RU2007101510A - Композиции для лечения воспаления и боли с использованием комбинации селективного ингибитора сох-2 и антагониста рецептора ltb4 - Google Patents
Композиции для лечения воспаления и боли с использованием комбинации селективного ингибитора сох-2 и антагониста рецептора ltb4 Download PDFInfo
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Claims (37)
1. Терапевтическая композиция, содержащая целекоксиб и по меньшей мере один антагонист рецептора LTB4, где антагонист рецептора LTB4 включает одно или более чем одно соединение, выбранное из группы, состоящей из 2-[(3S,4R)-3,4-дигидро-4-гидрокси-3-(фенилметил)-2Н-1-бензопиран-7-ил]-4-(трифторметил)бензойной кислоты; ее фармацевтически приемлемой соли и их смесей.
2. Терапевтическая композиция по п.1, где антагонист рецептора LTB4 включает 2-[(3S,4R)-3,4-дигидро-4-гидрокси-3-(фенилметил)-2Н-1-бензопиран-7-ил]-4-(трифторметил)бензойную кислоту.
3. Терапевтическая композиция по п.1. где антагонист рецептора LTB4 включает фармацевтически приемлемую соль 2-[(3S,4R)-3,4-дигидро-4-гидрокси-3-(фенилметил)-2Н-1-бензопиран-7-ил]-4-(трифторметил)бензойной кислоты.
4. Терапевтическая композиция по п.1, где антагонист рецептора LTB4 включает моноэтилендиаминовую соль 2-[(3S,4R)-3,4-дигидро-4-гидрокси-3-(фенилметил)-2Н-1-бензопиран-7-ил]-4-(трифторметил)бензойной кислоты.
5. Композиция по п.1, дополнительно содержащая фармацевтически приемлемый эксципиент.
6. Композиция по п.1, представляющая собой твердую лекарственную форму.
7. Композиция по п.6, где твердая лекарственная форма представляет собой пероральную лекарственную форму.
8. Композиция по п.7, где пероральная лекарственная форма выбрана из группы, состоящей из таблетки, капсулы, суппозитория, пилюли, гелевой капсулы и гранулированной композиции.
9. Композиция по п.8, где пероральная лекарственная форма представляет собой капсулу.
10. Композиция по п.9, где капсула представляет собой капсульную лекарственную форму с высвобождением по времени.
11. Композиция по п.8, где пероральная лекарственная форма представляет собой таблетированную лекарственную форму.
12. Композиция по п.11, где таблетированная лекарственная форма выбрана из группы, состоящей из многослойной таблетированной лекарственной формы, таблетированной лекарственной формы с замедленным высвобождением, таблетированной лекарственной формы из ядра и оболочки, осмотической таблетированной лекарственной формы и двухслойной таблетированной лекарственной формы.
13. Композиция по п.12, где таблетированная лекарственная форма представляет собой многослойную таблетированную лекарственную форму.
14. Композиция по п.12, где таблетированная лекарственная форма представляет собой двухслойную таблетированную лекарственную форму.
15. Композиция по п.12, где таблетированная лекарственная форма представляет собой таблетированную лекарственную форму с замедленным высвобождением.
16. Композиция по п.12, где таблетированная лекарственная форма представляет собой таблетированную лекарственную форму из ядра и оболочки.
17. Композиция по п.1, где целекоксиб и антагонист рецептора LTB4 присутствуют в гомогенной смеси.
18. Композиция по п.1, представляющая собой водную форму.
19. Композиция по п.18, где водная форма представляет собой сироп.
20. Композиция по п.18, где водная форма пригодна для парентерального введения.
21. Композиция по п.1, представляющая собой ингаляционную лекарственную форму.
22. Композиция по п.1, представляющая собой полутвердую лекарственную форму.
23. Композиция по п.22, где полутвердая форма пригодна для местного применения.
24. Композиция по п.1, представляющая собой суспензию.
25. Способ лечения, предупреждения или ингибирования воспаления, расстройства, связанного с воспалением, расстройства, связанного с болью, или боли у субъекта, нуждающегося в таком предупреждении, лечении или ингибировании, при котором этому субъекту вводят композицию, содержащую целекоксиб и соединение, являющееся антагонистом рецептора LTB4, где соединение, являющееся антагонистом рецептора LTB4, представляет собой одно или более чем одно соединение, выбранное из группы, состоящей из 2-[(3S,4R)-3,4-дигидро-4-гидрокси-3-(фенилметил)-2Н-1-бензопиран-7-ил]-4-(трифторметил)бензойной кислоты, ее фармацевтически приемлемой соли и их смесей.
26. Способ по п.25, где субъект представляет собой животное.
27. Способ по п.26, где животное представляет собой человека.
28. Способ по п.27 для лечения, предупреждения или ингибирования расстройства, связанного с воспалением.
29. Способ по п.27 для лечения, предупреждения или ингибирования воспаления.
30. Способ по п.27 для лечения, предупреждения или ингибирования боли.
31. Способ по п.27 для лечения, предупреждения или ингибирования расстройства, связанного с болью.
32. Способ по п.27, где расстройство, связанное с воспалением, представляет собой артрит.
33. Способ по п.32, где артрит представляет собой остеоартрит.
34. Способ по п.33, где артрит представляет собой ревматоидный артрит.
35. Способ по п.27 для предупреждения или лечения любого одного или более чем одного расстройства, выбранного из группы, состоящей из расстройства соединительной ткани и суставов, неопластического расстройства, сердечно-сосудистого расстройства, ушного расстройства, офтальмологического расстройства, респираторного расстройства, желудочно-кишечного расстройства, расстройства, связанного с ангиогенезом, иммунологических расстройств, аллергического расстройства, расстройства питания, инфекционных заболеваний и расстройств, эндокринного расстройства, метаболического расстройства, неврологического и нейродегенеративного расстройства, психиатрического расстройства, расстройства печени и желчного пузыря, скелетно-мышечного расстройства, мочеполового расстройства, гинекологического и родового расстройства, расстройства, связанного с повреждением и травмой, хирургического расстройства, зубного расстройства и расстройства ротовой полости, расстройства, связанного с половой дисфункцией, дерматологического расстройства, гематологического расстройства и расстройства, связанного с отравлением.
36. Способ по п.25, где количество антагониста рецептора LTB4 и количество целекоксиба вводят последовательно.
37. Способ по п.28, где количество антагониста рецептора LTB4 и количество целекоксиба вводят, по существу, одновременно.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US59007604P | 2004-07-22 | 2004-07-22 | |
US60/590,076 | 2004-07-22 |
Publications (1)
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RU2007101510A true RU2007101510A (ru) | 2008-08-27 |
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RU2007101510/15A RU2007101510A (ru) | 2004-07-22 | 2005-07-11 | Композиции для лечения воспаления и боли с использованием комбинации селективного ингибитора сох-2 и антагониста рецептора ltb4 |
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EP (1) | EP1773396A1 (ru) |
JP (1) | JP2008506768A (ru) |
KR (1) | KR20070035101A (ru) |
CN (1) | CN101014369A (ru) |
AR (1) | AR050351A1 (ru) |
AU (1) | AU2005266088A1 (ru) |
BR (1) | BRPI0513695A (ru) |
CA (1) | CA2574627A1 (ru) |
IL (1) | IL180638A0 (ru) |
MX (1) | MX2007000749A (ru) |
NO (1) | NO20070774L (ru) |
RU (1) | RU2007101510A (ru) |
TW (1) | TW200614985A (ru) |
WO (1) | WO2006011048A1 (ru) |
ZA (1) | ZA200700312B (ru) |
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US10849954B2 (en) * | 2014-11-11 | 2020-12-01 | Juntendo Educational Foundation | Preventive or therapeutic agent for age-related macular degeneration |
KR102631399B1 (ko) * | 2018-03-30 | 2024-02-01 | 씨지인바이츠 주식회사 | 폴마콕시브 및 프레가발린을 포함하는 통증 치료용 약제학적 조성물 |
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US5384318A (en) * | 1989-06-22 | 1995-01-24 | Pfizer Inc. | Substituted sulfonamides and related compounds in the treatment of asthma, arthritis and related diseases |
US5124350A (en) * | 1990-06-28 | 1992-06-23 | G. D. Searle & Co. | Leukotriene b4 antagonists |
US5246965A (en) * | 1991-06-11 | 1993-09-21 | Ciba-Geigy | Arylethers, their manufacture and methods of treatment |
MX9300312A (es) * | 1992-01-23 | 1993-07-31 | Pfizer | Antagonistas benzopiranicos y relacionado de ltb. |
EP0623122B1 (en) * | 1992-01-23 | 1997-03-05 | Pfizer Inc. | Benzopyran and related LTB4-antagonists. |
US5474995A (en) * | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
US5466823A (en) * | 1993-11-30 | 1995-11-14 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides |
HUT77515A (hu) * | 1994-10-13 | 1998-05-28 | Pfizer Inc. | Hidrogénezett benzopirán- és naftalinszármazékok, ezeket tartalmazó gyógyszerkészítmények és intermedierjeik |
US5633272A (en) * | 1995-02-13 | 1997-05-27 | Talley; John J. | Substituted isoxazoles for the treatment of inflammation |
US6342510B1 (en) * | 1995-06-12 | 2002-01-29 | G. D. Searle & Co. | Treatment of inflammation and inflammation-related disorders with a combination of a cyclooxygenase-2 inhibitors and a leukotriene B4 receptor antagonist |
EP0892791B1 (en) * | 1996-04-12 | 2003-03-05 | G.D. Searle & Co. | N-[[4-(5-METHYL-3-PHENYLISOXAZOL-4-YL]PHENYL]SULFONYLPROPYLAMIDE and its SODIUMSALT AS PRODRUGS OF COX-2 INHIBITORS |
JP2000508862A (ja) * | 1996-04-18 | 2000-07-11 | シーメンス アクチエンゲゼルシヤフト | 複数のデータ源により共通に利用される1つの伝送チャネルへのアクセス制御方法 |
US6417382B2 (en) * | 2000-01-12 | 2002-07-09 | Boehringer Ingelheim Pharma Kg | Process for preparing aryl-iminomethyl-carbamino acid esters |
US6436987B1 (en) * | 2000-06-08 | 2002-08-20 | Pfizer Inc. | Crystalline forms of (3S-trans)-2-[3,4-dihydro-4-hydroxy-3-(phenylmethyl)-2H-1-benzopyran-7-yl]-4-(trifluoromethyl)-benzoic acid |
AU4239302A (en) * | 2001-06-28 | 2003-01-02 | Pfizer Products Inc. | Benzoic acid substituted benzopyrans for the treatment of atherosclerosis |
EP1384723A1 (de) * | 2002-07-26 | 2004-01-28 | Boehringer Ingelheim Pharma GmbH & Co.KG | Neue 4-Hydroxy-2H-thieno[2,3-e]-1,2-thiazin-3-carboxamid-1,1-dioxide, Verfahren zu ihrer Herstellung und diese enthaltende Arzneimittel |
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US20080260817A1 (en) | 2008-10-23 |
IL180638A0 (en) | 2007-06-03 |
NO20070774L (no) | 2007-04-23 |
BRPI0513695A (pt) | 2008-05-13 |
AU2005266088A1 (en) | 2006-02-02 |
CN101014369A (zh) | 2007-08-08 |
TW200614985A (en) | 2006-05-16 |
MX2007000749A (es) | 2007-03-28 |
JP2008506768A (ja) | 2008-03-06 |
KR20070035101A (ko) | 2007-03-29 |
EP1773396A1 (en) | 2007-04-18 |
ZA200700312B (en) | 2008-05-28 |
CA2574627A1 (en) | 2006-02-02 |
WO2006011048A1 (en) | 2006-02-02 |
AR050351A1 (es) | 2006-10-18 |
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FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
Effective date: 20090417 |