methyl-5-(4-methylphenyl)-7H-[ 1 ,4]diazocino[2, 1 -g] [ 1 ,7]naphthridine-6- 13-dione (TAK-637), 5-[[(2R,3S)-2-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethoxy-3-(4- fluorophenyl)-4-mo ⁇ holinyl]methyl]-l,2-dihydro-3H-l,2,4-triazol-3-one (MK-869), lanepitant, dapitant and 3-[[2-methoxy-5-(trifluoromethoxy)phenyl]
  • celecoxib, rofecoxib and valdecoxib (xiv) Non-selective COX inhibitors (preferably with GI protection), e.g. nitroflurbiprofen (HCT-1026); (xv) coal-tar analgesics, in particular, paracetamol; (xvi) neuroleptics, such as droperidol; (xvii) Vanilloid receptor agonists, e.g.
  • Beta-adrenergic compounds such as propranolol
  • Local anaesthetics such as mexiletine
  • Corticosteroids such as dexamethasone
  • serotonin receptor agonists and antagonists such as dexamethasone
  • cholinergic (nicotinic) analgesics such as Tramadol®
  • PDEV inhibitors such as sildenafil, vardenafil or taladafil;
  • serotonin reuptake inhibitors e.g. fluoxetine, paroxetine, citalopram and sertraline
  • mixed serotonin-noradrenaline reuptake inhibitors e.g. milnacipran, venlafaxine and duloxetine
  • noradrenaline reuptake inhibitors e.g. reboxetine.
  • the present invention extends to a combination product comprising an alpha-2-delta ligand, or a pharmaceutically acceptable salt, ester or solvate thereof, and an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof, and one or more other therapeutic agents, such as those listed above, for simultaneous, separate or sequential use in the curative, prophylactic treatment of pain, particularly neuropathic pain.
  • the combination of the invention can be administered alone but one or both elements will generally be administered in an admixture with suitable pharmaceutical excipient(s), diluent(s) or carrier(s) selected with regard to the intended route of administration and standard pharmaceutical practice. I f appropriate, auxiliaries can be added. Auxiliaries are preservatives, anti-oxidants, flavours or colourants.
  • the compounds of the invention may be of immediate-, delayed-, modified-, sustained-, pulsed- or controlled-release type.
  • the elements of the combination of the present invention can be administered, for example but not limited to, the following route: orally, buccally or sublingually in the form of tablets, capsules, multi-and nano-particulates, gels, films (incl. muco-adhesive), powder, ovules, e lixirs, lozenges (including 1 iquid- filled), chews, solutions, suspensions and sprays.
  • the compounds of the invention may also be administered as osmotic dosage form, or in the form of a high energy dispersion or as coated particles or fast-dissolving, fast-disintegrating dosage form as described in Ashley Publications, 2001 by Liang and Chen.
  • the compounds of the invention may be administered as crystalline or amo ⁇ hous products, freeze dried or spray dried. Suitable formulations of the compounds of the invention may be in hydrophilic or hydrophobic matrix, ion-exchange resin complex, coated or uncoated form and other types as described in US 6,106,864 as desired.
  • Such pharmaceutical compositions may contain excipients such as microcrystalline cellulose, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate, glycine and starch (preferably corn, potato or tapioca starch), mannitol, disintegrants such as sodium starch glycolate, croscarmellose sodium and certain complex silicates, and granulation binders such as polyvinylpyrrolidone, hydroxypropylmethylcellulose (HPMC), triglycerides, hydroxypropylcellulose (HPC), bentonite sucrose, sorbitol, gelatin and acacia.
  • excipients such as microcrystalline cellulose, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate, glycine and starch (preferably corn, potato or tapioca starch), mannitol, disintegrants such as sodium starch glycolate, croscarmellose sodium and certain complex silicates, and granulation binders such as polyviny
  • lubricating agents may be added to solid compositions such as magnesium stearate, stearic acid, glyceryl behenate, PEG and talc or wetting agents, such as sodium lauryl sulphate. Additionally, polymers such as carbohydrates, phospoholipids and proteins may be included.
  • the solid dosage form such as tablets are manufactured by a standard p rocess, for example, direct compression or a wet, dry or melt granulation, melt congealing and extrusion process.
  • the tablet cores which may be mono or multi-layer may be coated with appropriate overcoats known in the art.
  • Solid compositions of a similar type may also be employed as fillers in capsules such as gelatin, starch or HPMC capsules.
  • Preferred excipients in this regard include lactose, starch, a cellulose, milk sugar or high molecular weight polyethylene glycols.
  • Liquid compositions may be employed as fillers in soft or hard capsules such as gelatin capsule.
  • the compounds of the invention may be combined with various sweetening or flavouring agents, colouring matter or dyes, with emulsifying and/or suspending agents and with diluents such as water, ethanol, propylene glycol, methylcellulose, alginic acid or sodium alginate, glycerin, oils, hydrocolloid agents and combinations thereof.
  • diluents such as water, ethanol, propylene glycol, methylcellulose, alginic acid or sodium alginate, glycerin, oils, hydrocolloid agents and combinations thereof.
  • formulations containing these compounds and excipients may be presented as a dry product for constitution with water or other suitable vehicles before use.
  • Liquid form preparations include solutions, suspensions, and emulsions, for example, water or water propylene glycol solutions.
  • liquid preparations can be formulated in solution in aqueous polyethylene glycol solution.
  • Aqueous solutions suitable for oral use can be prepared by dissolving the active component in water and adding suitable colorants, flavors, stabilizing and thickening agents as desired.
  • Aqueous suspensions suitable for oral use can be made by dispersing the finely divided active component in water with viscous material, such as natural or synthetic gums, resins, methylcellulose, sodium carboxymethylcellulose, and other well-known suspending agents.
  • the elements of the combination of the present invention can also be administered by injection, that is, intravenously, intramuscularly, infracutaneously, intraduodenally, or intraperitoneally, intraarterially, intrathecally, intraventricularly, intraurethrally, intrasternally, intracranially, intraspinally or subcutaneously, or they may be administered by infusion, needle-free injectors or implant injection techniques.
  • parenteral administration they are best used in the form of a sterile aqueous solution, suspension or emulsion (or system so that can include micelles) which may contain other substances known in the art, for example, enough salts or carbohydrates such as glucose to make the solution isotonic with blood.
  • aqueous solutions should be suitably buffered (preferably to a pH of from 3 to 9), if necessary.
  • parenteral administration they may be used in the form of a sterile non-aqueous system such as fixed oils, including mono- or diglycerides, and fatty acids, including oleic acid.
  • suitable parenteral formulations under sterile conditions for example lyophilisation is readily accomplished by standard pharmaceutical techniques well-known to those skilled in the art.
  • the active ingredient may be in powder form for constitution with a suitable vehicle (e.g. sterile, pyro gen- free water) before use.
  • the elements of the combination of the present invention can be administered intranasally or by inhalation. They are conveniently delivered in the form of a dry powder (either alone, as a mixture, for example a dry blend with lactose, or a mixed component particle, for example with phospholipids) from a dry powder inhaler or an aerosol spray presentation from a pressurised container, pump, spray, atomiser (preferably an atomiser using electrohydrodynamics to produce a fine mist) or nebuliser, with or without the use of a suitable propellant, e.g.
  • a dry powder either alone, as a mixture, for example a dry blend with lactose, or a mixed component particle, for example with phospholipids
  • atomiser preferably an atomiser using electrohydrodynamics to produce a fine mist
  • nebuliser e.g.
  • the dosage unit may be determined by providing a valve to deliver a metered amount.
  • the pressurised container, pump, spray, atomiser or nebuliser may contain a solution or suspension of the active compound, e.g. using a mixture of ethanol (optionally, aqueous ethanol) or a suitable agent for dispersing, solubilising or extending release and the propellant as the solvent, which may additionally contain a lubricant, e.g. sorbitan trioleate.
  • a lubricant e.g. sorbitan trioleate.
  • Capsules, blisters and cartridges for use in an inhaler or insufflator may be formulated to contain a powder mix of the compound of the invention, a suitable powder base such as lactose or starch and a performance modifier such as 1-leucine, mannitol or magnesium stearate.
  • the elements of the combination of the invention Prior to use in a dry powder formulation or suspension formulation for inhalation the elements of the combination of the invention will be micronised to a size suitable for delivery by inhalation (typically considered as less than 5 microns). Micronisation could be achieved by a range of methods, for example spiral jet milling, fluid bed jet milling, use of supercritical fluid crystallisation or by spray drying.
  • a suitable solution formulation for use in an atomiser using electrohydrodynamics to produce a fine mist may contain from l ⁇ g to lOmg of the compound of the invention per actuation and the actuation volume may vary from 1 to lOO ⁇ l.
  • a typical formulation may comprise the elements of the combination of the invention, propylene glycol, sterile water, ethanol and sodium chloride.
  • Alternative solvents may be used in place of propylene glycol, for example glycerol or polyethylene glycol.
  • the elements of the combination of the invention may be administered topically to the skin, mucosa, dermally or transdermally, for example, in the form of a gel, hydrogel, lotion, solution, cream, ointment, dusting powder, dressing, foam, film, skin patch, wafers, implant, sponges, fibres, bandage, microemulsions and combinations thereof.
  • the compounds of the invention can be suspended or dissolved in, for example, a mixture with one or more of the following: mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax , fixed oils, including synthetic mono- or diglycerides, and fatty acids, including oleic acid, water, sorbitan monostearate, a polyethylene glycol, liquid paraffin, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol, alcohols such as ethanol.
  • penetration enhancers may be used.
  • polymers such as niosomes or liposomes
  • phospolipids in the form of nanoparticles (such as niosomes or liposomes) or suspended or dissolved.
  • they may be delivered using iontophoresis, electroporation, phonophoresis and sonophoresis.
  • the elements of the combination of the invention can be administered rectally, for example in the form of a suppository or pessary. They may also be administered by vaginal route.
  • these compositions may be prepared by mixing the drug with a suitable non-irritant excipients, such as cocoa butter, synthetic glyceride esters or polyethylene glycols, which are solid at ordinary temperatures, but liquefy and/or dissolve in the cavity to release the drug.
  • a suitable non-irritant excipients such as cocoa butter, synthetic glyceride esters or polyethylene glycols, which are solid at ordinary temperatures, but liquefy and/or dissolve in the cavity to release the drug.
  • the compounds can be formulated as micronised suspensions in isotonic, pH adjusted, sterile saline, or, preferably, as solutions in isotonic, pH adjusted, sterile saline.
  • a polymer may be added such as crossed-linked polyacrylic acid, polyvinylalcohol, hyaluronic acid, a cellulosic polymer (e.g. hydroxypropylmethylcellulose, hydroxyethylcellulose, methyl cellulose), or a heteropolysaccharide polymer (e.g. gelan gum).
  • they may be formulated in an ointment such as petrolatum or mineral oil, inco ⁇ orated into bio-degradable (e.g.
  • Formulations may be optionally combined with a preservative, such as benzalkonium chloride.
  • a preservative such as benzalkonium chloride.
  • they may be delivered using iontophoresis. They may also be administered in the ear, using for example but not limited to the drops.
  • a pharmaceutical composition comprising a synergistic combination comprising an alpha-2-delta ligand, an NMDA, suitably NR2B, antagonist, or a pharmaceutically acceptable salt, ester or solvate thereof.
  • the composition is suitable for use in the treatment of pain, particularly neuropathic pain.
  • the element of the pharmaceutical preparation is preferably in unit dosage form.
  • the preparation is subdivided into unit doses containing appropriate quantities of the active component.
  • the unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, such as packeted tablets, capsules, and powders in vials or ampoules.
  • the unit dosage form can be a capsules, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.
  • the quantity of active component in a unit dose preparation may be varied or adjusted from 0.1 mg to 1 g according to the particular application and the potency of the active components. In medical use the drug may be administered three times daily as, for example, capsules of 100 or 300 mg.
  • the compounds utilized in the pharmaceutical method of this invention are administered at the initial dosage of about 0.01 mg to about 100 mg/kg daily.
  • a daily dose range of about 0.01 mg to about 100 mg/kg is preferred.
  • the dosages may be varied depending upon the requirements of the patient, the severity of the condition being treated, and the compounds being employed. Determination of the proper dosage for a particular situation is within the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compounds. Thereafter, the dosage is increased by small increments until the optimum effect under the circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day, if desired.
  • a combination according to the present invention or veterinarily acceptable salts, esters or solvates thereof is administered as a suitably acceptable formulation in accordance with normal veterinary practice and the veterinary surgeon will determine the dosing regimen and route of administration which will be most appropriate for a particular animal.
  • the reaction was heated to 75°C for 20 hours and then cooled to room temperature.
  • the reaction solution was extracted 3x with 4 L aliquots of IN HC1 and lx with 4 L of 0.2N NaOH.
  • the 20 L reactor was fitted with a distillation head. The organic layer was distilled to remove, in succession: 6.5 L of EtOAc, after which 8 L of heptane was added back to the reactor; 4 L of EtO Ac/heptane, after which 4 L of heptane was added to the reactor; and 4 L of EtO Ac/heptane, after which 8 L of heptane was added to the reactor.
  • reaction mixture was cooled to an internal temperature of 40°C, and the reactor contents were charged to a filter and filtered under 5 psig of nitrogen washing with 8 L of heptane.
  • the mixture was stirred for 1 hour at 0°C at which time 2.0 g (47 mmol) of lithium chloride was added in one portion, followed by 10 g (42 mmol) of (4S,5R)-4,5-diphenyl-2-oxazolidinone in four batches. Stirring was maintained throughout the solid additions.
  • the reaction mixture was stirred for 1 hour at 0°C, and for 1 hour at ambient temperature, and was vacuum filtered through a coarse frit and concentrated. The residue was partitioned between EtOAc/water, and the organics were dried over MgSO 4 and concentrated. To the residue was added 200 mL of MTBE and the mixture was warmed cautiously with swirling.
  • the titled acylated oxazolidinone may be used in the next step instead of (S)-3-((E)-2-Methyl-pent-2-enoyl)-4- phenyl-oxazolidin-2-one.
  • (2R, JR.4S)-3-(2, 3-Dimethyl-pentanoyl)-4-phenyl-oxazolidin-2-one A 20 L jacketed reactor was fit with a gas inlet and a 2 L dripping funnel. A nitrogen sweep was begun over the reactor and maintained throughout the process.
  • the organic layer was clarified through a plug of magnesol.
  • the organic layer was concentrated to give 822 g of a crude solid.
  • the crude solid was recrystallized from 8 L of 20% H 2 O in MeOH, filtered and dried in a vacuum oven to give 550 g of a white solid.
  • the layers were separated.
  • the aqueous layer was extracted 2x with 1 L aliquots of MTBE.
  • the organic phases were combined and concentrated to give a solid/oil mixture.
  • the solid/oil mixture was slurried in 1.7 L of hexane.
  • the slurry was filtered and the collected solids were washed with 1.7 L of hexane.
  • the hexane filtrates were extracted 2x with 1.35 L aliquots of IN NaOH.
  • the aqueous extracts were combined and exfracted with 800 mL of dichloromethane.
  • the aqueous layer was then acidified with 240 mL of concentrated hydrochloric acid.
  • the aqueous solution was extracted 2x with 1 L aliquots of dichloromethane.
  • Example 2 (3R.4R.5R)-3-Amino-4.5-dimethyl-octanoic acid (4S, 5R)-4, 5-Diphenyl-oxazolidin-2-one
  • 4S, 5R 4-Diphenyl-oxazolidin-2-one
  • 550 g (2.579 mol) of (lR,2S)-diphenyl-2-aminoethanol 457 g (3.868 mol, 1.5eq) of diethylcarbonate, 18 g (0.258 mol, O.leq) of NaOEt in 100 mL of EtOH and 3.5 L of toluene.
  • the reaction was heated until an internal temperature of 90°C was reached and EtOH distillation began.
  • the reaction mixture was cooled to room temperature and was extracted 3x with 3.5 L aliquots of IN HC1.
  • the combined aqueous extracts were filtered to give a white solid.
  • the recovered white solid was added back to the organic layer.
  • the 20 L reactor was fitted with a distillation head and the organic layer was distilled to remove in succession: 13.5 L of EtOAc, after which 5 L of heptane was added to the reactor; 5 L of EtOAc/heptane, after which 5 L of heptane was added to the reactor; and 2.7 L of EtOAc/heptane, after which 2.7L of heptane was added to the reactor.
  • the reaction mixture was transferred over a 2 hour period into another 22 L flask equipped with a mechanical stirrer, transfer line, vacuum line, and containing 4 L of 1 : 1 acetic acid:THF solution cooled in an ice-water bath.
  • the quenched solution was stirred for 30 minutes and then diluted with 4 L of 2M NH 4 OH in saturated aqueous NH 4 C1 and 2 L of water.
  • the biphasic mixture was stirred for 15 minutes and the phases separated.
  • the organic phase was washed 4x with 4 L aliquots of the 2M NH 4 OH solution.
  • the LiOH/water/H 2 ⁇ 2 solution was added dropwise to the vigorously stirred oxazolidinone/THF solution at such a rate as to maintain the reaction temp at 0°C to 5°C.
  • the addition funnel was recharged with approximately one quarter of the cold LiOH water/H 2 ⁇ 2 solution as required until all of the solution had been added to the reaction mixture (about 40 minutes for 0.45 mol scale). After the addition was completed, the mixture was stirred at 0°C to 5°C for 5 hours, during which the reaction mixture changed from a homogeneous solution to white slurry.
  • reaction mixture A solution of 341 g of Na 2 SO 3 and 188 g of NaHSO 3 in 2998 mL of deionized water (15 wt%) was added dropwise to the reaction mixture over about a 1.5 hour period (reaction was exothermic) via the addition funnel, while maintaining the reaction temperature at 0°C to 10°C. Following the addition, the reaction mixture was stirred at 0°C to 10°C for 1 hour. The reaction mixture was tested with potassium iodide-starch test paper to ensure the absence of peroxides. The reaction mixture was charged with 2000 mL of EtOAc and was stirred 5 minutes. The phases were separated and the aqueous phase was extracted with 2000 mL of EtOAc.
  • the addition funnel was charged portion-wise with a solution of 219.9 g of (2R,3R)-2,3-dimethyl-hexanoic acid in 350 mL of dry THF.
  • the entire dimethyl-hexanoic acid acid/THF solution was added dropwise to the stirred CDI/THF suspension at such a rate so as to control the evolution of CO 2 and to maintain the reaction at a temperature of 20°C to 25°C.
  • reaction mixture was stirred at 20°C to 25°C for 1 hour, during which the slurry became a pale yellow solution.
  • the malonate/MgCl 2 reaction mixture was cooled to 20°C to 25°C and the condenser was replaced with a 1 L addition funnel.
  • the addition funnel was charged portion- wise with the dimethylhexanoic acid CD I/THF reaction mixture. This entire reaction mixture was added dropwise to the stirred malonate/MgC ⁇ /THF reaction mixture over about 10 minutes. After the addition was completed, the reaction mixture was heated to 35°C to 40°C. Some effervescence was noted.
  • the reaction mixture was stirred at 35°C to 40°C for 16 hour.
  • reaction mixture was cooled to 20°C to 25°C.
  • the reaction mixture (a grey suspension) was added portion-wise to the aq. HC1 solution while maintaining an internal temperature of 20°C-25°C.
  • the reaction temperature was moderated with an ice/water bath; the reaction mixture pH was about 1.
  • the reaction mixture was stirred at 20°C to 25°C for 2 hours.
  • the reaction mixture was subsequently charged with 4000 mL of EtOAc and was stirred for 5 minutes. The phases were separated and the aqueous phase was exfracted with 2000 mL of EtOAc.
  • the combined organic extract was washed sequentially with: IN aq. HC1 (2x1500 mL); 1000 mL of water (incomplete phase separation); half saturated aq. Na 2 CO 3 (2x1500 mL); 1000 mL water; and brine (2x1000 mL).
  • the aqueous base wash removed unreacted malonate ester-acid.
  • the straw colored organic solution was concentrated under vacuum (35°C-40°C) to give a cloudy, pale yellow oil with some white solid present. The oil was redissolved in 1500 mL of n- heptane and was filtered.
  • Butyl lithium (32.7ml, 52.4mmol) was added to a solution of diisopropylamine (4.9 g, 48.5 mmol) in dry THF (20 mL) under nitrogen at 0°C and stirred for 20 minutes. The solution was cooled to - 78°C and 4.3 g (48.5mmol) of ethyl acetate was added. The solution was stirred at that temperature for 45 minutes. (2R,3R)-2,3-Dimethyl-hexanoyl chloride in dry THF (20 mL) was slowly added to the ethyl acetate enolate at -78°C and the resulting reaction mixture was allowed to warm to room temperature.
  • the reaction mixture was stirred at room temperature for 2.5 hours and was cooled to 0°C.
  • the reaction was quenched with a saturated solution of ammonium chloride and extracted into ethyl acetate. The solution was washed with brine, dried over MgSO 4 and concentrated. The resulting residue was filtered through a silica plug, eluting with 60/40 solution of hexane/ethyl acetate to afford 2.7 g (89.2% yield) of the title compound as an oil.
  • reaction mixture was cooled to 25°C, quenched with a saturated solution of ammonium chloride and extracted into ethyl acetate. The solution was washed with brine, dried over MgSO 4 and concentrated. The resulting residue was filtered through a silica plug, eluting with 60/40 solution of hexane/ethyl acetate to afford 1.3 g (87.8% yield) of the title compoxmd as an oil.
  • the aim of this experiment was to characterize the anti-allodynic effects of alphas- delta ligand administered in combination with a NR2B antagonist in mice.
  • 3- methylgabapentin (3M-GBP) as alpha-2-delta ligand, (-)-(R)-6- ⁇ 2-[4-(3-fluorophenyl)-4- hydroxy-1 -piperidinyl] -1 -hydroxyethyl-3, 4-dihydro-2(lH)-quinolinone (Compound A) as NR2B antagonist and the combination of 3-methylgabapentin, and Compound A were evaluated in mice partial sciatic nerve ligation-induced static allodynia assay.
  • mice Male ddY mice (16-18g), obtained from Japan SLC Inc. (Hamamatsu, Japan), were housed in groups of six. All animals were kept under a 12-hr light/dark cycle (lights on at 07h OOmin) with food and water ad libitum. All experiments were carried out by an observer unaware of drug treatments.
  • PSL Surgery in mice was made according to the method of Seltzer et al. (Pain 43, 1990, 205-218). Animals were anesthetized with isoflurane. After surgical preparation the right sciatic nerve is exposed at the upper-thigh level. The dorsal third to half of the sciatic nerve is tightly ligated with a 9-0 silk suture at a site just proximal to the sciatic bifurcation. In sham-operated mice the nerve is exposed, but not ligated. The wound is closed, layer to layer, using 6-0 silk sutures, and the mice are allowed to recover from the anesthetic. The general appearance and motor function are normal in the injured mice.
  • Suitable NR2B antagonists of the present invention may be prepared as described in the references or are obvious to those skilled in the art on the basis of these documents.
  • Suitable alpha-2-delta ligand compounds of the present invention may be prepared as described in the aforementioned patent literature references, or are obvious to those skilled in the art on the basis of these documents.

Abstract

L'invention concerne une combinaison synergique d'un ligand alpha-2-delta et un antagoniste du récepteur de NMDA, de préférence NR2B, ou des sels, des esters ou des solvates de ceux-ci pharmaceutiquement acceptables, des compositions pharmaceutiques associées et leur utilisation dans le traitement de la douleur, en particulier la douleur névropathique, et les troubles du système nerveux central.
PCT/IB2005/000988 2004-04-22 2005-04-11 Combinaisons comprenant des ligands alpha-2-delta et des antagonistes des recepteurs de nmda WO2005102390A2 (fr)

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WO2008055945A1 (fr) 2006-11-09 2008-05-15 Probiodrug Ag Dérivés 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one utiles en tant qu' inhibiteurs de la glutaminyl-cyclase dans le traitement des ulcères, du cancer et d'autres maladies
WO2008065141A1 (fr) 2006-11-30 2008-06-05 Probiodrug Ag Nouveaux inhibiteurs de glutaminylcyclase
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WO2011107530A2 (fr) 2010-03-03 2011-09-09 Probiodrug Ag Nouveaux inhibiteurs
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