DK2727588T3 - Baclofen- og acamprosat-baseret terapi af neurologiske lidelser - Google Patents

Baclofen- og acamprosat-baseret terapi af neurologiske lidelser Download PDF

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DK2727588T3
DK2727588T3 DK13196461.1T DK13196461T DK2727588T3 DK 2727588 T3 DK2727588 T3 DK 2727588T3 DK 13196461 T DK13196461 T DK 13196461T DK 2727588 T3 DK2727588 T3 DK 2727588T3
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baclofen
acamprosate
composition
drug
combination
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DK13196461.1T
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Daniel Cohen
Ilya Chumakov
Serguei Nabirochkin
Emmanuel Vial
Mickaël Guedj
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Pharnext
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/137Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
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    • A61K31/138Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
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    • A61K31/145Amines having sulfur, e.g. thiurams (>N—C(S)—S—C(S)—N< and >N—C(S)—S—S—C(S)—N<), Sulfinylamines (—N=SO), Sulfonylamines (—N=SO2)
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    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
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    • A61K31/196Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
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    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
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    • A61K31/27Esters, e.g. nitroglycerine, selenocyanates of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine
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    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/435Heterocyclic 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
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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Claims (12)

1. Sammensætning omfattende (i) baclofen eller et farmaceutisk acceptabelt salt deraf, eller arbaclofen placarbil eller 3-(p-chlorphenyl)-4-hydroxysmørsyre, og (ii) acamprosat eller et farmaceutisk acceptabelt salt deraf, eller homotaurin eller ethyldimethyl-ammonio-propansulfonat eller taurin, til anvendelse i behandlingen af multipel sklerose hos et individ med behov deraf.
2. Sammensætningen til anvendelse ifølge krav 1, yderligere omfattende mindst én forbindelse valgt fra sulfisoxazol, methimazol, prilocain, dyphyllin, quinacrin, carbenoxolon, aminocapronsyre, cabergolin, diethylcarbamazin, cinacalcet, cinnarizin, eplerenon, fenoldopam, leflunomid, levosimendan, sulodexid, terbinafin, zonisamid, etomidat, phenformin, trimetazidin, mexiletin, ifenprodil, moxifloxacin, bromocriptin eller torasemid, eller farmaceutisk acceptable salte deraf.
3. Sammensætningen til anvendelse ifølge krav 1 eller 2, hvor nævnte sammensætning omfatter mindst én af de følgende kombinationer af forbindelser: - baclofen og acamprosat, - baclofen og acamprosat og diethylcarbamazin, - baclofen og acamprosat og cinacalcet, - baclofen og acamprosat og sulfisoxazol, - baclofen og acamprosat og torasemid, - baclofen og acamprosat og ifenprodil, - baclofen og acamprosat og mexiletin, - baclofen og acamprosat og eplerenon, - baclofen og acamprosat og levosimendan, - baclofen og acamprosat og terbinafin, eller - baclofen og acamprosat og leflunomid, eller farmaceutisk acceptable salte deraf.
4. Sammensætningen til anvendelse ifølge krav 1, hvor nævnte sammensætning omfatter mindst én af de følgende kombinationer af forbindelser: - baclofen, acamprosat og donepezil, - baclofen, acamprosat og rivastigmin, - baclofen, acamprosat og memantin, - baclofen, acamprosat og gabapentin, eller farmaceutisk acceptable salte deraf.
5. Sammensætningen til anvendelse ifølge krav 1, omfattende (i) baclofen eller et farmaceutisk acceptabelt salt deraf, eller arbaclofen placarbil eller 3-(p-chlorphenyl)-4-hydroxysmørsyre, og (ii) acamprosat eller et farmaceutisk acceptabelt salt deraf, eller homotaurin eller ethyldimethyl-ammonio-propansulfonat eller taurin, som de eneste aktive midler.
6. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvilken yderligere omfatter en farmaceutisk acceptabel bærer eller excipiens.
7. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvor forbindelserne i nævnte sammensætning formuleres eller administreres sammen, separat eller sekventielt.
8. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvor nævnte sammensætning administreres gentagne gange til individet.
9. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvor forholdet acamprosat/baclofen (W:W) er omfattet mellem 0,05 og 1000.
10. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvor dosen af baclofen er mindre end 100 mg/dag.
11. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvor dosen af acamprosat er mindre end 1000 mg/dag.
12. Sammensætningen til anvendelse ifølge et hvilket som helst af de foregående krav, hvor et calciumsalt af acamprosat anvendes.
DK13196461.1T 2011-03-01 2012-03-01 Baclofen- og acamprosat-baseret terapi af neurologiske lidelser DK2727588T3 (da)

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EP11305217 2011-03-01
US201161468658P 2011-03-29 2011-03-29
US201161493606P 2011-06-06 2011-06-06
EP11305687 2011-06-06
EP12708113.1A EP2560631B1 (en) 2011-03-01 2012-03-01 Baclofen and acamprosate based therapy of neurogical disorders

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