HRP20020777A2 - Hydrophilic molecular disperse solutions of carvedilol - Google Patents
Hydrophilic molecular disperse solutions of carvedilol Download PDFInfo
- Publication number
- HRP20020777A2 HRP20020777A2 HRP20020777A HRP20020777A2 HR P20020777 A2 HRP20020777 A2 HR P20020777A2 HR P20020777 A HRP20020777 A HR P20020777A HR P20020777 A2 HRP20020777 A2 HR P20020777A2
- Authority
- HR
- Croatia
- Prior art keywords
- carvedilol
- preparation according
- solid
- pharmaceutically acceptable
- melt
- Prior art date
Links
- 229960004195 carvedilol Drugs 0.000 title claims description 100
- NPAKNKYSJIDKMW-UHFFFAOYSA-N carvedilol Chemical compound COC1=CC=CC=C1OCCNCC(O)COC1=CC=CC2=NC3=CC=C[CH]C3=C12 NPAKNKYSJIDKMW-UHFFFAOYSA-N 0.000 title claims 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 42
- 239000006104 solid solution Substances 0.000 claims description 40
- 229920001223 polyethylene glycol Polymers 0.000 claims description 27
- 239000002202 Polyethylene glycol Substances 0.000 claims description 24
- 238000002360 preparation method Methods 0.000 claims description 24
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims description 21
- 239000000377 silicon dioxide Substances 0.000 claims description 21
- 239000013543 active substance Substances 0.000 claims description 20
- 239000007787 solid Substances 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- -1 polyoxyethylene stearate Polymers 0.000 claims description 15
- 238000005507 spraying Methods 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 10
- 239000003814 drug Substances 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 9
- 229940079593 drug Drugs 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- SERLAGPUMNYUCK-DCUALPFSSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 claims description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 5
- 206010002383 Angina Pectoris Diseases 0.000 claims description 4
- 206010019280 Heart failures Diseases 0.000 claims description 4
- 206010020772 Hypertension Diseases 0.000 claims description 4
- 201000010099 disease Diseases 0.000 claims description 4
- 239000000905 isomalt Substances 0.000 claims description 4
- 235000010439 isomalt Nutrition 0.000 claims description 4
- HPIGCVXMBGOWTF-UHFFFAOYSA-N isomaltol Natural products CC(=O)C=1OC=CC=1O HPIGCVXMBGOWTF-UHFFFAOYSA-N 0.000 claims description 4
- 238000011321 prophylaxis Methods 0.000 claims description 4
- 235000021092 sugar substitutes Nutrition 0.000 claims description 4
- 239000003765 sweetening agent Substances 0.000 claims description 4
- 238000011282 treatment Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 3
- OGHNVEJMJSYVRP-UHFFFAOYSA-N carvedilol Chemical compound COC1=CC=CC=C1OCCNCC(O)COC1=CC=CC2=C1C1=CC=CC=C1N2 OGHNVEJMJSYVRP-UHFFFAOYSA-N 0.000 description 95
- 239000000155 melt Substances 0.000 description 32
- 239000000203 mixture Substances 0.000 description 29
- 238000009472 formulation Methods 0.000 description 17
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 16
- 238000007711 solidification Methods 0.000 description 14
- 230000008023 solidification Effects 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 13
- 230000002349 favourable effect Effects 0.000 description 11
- 238000009826 distribution Methods 0.000 description 10
- 239000000546 pharmaceutical excipient Substances 0.000 description 10
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 9
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 9
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 9
- 235000019359 magnesium stearate Nutrition 0.000 description 8
- 229920001993 poloxamer 188 Polymers 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
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- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 6
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 6
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
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- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
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- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 3
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000416 hydrocolloid Substances 0.000 description 3
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 229920003091 Methocel™ Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
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- SERLAGPUMNYUCK-OQPGPFOOSA-N (2r,3r,4r,5s)-6-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexane-1,2,3,4,5-pentol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-OQPGPFOOSA-N 0.000 description 1
- SERLAGPUMNYUCK-BLEZHGCXSA-N (2xi)-6-O-alpha-D-glucopyranosyl-D-arabino-hexitol Chemical compound OCC(O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-BLEZHGCXSA-N 0.000 description 1
- BTKQLFSKIFGYOF-MASOBFGXSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol dihydrate Chemical compound O.O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O BTKQLFSKIFGYOF-MASOBFGXSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 229920003084 Avicel® PH-102 Polymers 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 229920003151 Eudragit® RL polymer Polymers 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
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- DNKKLDKIFMDAPT-UHFFFAOYSA-N n,n-dimethylmethanamine;2-methylprop-2-enoic acid Chemical compound CN(C)C.CC(=C)C(O)=O.CC(=C)C(O)=O DNKKLDKIFMDAPT-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
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- 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
- A61K31/40—Heterocyclic 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
- A61K31/403—Heterocyclic 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/145—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Cardiology (AREA)
- Organic Chemistry (AREA)
- Heart & Thoracic Surgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00107093 | 2000-04-03 | ||
| PCT/EP2001/003502 WO2001074357A1 (fr) | 2000-04-03 | 2001-03-28 | Solutions dispersees moleculaires hydrophiles de carvedilol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20020777A2 true HRP20020777A2 (en) | 2004-12-31 |
Family
ID=8168348
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20020777 HRP20020777A2 (en) | 2000-04-03 | 2002-09-26 | Hydrophilic molecular disperse solutions of carvedilol |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US20010036959A1 (fr) |
| EP (1) | EP1272179B1 (fr) |
| JP (1) | JP2003528915A (fr) |
| KR (1) | KR100478793B1 (fr) |
| CN (1) | CN1189171C (fr) |
| AR (1) | AR029825A1 (fr) |
| AT (1) | ATE450257T1 (fr) |
| AU (2) | AU5622701A (fr) |
| BR (1) | BR0109779A (fr) |
| CA (1) | CA2401910C (fr) |
| CZ (1) | CZ20023625A3 (fr) |
| DE (1) | DE60140662D1 (fr) |
| HR (1) | HRP20020777A2 (fr) |
| HU (1) | HUP0300342A3 (fr) |
| IL (1) | IL151642A0 (fr) |
| MA (1) | MA26888A1 (fr) |
| MX (1) | MXPA02009725A (fr) |
| NO (1) | NO20024733D0 (fr) |
| NZ (1) | NZ521232A (fr) |
| PL (1) | PL358103A1 (fr) |
| RU (1) | RU2248204C2 (fr) |
| WO (1) | WO2001074357A1 (fr) |
| YU (1) | YU72602A (fr) |
| ZA (1) | ZA200207304B (fr) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2327685C (fr) * | 1998-04-03 | 2008-11-18 | Bm Research A/S | Composition a liberation lente |
| EP2957281A1 (fr) | 2001-09-21 | 2015-12-23 | Egalet Ltd. | Systeme de liberation a base de polymere |
| WO2003024426A1 (fr) * | 2001-09-21 | 2003-03-27 | Egalet A/S | Dispersions solides a liberation controlee |
| US20040253310A1 (en) | 2001-09-21 | 2004-12-16 | Gina Fischer | Morphine polymer release system |
| RU2308449C2 (ru) * | 2001-09-28 | 2007-10-20 | Ф.Хоффманн-Ля Рош Аг | Псевдополиморфные формы карведилола |
| US8101209B2 (en) | 2001-10-09 | 2012-01-24 | Flamel Technologies | Microparticulate oral galenical form for the delayed and controlled release of pharmaceutical active principles |
| AR038681A1 (es) * | 2002-02-14 | 2005-01-26 | Solvay Pharm Bv | Formulacion oral de solucion solida de una sustancia activa pobremente soluble en agua |
| CA2483054A1 (fr) * | 2002-04-30 | 2003-11-13 | Sb Pharmco Puerto Rico Inc. | Monocitrate monohydrate de carvedilol |
| US20050261335A1 (en) * | 2002-05-03 | 2005-11-24 | Wei Chen | Carvedilol formulations |
| JP2005533822A (ja) * | 2002-06-27 | 2005-11-10 | エスビー・ファルムコ・プエルト・リコ・インコーポレイテッド | 臭化水素酸カルベジロール |
| JP2005533823A (ja) * | 2002-06-27 | 2005-11-10 | エスビー・ファルムコ・プエルト・リコ・インコーポレイテッド | リン酸カルベジロール塩および／またはその溶媒和物、対応する組成物、および／または治療方法 |
| AU2003275953A1 (en) * | 2002-11-08 | 2004-06-07 | Egalet A/S | Controlled release carvedilol compositions |
| WO2004069180A2 (fr) | 2003-01-31 | 2004-08-19 | Smithkline Beecham Corporation | Compositions solides de dispersion |
| EP2301526B1 (fr) * | 2003-03-26 | 2016-03-23 | Egalet Ltd. | Système de libération contrôlée de morphine |
| EP1610768B1 (fr) * | 2003-03-26 | 2008-07-02 | Egalet A/S | Compositions matricielles pour administration controlee de substances medicamenteuses |
| MXPA06000370A (es) * | 2003-07-09 | 2006-03-28 | Chong Kun Dang Pharm Corp | Dispersion solida de tacrolimus. |
| BRPI0413927B8 (pt) * | 2003-08-29 | 2021-05-25 | Lifecycle Pharma As | composição farmacêutica compreendendo tacrolimus, forma de dosagem, uso da composição, e, método para a preparação da composição |
| SI1663217T1 (sl) * | 2003-08-29 | 2010-10-29 | Lifecycle Pharma As | Trdne disperzije, ki vsebujejo takrolimus |
| EP1686967A4 (fr) * | 2003-11-25 | 2012-08-08 | Smithkline Beecham Cork Ltd | Base libre de carvedilol, ses sels, formes anhydres ou solvats, compositions pharmaceutiques correspondantes, formulations a liberation controlee, et methodes de traitement ou d'administration |
| EP1691789B1 (fr) * | 2003-11-25 | 2017-12-20 | SmithKline Beecham (Cork) Limited | Base libre de carvedilol, ses sels, formes anhydres ou solvates, compositions pharmaceutiques correspondantes, formulations a liberation controlee, et procedes de traitement ou d'administration |
| EP1686986A4 (fr) * | 2003-11-25 | 2009-05-27 | Sb Pharmco Inc | Sels de carvedilol, compositions correspondantes, procedes d'administration et/ou de traitement |
| WO2005065657A2 (fr) * | 2003-12-31 | 2005-07-21 | Pfizer Products Inc. | Compositions solides a base de medicaments peu solubles et de poloxameres |
| BRPI0418294A (pt) * | 2003-12-31 | 2007-05-02 | Pfizer Prod Inc | composições sólidas farmacêuticas estabilizadas de medicamentos de baixa solubilidade, poloxámeros e polìmeros estabilizantes |
| NZ563846A (en) * | 2005-06-03 | 2010-03-26 | Egalet As | A drug delivery system for delivering active substances dispersed in a dispersion medium |
| US8367112B2 (en) * | 2006-02-28 | 2013-02-05 | Alkermes Pharma Ireland Limited | Nanoparticulate carverdilol formulations |
| US20090028935A1 (en) * | 2006-12-01 | 2009-01-29 | Kristin Arnold | Carvedilol forms, compositions, and methods of preparation thereof |
| WO2008070072A2 (fr) * | 2006-12-01 | 2008-06-12 | Mutual Pharmaceutical Company, Inc. | Formes, compositions de carvédilol, et leurs procédés de préparation |
| US20080138404A1 (en) * | 2006-12-06 | 2008-06-12 | Biovail Laboratories International S.R.L. | Extended release formulations of carvedilol |
| CA2930487A1 (fr) * | 2007-01-16 | 2008-07-24 | Egalet Ltd. | Utilisation (i) d'un polyglycol et (ii) d'une substance medicamenteuse active dans la preparation d'une composition pharmaceutique destinee (i) a reduire le risque de liberation massive induite par l'alcool et/ou (ii) a reduire le risque de toxicomanie medicamenteuse |
| BRPI0701904A2 (pt) * | 2007-04-27 | 2008-12-09 | Libbs Farmaceutica Ltda | forma farmacÊutica de liberaÇço controlada de princÍpios ativos com solubilidade dependente do baixo ph do meio e processo para preparar a forma farmacÊutica |
| WO2008148798A2 (fr) | 2007-06-04 | 2008-12-11 | Egalet A/S | Compositions pharmaceutiques à libération contrôlée pour un effet prolongé |
| ATE539769T1 (de) * | 2008-03-04 | 2012-01-15 | Lupin Ltd | Stabile pharmazeutische zusammensetzungen mit carvedilol |
| ES2330404B1 (es) * | 2008-05-19 | 2010-09-22 | Universidad De Barcelona | Solucion acuosa para la preservacion de tejidos y organos. |
| WO2010089132A1 (fr) | 2009-02-06 | 2010-08-12 | Egalet A/S | Composition à libération immédiate résistant à une maltraitance par prise d'alcool |
| NZ597283A (en) | 2009-06-24 | 2013-07-26 | Egalet Ltd | Controlled release formulations |
| WO2011154009A1 (fr) * | 2010-06-10 | 2011-12-15 | Lifecycle Pharma A/S | Composition comprenant un principe actif sous une forme amorphe et une substance poreuse adsorbante |
| US9549899B2 (en) | 2012-07-06 | 2017-01-24 | Egalet Ltd. | Abuse deterrent pharmaceutical compositions for controlled release |
| KR102158339B1 (ko) | 2016-02-05 | 2020-09-21 | 삼진제약주식회사 | 인습성이 개선된 카르베딜롤 속방성 제제 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2815926A1 (de) * | 1978-04-13 | 1979-10-18 | Boehringer Mannheim Gmbh | Neue carbazolyl-(4)-oxy-propanolamin-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| DE3319027A1 (de) * | 1983-05-26 | 1984-11-29 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur herstellung von optisch aktiven carbazol-derivaten, neue r- und s-carbazol-derivate, sowie arzneimittel, die diese verbindungen enthalten |
| US5258185A (en) * | 1989-08-23 | 1993-11-02 | Bauer Kurt H | Highly active, rapidly absorbable formulations of glibenclamide, processes for the production thereof and their use |
| US5281420A (en) * | 1992-05-19 | 1994-01-25 | The Procter & Gamble Company | Solid dispersion compositions of tebufelone |
| US5760069A (en) * | 1995-02-08 | 1998-06-02 | Boehringer Mannheim Pharmaceuticals Corporation-Smithkline Beecham Corporation Limited Partnership #1 | Method of treatment for decreasing mortality resulting from congestive heart failure |
| GB9514473D0 (en) * | 1995-07-14 | 1995-09-13 | Glaxo Lab Sa | Chemical compounds |
| DE19637082A1 (de) * | 1996-09-12 | 1998-03-19 | Boehringer Mannheim Gmbh | Schnellzerfallende Pellets |
| IL131713A (en) * | 1997-03-11 | 2004-08-31 | Arakis Ltd | Dosage forms comprising separate portions of r- and s-enantiomers |
| DE19809242A1 (de) * | 1998-03-05 | 1999-09-09 | Basf Ag | Verfahren zur Herstellung von festen, sphärischen Formkörpern, enthaltend pharmazeutische Wirkstoffe in einer Bindemittelmatrix |
| US6852337B2 (en) * | 1998-04-09 | 2005-02-08 | Roche Diagnostics Gmbh | Carvedilol-galenics |
| DE19816036A1 (de) * | 1998-04-09 | 1999-10-14 | Roche Diagnostics Gmbh | Verfahren zur Herstellung schnellauflösender pharmazeutischer Zubereitungen von schwerlöslichen Wirkstoffen |
| US6664284B2 (en) * | 1998-07-23 | 2003-12-16 | Roche Diagnostics Gmbh | Stabilized carvedilol injection solution |
| US6395300B1 (en) * | 1999-05-27 | 2002-05-28 | Acusphere, Inc. | Porous drug matrices and methods of manufacture thereof |
| PL371409A1 (en) * | 2002-01-15 | 2005-06-13 | Teva Pharmaceutical Industries Ltd. | Crystalline solids of carvedilol and processes for their preparation |
-
2001
- 2001-03-26 US US09/817,308 patent/US20010036959A1/en not_active Abandoned
- 2001-03-28 JP JP2001572101A patent/JP2003528915A/ja not_active Ceased
- 2001-03-28 RU RU2002129571/15A patent/RU2248204C2/ru not_active IP Right Cessation
- 2001-03-28 AT AT01929462T patent/ATE450257T1/de not_active IP Right Cessation
- 2001-03-28 IL IL15164201A patent/IL151642A0/xx unknown
- 2001-03-28 WO PCT/EP2001/003502 patent/WO2001074357A1/fr not_active Application Discontinuation
- 2001-03-28 KR KR10-2002-7013230A patent/KR100478793B1/ko not_active IP Right Cessation
- 2001-03-28 AU AU5622701A patent/AU5622701A/xx active Pending
- 2001-03-28 CZ CZ20023625A patent/CZ20023625A3/cs unknown
- 2001-03-28 EP EP01929462A patent/EP1272179B1/fr not_active Revoked
- 2001-03-28 NZ NZ521232A patent/NZ521232A/en unknown
- 2001-03-28 HU HU0300342A patent/HUP0300342A3/hu unknown
- 2001-03-28 MX MXPA02009725A patent/MXPA02009725A/es active IP Right Grant
- 2001-03-28 DE DE60140662T patent/DE60140662D1/de not_active Expired - Fee Related
- 2001-03-28 BR BR0109779-2A patent/BR0109779A/pt not_active Application Discontinuation
- 2001-03-28 YU YU72602A patent/YU72602A/sh unknown
- 2001-03-28 CA CA002401910A patent/CA2401910C/fr not_active Expired - Fee Related
- 2001-03-28 AU AU2001256227A patent/AU2001256227B2/en not_active Ceased
- 2001-03-28 PL PL01358103A patent/PL358103A1/xx not_active Application Discontinuation
- 2001-03-28 CN CNB018074278A patent/CN1189171C/zh not_active Expired - Fee Related
- 2001-03-30 AR ARP010101538A patent/AR029825A1/es not_active Application Discontinuation
-
2002
- 2002-08-08 US US10/214,697 patent/US20030004205A1/en not_active Abandoned
- 2002-09-11 ZA ZA200207304A patent/ZA200207304B/en unknown
- 2002-09-26 HR HRP20020777 patent/HRP20020777A2/hr not_active Application Discontinuation
- 2002-10-01 MA MA26845A patent/MA26888A1/fr unknown
- 2002-10-02 NO NO20024733A patent/NO20024733D0/no unknown
-
2005
- 2005-08-16 US US11/204,614 patent/US20050271721A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CZ20023625A3 (cs) | 2003-04-16 |
| MA26888A1 (fr) | 2004-12-20 |
| ZA200207304B (en) | 2003-12-11 |
| AR029825A1 (es) | 2003-07-16 |
| US20050271721A1 (en) | 2005-12-08 |
| JP2003528915A (ja) | 2003-09-30 |
| NO20024733L (no) | 2002-10-02 |
| WO2001074357A1 (fr) | 2001-10-11 |
| ATE450257T1 (de) | 2009-12-15 |
| US20030004205A1 (en) | 2003-01-02 |
| EP1272179A1 (fr) | 2003-01-08 |
| AU5622701A (en) | 2001-10-15 |
| PL358103A1 (en) | 2004-08-09 |
| EP1272179B1 (fr) | 2009-12-02 |
| IL151642A0 (en) | 2003-04-10 |
| BR0109779A (pt) | 2003-01-21 |
| YU72602A (sh) | 2005-03-15 |
| KR100478793B1 (ko) | 2005-03-24 |
| RU2248204C2 (ru) | 2005-03-20 |
| KR20030019339A (ko) | 2003-03-06 |
| DE60140662D1 (de) | 2010-01-14 |
| AU2001256227B2 (en) | 2005-09-01 |
| HUP0300342A2 (hu) | 2003-06-28 |
| NZ521232A (en) | 2004-05-28 |
| HUP0300342A3 (en) | 2005-07-28 |
| CN1420771A (zh) | 2003-05-28 |
| CA2401910A1 (fr) | 2001-10-11 |
| MXPA02009725A (es) | 2003-03-27 |
| US20010036959A1 (en) | 2001-11-01 |
| RU2002129571A (ru) | 2004-03-27 |
| CN1189171C (zh) | 2005-02-16 |
| NO20024733D0 (no) | 2002-10-02 |
| CA2401910C (fr) | 2008-04-15 |
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| A1OB | Publication of a patent application | ||
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| OBST | Application withdrawn |