EP2049093A2 - Pharmaceutical composition containing saredutant and a selective inhibitor of serotonin recapture or an inhibitor of serotonin/norepinephrine recapture in combination - Google Patents

Pharmaceutical composition containing saredutant and a selective inhibitor of serotonin recapture or an inhibitor of serotonin/norepinephrine recapture in combination

Info

Publication number
EP2049093A2
EP2049093A2 EP07823369A EP07823369A EP2049093A2 EP 2049093 A2 EP2049093 A2 EP 2049093A2 EP 07823369 A EP07823369 A EP 07823369A EP 07823369 A EP07823369 A EP 07823369A EP 2049093 A2 EP2049093 A2 EP 2049093A2
Authority
EP
European Patent Office
Prior art keywords
disorder
pharmaceutically acceptable
saredutant
combination
pharmaceutical composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP07823369A
Other languages
German (de)
French (fr)
Inventor
Guy Griebel
Caroline Cohen
Caroline Louis
Lisa Arvanitis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanofi SA
Original Assignee
Sanofi Aventis France
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FR0607050A external-priority patent/FR2904221B1/en
Priority claimed from FR0700863A external-priority patent/FR2912057B1/en
Application filed by Sanofi Aventis France filed Critical Sanofi Aventis France
Publication of EP2049093A2 publication Critical patent/EP2049093A2/en
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/15—Oximes (>C=N—O—); Hydrazines (>N—N<); Hydrazones (>N—N=) ; Imines (C—N=C)
    • 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
    • A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • 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
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • 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
    • A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
    • 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
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4525—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • the present invention relates to pharmaceutical compositions containing in combination (S) - (-) - N- [4- (4-acetamido-4-phenylpiperidin-1-yl) -2- (3,4-dichlorophenyl) butyl] ] N-methylbenzamide or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor.
  • compound A hereinafter referred to as compound A, and its pharmaceutically acceptable salts have been described as antagom 'sts nonpeptide, potent and selective NK2 receptors of neurokinin A (Life Sciences, 1992, 50 (15), PL101-PL106) and can be prepared according to patents EP 0 474 561 or US 5 236 921.
  • the salts are salts with conventional pharmaceutically acceptable inorganic or organic acids such as hydrochloride, hydrobromide, sulfate, hydrogen sulfate, dihydrogenphosphate, methanesulfonate, methylsulfate, acetate, oxalate, maleate, fumarate, succinate, naphthalene
  • selective serotonin reuptake inhibitor is meant a compound such as, for example: - ( ⁇ ) N-methyl-3-phenyl-3- [4- (trifluoromethyl) ) phenoxy] propan-1-amine, whose international nonproprietary name is fluoxetine, of formula: hereinafter referred to as compound B, and its pharmaceutically acceptable salts which may be prepared according to US Pat. No. 4,314,081; 1- [3- (dimethylamino) propyl] -1- (4-fluorophenyl) -1,3-dihydro-2-benzofuran-5-carbonitrile, the international nonproprietary name of which is citalopram and its pharmaceutically acceptable salts, which may be prepared according to the patent
  • selective serotonin / norepinephrine reuptake inhibitor is meant a compound such as, for example:
  • compositions containing such combinations may be useful for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, non-depressive disorder. specified, bipolar disorder
  • bipolar disorder II bipolar disorder II, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
  • compositions containing such combinations may be useful for the manufacture of medicaments for the prevention and treatment of a major depressive disorder.
  • pharmaceutical compositions containing such combinations may be useful for the manufacture of medicaments for the treatment of sexual dysfunction associated with major depressive disorder.
  • disorders of sexual desire that is to say, disorder: lowering of sexual desire and disorder: sexual aversion
  • disorders of sexual arousal that is to say the disorder of sexual arousal in women and erectile dysfunction in men
  • disorders of orgasm ie orgasm disorder in women, orgasm disorder in men, and premature ejaculation
  • sexual disorders with pain ie dyspareunia and vaginismus
  • dysfunction sexual dysfunction due to a general medical condition, substance-induced sexual dysfunction, and unspecified sexual dysfunction.
  • the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with a serotonin reuptake inhibitor. and norepinephrine, as well as at least one pharmaceutically acceptable excipient.
  • the present invention relates to pharmaceutical compositions containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor chosen from fluoxetine, citalopram, escitalopram, paroxetine, sertraline and fluvoxamine, or a pharmaceutically acceptable salt thereof and at least one pharmaceutically acceptable excipient.
  • a selective serotonin reuptake inhibitor chosen from fluoxetine, citalopram, escitalopram, paroxetine, sertraline and fluvoxamine, or a pharmaceutically acceptable salt thereof and at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with fluoxetine or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with citalopram or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitalopram or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its salts pharmaceutically acceptable, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with sertraline or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
  • the present invention relates to pharmaceutical compositions containing in combination the saredutant or one of its pharmaceutically acceptable salts with fluvoxamine or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
  • the present invention relates to pharmaceutical compositions containing in combination the saredutant or one of its pharmaceutically acceptable salts with a serotonin / norepinephrine reuptake inhibitor, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran, or one of their pharmaceutically acceptable salts and at least one pharmaceutically acceptable excipient.
  • a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran, or one of their pharmaceutically acceptable salts and at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with venlafaxine or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with duloxetine or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
  • compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with milnacipran or one of its salts. pharmaceutically acceptable, as well as at least one pharmaceutically acceptable excipient.
  • the present invention relates to the combination of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor.
  • the present invention relates to the combination of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor selected from fmoxetine, citalopram, escitalopram, paroxetine, sertraline and fluvoxamine or a pharmaceutically acceptable salt thereof.
  • the subject of the present invention is the combination of saredutant or a pharmaceutically acceptable salt thereof with a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran or one of their pharmaceutically acceptable salts.
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with an inhibitor of the reuptake of serotonin / norepinephrine or a pharmaceutically acceptable salt thereof for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, unspecified depressive disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
  • mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, unspecified depressive disorder, bipolar I disorder, bipolar
  • the present invention relates to the use of a pharmaceutical composition containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with a reuptake inhibitor.
  • serotonin / norepinephrine or a pharmaceutically acceptable salt thereof for the manufacture of medicaments for the prevention and treatment of a major depressive disorder.
  • the subject of the present invention is the use of a pharmaceutical composition containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with a reuptake inhibitor.
  • serotonin / norepinephrine or a pharmaceutically acceptable salt thereof for the manufacture of medicaments for the treatment of sexual dysfunction associated with a major depressive disorder.
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitolopram or one of its pharmaceutically acceptable salts, for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, unspecified depressive disorder, bipolar I disorder, bipolar disorder II, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
  • mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, unspecified depressive disorder, bipolar I disorder, bipolar disorder II, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitolopram or one of its pharmaceutically acceptable salts, for the manufacture of medicines for the prevention and treatment of a major depressive disorder.
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitolopram or one of its pharmaceutically acceptable salts, for the manufacture of drugs for the treatment of sexual dysfunction associated with major depressive disorder.
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its pharmaceutically acceptable salts, for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, resistant depressive disorder, dysthymic disorder, non-depressive disorder specified, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
  • mood disorders selected from major depressive disorder, resistant depressive disorder, dysthymic disorder, non-depressive disorder specified, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its pharmaceutically acceptable salts, for the manufacture of medicaments intended for the prevention and treatment of a major depressive disorder.
  • the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its pharmaceutically acceptable salts, for the manufacture of medicaments for the treatment of sexual dysfunction associated with major depressive disorder.
  • the present invention relates to the use of the combination of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine inhibitor or a pharmaceutically acceptable salt thereof, for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, non-specified depressive disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, mood disorder unspecified ; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
  • mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, non-specified depressive disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, un
  • excipients are selected according to the pharmaceutical form and the desired mode of administration, from the usual excipients which are known to those skilled in the art.
  • compositions of the present invention for oral, sublingual, subcutaneous, intramuscular, intravenous, topical, local, intratracheal, intranasal, transdermal or rectal administration, the principles
  • the active ingredients can be administered in unit dosage form, in admixture with conventional pharmaceutical excipients, to animals and humans for the prevention or treatment of the above disorders or diseases.
  • Suitable unit dosage forms include oral forms such as tablets, soft or hard capsules, powders, granules and oral solutions or suspensions, sublingual, oral, intratracheal, intraocular forms of administration. , intranasal, inhalation, topical, transdermal, subcutaneous, intramuscular or intravenous administration forms, rectal administration forms and implants.
  • the compounds according to the invention can be used in creams, gels, ointments or lotions.
  • the active ingredient or active ingredients are generally formulated in dosage units.
  • the dosage unit contains 2.5 to 500 mg, preferably 10 to 250 mg, preferably 10 to 150 mg per dosage unit, for daily administrations, one or more times per day.
  • these assays are examples of average situations, there may be special cases where higher or lower dosages are appropriate, such assays also belong to the invention.
  • the dosage appropriate to each patient is determined by the physician according to the mode of administration, the age, the weight and the response of said patient.
  • the compound A and the other active ingredient according to the invention can be administered simultaneously, separately or spread over time.
  • Extended use over time is understood to mean the sequential administration of the first compound of the composition according to the invention, included in a pharmaceutical form, and then of the second compound of the composition according to the invention, included in a pharmaceutical form. separate.
  • the lapse of time elapsed between the administration of the first compound of the composition according to the invention and the administration of the second compound of the same composition according to the invention does not exceed usually not 24 hours.
  • the unit dosage forms containing either only one of the constituent compounds of the composition according to the invention, or the combination of the two compounds which can be used in the various types of use described above, may for example be appropriate for the oral, nasal, parenteral or transdermal administration.
  • two different dosage forms may be for the same route of administration or a different route of administration (oral and transdermal). or oral and nasal or parenteral and transdermal etc.).
  • the invention therefore also relates to a kit containing compound A and the other active ingredient according to the invention wherein said compound A, and the other active ingredient according to the invention are in separate compartments and in similar or different packages. and are intended to be administered simultaneously, separately or spread over time.
  • the increase in the pharmacological effects of a combination according to the invention of compound A and fluoxetine (compound B) has been demonstrated in animals.
  • the combination was administered intraperitoneally by two simultaneous administrations of compound A (3 mg / kg) and then compound B (2.5 mg / kg).
  • the doses of the compounds being expressed as free base.
  • the effects of a combination of the saredutant with Pescitalopram according to the invention are evaluated in randomized, double-blind, multicenter, eight-week clinical trials comparing a fixed-dose group of saredutant once daily with a dose fixed escitalopram once daily with a group receiving saredutant placebo in combination with a fixed dose of escitalopram and another group receiving placebo saredutant with placebo escitalopram.
  • Hamilton depression rating scale It measures the change in total score on the Hamilton depression rating scale includes 17 items (HAM-D, English Hamilton Depression Rating Scale) between the last visit (under 56 th day) and first visit (before the start of treatment) compared to the placebo group.
  • the Hamilton Depression Rating Scale is defined by Hamilton M., J. Neurol.
  • CSFQ is defined by Clayton AH et al., Psychopharmacol.

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Reproductive Health (AREA)
  • Endocrinology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pregnancy & Childbirth (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

The object of the present invention is pharmaceutical compositions containing (S)-(-)-N-[4-(4-acetamido-4-phenylpiperidin-l-yl)-2-(3,4-dichlorophenyl)butyl]-N-methylbenzamide or one of its pharmaceutically acceptable salts in combination with a selective inhibitor for serotonin recapture or with an inhibitor of serotonin/norepinephrine recapture.

Description

COMPOSITION PHARMACEUTIQUE CONTENANT EN ASSOCIATION LE SAREDUTANT ET UN INHIBITEUR SELECTIF DE LA RECAPTURE DE LA SEROTONINE OU UN INHIBITEUR DE LA RECAPTURE DE LA SEROTONINE/NOREPINEPHRINE. PHARMACEUTICAL COMPOSITION CONTAINING IN ASSOCIATION SAREDUTANT AND A SELECTIVE SEROTONIN RECAPTURE INHIBITOR OR A SEROTONIN / NOREPINEPHRINE RECAPTURE INHIBITOR.
La présente invention a pour objet des compositions pharmaceutiques contenant en association le (S)-(-)-N-[4-(4-acétamido-4-phénylpipéridin-l-yl)-2-(3,4- dichlorophényl)butyl]~N-méthylbenzamide ou l'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine.The present invention relates to pharmaceutical compositions containing in combination (S) - (-) - N- [4- (4-acetamido-4-phenylpiperidin-1-yl) -2- (3,4-dichlorophenyl) butyl] ] N-methylbenzamide or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor.
Le (S)-(-)-N-[4-(4-acétamido-4-phénylpipéridin- 1 -yl)-2-(3,4-dichlorophényl) butyl]-N-méthylbenzamide dont la dénomination commune internationale est saredutant, de formule :(S) - (-) - N- [4- (4-acetamido-4-phenylpiperidin-1-yl) -2- (3,4-dichlorophenyl) butyl] -N-methylbenzamide International Trade Name Sarmutant , of formula:
ci-après dénommé composé A, et ses sels pharmaceutiquement acceptables ont été décrits comme des antagom'stes non peptidiques, puissants et sélectifs des récepteurs NK2 de la neurokinine A (Life Sciences, 1992, 50(15), PL101-PL106) et peuvent être préparés selon les brevets EP O 474 561 ou US 5 236 921. hereinafter referred to as compound A, and its pharmaceutically acceptable salts have been described as antagom 'sts nonpeptide, potent and selective NK2 receptors of neurokinin A (Life Sciences, 1992, 50 (15), PL101-PL106) and can be prepared according to patents EP 0 474 561 or US 5 236 921.
Les sels sont les sels avec des acides minéraux ou organiques pharmaceutiquement acceptables classiques tels que le chlorhydrate, le bromhydrate, le sulfate, l'hydrogénosulfate, le dihydrogénophosphate, le méthanesulfonate, le méthylsulfate, l'acétate, l'oxalate, le maléate, le fumarate, le succinate, le naphtalène-The salts are salts with conventional pharmaceutically acceptable inorganic or organic acids such as hydrochloride, hydrobromide, sulfate, hydrogen sulfate, dihydrogenphosphate, methanesulfonate, methylsulfate, acetate, oxalate, maleate, fumarate, succinate, naphthalene
2-sulfonate, le glyconate, le gluconate, le citrate, l'iséthionate, le benzènesulfonate, le paratoluènesulfonate .2-sulfonate, glyconate, gluconate, citrate, isethionate, benzenesulfonate, paratoluenesulfonate.
Par inhibiteur sélectif de la recapture de la sérotonine (SSRI de l'anglais Sélective Serotonin Reuptake Inhibitor) on entend un composé tel que, par exemple : - le (±) N-méthyl-3-phényl-3-[4-(trifluorométhyl)phénoxy]propan-l -aminé, dont la dénomination commune internationale est fluoxetine, de formule : ci-après dénommé composé B, et ses sels pharmaceutiquement acceptables qui peuvent être préparés selon le brevet US 4 314 081; - le l-[3-(diméthylammo)propyl]-l-(4-fluorophényl)-l,3-dihydro-2-benzofuran-5- carbonitrile, dont la dénomination commune internationale est citalopram et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon le brevetBy selective serotonin reuptake inhibitor (SSRI) is meant a compound such as, for example: - (±) N-methyl-3-phenyl-3- [4- (trifluoromethyl) ) phenoxy] propan-1-amine, whose international nonproprietary name is fluoxetine, of formula: hereinafter referred to as compound B, and its pharmaceutically acceptable salts which may be prepared according to US Pat. No. 4,314,081; 1- [3- (dimethylamino) propyl] -1- (4-fluorophenyl) -1,3-dihydro-2-benzofuran-5-carbonitrile, the international nonproprietary name of which is citalopram and its pharmaceutically acceptable salts, which may be be prepared according to the patent
US 4 136 193 ;US 4,136,193;
- le S-(+)-l-[3-(diméthylamino)propyl]-l-(4-fluorophényl)-l,3-dihydro-2-benzofuran- 5-carbonitrile dont la dénomination commune internationale est escitalopram et ses sels pharmaceutiquement acceptables qui peuvent être préparés selon le brevet EP O 347 066 or US 4,943,590 ;S - (+) - 1- [3- (dimethylamino) propyl] -1- (4-fluorophenyl) -1,3-dihydro-2-benzofuran-5-carbonitrile, the international nonproprietary name of which is escitalopram and its salts pharmaceutically acceptable compounds which can be prepared according to EP 0 347 066 or US Pat. No. 4,943,590;
- le trans-(-)-3-[(l,3-benzodioxol-5-yloxy)méthyl]-4-(4-fluorophényl)pipéridine, dont la dénomination commune internationale est paroxetine et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon les brevets US 3 912 743 et US 4 007 196 ; - le (lS-cis)-4-(3,4-dichlorophényl)-l,253,4-tétrahydro-N-méthyl-l-naphtalèneamine, dont la dénomination commune internationale est sertraline et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon le brevet US 4 536 518 ;trans - (-) - 3 - [(1,3-benzodioxol-5-yloxy) methyl] -4- (4-fluorophenyl) piperidine, the international nonproprietary name of which is paroxetine and its pharmaceutically acceptable salts, which may be prepared according to US Pat. Nos. 3,912,743 and 4,007,196; - the (lS-cis) -4- (3,4-dichlorophenyl) -l, 2 5 3,4-tetrahydro-N-methyl-l-naphthalenamine, whose international nonproprietary name is sertraline and pharmaceutically acceptable salts thereof, which may be prepared according to US Patent 4,536,518;
- le 5-méthoxy-l-[4-(trifluorométhyl)phényl]-l-pentanone-0-(2-aminoéthyl)oxime, dont la dénomination commune internationale est fluvoxamine et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon le brevet US 4 085 225 ;5-methoxy-1- [4- (trifluoromethyl) phenyl] -1-pentanone-O- (2-aminoethyl) oxime, whose international nonproprietary name is fluvoxamine and its pharmaceutically acceptable salts, which may be prepared according to the patent U.S. 4,085,225;
Par inhibiteur de la recapture de la sérotonine/norépinephrine (SNRI de l'anglais Sélective Serotonin/Norepinephrine Reuptake Inhibitor) on entend un composé tel que, par exemple :By selective serotonin / norepinephrine reuptake inhibitor (SNRI) is meant a compound such as, for example:
- le l-[2-diméthylamino-l-(4-méthoxyphényl)éthyl]cyclohexan-l-ol dont la dénomination commune internationale est venlafaxine, et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon le brevet EP 0 112 669 ; - le (+)-(S)-N-méthyl-3-(l-naphtyloxy)-3-(thiophen-2-yl)ρropan-l-amine dont la dénomination commune internationale est duloxetine, et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon le brevet EP 0 273 658 ;1- [2-dimethylamino-1- (4-methoxyphenyl) ethyl] cyclohexan-1-ol, whose international non-proprietary name is venlafaxine, and its pharmaceutically acceptable salts, which may be prepared according to EP 0 112 669; (+) - (S) -N-methyl-3- (1-naphthyloxy) -3- (thiophen-2-yl) -propan-1-amine, the international nonproprietary name of which is duloxetine, and its salts pharmaceutically acceptable, which can be prepared according to EP 0 273 658;
- le (lR52R)-2-(aminométhyl)-N,N-diéthyl-l-phénylcyclopropane-l-carboxamide dont la dénomination commune internationale est milnacipran, et ses sels pharmaceutiquement acceptables, qui peuvent être préparés selon le brevet US 4(lR 5 2R) -2- (aminomethyl) -N, N-diethyl-1-phenylcyclopropane-1-carboxamide, whose international non-proprietary name is milnacipran, and its pharmaceutically acceptable salts, which may be prepared according to US Pat.
478 836 ;478,836;
II a maintenant été trouvé de façon surprenante que l'association du saredutant avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine augmente significativement les effets pharmacologiques de chacun des composés utilisés seuls, notamment les effets antidépressifs.It has now surprisingly been found that the combination of saredutant with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor significantly increases the pharmacological effects of each of the compounds used alone, particularly the antidepressant effects.
Ainsi, les compositions pharmaceutiques contenant de telles associations peuvent être utiles pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaireThus, pharmaceutical compositions containing such combinations may be useful for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, non-depressive disorder. specified, bipolar disorder
I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.I, bipolar disorder II, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
En particulier les compositions pharmaceutiques contenant de telles associations peuvent être utiles pour la fabrication de médicaments destinés à la prévention et au traitement d'un trouble dépressif majeur. En particulier également les compositions pharmaceutiques contenant de telles associations peuvent être utiles pour la fabrication de médicaments destinés au traitement des dysfonctions sexuelles associés à un trouble dépressif majeur.In particular, pharmaceutical compositions containing such combinations may be useful for the manufacture of medicaments for the prevention and treatment of a major depressive disorder. In particular also pharmaceutical compositions containing such combinations may be useful for the manufacture of medicaments for the treatment of sexual dysfunction associated with major depressive disorder.
Par dysfonctions sexuelles on entend toutes pathologies telles que définies par l'American Psychiatrie Association - DSM-IV-TR, Manuel diagnostique et statistique des troubles mentaux, 4ème édition, texte révisé (Washington DC, 2000), pages 617-Sexual dysfunction refers to all conditions as defined by the American Psychiatric Association - DSM-IV-TR, Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Revised Text (Washington DC, 2000), pages 617-
654 et qui incluent les troubles du désir sexuel (c'est-à-dire le trouble : baisse du désir sexuel et le trouble : aversion sexuelle), les troubles de l'excitation sexuelle (c'est-à- dire le trouble de l'excitation sexuelle chez la femme et le trouble de l'érection chez l'homme), les troubles de l'orgasme (c'est-à-dire le trouble de l'orgasme chez la femme, le trouble de l'orgasme chez l'homme, et l'éjaculation précoce), les troubles sexuels avec douleurs (c'est-à-dire la dyspareunie et le vaginisme), la dysfonction sexuelle due à une affection médicale générale, la dysfonction sexuelle induite par une substance, et les dysfonctions sexuelles non spécifiées.654 and which include disorders of sexual desire (that is to say, disorder: lowering of sexual desire and disorder: sexual aversion), disorders of sexual arousal (that is to say the disorder of sexual arousal in women and erectile dysfunction in men), disorders of orgasm (ie orgasm disorder in women, orgasm disorder in men, and premature ejaculation), sexual disorders with pain (ie dyspareunia and vaginismus), dysfunction sexual dysfunction due to a general medical condition, substance-induced sexual dysfunction, and unspecified sexual dysfunction.
Ainsi selon un de ses aspects, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine, ainsi qu'au moins un excipient pharmaceutiquement acceptable.Thus according to one of its aspects, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with a serotonin reuptake inhibitor. and norepinephrine, as well as at least one pharmaceutically acceptable excipient.
En particulier, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular, the present invention relates to pharmaceutical compositions containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine choisi parmi la fluoxetine, le citalopram, l'escitalopram, la paroxetine, la sertraline et la fluvoxamine, ou l'un de leurs sels pharmaceutiquement acceptables ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor chosen from fluoxetine, citalopram, escitalopram, paroxetine, sertraline and fluvoxamine, or a pharmaceutically acceptable salt thereof and at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la fluoxetine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with fluoxetine or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec le citalopram ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with citalopram or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec l'escitalopram ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitalopram or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient. .
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la paroxetine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its salts pharmaceutically acceptable, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la sertraline ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with sertraline or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la fluvoxamine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the present invention relates to pharmaceutical compositions containing in combination the saredutant or one of its pharmaceutically acceptable salts with fluvoxamine or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur de la recapture de la sérotonine/norépinephrine, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the present invention relates to pharmaceutical compositions containing in combination the saredutant or one of its pharmaceutically acceptable salts with a serotonin / norepinephrine reuptake inhibitor, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur de la recapture de la sérotonine/norépinephrine choisi parmi la venlafaxine, la duloxetine et le milnacipran, ou l'un de leurs sels pharmaceutiquement acceptables ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran, or one of their pharmaceutically acceptable salts and at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la venlafaxine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with venlafaxine or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la duloxetine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with duloxetine or one of its pharmaceutically acceptable salts, as well as at least one pharmaceutically acceptable excipient.
En particulier également, la présente invention a pour objet des compositions pharmaceutiques contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec le milnacipran ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.In particular also, the subject of the present invention is pharmaceutical compositions containing, in combination, saredutant or one of its pharmaceutically acceptable salts with milnacipran or one of its salts. pharmaceutically acceptable, as well as at least one pharmaceutically acceptable excipient.
Selon un autre de ses aspects, la présente invention a pour objet l'association du saredutant ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine .In another aspect, the present invention relates to the combination of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor.
En particulier, la présente invention a pour objet l'association du saredutant ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine choisi parmi la fmoxétine, le citalopram, Pescitalopram, la paroxetine, la sertraline et la fluvoxamine ou l'un de leurs sels pharmaceutiquement acceptables.In particular, the present invention relates to the combination of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor selected from fmoxetine, citalopram, escitalopram, paroxetine, sertraline and fluvoxamine or a pharmaceutically acceptable salt thereof.
En particulier également, la présente invention a pour objet l'association du saredutant ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur de la recapture de la sérotonine/norépinephrine choisi parmi la venlafaxine, la duloxetine et le milnacipran ou l'un de leurs sels pharmaceutiquement acceptables.In particular also, the subject of the present invention is the combination of saredutant or a pharmaceutically acceptable salt thereof with a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran or one of their pharmaceutically acceptable salts.
Selon un autre de ses aspects la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine ou l'un de leurs sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance. En particulier, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine ou l'un de leurs sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement d'un trouble dépressif majeur. En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine ou l'un de leurs sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés au traitement des dysfonctions sexuelles associées à un trouble dépressif majeur.According to another of its aspects, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with an inhibitor of the reuptake of serotonin / norepinephrine or a pharmaceutically acceptable salt thereof for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, unspecified depressive disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance. In particular, the present invention relates to the use of a pharmaceutical composition containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with a reuptake inhibitor. serotonin / norepinephrine or a pharmaceutically acceptable salt thereof for the manufacture of medicaments for the prevention and treatment of a major depressive disorder. In particular also, the subject of the present invention is the use of a pharmaceutical composition containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor or with a reuptake inhibitor. serotonin / norepinephrine or a pharmaceutically acceptable salt thereof for the manufacture of medicaments for the treatment of sexual dysfunction associated with a major depressive disorder.
En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec l'escitolopram ou l'un de ses sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.In particular also, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitolopram or one of its pharmaceutically acceptable salts, for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, unspecified depressive disorder, bipolar I disorder, bipolar disorder II, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec l'escitolopram ou l'un de ses sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement d'un trouble dépressif majeur.In particular also, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitolopram or one of its pharmaceutically acceptable salts, for the manufacture of medicines for the prevention and treatment of a major depressive disorder.
En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec l'escitolopram ou l'un de ses sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés au traitement des dysfonctions sexuelles associées à un trouble dépressif majeur.In particular also, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with escitolopram or one of its pharmaceutically acceptable salts, for the manufacture of drugs for the treatment of sexual dysfunction associated with major depressive disorder.
En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec la paroxetine ou l'un de ses sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.In particular also, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its pharmaceutically acceptable salts, for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, resistant depressive disorder, dysthymic disorder, non-depressive disorder specified, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec la paroxetine ou l'un de ses sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement d'un trouble dépressif majeur.In particular also, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its pharmaceutically acceptable salts, for the manufacture of medicaments intended for the prevention and treatment of a major depressive disorder.
En particulier également, la présente invention a pour objet l'utilisation d'une composition pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec la paroxetine ou l'un de ses sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés au traitement des dysfonctions sexuelles associées à un trouble dépressif majeur.In particular also, the subject of the present invention is the use of a pharmaceutical composition containing, in combination, saredutant or one of its pharmaceutically acceptable salts with paroxetine or one of its pharmaceutically acceptable salts, for the manufacture of medicaments for the treatment of sexual dysfunction associated with major depressive disorder.
Selon un autre de ses aspects, la présente invention a pour objet l'utilisation de l'association du saredutant ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la sérotonine/norépinephrine ou l'un de leurs sels pharmaceutiquement acceptables, pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.According to another of its aspects, the present invention relates to the use of the combination of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine inhibitor or a pharmaceutically acceptable salt thereof, for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive resistant disorder, dysthymic disorder, non-specified depressive disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, mood disorder unspecified ; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
Les excipients sont choisis selon la forme pharmaceutique et le mode d'administration souhaité, parmi les excipients habituels qui sont connus de l'homme du métier.The excipients are selected according to the pharmaceutical form and the desired mode of administration, from the usual excipients which are known to those skilled in the art.
Dans les compositions pharmaceutiques de la présente invention pour l'administration orale, sublinguale, sous-cutanée, intramusculaire, intra- veineuse, topique, locale, intra-trachéale, intranasale, transdermique ou rectale, les principes actifs peuvent être administrés sous forme unitaire d'administration, en mélange avec des excipients pharmaceutiques classiques, aux animaux et aux êtres humains pour la prévention ou le traitement des troubles ou des maladies ci-dessus.In the pharmaceutical compositions of the present invention for oral, sublingual, subcutaneous, intramuscular, intravenous, topical, local, intratracheal, intranasal, transdermal or rectal administration, the principles The active ingredients can be administered in unit dosage form, in admixture with conventional pharmaceutical excipients, to animals and humans for the prevention or treatment of the above disorders or diseases.
Les formes unitaires d'administration appropriées comprennent les formes par voie orale telles que les comprimés, les gélules molles ou dures, les poudres, les granules et les solutions ou suspensions orales, les formes d'administration sublinguale, buccale, intra-trachéale, intraoculaire, intranasale, par inhalation, les formes d'administration topique, transdermique, sous-cutanée, intramusculaire ou intraveineuse, les formes d'administration rectale et les implants. Pour l'application topique, on peut utiliser les composés selon l'invention dans des crèmes, gels, pommades ou lotions.Suitable unit dosage forms include oral forms such as tablets, soft or hard capsules, powders, granules and oral solutions or suspensions, sublingual, oral, intratracheal, intraocular forms of administration. , intranasal, inhalation, topical, transdermal, subcutaneous, intramuscular or intravenous administration forms, rectal administration forms and implants. For topical application, the compounds according to the invention can be used in creams, gels, ointments or lotions.
Dans les compositions pharmaceutiques de la présente invention, le principe actif ou les principes actifs sont généralement formulés en unités de dosage. L'unité de dosage contient 2,5 à 500 mg, avantageusement de 10 à 250 mg, de préférence de 10 à 150 mg par unité de dosage, pour les administrations quotidiennes, une ou plusieurs fois par jour. Bien que ces dosages soient des exemples de situations moyennes, il peut y avoir des cas particuliers où des dosages plus élevés ou plus faibles sont appropriés, de tels dosage appartiennent également à l'invention. Selon la pratique habituelle, le dosage approprié à chaque patient est déterminé par le médecin selon le mode d'administration, l'âge, le poids et la réponse dudit patient.In the pharmaceutical compositions of the present invention, the active ingredient or active ingredients are generally formulated in dosage units. The dosage unit contains 2.5 to 500 mg, preferably 10 to 250 mg, preferably 10 to 150 mg per dosage unit, for daily administrations, one or more times per day. Although these assays are examples of average situations, there may be special cases where higher or lower dosages are appropriate, such assays also belong to the invention. According to the usual practice, the dosage appropriate to each patient is determined by the physician according to the mode of administration, the age, the weight and the response of said patient.
Selon un autre aspect de l'invention, le composé A et l'autre principe actif selon l'invention peuvent être administrés de manière simultanée, séparée ou étalée dans le temps.According to another aspect of the invention, the compound A and the other active ingredient according to the invention can be administered simultaneously, separately or spread over time.
On entend par "utilisation simultanée", l'administration des composés de la composition selon l'invention compris dans une seule et même forme pharmaceutique.By "simultaneous use" is meant the administration of the compounds of the composition according to the invention included in one and the same pharmaceutical form.
On entend par "utilisation séparée" l'administration, en même temps, des deux composés de la composition selon l'invention, chacun compris dans une forme pharmaceutique distincte.By "separate use" is meant the administration, at the same time, of the two compounds of the composition according to the invention, each comprised in a separate pharmaceutical form.
On entend par "utilisation étalée dans le temps", l'administration successive du premier composé de la composition selon l'invention, compris dans une forme pharmaceutique, puis, du deuxième composé de la composition selon l'invention, compris dans une forme pharmaceutique distincte."Extended use over time" is understood to mean the sequential administration of the first compound of the composition according to the invention, included in a pharmaceutical form, and then of the second compound of the composition according to the invention, included in a pharmaceutical form. separate.
Dans le cas de cette "utilisation étalée dans le temps", le laps de temps écoulé entre l'administration du premier composé de la composition selon l'invention et l'administration du deuxième composé de la même composition selon l'invention n'excède généralement pas 24 heures. Les formes pharmaceutiques unitaires contenant soit un seul des composés constitutifs de la composition selon l'invention, soit l'association des 2 composés qui peuvent être mis en œuvre dans les différents types d'utilisation décrits ci-dessus peuvent par exemple être appropriées à l'administration orale, nasale, parentérale ou transdermique.In the case of this "use spread over time", the lapse of time elapsed between the administration of the first compound of the composition according to the invention and the administration of the second compound of the same composition according to the invention does not exceed usually not 24 hours. The unit dosage forms containing either only one of the constituent compounds of the composition according to the invention, or the combination of the two compounds which can be used in the various types of use described above, may for example be appropriate for the oral, nasal, parenteral or transdermal administration.
Aussi, dans le cas d'une "utilisation séparée" et d'une "utilisation étalée dans le temps", deux formes pharmaceutiques distinctes peuvent être destinées à la même voie d'administration ou à une voie d'administration différente (orale et transdermique ou orale et nasale ou parentérale et transdermique etc.). L'invention concerne donc également une trousse contenant le composé A et l'autre principe actif selon l'invention dans laquelle ledit composé A, et l'autre principe actif selon l'invention sont dans des compartiments distincts et dans des conditionnements semblables ou différents, et sont destinés à être administrés de manière simultanée, séparée ou étalée dans le temps. De manière particulière et non limitative, l'augmentation des effets pharmacologiques d'une association selon l'invention du composé A et de la fluoxetine (composé B) a été mise en évidence chez l'animal.Also, in the case of "separate use" and "spread use over time", two different dosage forms may be for the same route of administration or a different route of administration (oral and transdermal). or oral and nasal or parenteral and transdermal etc.). The invention therefore also relates to a kit containing compound A and the other active ingredient according to the invention wherein said compound A, and the other active ingredient according to the invention are in separate compartments and in similar or different packages. and are intended to be administered simultaneously, separately or spread over time. In a particular and non-limiting way, the increase in the pharmacological effects of a combination according to the invention of compound A and fluoxetine (compound B) has been demonstrated in animals.
De manière particulière aussi, les effets d'une association selon l'invention du composé A et d'un inhibiteur sélectif de la recapture de la sérotonine sont étudiés au cours d'études cliniques.Particularly also, the effects of an association according to the invention of compound A and a selective serotonin reuptake inhibitor are studied in clinical studies.
EXEMPLE 1EXAMPLE 1
On utilise le test in- vivo chez le rat DRL-72 s (de l'anglais Differential Reinforcement of Low-rate-72 seconds) selon la technique décrite par C. Louis et al., Neuropsychopharmacology, 2006,1-8. Effets comparés sur le pourcentage de récompenses obtenues (appuis renforcés) par rapport au nombre total d'appuis chez le rat après administration par voie intra péritonéale du composé A seul, du composé B seul et de l'association composé A + composé B versus le contrôle (solvant seul).The in vivo test was used in the rat DRL-72 s (English Differential Reinforcement of Low-rate-72 seconds) according to the technique described by C. Louis et al., Neuropsychopharmacology, 2006, 1-8. Comparative effects on the percentage of rewards obtained (increased support) relative to the total number of supports in the rat after intraperitoneal administration of compound A alone, compound B alone and the combination compound A + compound B versus control (solvent only).
Au préalable, on a déterminé les doses minimales actives du composé A seul et du composé B seul dans le test DRL-72 s, à savoir :Beforehand, the minimum active doses of compound A alone and compound B alone in the DRL-72s test were determined, namely:
- composé A : 10 mg/kg par voie intrapéritonéale ;compound A: 10 mg / kg intraperitoneally;
- composé B : 5 mg/kg par voie intrapéritonéalecompound B: 5 mg / kg intraperitoneally
Pour la présente étude une dose faiblement active de composé A seul et une dose inactive de composé B seul et de composé A + composé B ont été sélectionnées. Le composé A seul à la dose de 3 mg/kg et le composé B seul à la dose de 2,5 mg/kg ont été dissous dans une solution aqueuse de chlorure de sodium à 0,9% (poids/volume) contenant du Tween 80® à 0,1% (v/v) et administrés par voie intra péritonéale sous un volume final de 1 ml/kg ;For the present study a low active dose of compound A alone and an inactive dose of compound B alone and compound A + compound B were selected. Compound A alone at the dose of 3 mg / kg and compound B alone at the dose of 2.5 mg / kg were dissolved in a 0.9% aqueous solution of sodium chloride. (weight / volume) containing Tween 80® 0.1% (v / v) and administered intraperitoneally in a final volume of 1 ml / kg;
L'association a été administrée par voie intrapéritonéale par deux administrations simultanées du composé A (3 mg/kg) puis du composé B (2,5 mg/kg).The combination was administered intraperitoneally by two simultaneous administrations of compound A (3 mg / kg) and then compound B (2.5 mg / kg).
Les doses des composés étant exprimées sous forme de base libre.The doses of the compounds being expressed as free base.
Pour le besoin du test, on mesure pour chaque animal l'effet du composé A seul, l'effet du composé B seul et l'effet de l'association composé A + composé B, comparé à l'effet du solvant (contrôle).For the purpose of the test, the effect of compound A alone, the effect of compound B alone and the effect of compound A + compound B, compared with the effect of the solvent (control), were measured for each animal. .
Chaque rat (n=8) reçoit donc quatre injections étalées dans le temps à savoir le solvant (contrôle), le composé A seul, le composé B seul et l'association composé A + composé B.Each rat (n = 8) thus receives four injections spread over time, namely the solvent (control), compound A alone, compound B alone and the compound A + compound B combination.
Les résultats obtenus sont rassemblés dans le Tableau I et sont exprimés en pourcentage de récompenses obtenues par rapport au nombre total d'appuis pendant la durée du test (1 heure), sous forme de moyenne ± ESM (erreur standard à la moyenne).The results obtained are collated in Table I and are expressed as a percentage of rewards obtained relative to the total number of supports during the test duration (1 hour), in the form of mean ± ESM (standard error to the mean).
TABLEAU ITABLE I
* p < 0,05 versus contrôle* p <0.05 versus control
Les résultats obtenus montrent que :The results obtained show that:
- le composé A administré seul à la dose de 3 mg / kg modifie peu le nombre de pourcentage de récompenses obtenues par rapport au contrôle, de plus cette augmentation n'est pas statistiquement significative- Compound A administered alone at a dose of 3 mg / kg has little effect on the number of percentages of reward obtained compared to control, and this increase is not statistically significant
- le composé B administré seul à la dose de 2,5 mg / kg ne modifie pas le nombre de pourcentage de récompenses obtenues par rapport au contrôle. - l'association du composé A et du composé B augmente nettement le nombre de pourcentage de récompenses obtenues par rapport au contrôle et cette augmentation est statistiquement significative.- Compound B administered alone at a dose of 2.5 mg / kg does not modify the number of percentages of rewards obtained with respect to the control. the combination of the compound A and the compound B significantly increases the number of percentages of rewards obtained with respect to the control and this increase is statistically significant.
Ainsi l'association du composé A et du composé B selon l'invention, montre de manière inattendue ses effets positifs sur le comportement des animaux dans ce test, permettant de confirmer le potentiel anti-dépressif de l'association pour une application en thérapeutique.Thus the combination of compound A and compound B according to the invention unexpectedly shows its positive effects on the behavior of animals in this test, making it possible to confirm the anti-depressive potential of the combination for an application in therapy.
EXEMPLE 2EXAMPLE 2
Les effets d'une association selon l'invention du saredutant avec Pescitalopram sont évalués au cours d'études cliniques de huit semaines, multicentriques randomisées, en double-aveugle comparant un groupe recevant une dose fixe de saredutant une fois par jour associée à une dose fixe d'escitalopram une fois par jour avec un groupe recevant du placebo saredutant associé à une dose fixe d'escitalopram et avec un autre groupe recevant du placebo saredutant associé avec du placebo escitalopram.The effects of a combination of the saredutant with Pescitalopram according to the invention are evaluated in randomized, double-blind, multicenter, eight-week clinical trials comparing a fixed-dose group of saredutant once daily with a dose fixed escitalopram once daily with a group receiving saredutant placebo in combination with a fixed dose of escitalopram and another group receiving placebo saredutant with placebo escitalopram.
Ces études cliniques sont effectuées sur des patients adultes, maies ou femelles, présentant un trouble dépressif majeur tel que défini par les critères du Diagnostic andThese clinical studies are carried out on adult patients, male or female, presenting a major depressive disorder as defined by the criteria of the Diagnosis and Diagnosis.
Statistical Manual of Mental Disorders, 4ème édition, texte révisé (DSM-IV-TR) et confirmé par les critères du Mini Internationl Neuropsychiatrie Interview (MINI), Lecrubier Y. et al, Eur. Psychiatr., 1997, 12, 224-231.Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria and confirmed by the Internationl Mini Neuropsychiatric Interview (MINI) Lecrubier Y. et al, Eur. Psychiatr., 1997, 12, 224-231.
On mesure le changement du score total sur l'échelle d'évaluation de la dépression d'Hamilton comprenant 17 items (HAM-D, de l'anglais Hamilton Dépression Rating Scale) entre la dernière visite (prévue au 56ème jour) et la première visite (avant le début du traitement) par rapport au groupe placebo. L'échelle d'évaluation de la dépression d'Hamilton est définie par Hamilton M., J. Neurol.It measures the change in total score on the Hamilton depression rating scale includes 17 items (HAM-D, English Hamilton Depression Rating Scale) between the last visit (under 56 th day) and first visit (before the start of treatment) compared to the placebo group. The Hamilton Depression Rating Scale is defined by Hamilton M., J. Neurol.
Neurosurg. Psychiatry, 1960, 23, 56-62.Neurosurg. Psychiatry, 1960, 23, 56-62.
On mesure aussi le changement du score total du CSFQ comprenant 14 items (de l'anglais Changes in Sexual Functioning Questionnaire) entre la dernière visiteWe also measure the change in the total score of the CSFQ including 14 items (of the English Changes in Sexual Functioning Questionnaire) between the last visit
(prévue au 56ème jour) et la première visite (avant le début du traitement) par rapport au groupe placebo. Le CSFQ est définie par Clayton AH et al., Psychopharmacol.(under 56th day) and the first visit (before start of treatment) compared with the placebo group. CSFQ is defined by Clayton AH et al., Psychopharmacol.
Bull, 1997, 33, 731-745.Bull, 1997, 33, 731-745.
EXEMPLE 3EXAMPLE 3
Les effets d'une association selon l'invention du saredutant avec la paroxetine sont évalués au cours d'études cliniques de huit semaines, multicentriques, randomisées, en double aveugle comparant un groupe recevant une dose fixe de saredutant une fois par jour associée à une dose fixe de paroxetine une fois par jour avec un groupe recevant du placebo saredutant associé à une dose fixe de paroxetine et avec un autre groupe recevant du placebo saredutant associé avec du placebo paroxetine.The effects of an association according to the invention of saredutant with paroxetine are evaluated in eight-week, multicenter, randomized, double-blind clinical trials comparing a group receiving a fixed dose of saredutant once daily associated with a fixed dose of paroxetine once a day with a placebo group saredutant with a fixed dose of paroxetine and another group receiving placebo saredutant with placebo paroxetine.
Ces études cliniques sont effectuées sur des patients adultes, maies ou femelles, présentant un trouble dépressif majeur tel que défini par les critères du Diagnostic andThese clinical studies are carried out on adult patients, male or female, presenting a major depressive disorder as defined by the criteria of the Diagnosis and Diagnosis.
Statistical Manual of Mental Disorders, 4ème édition, texte révisé (DSM-IV-TR) et confirmé par les critères du Mini Internationl Neuropsychiatrie Interview (MINI),Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria and confirmed by the Internationl Mini Neuropsychiatric Interview (MINI)
Lecrubier Y. et al., Eur. Psychiatr., 1997, .12, 224-231.Lecrubier Y. et al., Eur. Psychiatr., 1997, 12, 224-231.
On mesure le changement du score total sur l'échelle d'évaluation de la dépression d'Hamilton comprenant 17 items (HAM-D, de l'anglais HamiltonThe change in total score is measured on the Hamilton Depression Rating Scale of 17 items (Hamilton HAM-D)
Dépression Rating Scale) entre la dernière visite (prévue au 56ème jour) et la première visite (avant le début du traitement) par rapport au groupe placebo. L'échelle d'évaluation de la dépression d'Hamilton est définie par Hamilton M., J. Neurol. Neurosurg. Psychiatry, 1960, 23, 56-62. On mesure aussi le changement du score total du CSFQ comprenant 14 items (de l'anglais Changes in Sexual Functioning Questionnaire) entre la dernière visite (prévue au 56ème jour) et la première visite (avant le début du traitement) par rapport au groupe placebo. Le CSFQ est définie par Clayton AH et al., Psychopharmacol. Bull., 1997, 33, 731-745. EXAMPLE 4 : Gélule à 30 mg de saredutant.Depression Rating Scale) between the last visit (under 56 th day) and the first visit (before the start of treatment) compared to placebo. The Hamilton Depression Rating Scale is defined by Hamilton M., J. Neurol. Neurosurg. Psychiatry, 1960, 23, 56-62. We also measure the change in the total score of the CSFQ including 14 items (of the English Changes in Sexual Functioning Questionnaire) between the last visit (scheduled for the 56 th day) and the first visit (before the start of treatment) compared to the group placebo. CSFQ is defined by Clayton AH et al., Psychopharmacol. Bull., 1997, 33, 731-745. EXAMPLE 4: 30 mg capsule of saredutant.
Saredutant (exprimé en base) 30,0 mgSaredutant (expressed as base) 30.0 mg
Lactose monohydrate (200 mesh) QSP 400,0 mgLactose monohydrate (200 mesh) QSP 400.0 mg
Croscarmellose sodium 8,0 mgCroscarmellose sodium 8.0 mg
Stéarate de magnésium 4,0 mg Eau purifiée* QSMagnesium Stearate 4.0 mg Purified Water * QS
Pour une gélule opaque de taille 0, remplie à 400,0 mgFor an opaque capsule size 0, filled to 400.0 mg
* évaporée au séchage après la granulation humide. EXAMPLE 5 : Gélule à 100 mg de saredutant. Saredutant (exprimé en base) 100,0 mg Lactose monohydrate (200 mesh) QSP 400,0 mg* evaporated on drying after wet granulation. EXAMPLE 5: Capsule 100 mg of saredutant. Saredutant (expressed as base) 100.0 mg Lactose monohydrate (200 mesh) QSP 400.0 mg
Croscarmellose sodium 8,0 mgCroscarmellose sodium 8.0 mg
Stéarate de magnésium 4,0 mgMagnesium stearate 4.0 mg
Eau purifiée* QSPurified water * QS
Pour une gélule opaque de taille 0, remplie à 400,0 mg * évaporée au séchage après la granulation humide. For an opaque capsule size 0, filled to 400.0 mg * evaporated on drying after wet granulation.

Claims

REVENDICATIONS
1. Compositions pharmaceutique contenant en association le saredutant ou l'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine, ainsi qu'au moins un excipient pharmaceutiquement acceptable. 1. Pharmaceutical compositions containing in combination saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor, and at least one pharmaceutically acceptable excipient .
2. Composition pharmaceutique selon la revendication 1 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine, ainsi qu'au moins un excipient pharmaceutiquement acceptable.2. Pharmaceutical composition according to claim 1, containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective serotonin reuptake inhibitor, as well as at least one pharmaceutically acceptable excipient.
3. Composition pharmaceutique selon la revendication 1 ou la revendication 2 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la fecapture de la sérotonine choisi parmi la fluoxetine, le citalopram, l'escitalopram, la paroxetine, la sertraline et la fluvoxamine, ou l'un de leurs sels pharmaceutiquement acceptables ainsi qu'au moins un excipient pharmaceutiquement acceptable. 3. Pharmaceutical composition according to claim 1 or claim 2 containing in combination the saredutant or one of its pharmaceutically acceptable salts with a selective inhibitor of the fecapture of serotonin selected from fluoxetine, citalopram, escitalopram, paroxetine , sertraline and fluvoxamine, or a pharmaceutically acceptable salt thereof and at least one pharmaceutically acceptable excipient.
4. Composition pharmaceutique selon la revendication 3 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la fluoxetine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.4. Pharmaceutical composition according to claim 3 containing in combination the saredutant or one of its pharmaceutically acceptable salts with fluoxetine or one of its pharmaceutically acceptable salts, and at least one pharmaceutically acceptable excipient.
5. Composition pharmaceutique selon la revendication 3 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec le citalopram ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.5. Pharmaceutical composition according to claim 3 containing in combination the saredutant or one of its pharmaceutically acceptable salts with citalopram or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
6. Composition pharmaceutique selon la revendication 3 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec V escitalopram ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.6. Pharmaceutical composition according to claim 3 containing in combination the saredutant or one of its pharmaceutically acceptable salts with V escitalopram or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
7. Composition pharmaceutique selon la revendication 3 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la paroxetine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable. 7. Pharmaceutical composition according to claim 3 containing in combination the saredutant or one of its pharmaceutically acceptable salts with paroxetine or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
8. Composition pharmaceutique selon la revendication 3 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la sertraline ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable. 8. Pharmaceutical composition according to claim 3 containing in combination the saredutant or one of its pharmaceutically acceptable salts with sertraline or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
9. Composition pharmaceutique selon la revendication 3 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la fluvoxamine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.9. Pharmaceutical composition according to claim 3 containing in combination the saredutant or one of its pharmaceutically acceptable salts with fluvoxamine or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
10. Composition pharmaceutique selon la revendication 1 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur de la recapture de la sérotonine/norépinephrine, ainsi qu'au moins un excipient pharmaceutiquement acceptable.10. Pharmaceutical composition according to claim 1, containing in combination the saredutant or one of its pharmaceutically acceptable salts with a serotonin / norepinephrine reuptake inhibitor, as well as at least one pharmaceutically acceptable excipient.
11. Composition pharmaceutique selon la revendication 1 ou la revendication 10 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec un inhibiteur de la recapture de la sérotonin/norépinephrine choisi parmi la venlafaxine, la duloxetine et le milnacipran, ou l'un de leurs sels pharmaceutiquement acceptables ainsi qu'au moins un excipient pharmaceutiquement acceptable.11. A pharmaceutical composition according to claim 1 or claim 10 containing in combination the saredutant or a pharmaceutically acceptable salt thereof with a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran, or one of their pharmaceutically acceptable salts and at least one pharmaceutically acceptable excipient.
12. Composition pharmaceutique selon la revendication 11 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la venlafaxine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.12. Pharmaceutical composition according to claim 11 containing in combination the saredutant or one of its pharmaceutically acceptable salts with venlafaxine or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
13. Composition pharmaceutique selon la revendication 11 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec la duloxetine ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.13. Pharmaceutical composition according to claim 11 containing in combination the saredutant or one of its pharmaceutically acceptable salts with duloxetine or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
14. Composition pharmaceutique selon la revendication 11 contenant en association le saredutant ou l'un des ses sels pharmaceutiquement acceptables avec le milnacipran ou l'un de ses sels pharmaceutiquement acceptables, ainsi qu'au moins un excipient pharmaceutiquement acceptable.14. Pharmaceutical composition according to claim 11 containing in combination the saredutant or one of its pharmaceutically acceptable salts with milnacipran or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.
15. Association du saredutant ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine ou avec un inhibiteur de la recapture de la sérotonine/norépinephrine.15. Association of saredutant or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor or with a serotonin / norepinephrine reuptake inhibitor.
16. Association du saredutant selon la revendication 15 ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur sélectif de la recapture de la sérotonine choisi parmi la fluoxétine, le citalopram, l'escitalopram, la paroxetine, la sertraline et la fluvoxamine ou l'un de leurs sels pharmaceutiquement acceptables.16. Association of saredutant according to claim 15 or a pharmaceutically acceptable salt thereof with a selective serotonin reuptake inhibitor selected from fluoxetine, citalopram, escitalopram, paroxetine, sertraline and fluvoxamine or a pharmaceutically acceptable salt thereof.
17. Association du saredutant selon la revendication 15 ou d'un de ses sels pharmaceutiquement acceptables avec un inhibiteur de la recapture de la sérotonine/norépinéphrine choisi parmi la venlafaxine, la duloxetine et le milnacipran ou l'un de leurs sels pharmaceutiquement acceptables.17. A combination of saredutant according to claim 15 or a pharmaceutically acceptable salt thereof with a serotonin / norepinephrine reuptake inhibitor selected from venlafaxine, duloxetine and milnacipran or a pharmaceutically acceptable salt thereof.
18. Utilisation d'une composition pharmaceutique selon l'une quelconque des revendications 1 à 14 pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.18. Use of a pharmaceutical composition according to any one of claims 1 to 14 for the manufacture of medicaments for the prevention and treatment of mood disorders selected from major depressive disorder, depressive disorder resistant, the disorder dysthymic disorder, non-specific depressive disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, mood disorder induced by substance, unspecified mood disorder; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
19. Utilisation selon la revendication 18 pour la prévention et le traitement d'un trouble dépressif majeur. 19. Use according to claim 18 for the prevention and treatment of a major depressive disorder.
20. Utilisation selon la revendication 19 pour le traitement des dysfonctions sexuelles associées à un trouble dépressif majeur.20. Use according to claim 19 for the treatment of sexual dysfunction associated with a major depressive disorder.
21. Utilisation d'une composition pharmaceutique selon la revendication 6 pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I, le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.21. Use of a pharmaceutical composition according to claim 6 for the manufacture of medicaments for the prevention and treatment of mood disorders chosen from major depressive disorder, resistant depressive disorder, dysthymic disorder, non-depressive disorder. specified, bipolar I disorder, bipolar II disorder, cyclothymic disorder, unspecified bipolar disorder, mood disorder due to a general medical condition, substance-induced mood disorder, unspecified mood; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
22. Utilisation selon la revendication 21 pour la prévention et le traitement d'un trouble dépressif majeur. 22. Use according to claim 21 for the prevention and treatment of a major depressive disorder.
23. Utilisation selon la revendication 22 pour le traitement des dysfonctions sexuelles associées à un trouble dépressif majeur. 23. Use according to claim 22 for the treatment of sexual dysfunctions associated with a major depressive disorder.
24. Utilisation d'une composition pharmaceutique selon la revendication 7 pour la fabrication de médicaments destinés à la prévention et au traitement des troubles de l'humeur choisis parmi le trouble dépressif majeur, le trouble dépressif résistant, le trouble dysthymique, le trouble dépressif non spécifié, le trouble bipolaire I5 le trouble bipolaire II, le trouble cyclothymique, le trouble bipolaire non spécifié, le trouble de l'humeur dû à une affection médicale générale, le trouble de l'humeur induit par une substance, le trouble de l'humeur non spécifié ; des troubles anxieux choisis parmi l'attaque de panique, l'agoraphobie, la phobie sociale, le trouble obsessionnel compulsif, l'état de stress post-traumatique, l'état de stress aigu, le trouble anxieux généralisé, le trouble anxieux induit par une substance.24. Use of a pharmaceutical composition according to claim 7 for the manufacture of medicaments for the prevention and treatment of mood disorders chosen from major depressive disorder, depressive resistant disorder, dysthymic disorder, non-depressive disorder. specified, bipolar I 5 bipolar II disorder, cyclothymic disorder, bipolar disorder not otherwise specified, mood disorder due to a general medical condition, the mood disorder substance induced disorder or the unspecified mood; anxiety disorders selected from panic attack, agoraphobia, social phobia, obsessive-compulsive disorder, post-traumatic stress disorder, acute stress disorder, generalized anxiety disorder, anxiety disorder induced by a substance.
25. Utilisation selon la revendication 24 pour le traitement et la prévention d'un trouble dépressif majeur.25. Use according to claim 24 for the treatment and prevention of a major depressive disorder.
26. Utilisation selon la revendication 25 pour le traitement des dysfonctions sexuelles associées à un trouble dépressif majeur. 26. Use according to claim 25 for the treatment of sexual dysfunctions associated with a major depressive disorder.
EP07823369A 2006-07-31 2007-07-30 Pharmaceutical composition containing saredutant and a selective inhibitor of serotonin recapture or an inhibitor of serotonin/norepinephrine recapture in combination Withdrawn EP2049093A2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0607050A FR2904221B1 (en) 2006-07-31 2006-07-31 PHARMACEUTICAL COMPOSITION CONTAINING IN ASSOCIATION SAREDUTANT AND FLUOXETINE.
FR0700863A FR2912057B1 (en) 2007-02-07 2007-02-07 PHARMACEUTICAL COMPOSITION COMPRISING SAREDUTANT AND A SELECTIVE SEROTONIN RECAPTURE INHIBITOR OR SEROTONIN / NOREPINEPHRINE RECAPTURE INHIBITOR
PCT/FR2007/001314 WO2008017753A2 (en) 2006-07-31 2007-07-30 Pharmaceutical composition containing saredutant and a selective inhibitor of serotonin recapture or an inhibitor of serotonin/norepinephrine recapture in combination

Publications (1)

Publication Number Publication Date
EP2049093A2 true EP2049093A2 (en) 2009-04-22

Family

ID=39001699

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07823369A Withdrawn EP2049093A2 (en) 2006-07-31 2007-07-30 Pharmaceutical composition containing saredutant and a selective inhibitor of serotonin recapture or an inhibitor of serotonin/norepinephrine recapture in combination

Country Status (23)

Country Link
US (2) US20080033014A1 (en)
EP (1) EP2049093A2 (en)
JP (1) JP2009545573A (en)
KR (1) KR20090034368A (en)
AR (1) AR062142A1 (en)
AU (1) AU2007283530A1 (en)
BR (1) BRPI0714862A2 (en)
CA (1) CA2658614A1 (en)
CL (1) CL2007002217A1 (en)
CO (1) CO6150152A2 (en)
CR (1) CR10579A (en)
EA (1) EA200970167A1 (en)
EC (1) ECSP099093A (en)
GT (1) GT200900018A (en)
IL (1) IL196570A0 (en)
MA (1) MA30645B1 (en)
MX (1) MX2009001219A (en)
NO (1) NO20090924L (en)
PE (1) PE20080431A1 (en)
TN (1) TN2009000008A1 (en)
TW (1) TW200817003A (en)
UY (1) UY30517A1 (en)
WO (1) WO2008017753A2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2912057B1 (en) * 2007-02-07 2009-04-17 Sanofi Aventis Sa PHARMACEUTICAL COMPOSITION COMPRISING SAREDUTANT AND A SELECTIVE SEROTONIN RECAPTURE INHIBITOR OR SEROTONIN / NOREPINEPHRINE RECAPTURE INHIBITOR
WO2012145234A2 (en) * 2011-04-21 2012-10-26 Emory University Cyclopropyl derivatives and methods of use

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1422263A (en) * 1973-01-30 1976-01-21 Ferrosan As 4-phenyl-piperidine compounds
US4314081A (en) * 1974-01-10 1982-02-02 Eli Lilly And Company Arloxyphenylpropylamines
NL7503310A (en) * 1975-03-20 1976-09-22 Philips Nv CONNECTIONS WITH ANTIDEPRESSIVE ACTION.
GB1526331A (en) * 1976-01-14 1978-09-27 Kefalas As Phthalanes
US4536518A (en) * 1979-11-01 1985-08-20 Pfizer Inc. Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine
FR2508035A1 (en) * 1981-06-23 1982-12-24 Fabre Sa Pierre ARYL-1-AMINOMETHYL-2 CYCLOPROPANES CARBOXAMIDE (Z) DERIVATIVES, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS USEFUL IN THE TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS
GB8814057D0 (en) * 1988-06-14 1988-07-20 Lundbeck & Co As H New enantiomers & their isolation
US4902710A (en) * 1988-12-14 1990-02-20 Eli Lilly And Company Serotonin and norepinephrine uptake inhibitors
IL99320A (en) * 1990-09-05 1995-07-31 Sanofi Sa Arylalkylamines, their preparation and pharmaceutical compositions containing them
GB9402029D0 (en) * 1994-02-03 1994-03-30 Smithkline Beecham Plc Novel formulation
WO1996024353A1 (en) * 1995-02-10 1996-08-15 Eli Lilly And Company Methods of treating or preventing psychiatric disorders
FR2792835B3 (en) * 1999-04-27 2001-05-25 Sanofi Sa USE OF SAREDUTANT FOR THE PREPARATION OF MEDICINES USEFUL IN THE TREATMENT OR PREVENTION OF ALL MOOD DISORDERS, ADAPTATION DISORDERS OR MIXED ANXIETY-DEPRESSION DISORDERS
AR021155A1 (en) * 1999-07-08 2002-06-12 Lundbeck & Co As H TREATMENT OF NEUROTIC DISORDERS
WO2007047576A1 (en) * 2005-10-14 2007-04-26 The Board Of Trustees Of The University Of Illinois Pharmacological treatments for sleep disorders
FR2912057B1 (en) * 2007-02-07 2009-04-17 Sanofi Aventis Sa PHARMACEUTICAL COMPOSITION COMPRISING SAREDUTANT AND A SELECTIVE SEROTONIN RECAPTURE INHIBITOR OR SEROTONIN / NOREPINEPHRINE RECAPTURE INHIBITOR

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2008017753A2 *

Also Published As

Publication number Publication date
TN2009000008A1 (en) 2010-08-19
MA30645B1 (en) 2009-08-03
WO2008017753A3 (en) 2009-02-19
PE20080431A1 (en) 2008-05-26
GT200900018A (en) 2010-08-23
WO2008017753A2 (en) 2008-02-14
AU2007283530A1 (en) 2008-02-14
AR062142A1 (en) 2008-10-15
CL2007002217A1 (en) 2008-03-07
CR10579A (en) 2009-03-20
ECSP099093A (en) 2009-02-27
IL196570A0 (en) 2009-11-18
UY30517A1 (en) 2008-02-29
JP2009545573A (en) 2009-12-24
EA200970167A1 (en) 2009-08-28
KR20090034368A (en) 2009-04-07
US20080033014A1 (en) 2008-02-07
CA2658614A1 (en) 2008-02-14
MX2009001219A (en) 2009-02-13
NO20090924L (en) 2009-03-18
TW200817003A (en) 2008-04-16
CO6150152A2 (en) 2010-04-20
US20090227632A1 (en) 2009-09-10
BRPI0714862A2 (en) 2013-07-02

Similar Documents

Publication Publication Date Title
US6169105B1 (en) Potentiation of drug response
WO2006096435A1 (en) Pharmaceutical compositions for the treatment and/or prevention of depression
EP1641461B1 (en) Combination product comprising an antagonist or inverse agonist of histamine receptor h&lt;sb&gt;3&lt;/sb&gt; and an antipsychotic or antidepressant agent, and use thereof for the preparation of a medicament that prevents the adverse effects of psychotropic drugs
HU225534B1 (en) Pharmaceutical compositions comprising mirtazapine and one or more selective serotonin reuptake inhibitors
FR2804604A1 (en) USE OF A CENTRAL CANNABINOID RECEPTOR ANTAGONIST FOR THE PREPARATION OF USEFUL DRUGS TO FACILITATE THE STOPPAGE OF TOBACCO CONSUMPTION
WO2023278824A1 (en) Methods for treating depressive states
KR20020025252A (en) Methods of Using Rapid-Onset Selective Serotonin Reuptake Inhibitors for Treating Sexual Dysfunction
US20050119249A1 (en) Method of treating neurodegenerative diseases using D4 and 5-HT2A antagonists, inverse agonists or partial agonists
US20020165217A1 (en) Combination treatment for anxiety and depression
KR20090036114A (en) Treating psychological conditions using muscarinic receptor m1 antagonists
Khawaja et al. Cardiovascular effects of selective serotonin reuptake inhibitors and other novel antidepressants
EP2049093A2 (en) Pharmaceutical composition containing saredutant and a selective inhibitor of serotonin recapture or an inhibitor of serotonin/norepinephrine recapture in combination
FR2912057A1 (en) PHARMACEUTICAL COMPOSITION COMPRISING SAREDUTANT AND A SELECTIVE SEROTONIN RECAPTURE INHIBITOR OR SEROTONIN / NOREPINEPHRINE RECAPTURE INHIBITOR
CN101495109A (en) Pharmaceutical composition comprising, in combination, saredutant and a selective serotonin reuptake inhibitor or a serotonin/norepinephrine reuptake inhibitor
EP2012792B1 (en) Use of a compound inducing an increase of free serotonin rate in the body, for preparing a medicine for treating skeletal muscle degeneration of genetic origin
FR2758460A1 (en) USE OF ADRENERGIC BETA-3 RECEPTOR AGONISTS FOR THE PREPARATION OF HEALING MEDICINAL PRODUCTS
US6403650B1 (en) Treatment of pulmonary hypertension
FR2912058A1 (en) Treatment or prevention of sexual dysfunction, e.g. lack of sexual desire or erectile dysfunction, uses neurokinin A NK2 receptor antagonist, e.g. sareductant
WO2007034056A1 (en) ASSOCIATION OF ß3 RECEPTOR AGONIST AND MONOAMINE REUPTAKE INHIBITORS, PHARMACEUTICAL COMPOSITION CONTAINING SAME AND THERAPEUTIC USE THEREOF
EP2012793B1 (en) Use of a tricyclic compound for preparing a medicament for treating skeletal muscle degeneration of genetic origin

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK RS

17P Request for examination filed

Effective date: 20090819

RAX Requested extension states of the european patent have changed

Extension state: RS

Payment date: 20090819

Extension state: MK

Payment date: 20090819

Extension state: HR

Payment date: 20090819

Extension state: BA

Payment date: 20090819

Extension state: AL

Payment date: 20090819

RBV Designated contracting states (corrected)

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

17Q First examination report despatched

Effective date: 20091023

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: SANOFI

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: SANOFI

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: SANOFI

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20130201