UA78854C2 - Crystal for an oral solid drug and oral solid drug for dysuria treatment containing the same - Google Patents
Crystal for an oral solid drug and oral solid drug for dysuria treatment containing the same Download PDFInfo
- Publication number
- UA78854C2 UA78854C2 UAA200503153A UA2005003153A UA78854C2 UA 78854 C2 UA78854 C2 UA 78854C2 UA A200503153 A UAA200503153 A UA A200503153A UA 2005003153 A UA2005003153 A UA 2005003153A UA 78854 C2 UA78854 C2 UA 78854C2
- Authority
- UA
- Ukraine
- Prior art keywords
- dysuria
- medicinal preparation
- degree
- urethral
- kmo
- Prior art date
Links
- 206010013990 dysuria Diseases 0.000 title claims abstract description 52
- 239000007787 solid Substances 0.000 title claims abstract description 40
- 239000003814 drug Substances 0.000 title claims abstract description 22
- 229940079593 drug Drugs 0.000 title claims abstract description 18
- 239000013078 crystal Substances 0.000 title abstract description 17
- 239000004480 active ingredient Substances 0.000 claims abstract description 40
- 230000000694 effects Effects 0.000 claims abstract description 10
- -1 indoline compound Chemical class 0.000 claims abstract description 9
- 239000000126 substance Substances 0.000 claims description 41
- 238000002360 preparation method Methods 0.000 claims description 40
- 239000002775 capsule Substances 0.000 claims description 29
- 201000010099 disease Diseases 0.000 claims description 15
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 15
- 239000000843 powder Substances 0.000 claims description 15
- 229940126601 medicinal product Drugs 0.000 claims description 14
- 229940122041 Cholinesterase inhibitor Drugs 0.000 claims description 10
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 claims description 10
- 239000000812 cholinergic antagonist Substances 0.000 claims description 10
- 230000001713 cholinergic effect Effects 0.000 claims description 10
- 239000000544 cholinesterase inhibitor Substances 0.000 claims description 10
- 239000000932 sedative agent Substances 0.000 claims description 10
- 239000003242 anti bacterial agent Substances 0.000 claims description 9
- 239000002260 anti-inflammatory agent Substances 0.000 claims description 9
- 229940121363 anti-inflammatory agent Drugs 0.000 claims description 9
- 239000003163 gonadal steroid hormone Substances 0.000 claims description 9
- 229940123934 Reductase inhibitor Drugs 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 210000005036 nerve Anatomy 0.000 claims description 8
- 206010046459 urethral obstruction Diseases 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- 230000027939 micturition Effects 0.000 claims description 7
- 230000001624 sedative effect Effects 0.000 claims description 7
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 6
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 6
- 201000004240 prostatic hypertrophy Diseases 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 6
- 210000003708 urethra Anatomy 0.000 claims description 6
- 208000000693 Neurogenic Urinary Bladder Diseases 0.000 claims description 5
- 206010029279 Neurogenic bladder Diseases 0.000 claims description 5
- 206010060862 Prostate cancer Diseases 0.000 claims description 4
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000002441 X-ray diffraction Methods 0.000 claims description 4
- 239000002552 dosage form Substances 0.000 claims description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 4
- 201000009160 urethral calculus Diseases 0.000 claims description 3
- 230000000844 anti-bacterial effect Effects 0.000 claims description 2
- 230000003110 anti-inflammatory effect Effects 0.000 claims description 2
- 239000004575 stone Substances 0.000 claims description 2
- 208000012931 Urologic disease Diseases 0.000 claims 3
- 208000014001 urinary system disease Diseases 0.000 claims 3
- 230000001078 anti-cholinergic effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 12
- 229940124597 therapeutic agent Drugs 0.000 abstract description 4
- 238000000634 powder X-ray diffraction Methods 0.000 abstract description 2
- PNCPYILNMDWPEY-QGZVFWFLSA-N silodosin Chemical compound N([C@@H](CC=1C=C(C=2N(CCCO)CCC=2C=1)C(N)=O)C)CCOC1=CC=CC=C1OCC(F)(F)F PNCPYILNMDWPEY-QGZVFWFLSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 32
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 229920002472 Starch Polymers 0.000 description 15
- 239000000203 mixture Substances 0.000 description 15
- 239000008107 starch Substances 0.000 description 15
- 235000019698 starch Nutrition 0.000 description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000002904 solvent Substances 0.000 description 9
- 235000019359 magnesium stearate Nutrition 0.000 description 8
- 229940126701 oral medication Drugs 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 5
- 238000009776 industrial production Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000013557 residual solvent Substances 0.000 description 5
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000012046 mixed solvent Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000008194 pharmaceutical composition Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 229940125723 sedative agent Drugs 0.000 description 3
- 210000001635 urinary tract Anatomy 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- 206010020853 Hypertonic bladder Diseases 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 208000034189 Sclerosis Diseases 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 206010065584 Urethral stenosis Diseases 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 230000036772 blood pressure Effects 0.000 description 2
- 208000013507 chronic prostatitis Diseases 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 210000003205 muscle Anatomy 0.000 description 2
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 201000007094 prostatitis Diseases 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000012453 solvate Substances 0.000 description 2
- 201000001988 urethral stricture Diseases 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 208000003174 Brain Neoplasms Diseases 0.000 description 1
- 208000014644 Brain disease Diseases 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 206010063057 Cystitis noninfective Diseases 0.000 description 1
- 208000032274 Encephalopathy Diseases 0.000 description 1
- 208000026602 Hinman syndrome Diseases 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
- 208000001089 Multiple system atrophy Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 206010031127 Orthostatic hypotension Diseases 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 206010036968 Prostatic pain Diseases 0.000 description 1
- 206010037195 Psychogenic dysuria Diseases 0.000 description 1
- 208000029033 Spinal Cord disease Diseases 0.000 description 1
- 206010046477 Urethral syndrome Diseases 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 201000003139 chronic cystitis Diseases 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002476 indolines Chemical class 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 206010025005 lumbar spinal stenosis Diseases 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000008184 oral solid dosage form Substances 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 208000027232 peripheral nervous system disease Diseases 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 210000002307 prostate Anatomy 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 230000016160 smooth muscle contraction Effects 0.000 description 1
- 210000005070 sphincter Anatomy 0.000 description 1
- 208000020431 spinal cord injury Diseases 0.000 description 1
- 208000005198 spinal stenosis Diseases 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
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
- A61K31/33—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
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Urology & Nephrology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Indole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Steroid Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002262157 | 2002-09-06 | ||
| PCT/JP2003/011345 WO2004022538A1 (fr) | 2002-09-06 | 2003-09-05 | Cristal pour medicament solide a administration orale et medicament solide a administration orale destine au traitement de la dysurie contenant ce cristal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA78854C2 true UA78854C2 (en) | 2007-04-25 |
Family
ID=31973150
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UAA200503153A UA78854C2 (en) | 2002-09-06 | 2003-05-09 | Crystal for an oral solid drug and oral solid drug for dysuria treatment containing the same |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US20060142374A1 (fr) |
| EP (1) | EP1541554B1 (fr) |
| JP (1) | JP4532274B2 (fr) |
| KR (1) | KR100670592B1 (fr) |
| CN (1) | CN1321111C (fr) |
| AT (1) | ATE416159T1 (fr) |
| AU (1) | AU2003264385B2 (fr) |
| BR (1) | BR0314338A (fr) |
| CA (1) | CA2496780C (fr) |
| DE (1) | DE60325074D1 (fr) |
| ES (1) | ES2316858T3 (fr) |
| HK (1) | HK1084396A1 (fr) |
| HR (1) | HRP20050214B1 (fr) |
| IL (1) | IL167168A (fr) |
| IS (1) | IS2640B (fr) |
| MX (1) | MXPA05002549A (fr) |
| NO (2) | NO329855B1 (fr) |
| NZ (1) | NZ538598A (fr) |
| PL (1) | PL375701A1 (fr) |
| RU (1) | RU2347774C2 (fr) |
| TW (1) | TW200407126A (fr) |
| UA (1) | UA78854C2 (fr) |
| WO (1) | WO2004022538A1 (fr) |
| ZA (1) | ZA200501884B (fr) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101077061B1 (ko) * | 2002-12-16 | 2011-10-26 | 깃세이 야쿠힌 고교 가부시키가이샤 | 경구고형의약 |
| CA2557758C (fr) * | 2004-03-05 | 2013-09-10 | Kissei Pharmaceutical Co., Ltd. | Composition therapeutique destinee a prevenir ou a traiter une vessie hyperactive qui accompagne un trouble nerveux |
| JPWO2006038611A1 (ja) * | 2004-10-05 | 2008-05-15 | キッセイ薬品工業株式会社 | 下部尿路閉塞疾患に伴う蓄尿障害の予防及び／又は治療剤 |
| KR20070059152A (ko) * | 2004-10-06 | 2007-06-11 | 깃세이 야쿠힌 고교 가부시키가이샤 | 전립선 비대증에 대한 수술요법으로의 이행 예방용 의약조성물 |
| UA93669C2 (ru) * | 2005-02-02 | 2011-03-10 | Тева Фармасьютикл Индастриз, Лтд. | Способ приготовления полипептидной смеси c использованием гидрогенолиза |
| SI1848415T1 (sl) * | 2005-02-17 | 2013-08-30 | Teva Pharmaceutical Industries Ltd. | Kombinacijska terapija z glatiramer acetatom in razagilinom za zdravljenje muliple skleroze |
| US7750051B2 (en) * | 2006-12-14 | 2010-07-06 | Teva Pharmaceutical Industries, Ltd. | Crystalline solid rasagiline base |
| US20100076010A1 (en) * | 2007-02-26 | 2010-03-25 | Concert Pharmaceuticals, Inc. | Alpha 1a-adrenoceptor antagonists |
| WO2008106125A2 (fr) * | 2007-02-26 | 2008-09-04 | Concert Pharmaceuticals, Inc. | Antagonistes du récepteur alpha 1a-adrénergique |
| WO2008106536A1 (fr) * | 2007-02-28 | 2008-09-04 | Kissei Pharmaceuticals Co., Ltd. | Utilisation de silodosine administrée une fois par jour pour le traitement d'une hyperplasie prostatique bénigne |
| AU2009260733B2 (en) * | 2008-06-19 | 2015-01-29 | Teva Pharmaceutical Industries, Ltd. | Process for purifying rasagiline base |
| WO2012000926A1 (fr) | 2010-06-28 | 2012-01-05 | Ratiopharm Gmbh | Composés d'inclusion silodosine et cyclodextrine |
| EP2595607A2 (fr) | 2010-07-23 | 2013-05-29 | Ratiopharm GmbH | Médicament d'administration orale contenant un mélange de silodosine et d'un copolymère basique |
| WO2012014186A1 (fr) | 2010-07-30 | 2012-02-02 | Ranbaxy Laboratories Limited | Procédé de préparation de silodosin et de nouveaux intermédiaires de celui-ci |
| CN102229557B (zh) * | 2010-08-05 | 2013-03-27 | 南京海纳医药科技有限公司 | 西洛多辛的半水合物晶体、制备方法和包含它的药物组合物 |
| CN102229558B (zh) * | 2010-08-05 | 2013-05-08 | 南京海纳医药科技有限公司 | 西洛多辛的晶型δ、它的制备方法和包含它的药物组合物 |
| CN102010359B (zh) * | 2010-09-10 | 2013-01-23 | 北京阳光诺和药物研究有限公司 | β晶型西洛多辛的制备方法 |
| WO2012077138A1 (fr) | 2010-12-09 | 2012-06-14 | Panacea Biotec Limited | Procédés de cristallisation du (r)-1-(3-hydroxypropyl)-5-[2-[2-(2,2,2- trifluoroéthoxy)phénoxy]éthylamino]propyl]indoline-7-carboxamide |
| ES2492673T3 (es) | 2010-12-23 | 2014-09-10 | Sandoz Ag | Formas cristalinas de un ingrediente farmacéutico activo |
| CN102283816B (zh) * | 2011-08-05 | 2013-09-11 | 北京海步国际医药科技发展有限公司 | 西洛多辛缓释片剂及其制备方法 |
| WO2013061338A1 (fr) * | 2011-08-24 | 2013-05-02 | Cadila Healthcare Limited | Compositions pharmaceutiques de silodosine |
| WO2013072935A2 (fr) | 2011-10-10 | 2013-05-23 | Cadila Healthcare Limited | Procédé de préparation du silodosin |
| WO2014157137A1 (fr) * | 2013-03-26 | 2014-10-02 | キッセイ薬品工業株式会社 | Préparation pour l'administration orale avec l'amertume de la silodosine masquée |
| CN103159664B (zh) * | 2013-03-29 | 2016-03-23 | 深圳市海滨制药有限公司 | 一种赛洛多辛原料药及其制备方法、药物组合物 |
| WO2015015512A2 (fr) * | 2013-07-29 | 2015-02-05 | Ind-Swift Laboratories Limited | Procédé de préparation de silodosine et de sa forme gamma |
| JP2015117192A (ja) * | 2013-12-17 | 2015-06-25 | 東和薬品株式会社 | シロドシンγ型結晶及びその製造方法 |
| EP3103794A4 (fr) | 2014-02-06 | 2017-10-04 | UBE Industries, Ltd. | Procédé de production d'un composé indoline |
| KR20150127996A (ko) * | 2014-05-08 | 2015-11-18 | 한미정밀화학주식회사 | 실로도신 감마형 결정의 제조방법 |
| KR101725393B1 (ko) * | 2014-07-24 | 2017-04-27 | 주식회사 경보제약 | 실로도신의 제조 방법 및 신규 중간체 |
| KR101673160B1 (ko) | 2014-10-24 | 2016-11-07 | 보령제약 주식회사 | 실로도신 γ 결정형의 제조방법 |
| JP2016147811A (ja) * | 2015-02-10 | 2016-08-18 | ダイト株式会社 | シロドシンγ型結晶の製造方法 |
| ES2607639B1 (es) | 2015-09-30 | 2018-02-28 | Urquima, S.A | Sal de ácido maleico de un intermedio de silodosina |
| KR101733084B1 (ko) | 2016-07-27 | 2017-05-08 | (주)다산메디켐 | 실로도신의 결정형의 제조방법 |
| EP3354283B1 (fr) | 2017-06-20 | 2019-08-07 | Alfred E. Tiefenbacher (GmbH & Co. KG) | Composition de capsule pharmaceutique comprenant de la silodosine |
| JP2018035199A (ja) * | 2017-12-07 | 2018-03-08 | 東和薬品株式会社 | シロドシンγ型結晶及びその製造方法 |
| CN107903201B (zh) * | 2017-12-27 | 2020-09-25 | 浙江天宇药业股份有限公司 | 一种β晶型西洛多辛的制备方法 |
| CN111410626B (zh) * | 2019-01-04 | 2022-11-04 | 上海汇伦医药股份有限公司 | 赛洛多辛α-晶型的制备方法 |
| CN109824569B (zh) * | 2019-04-04 | 2022-09-20 | 重庆医药高等专科学校 | 一种西罗多辛晶型i及其制备方法 |
| WO2020237643A1 (fr) * | 2019-05-31 | 2020-12-03 | 上海汇伦生命科技有限公司 | Procédé de préparation d'une forme cristalline alpha de silodosine |
| CN114601826B (zh) * | 2022-03-31 | 2024-06-04 | 乐泰药业有限公司 | 一种用于治疗前列腺增生的药物制剂及其制备方法和质量检测方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE122010000031I1 (de) * | 1992-12-02 | 2010-10-21 | Kissei Pharmaceutical | Indolin Verbindungen zur Behandlung von Dysurien |
| JP3331048B2 (ja) * | 1994-06-01 | 2002-10-07 | キッセイ薬品工業株式会社 | インドール誘導体 |
| WO1999015202A1 (fr) * | 1997-09-22 | 1999-04-01 | Kissei Pharmaceutical Co., Ltd. | Medicaments contre la dysurie resultant d'une hypertrophie de la prostate |
| AU3011299A (en) * | 1998-03-23 | 1999-10-18 | Merck & Co., Inc. | Combination therapy for the treatment of benign prostatic hyperplasia |
| JP4324266B2 (ja) * | 1999-02-26 | 2009-09-02 | キッセイ薬品工業株式会社 | α１Ａアドレナリン受容体の変異体、当該変異体を用いた測定方法及び前立腺肥大に伴う排尿困難症治療剤 |
| JP4921646B2 (ja) * | 2001-03-08 | 2012-04-25 | キッセイ薬品工業株式会社 | １−（３−ベンジルオキシプロピル）−５−（２−置換プロピル）インドリン誘導体およびその使用方法 |
| CA2583660C (fr) * | 2004-10-27 | 2013-02-12 | Toshiaki Yamaguchi | Derive duindoline et procede de synthese dudit derive |
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