AU2002211758A1

AU2002211758A1 - Methods for modulating bladder function

Info

Publication number: AU2002211758A1
Application number: AU2002211758A
Authority: AU
Inventors: Thomas Michael Argentieri; Mark Robert Bowlby; Jeffrey Howard Sheldon
Original assignee: American Home Products Corp
Current assignee: Wyeth LLC
Priority date: 2000-10-17
Filing date: 2001-10-16
Publication date: 2002-04-29
Also published as: NZ525301A; CA2425742A1; US6348486B1; CA2450467C; EP1326597A2; US7160684B2; DE60116352D1; IL155090A0; CN1287781C; JP2004529611A; WO2002032419A2; DK1326597T3; CN1469739A; PL360903A1; MXPA03003339A; EP1328550A2; HUP0303288A2; JP2004511516A; AR030901A1; NO20031580L

Description

METHODS FOR MODULATING BLADDER FUNCTION

This invention relates to novel methods for modulating bladder tissues utilizing compounds which modulate the KCNQ family of potassium channels, particularly compounds which open or agonize the channels. The methods of this invention include the treatment, prevention, inhibition and amelioration of urge urinary incontinence also known as bladder instability, neurogenic bladder, voiding dysfunction, hyperactive bladder or detrusor overactivity. The methods of this invention also include the prevention and treatment of mixed stress and urge urinary incontinence, including that associated with secondary conditions such as prostate hypertrophy.

Background of the Invention

U.S. Patent No. 5,384,330 (Dieter et al.) (EP 0554543B) teaches pharmacologically active 1 ,2,4-triaminobenzene derivatives of the General Formula:

and their properties as anti-epileptic, muscle relaxing, fever-reducing and peripheral analgesic agents.

U.S. Patent No. 5,565,483 (Hewawasam et al.) (EP 0747354B) teaches compounds of the formulae:

(II) wherein: R is hydrogen, hydroxy or fluoro; R¹, R², R³ and R⁴ each are independently hydrogen, C^ alkyl, halogen, trifluoromethyl, phenyl, p-methylphenyl or p-trifluoromethyl- phenyl; or R¹ and R², R² and R³ or R³ and R⁴ are joined together to form a benzo fused ring; R⁵ is hydrogen or d-₄ alkyl; and R⁶ is chlorine or trifluoromethyl; or a nontoxic pharmaceutically acceptable salt, solvate or hydrate thereof, which are potassium channel openers useful for treating ischemia, convulsions and asthma.

The article Modulation of KCNQ2/3 Potassium Channels by the Novel Anticonvulsant Retigabine, Main et al., Molecular Pharmacology, 58: pp. 253-262, 2000, describes the actions of retigabine (D23129; N-[2-amino-4-(4-fluorobenzylamino)- phenyl]carbamic acid ethyl ester) in modulating the KCNQ2/3 potassium channels in oocytes in a 3-fold manner, i.e. retigabine shifts the voltage dependence of channel activation to more hyperpolarized membrane potentials, increases the rate of channel activation and slows channel deactivation. The article "KCNQ4 Channel Inactivation by BMS-204352 and Retigabine" R L Schroder et al Neuropharmacology 40, 888-898 (2000) describes the activation of KCNQ4 channels in a reversible and concentration- dependent manner using retigabine and BMS-204352; (3S)-(+)-(5-chloro-2-methoxy- phenyl)-1 ,3-dihydro-3-fluoro-6-(trifluoro-methyl))-2H-indol-2-one.

U.S. Patent No. 5,849,789 and 5,852,053 (both to Rostock et al.) teache the use of retigabine for the treatment of neurodegenerative disorders, including those associated with stroke.

U.S. Patent No. 5,914,425 (Meisel et al.) teaches novel crystalline forms of retigabine.

U.S. Patent No. 6,1 17,900 teaches the use of retigabine, also known as N-[2- amino-4-(4-fluorobenzylamino)-phenyl]carbamic acid ethyl ester, for the treatment of neuropathic pain. Description of the Invention

This invention comprises methods for modulating urinary bladder tissues in a mammal, particularly including uses thereof for maintaining urinary bladder control, the methods comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound which acts as an agonist or opener of the KCNQ family of potassium channels, including the KCNQ2, KCNQ3, KCNQ4, and KCNQ5 potassium channels, alone or in combination. A particular embodiment of this invention includes use in the methods described herein of one or more agonists or openers of KCNQ2/3 potassium channels. Another series of methods of this invention comprises use of one or more agonists or openers of KCNQ3/5 potassium channels.

Among the compounds useful in the methods of this invention are those disclosed in U.S. Patent No. 5,384,330 (Dieter et al.) and EP 0554543B, the contents of which are incorporated herein by reference. The compounds include those of the formula:

wherein:

R- is selected from hydrogen, Ci — C₆-alkyl, C₂ — C₆-alkanoyl or the radical Ar;

R₂ is selected from hydrogen or d — C₆-alkyl;

R₃ is selected from d — C₆-alkoxy, NH₂, d — C₆-alkylamino, d — C₆-dialkylamino, amino substituted by the radical Ar, d — C₆-alkyl, C₂ — C₆-alkenyl, C₂ — C₆- alkynyl, the radical Ar or the radical ArO-; R is selected from hydrogen, Ci — C₆-alkyl or the radical Ar; R₅ is selected from hydrogen or d — C₆-alkyl or the radical Ar; Alk indicates a straight or branched alkylene group with 1 -9 carbon atoms, which can also be substituted by the radical Ar; Ar is a phenyl radical substituted by the radicals R₆, R₇ and/or R₈ where these radicals R₆, R₇ and R₈ are the same or different and represent H, d-C₆- alkyl, C₃-C₇-cycloalkyl, hydroxy, d-C₆-alkoxy, C₂-C₆-alkanoyloxy, halogen, hydroxy, d-C₆-halogenoalkyl, -CN, -NH₂, -NH — d-C₆-alkyl, -N(d-C₆-alkyl)₂, -CO₂H, -CO— d-C₆-alkyl, -CO— O— C d-alkyl, -COAr,

-CO— OAr, -CONH₂, -CONH— d-C₆-alkyl, -CON(C_rC₆-alkyl)₂, -CONHAr, -NH-CO— C_rC₆-alkyl, -NHCO— Ar, -NHCO-C_rC₆-alkoxy, -N-H-CO-Ar, -NHCO— NH₂, -NHCO— N(-d-C₆-alkyl)₂, -NHCO-NHAr, -NH-SO₂-d-C₆- alkyl, -NH— SO₂Ar, -NH— SO₂-nitrophenyl, -SO₂-OH, -SO₂— d-C₆-alkyl, -SO₂-Ar, -SO₂— Cj-Ce-alkoxy, -SO₂-OAr, -SO₂-NH₂, -SO₂-NH-d-C₆-alkyl,

-SO₂— N(d-C₆-alkyl)₂, -SO₂-NHAr, -SO₂-C_rC₆-alkoxy; n is 0 or 1 ; or a pharmaceutically acceptable salt thereof.

The alkyl groups, halogenalkyl groups, alkenyl groups, alkynyl groups, alkoxy groups, alkylamino groups, alkanoyl amino groups, alkanoyloxy groups and alkanoyl groups in general can be straight or branched. The same also applies to alkyl and alkyloxy groups (=alkoxy groups) if these are components of more complicated radicals for example in the form of a monoalkyl- or dialkylamino group, alkanoylamino group, carbalkoxy group, alkylcarbonyl group and analogous groups. The C₃ — C₇-cycloalkyl group is preferably cyclopentyl or cyclohexyl. C₂ — C₆-alkenyl preferably represents allyl. C₂ — C₆-alkynyl preferably represents propargyl.

The halogen atoms are chlorine, bromine or fluorine, in particular chlorine of fluorine. The alkyl and alkoxy groups as such or as components of groups of more complicated radicals consist in particular of 1 -4 carbon atoms, preferably 1 or 2 carbon atoms. Alkanoyl groups, such as alkanoylamino groups or alkanoyloxy groups consist in particular of 2-4, preferably 2-3 carbon atoms. Alk consists in particular of 1 -3, preferably 1 or 2 carbon atoms.

Among the more preferred compounds of this group are: 2-Amino-4-(4-fluorobenzylamino)-1 -ethoxycarbonylaminobenzene; 2-Amino-4-(4-trifluoromethylbenzylamino)-1 -ethoxycarbonylamino-benzene; 2-Amino-4-benzylamino-1 -ethoxycarbonylamino-benzene; 2-Amino-4-(3,5-dichlorobenzylamino)-1 -ethoxycarbonylamino benzene; 2-Amino-4-(3,5-dichlorobenzylamino)-1 -propyloxycarbonylamino benzene; 2-Amino-(2-chlorobenzylamino)-1 -(diethylcarbamoylamino) benzene; 2-Amino-4-(2,4-dichlorobenzylamino)-1 -(dimethylcarbamoylamino) benzene; and

1 ,2-Diacetylamino-4-(4-fluorobenzylamino) benzene.

Among the most preferred compounds for use in the methods of this invention are N-[2-amino-4-(4-fluorobenzylamino)-phenyl]carbamic acid and its pharmaceutically acceptable salts and ester forms. Of particular preference is retigabine, also known as

N-[2-amino-4-(4-fluorobenzylamino)-phenyl]carbamic acid ethyl ester (CAS Registry No.

150812-12-7), having the formula:

Also useful in the methods of this invention are the metabolite forms of retigabine which may be isolated from blood, urine or feces of recipients of N-[2-amino-4-(4- fluorobenzylamino)-phenyl]carbamic acid ethyl ester. The metabolites include the glucoside of retigabine, [4-(4-Fluoro-benzylamino)-2-(3,4,5-trihydroxy-6-hydroxymethyl- tetrahydropyran-2-ylamino)-phenyl]-carbamic acid ethyl ester, as well as its two glucoronide analogs, 6-[2-Ethoxycarbonylamino-5-(4-fluoro-benzylamino)-phenylamino]- 3,4,5Jrihydroxy-tetrahydro-pyran-2-carboxylic acid and 6-[(3-Amino-4-ethoxycarbonyl- amino-phenyl)-(4-fluoro-benzyl)-amino]-3,4,5Jrihydroxy-tetrahydro-pyran-2-carboxylic acid. Further metabolites include Λ/-[2-Amino-4-(4-fluoro-benzylamino)-phenyl]- acetamide, its cyclized analog (4-Fluoro-benzyl)-2-methyl-1 Hbenzoimidazol-5-yl)amine and the glucoronide analogs of Λ/-[2-Amino-4-(4-fluoro-benzylamino)-phenyl]acetamide, 6-[(4-Acetylamino-3-amino-phenyl)-(4-fluoro-benzyl)-amino]-3,4₁5-trihydroxy-tetrahydro- pyran-2-carboxylic acid and 6-[2-Acetylamino-5-(4-fluoro-benzylamino)-phenylamino]- 3,4,5Jrihydroxy-tetrahydro-pyran-2-carboxylic acid. Also useful in the methods of this invention are the compounds disclosed in U.S. Patent No. 5,565,483 (Hewawasam et al.), which issued on October 15, 1996, and EP 0747354B, the contents of which are incorporated herein by reference. These compounds include the substituted 3-phenyl oxindole compounds having the formulae:

wherein:

R is hydrogen, hydroxy or fluoro;

R¹, R², R³ and R⁴ each are independently hydrogen, Cι. alkyl, halogen, trifluoromethyl, phenyl, p-methylphenyl or p-trifluoromethylphenyl; or R¹ and R², R² and R³ or R³ and R⁴ are joined together to form a benzo fused ring;

R⁵ is hydrogen or C₁-₄ alkyl; and

R⁶ is chlorine or trifluoromethyl; or a nontoxic pharmaceutically acceptable salt, solvate or hydrate thereof, and optical forms thereof.

One group of the substituted 3-phenyl oxindole compounds useful with this invention include those described above wherein R is hydrogen. Another subgroup of these compounds include those in which R¹, R², R³ and R⁴ are each independently selected from H, Ci to C alkyl, halogen or trifluoromethyl, and when R¹ and R⁴ are H; R² or R³ is phenyl, p-methoxyphenyl or trifluormethylphenyl; or R¹ and R², R² and R³, or R³ and R⁴ are joined together to form a benzo fused ring; R5 is H or d to C alkyl; and R⁶ is chlorine or trifluoromethyl, or a pharmaceutically acceptable salt form thereof.

Non-limiting examples of these substituted 3-phenyl oxindole compounds are: (+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one; (±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one; (±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-4,6-dichloro-1 ,3-dihydro-3-hydroxy-2-H-indol-2-one; (±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-7-(trifluoromethyl)-2H-indol-2- one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-4-trifluoromethyl)2H-indol-2-one;

(±)-1 ,3-Dihydro-3-hydroxy-3-[2-hydroxy-5-(trifluoromethyl)phenyl]-6-(trifluoromethyl)-2H- indol-2-one; (±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-4,6-bis(trif luoromethyl)-2H-indol-

2-one;

(^^-(δ-Chloro^-methoxypheny -l ^-dihydro-S-hydroxy-θ-^rifluoromethy ^H-indol^- one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one;

(-)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-(trifluoromethyl)-2H-indol-2-one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-benz[g]indol-2one; (±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-phenyl-2H-indol-2-one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[g]indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-phenyl-2H-indol-2-one;

(+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-iodo-2H-indol-2one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-(4-methylphenyl)-2H-indol-2-one; (±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-7-(trifluoromethyl)-2H-indol-2-one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[e]indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-5-methyl-2H-indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-4,6-bis(trifluoromethyl)-2H-indol-

2-one; (±)-5-Bromo-3-(5-chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-2H-indol-2one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-[4-(trifluoromethyl)phenyl]-2H-indol-2- one; (±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-indol-2-one;

(±)-5-Bromo-3-(5-chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-indol-2-one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-4,6-dichloro-1 ,3-dihydro-2H-indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-6-iodo-2H-indol-2-one;

(±)-3-(5-Chloro-hydroxyphenyl)-1 ,3-dihydro-6-iodo-2H-indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-benz[f]indol-2one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-benz[f]indol-2one; and

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[f]indol-2-one; and the pharmaceutically acceptable salt forms thereof.

Among the more preferred compounds of this group are:

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-(trifluoromethyl)-2H-indol-2-one; (±)-3-(5-Chloro-2-hydroxyp eny - ,3- ihy ro-3- y roxy-2H-benz[g]indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-phenyl-2H-indol-2-one; and

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[f]indol-2-one.

Pharmaceutically acceptable salt forms of these substituted 3-phenyl oxindole compounds include those formed as base addition, including those formed using suitable inorganic bases, such as alkali and alkaline earth metal bases, such as sodium, potassium, magnesium and calcium metallic cations. The compounds may be administered as described in U.S. Patent No. 5,565,483. A pharmaceutically effective amount in mammals, including man, may be from about 0J μg/kg to about 100 mg/kg of body weight. Parenteral administration may be completed at an effective dose of from about 1 μg/kg to about 10 mg/kg of body weight. The methods of this invention are useful for inducing, assisting or maintaining desirable bladder control in a mammal experiencing or susceptible to bladder instability or urinary incontinence. These methods include prevention, treatment or inhibition of bladder-related urinary conditions and bladder instability, including nocturnal enuresis, nocturia, voiding dysfunction and urinary incontinence. Also treatable or preventable with the methods of this invention is bladder instability secondary to prostate hypertrophy. The compounds described herein are also useful in promoting the temporary delay of urination whenever desirable. The compounds of this invention may also be utilized to stabilize the bladder and treat or prevent incontinence which urge urinary incontinence, stress urinary incontinence or a combination of urge and stress incontinence in a mammal, which may also be referred to as mixed urge and stress incontinence. These methods include assistance in preventing or treating urinary incontinence associated with secondary conditions such as prostate hypertrophy.

These methods may be utilized to allow a recipient to control the urgency and frequency of urination. The methods of this invention include the treatment, prevention, inhibition and amelioration of urge urinary incontinence also known as bladder instability, neurogenic bladder, voiding dysfunction, hyperactive bladder, detrusor overactivity, detrusor hyper-reflexia or uninhibited bladder.

As described above, methods of this invention include treatments, prevention, inhibition or amelioration of hyperactive or unstable bladder, neurogenic bladder or hyperreflexic bladder. These uses include, but are not limited to, those for bladder activities and instabilities in which the urinary urgency is associated with prostatitis, prostatic hypertrophy, interstitial cystitis, urinary tract infections or vaginitis. The methods of this invention may also be used to assist in inhibition or correction of the conditions of Frequency-Urgency Syndrome, and lazy bladder, also known as infrequent voiding syndrome.

The methods of this invention may also be used to treat, prevent, inhibit, or limit the urinary incontinence, urinary instability or urinary urgency associated with or resulting from administrations of other medications, including diuretics, vasopressin antagonists, anticholinergic agents, sedatives or hypnotic agents, narcotics, alpha-adrenergic agonists, alpha-adrenergic antagonists, or calcium channel blockers. The methods of this invention are useful for inducing or assisting in urinary bladder control or preventing or treating the maladies described herein in humans in need of such relief, including adult and pediatric uses. However, they may also be utilized for veterinary applications, particularly including canine and feline bladder control methods. If desired, the methods herein may also be used with farm animals, such as ovine, bovine, porcine and equine breeds.

The applications may utilize conventional oral, rectal, parenteral or intravenous delivery methods as conventionally utilized in veterinary practice. Most preferable in most instance for home use with companion animals are oral tablets or capsules or neat compound or powdered or granular pharmaceutical formulations which may be mixed with chewable or liquid veterinary formulations or food materials or liquids acceptable to the animal in question.

As used herein, the terms "pharmaceutically effective amount" or "therapeutically effective amount" mean the total amount of each active component of the pharmaceutical composition or method that is sufficient to show a meaningful patient benefit, i.e., treatment, prevention or amelioration of urinary incontinence or the excessive or undesirable urge to urinate, or a decrease in the frequency of incidence of urinary incontinence. When applied to an individual active ingredient, administered alone, the term refers to that ingredient alone. When applied to a combination, the term refers to combined amounts of the active ingredients that result in the therapeutic effect, whether administered in combination, serially or simultaneously.

The methods of this invention may be accomplished with a daily dose of the active compounds described above from U.S. Patent No. 5,384,330 of from about 0J mg/kg to about 10 mg/kg. Doses may be administered as a single regimen, such as only prior to bedtime or before travel, or as a continuous regimen divided by two or more doses over the course of a day. Human administration may be at dosages of from about 10 mg BID to about 1000 mg BID, preferably from about 50 mg BID to about 500 mg BID, more preferably at a dose of from about 100 mg BID to about 300 mg BID. The KCNQ potassium channel agonists of this invention may also be administered in the methods of this invention in combination with pharmaceutically effective amounts of other medicinal agents useful for bladder control or the treatment or inhibition of urinary incontinence. For instance, the compounds may be administered with desmopressin acetate, available as DDAVP^® Nasal Spray and DDAVP^® tablets from Aventis Pharmaceuticals, as well as a desmopressin acetate rhinal tube from Ferring Pharmaceuticals Inc. Other combination products include tolterodine tartrate (available as DETROL™ tablets from Pharmacia & Upjohn), oxybutinin chloride (available in the form of DITROPAN^® tablets and syrup and DITROPAN XL^® extended release tablets from ALZA Pharmaceuticals), propanthaline bromide (available in tablet form from Roxane Laboratories, Inc.), hyoscyamine and hyoscyamine sulfate (available, respectively, as CYSTOPAZ^® tablets and CYSTOPAZ-M^® timed release capsules from PolyMedica Pharmaceuticals (U.S.A.), Inc.), hyoscyamine hydrobromide, flavoxate HCI (available in URISPAS^® 100 mg tablets from ALZA Pharmaceuticals), imipramine HCI (available in 10 mg, 25 mg and 50 mg tablets from Geneva Pharmaceuticals, Inc.), phenylpropanolamine, midodrine HCI (available in 2.5 mg and 5 mg PROAMATINE^® tablets from Shire US Inc.), phenoxybenzamine HCI (available as DIBENZYLINE^® capsules from WellSpring Pharmaceuticals Corporation), and prazosin HCI (available in MINIPRESS^® capsules from Pfizer Inc.). Each of these medicaments may be administered in the pharmaceutically effective amounts and regimens known in the art, including those listed in the Physicians' Desk Reference, 55 Edition, 2001 , published by Medical Economics Company, Inc. at Monvale, NJ 07645-1742, the relevant portions of which are incorporated herein by reference. The KCNQ channel agonists of this invention may also be used in conjunction with one or more compounds which act as vasopressin agonists including, but not limited to those described in U.S. Patent No. 6,194,407 (Failli et al.), U.S. Patent No. 6,090,803 (Failli et al.), U.S. Patent No. 6,096,736 (Ogawa et al.), and U.S. Patent No. 6,096,735 (Ogawa et al.).

Compounds as described in U.S. Patent No. 5,384,330, including retigabine, can be administered orally using conventional pharmaceutical excipients or carriers, preferably coated or contained in hard or soft gelatin capsules. Examples of oral formulations contained in hard gelatin capsules can include those in which the active compound comprises from about 45% to 50%, by weight, of the formulation. Microcrystalline cellulose comprises from about 43% to about 47%, povidone comprises from about 3% to about 4%, and silicon dioxide and magnesium stearate each comprise from about 0.3% to about 0.7%, each by weight. Specific examples of capsules containing 50 mg, 100 mg and 200 mg may be formulated utilizing the following lists of components.

50 mg Retigabine Capsules

Ingredient Amount/Capsule

Retigabine 50.0 mg

Microcrystalline Cellulose, NF 45.5 mg

Povidone, USP 3.5 mg

Silicon Dioxide, Colloidal, anhydrous, NF 0.5 mg

Magnesium Stearate, EP 0.5 mg

Theoretical Fill Weight 100.0 mg

100 mg Retigabine Capsules

Ingredient Amount/Capsule

Retigabine 100.0 mg

Microcrystalline Cellulose, NF 91.0 mg

Povidone, USP 7.0 mg

Silicon Dioxide, Colloidal, anhydrous, NF 1.0 mg

Magnesium Stearate, EP 1.0 mg

Theoretical Fill Weight 200.0 mg

200 mg Retigabine Capsules

Ingredient Amount/Capsule

Retigabine 200.0 mg

Microcrystalline Cellulose, NF 182.0 mg

Povidone, USP 14.0 mg

Silicon Dioxide, Colloidal, anhydrous, NF 2.0 mg

Magnesium Stearate, EP 2.0 mg

Theoretical Fill Weight 400.0 mg The ingredients in the formulations above can be prepared using the following steps.

1 ) Weigh separately the active ingredient (retigabine), preferably screened through an 800 micron screen, and the microcrystalline cellulose components.

2) Prepare a granulation solution by dissolving the Povidone, USP in purified water.

3) Place the ingredients from Step 1 into a suitable blender and mix thoroughly.

4) Screen the mixture from Step 3 through a 1000 μm screen and place the screened mixture into the vessel of a fluidized bed granulator.

5) Heat the ingredients in the fluid bed granulator up to 27°C product temperature while mixing.

6) Add the granulation solution from Step 2 to the fluid bed.

7) Dry the granulate in the fluid bed.

8) Weigh the colloidal silicon dioxide component, preferably screened through a 1000 μm screen, and the magnesium stearate component, preferably screened through a 600 μm screen.

9) Add the silicon dioxide and magnesium stearate components to the fluid bed granulator's vessel containing the dried granulate from Step 7 and mix the components thoroughly.

10) Screen the mixed components from Step 9, preferably through a 800μm screen.

1 1 ) Transfer the final screened components into a suitable blender and mix thoroughly. The final component mixture from Step 1 1 can then be coated, encapsulated or compressed into tablets utilizing conventional tablet excipients or carriers, as desired. It will be understood that oral dosage forms within the scope of this invention can be prepared using the components listed above in respective amounts according the dose of active ingredient in the particular formulation. For veterinary uses, the final mixture of Step 1 1 can be administered neat or mixed into foods acceptable to the animal in question. Further, the mixtures can be formulated into tablets, capsules or coated products, as described above, or integrated into conventional veterinary medicaments or food products.

For intravenous administration, the compounds from U.S. Patent No. 5,384,330 described herein may be prepared and maintained in conventional lyophylized formulations and reconstituted prior to administration with an intravenously acceptable saline solution, such as a 0.9% saline solution. The pH of the intravenous formulation can be adjusted, as needed, with an intravenous and pharmaceutically acceptable acid, such as methanesulfonic acid.

KNCQ1 , 3 and 5 expression and M-current activity in rat urinary bladder

Using quantitative rtPCR, the expression of KCNQ1 , KCNQ3 and KCNQ5 potassium channels was identified in the rat urinary bladder. The highest levels of expression were seen in KCNQ5 (0.2+0J ng KCNQ5 mRNA/GAPDH mRNA). To further probe M-current activity in the bladder, retigabine (10μM, M-current agonist) was tested in isolated bladder smooth muscle cells using standard patch-clamp techniques. Exposure to retigabine significantly increased an outward current that was insensitive to iberiotoxin and was associated with a membrane hyperpolarization of 17.8 ± 3.0 mV (n=5). This hyperpolarization was reversed by the addition of linopirdine (50μM an M- current antagonist) to the tissue bath. Retigabine relaxed isolated carbachol contracted rat bladder strips with an IC₅₀ of 3.5+0.9 μM (n=14). This relaxation was reversed by the M-current blockers linopirdine and XE-991.

Claims

CLAIMS:

1 . A method of inducing or maintaining bladder control in a mammal, the method comprising administering to a mammal in need thereof a pharmacologically effective amount of a KCNQ potassium channel agonist.

2. A method of treatment or prevention of urinary incontinence in a mammal, the method comprising administering to a mammal in need thereof a pharmacologically effective amount of a KCNQ potassium channel agonist.

3. A method according to Claim 2 wherein the urinary incontinence is urge incontinence.

4. A method according to Claim 2 wherein the urinary incontinence is secondary to prostate hypertrophy.

5. A method according to Claim 2 wherein the urinary incontinence is mixed urge and stress incontinence.

6. A method according to any one of Claims 1 to 5 wherein the KCNQ potassium channel is a KCNQ4 potassium channel.

7. A method according to any one of Claims 1 to 5 wherein the KCNQ potassium channel is a KCNQ2/3 potassium channel.

8. A method according to any one of Claims 1 to 5 wherein the KCNQ potassium channel is a KCNQ3/5 potassium channel.

9. A method according to any one of Claims 1 to 8 wherein the mammal is a human.

10. A method according to any one of Claims 1 to 8 wherein the mammal is feline or canine.

11. A method according to any one of Claims 1 to 10 in which the KCNQ potassium channel agonist is a compound of the formula (I):

wherein:

Rj is selected from hydrogen, Ci — C₆-alkyl, C₂ — C₆-alkanoyl or the radical Ar; R₂ is selected from hydrogen or d — C₆-alkyl;

R₃ is selected from d — C₆-alkoxy, NH₂, d — C₆-alkylamino, Ci — C₆-dialkylamino, amino substituted by the radical Ar, Ci — C₆-alkyl, C₂ — C₆-alkenyl, C₂ — C₆-alkynyl, the radical Ar or the radical ArO-;

R₄ is selected from hydrogen, Ci — C₆-alkyl or the radical Ar; R₅ is selected from hydrogen or Ci — C₆-alkyl or the radical Ar; Alk indicates a straight or branched alkylene group with 1 -9 carbon atoms, which can also be substituted by the radical Ar; Ar is a phenyl radical substituted by the radicals R_s, R₇ and/or R₈ where these radicals R₆, R₇ and R₈ are the same or different and represent H, d — C₆-alkyl, C₃ — C₇- cycloalkyl, hydroxy, d — C₆-alkoxy, C₂ — C₆-alkanoyloxy, halogen, hydroxy, d — C₆- halogenoalkyl, -CN, -NH₂, -NH— Ci— C₆-alkyl, -N(d— C₆-alkyl)₂, -CO₂H, -CO— d— Ce- alkyl, -CO— O— d— Ce-alkyl, -COAr, -CO— OAr, -CONH₂, -CONH— d— C₆-alkyl, -CON(d— C₆-alkyl)₂, -CONHAr, -NH— CO— d— C₆-alkyl, -NHCO— Ar, -NHCO— d-Ce-alkoxy, -N— H— CO— Ar, -NHCO— H₂, -NHCO— N(-d— C₆-alkyl)₂, -NHCO— NHAr, -NH— SO₂— C— 1— C₆-alkyl, -NH— SO₂Ar, -NH— SO₂-nitrophenyl, -SO₂— OH, -SO₂— d— Ce-alkyl, -SO₂-Ar, -SO₂— d— C₆-alkoxy, -SO₂— OAr, -SO₂— NH₂, -SO₂— NH— d— Ce-alkyl, -S0₂— N(d— C₆-alkyl)₂, -SO₂— NHAr, -SO₂— d— C₆-alkoxy; n is 0 or 1 ; or a pharmaceutically acceptable salt thereof.

12. A method according to Claim 1 1 in which the compound of formula I is selected from the group of:

2-Amino-4-(4-fluorobenzylamino)-1 -ethoxycarbonylaminobenzene; 2-Amino-4-(4-trifluoromethylbenzylamino)-1 -ethoxycarbonylamino-benzene; 2-Amino-4-benzylamino-1 -ethoxycarbonylamino-benzene;

2-Amino-4-(3,5-dichlorobenzylamino)-1 -ethoxycarbonylamino benzene; 2-Amino-4-(3,5-dichlorobenzylamino)-1 -propyloxycarbonylamino benzene; 2-Amino-(2-chlorobenzylamino)-1 -(diethylcarbamoylamino) benzene; 2-Amino-4-(2,4-dichlorobenzylamino)-1 -(dimethylcarbamoylamino) benzene; or 1 ,2-Diacetylamino-4-(4-fluorobenzylamino) benzene; or a pharmaceutically acceptable salt thereof.

13. A method according to Claim 1 1 in which the compound of formula I is N-[2-amino-4-(4-fluorobenzylamino)-phenyl]carbamic acid or a pharmaceutically acceptable salt or ester form thereof.

14. A method according to Claim 13 wherein the pharmaceutically acceptable ester form is N-[2-amino-4-(4-fluorobenzylamino)-phenyl]carbamic acid ethyl ester.

15. A method according to Claim 13 or Claim 14 wherein the pharmacologically effective amount is from about 0J mg/kg to about 10 mg/kg.

16. A method according to Claim 13 or Claim 14 wherein the pharmacologically effective amount is from about 10 mg BID to about 1000 mg BID.

17. A method according to Claim 13 or Claim 14 wherein the pharmacologically effective amount is from about 50 mg BID to about 500 mg BID.

18. A method according to Claim 13 or Claim 14 wherein the pharmacologically effective amount is from about 100 mg BID to about 300 mg BID.

19. A method according to any one of Claims 1 to 10 in which the KCNQ potassium channel agonist is a compound of the formula (II)::

wherein:

R is hydrogen, hydroxy or fluoro;

R¹, R², R³ and R⁴ each are independently hydrogen, d-₄ alkyl, halogen, trifluoromethyl, phenyl, p-methylphenyl or p-trifluoromethylphenyl; or R¹ and R², R² and R³ or R³ and R⁴ are joined together to form a benzo fused ring;

R⁵ is hydrogen or d-₄ alkyl; and

R⁶ is chlorine or trifluoromethyl; or a nontoxic pharmaceutically acceptable salt, solvate or hydrate thereof..

20. A method according to Claim 19 in which the compound of formula II is selected from the group of: (+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one;

(i)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-6-(thfluoromethyl)-2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one; (±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-(trifluoromethyl)-2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-4,6-dichloro-1 ,3-dihydro-3-hydroxy-2-H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-7-(thfluoromethyl)-2H-indol-2- one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-4-trifluoromethyl)2H-indol-2-one; (+)-1 ,3-Dihydro-3-hydroxy-3-[2-hydroxy-5-(trifluoromethyl)phenyl]-6-(trifluoromethyl)-2H- indol-2-one; (+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-4,6-bis(trifluoromethyl)-2H-indol-

2-one;

(-)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)-2H-indol-2- one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)2H-indol-2- one;

(-)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-6-(trifluoromethyl)2H-indol-2- one;

(+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-(trifluoromethyl)2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-benz[g]indol-2one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-phenyl-2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[g]indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-phenyl-2H-indol-2-one;

(+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-6-iodo-2H-indol-2one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-(4-methylphenyl)-2H-indol-2-one;

(+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-7-(trifluoromethyl)-2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[e]indol-2-one;

(+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-5-methyl-2H-indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-4,6-bis(trifluoromethyl)-2H-indol-

2-one;

(+)-5-Bromo-3-(5-chloro-2-methoxyphenyl)-1 ,3-dihydro-3-fluoro-2H-indol-2one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-6-[4-(trifluoromethyl)phenyl]-2H-indol-2- one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-indol-2-one;

(+)-5-Bromo-3-(5-chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-indol-2-one;

(+)-3-(5-Chloro-2-hydroxyphenyl)-4,6-dichloro-1 ,3-dihydro-2H-indol-2-one;

(±)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-6-iodo-2H-indol-2-one;

(+)-3-(5-Chloro-hydroxyphenyl)-1 ,3-dihydro-6-iodo-2H-indol-2-one;

(+)-3-(5-Chloro-2-methoxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-benz[f]indol-2one;

(±)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-3-hydroxy-2H-benz[f]indol-2one; and

(+)-3-(5-Chloro-2-hydroxyphenyl)-1 ,3-dihydro-2H-benz[f]indol-2-one; and the pharmaceutically acceptable salt forms thereof. medicament for inducing or maintaining bladder control in a mammal.

22. Use of a KCNQ potassium channel agonist in the preparation of a medicament for the treatment or prevention of urinary incontinence in a mammal.