JP2010522139A5 - - Google Patents

Download PDF

Info

Publication number
JP2010522139A5
JP2010522139A5 JP2009541901A JP2009541901A JP2010522139A5 JP 2010522139 A5 JP2010522139 A5 JP 2010522139A5 JP 2009541901 A JP2009541901 A JP 2009541901A JP 2009541901 A JP2009541901 A JP 2009541901A JP 2010522139 A5 JP2010522139 A5 JP 2010522139A5
Authority
JP
Japan
Prior art keywords
aminomethyl
ligand
nsaid
methyl
carboxymethyl
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.)
Granted
Application number
JP2009541901A
Other languages
English (en)
Other versions
JP5308350B2 (ja
JP2010522139A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2007/011313 external-priority patent/WO2008077599A1/en
Publication of JP2010522139A publication Critical patent/JP2010522139A/ja
Publication of JP2010522139A5 publication Critical patent/JP2010522139A5/ja
Application granted granted Critical
Publication of JP5308350B2 publication Critical patent/JP5308350B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (17)

  1. 非ステロイド系抗炎症薬(NSAID)の投与前、投与中、または投与後と組み合わせて、下部尿路機能障害を患う対象の尿失禁の治療に使用する、α2δカルシウム・チャンネル・サブユニット(A2d)リガンド。
  2. (1R,5R,6S)−6−アミノメチル−6−カルボキシメチル−ビシクロ[3.2.0]ヘプタン、3−(1−アミノメチル−シクロヘキシルメチル)−4H−1,2,4−オキサジアゾール−5−オン、5−(1−アミノメチル−シクロヘキシルメチル)−1H−テトラゾール、(3S,4S)−(1−アミノメチル−1−カルボキシメチル−3,4−ジメチル−シクロペンタン、(1α,3α,5α)−(3−アミノメチル−3−カルボキシメチル−ビシクロ[3.2.0]ヘプタン、(3S,5R)−3−アミノメチル−5−メチル−オクタン酸、(3S,5R)−3−アミノ−5−メチル−ヘプタン酸、(3S,5R)−3−アミノ−5−メチル−オクタン酸、(3S,5R)−3−アミノ−5−メチル−ノナン酸、(2S,4S)−4−(3−クロロフェノキシ)−プロリンまたは(2S,4S)−4−(3−フルオロベンジル)−プロリン、もしくはそれらの2つ以上の混合物であることを特徴とする請求項1記載のA2dリガンド。
  3. ガバペンチンまたはプレガバリンであることを特徴とする請求項1記載のA2dリガンド。
  4. α2δカルシウム・チャンネル・サブユニット(A2d)リガンドの投与前、投与中、または投与後と組み合わせて、下部尿路機能障害を患う対象の尿失禁の治療に使用するための非ステロイド系抗炎症薬(NSAID)。
  5. COX阻害剤であることを特徴とする請求項4記載のNSAID。
  6. セレコキシブ、ジクロフェナク、ジフルニサル、フルルビプロフェン、ナプロキセン、ニメスリドまたはスリンダクであることを特徴とする請求項4または5記載のNSAID。
  7. 下部尿路機能障害を患う対象の尿失禁の治療において、同時に、または連続して使用する 、α2δカルシウム・チャンネル・サブユニット(A2d)リガンドおよび非ステロイド系抗炎症薬(NSAID)。
  8. 前記A2dリガンドが、(1R,5R,6S)−6−アミノメチル−6−カルボキシメチル−ビシクロ[3.2.0]ヘプタン、3−(1−アミノメチル−シクロヘキシルメチル)−4H−1,2,4−オキサジアゾール−5−オン、5−(1−アミノメチル−シクロヘキシルメチル)−1H−テトラゾール、(3S,4S)−(1−アミノメチル−1−カルボキシメチル−3,4−ジメチル−シクロペンタン、(1α,3α,5α)−(3−アミノメチル−3−カルボキシメチル−ビシクロ[3.2.0]ヘプタン、(3S,5R)−3−アミノメチル−5−メチル−オクタン酸、(3S,5R)−3−アミノ−5−メチル−ヘプタン酸、(3S,5R)−3−アミノ−5−メチル−オクタン酸, (3S,5R)−3−アミノ−5−メチル−ノナン酸、(2S,4S)−4−(3−クロロフェノキシ)−プロリンまたは(2S,4S)−4−(3−フルオロベンジル)−プロリン、もしくはそれらの2つ以上の混合物であることを特徴とする請求項7記載のA2dリガンドおよびNSAID。
  9. 前記A2dリガンドが、ガバペンチンまたはプレガバリンであることを特徴とする請求項7記載のA2dリガンドおよびNSAID。
  10. 前記NSAIDが、COX阻害剤であることを特徴とする請求項7〜9いずれか1項記載のA2dリガンドおよびNSAID。
  11. 前記NSAIDが、セレコキシブ、ジクロフェナク、ジフルニサル、フルルビプロフェン、ナプロキセン、ニメスリドまたはスリンダクであることを特徴とする請求項7〜10いずれか1項記載のA2dリガンドおよびNSAID。
  12. 非ステロイド系抗炎症薬(NSAID)の投与前、投与中、または投与後と組み合わせて、下部尿路機能障害を患う対象の尿失禁を治療するための医薬組成物であって
    α2δカルシウム・チャンネル・サブユニット(A2d)リガンドを含む、医薬組成物
  13. α2δカルシウム・チャンネル・サブユニット(A2d)リガンドの投与前、投与中、または投与後と組み合わせて、下部尿路機能障害を患う対象の尿失禁を治療するための医薬組成物であって
    非ステロイド系抗炎症薬(NSAID)を含む、医薬組成物
  14. 前記A2dリガンドが、(1R,5R,6S)−6−アミノメチル−6−カルボキシメチル−ビシクロ[3.2.0]ヘプタン、3−(1−アミノメチル−シクロヘキシルメチル)−4H−1,2,4−オキサジアゾール−5−オン、5−(1−アミノメチル−シクロヘキシルメチル)−1H−テトラゾール、(3S,4S)−(1−アミノメチル−1−カルボキシメチル−3,4−ジメチル−シクロペンタン、(1α,3α,5α)−(3−アミノメチル−3−カルボキシメチル−ビシクロ[3.2.0]ヘプタン、(3S,5R)−3−アミノメチル−5−メチル−オクタン酸、(3S,5R)−3−アミノ−5−メチル−ヘプタン酸、(3S,5R)−3−アミノ−5−メチル−オクタン酸, (3S,5R)−3−アミノ−5−メチル−ノナン酸、(2S,4S)−4−(3−クロロフェノキシ)−プロリンまたは(2S,4S)−4−(3−フルオロベンジル)−プロリン、もしくはそれらの2つ以上の混合物であることを特徴とする請求項12または13記載の医薬組成物
  15. 前記A2dリガンドが、ガバペンチンまたはプレガバリンであることを特徴とする請求項12または13記載の医薬組成物
  16. 前記NSAIDが、COX阻害剤であることを特徴とする請求項12〜15いずれか1項記載の医薬組成物
  17. 前記NSAIDが、セレコキシブ、ジクロフェナク、ジフルニサル、フルルビプロフェン、ナプロキセン、ニメスリドまたはスリンダクであることを特徴とする請求項12〜16いずれか1項記載の医薬組成物
JP2009541901A 2006-12-22 2007-12-21 α2δリガンドおよびNSAIDを用いた下部尿路機能障害の併用療法 Expired - Fee Related JP5308350B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US87171906P 2006-12-22 2006-12-22
US60/871,719 2006-12-22
PCT/EP2007/011313 WO2008077599A1 (en) 2006-12-22 2007-12-21 COMBINATION THERAPY OF LOWER URINARY TRACT DISORDERS WITH α2δ LIGANDS AND NSAIDS

Publications (3)

Publication Number Publication Date
JP2010522139A JP2010522139A (ja) 2010-07-01
JP2010522139A5 true JP2010522139A5 (ja) 2011-02-17
JP5308350B2 JP5308350B2 (ja) 2013-10-09

Family

ID=39272500

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009541901A Expired - Fee Related JP5308350B2 (ja) 2006-12-22 2007-12-21 α2δリガンドおよびNSAIDを用いた下部尿路機能障害の併用療法

Country Status (26)

Country Link
US (1) US20080153888A1 (ja)
EP (1) EP2125021B8 (ja)
JP (1) JP5308350B2 (ja)
KR (1) KR20090092307A (ja)
CN (2) CN101600458A (ja)
AT (1) ATE511860T1 (ja)
AU (1) AU2007338367B2 (ja)
BR (1) BRPI0720351A2 (ja)
CA (1) CA2673545A1 (ja)
CY (1) CY1111783T1 (ja)
DK (1) DK2125021T3 (ja)
EA (1) EA017171B1 (ja)
ES (1) ES2367881T3 (ja)
HK (1) HK1155663A1 (ja)
HR (1) HRP20110634T1 (ja)
IL (1) IL198891A (ja)
MX (1) MX2009006575A (ja)
NO (1) NO20092581L (ja)
NZ (1) NZ577097A (ja)
PL (1) PL2125021T3 (ja)
PT (1) PT2125021E (ja)
RS (1) RS51940B (ja)
SI (1) SI2125021T1 (ja)
UA (1) UA94979C2 (ja)
WO (1) WO2008077599A1 (ja)
ZA (1) ZA200905038B (ja)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2735913A1 (en) 2008-09-04 2010-03-11 Neurosearch A/S A method for combating adverse effects arising from antipsychotic treatment
US9415048B2 (en) * 2010-07-08 2016-08-16 Wellesley Pharmaceuticals, Llc Pharmaceutical formulation for reducing frequency of urination and method of use thereof
US20130323288A1 (en) * 2010-07-08 2013-12-05 Wellesley Pharmaceuticals, Llc Pharmaceutical formulation for bedwetting and method of use thereof
CN102648915B (zh) * 2011-02-28 2015-04-15 鲁南制药集团股份有限公司 一种治疗或预防神经病理性疼痛的药物组合物
ITMI20121263A1 (it) 2012-07-19 2014-01-20 Recordati Ind Chimica E Farma Ceutica S P A Forma farmaceutica multistrato
US10792326B2 (en) 2013-06-28 2020-10-06 Wellesley Pharmaceuticals, Llc Pharmaceutical formulation for bedwetting and method of use thereof
CR20160573A (es) 2014-06-16 2017-03-14 Farmacéuticos Rayere S A Composición farmaceutica que combina un anticonvulsivante y un derivado del ácido nicotínico

Family Cites Families (125)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4018830A (en) * 1969-09-22 1977-04-19 Merck & Co., Inc. Phenylthioaralkylamines
US3840597A (en) 1971-02-24 1974-10-08 Riker Laboratories Inc Substituted 2-phenoxy alkane-sulfonanilides
DE2460891C2 (de) 1974-12-21 1982-09-23 Gödecke AG, 1000 Berlin 1-Aminomethyl-1-cycloalkanessigsäuren und deren Ester, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel
GB1561411A (en) 1977-02-25 1980-02-20 Science Union & Cie 2-phenoxyphenyl pyrrolidines and pharmaceutical compositions containing them
DE2756113A1 (de) 1977-12-16 1979-06-21 Thomae Gmbh Dr K Neue 4-hydroxy-2h-1,2-benzothiazin- 3-carboxamid-1,1-dioxide, verfahren zu ihrer herstellung und diese enthaltende arzneimittel
US4885367A (en) 1987-11-19 1989-12-05 Taisho Pharmaceutical Co., Ltd. Sulfonanilide compounds
US6197819B1 (en) 1990-11-27 2001-03-06 Northwestern University Gamma amino butyric acid analogs and optical isomers
ZA923283B (en) * 1991-05-29 1993-01-27 Akzo Nv Phenoxyphenyl derivatives
EP0641330B1 (en) 1992-05-20 2001-10-17 Northwestern University Gaba and l-glutamic acid analogs for antiseizure treatment
ES2089736T3 (es) 1992-10-28 1996-10-01 Shionogi & Co Derivados de bencilideno.
WO1994015932A1 (en) 1993-01-15 1994-07-21 G.D. Searle & Co. Novel 3,4-diaryl thiophenes and analogs thereof having use as antiinflammatory agents
CA2113787A1 (en) 1993-01-29 1994-07-30 Nobuyuki Hamanaka Carbocyclic sulfonamides
US5380738A (en) 1993-05-21 1995-01-10 Monsanto Company 2-substituted oxazoles further substituted by 4-fluorophenyl and 4-methylsulfonylphenyl as antiinflammatory agents
US5474995A (en) 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
US5344991A (en) * 1993-10-29 1994-09-06 G.D. Searle & Co. 1,2 diarylcyclopentenyl compounds for the treatment of inflammation
CA2276945C (en) 1993-11-30 2006-08-01 G.D. Searle & Co. Tricyclic-substituted pyrazolyl benzenesulfonamides and pharmaceutical compositions thereof
US5475018A (en) 1993-11-30 1995-12-12 G. D. Searle & Co. 1,5-diphenyl pyrazole compounds for treatment of inflammation
US5466823A (en) 1993-11-30 1995-11-14 G.D. Searle & Co. Substituted pyrazolyl benzenesulfonamides
AU2424895A (en) 1994-05-04 1995-11-29 G.D. Searle & Co. Substituted spirodienes for the treatment of inflammation
US5418254A (en) 1994-05-04 1995-05-23 G. D. Searle & Co. Substituted cyclopentadienyl compounds for the treatment of inflammation
US5486534A (en) 1994-07-21 1996-01-23 G. D. Searle & Co. 3,4-substituted pyrazoles for the treatment of inflammation
EP1125932A3 (en) 1994-07-27 2001-08-29 G.D. Searle & Co. Substituted thiazoles for the treatment of inflammation
US5616601A (en) 1994-07-28 1997-04-01 Gd Searle & Co 1,2-aryl and heteroaryl substituted imidazolyl compounds for the treatment of inflammation
US5620999A (en) 1994-07-28 1997-04-15 Weier; Richard M. Benzenesulfonamide subtituted imidazolyl compounds for the treatment of inflammation
US5521213A (en) 1994-08-29 1996-05-28 Merck Frosst Canada, Inc. Diaryl bicyclic heterocycles as inhibitors of cyclooxygenase-2
US5547975A (en) 1994-09-20 1996-08-20 Talley; John J. Benzopyranopyrazolyl derivatives for the treatment of inflammation
US5739166A (en) 1994-11-29 1998-04-14 G.D. Searle & Co. Substituted terphenyl compounds for the treatment of inflammation
JP2636819B2 (ja) 1994-12-20 1997-07-30 日本たばこ産業株式会社 オキサゾール系複素環式芳香族化合物
JP3181190B2 (ja) 1994-12-20 2001-07-03 日本たばこ産業株式会社 オキサゾール誘導体
US5596008A (en) 1995-02-10 1997-01-21 G. D. Searle & Co. 3,4-Diaryl substituted pyridines for the treatment of inflammation
JP3267300B2 (ja) 1995-02-13 2002-03-18 ジー.ディー.サール アンド カンパニー 炎症の治療のための置換イソオキサゾール
US5633272A (en) 1995-02-13 1997-05-27 Talley; John J. Substituted isoxazoles for the treatment of inflammation
US5731343A (en) 1995-02-24 1998-03-24 The Scripps Research Institute Method of use of radicicol for treatment of immunopathological disorders
WO1996037479A1 (en) 1995-05-26 1996-11-28 F. Hoffmann La Roche Ag Cyclohexanone oxime derivatives
EP0828718A1 (en) 1995-06-02 1998-03-18 G.D. SEARLE & CO. Heterocyclo substituted hydroxamic acid derivatives as cyclooxygenase-2 and 5-lipoxygenase inhibitors
US5643933A (en) 1995-06-02 1997-07-01 G. D. Searle & Co. Substituted sulfonylphenylheterocycles as cyclooxygenase-2 and 5-lipoxygenase inhibitors
US5968974A (en) 1995-07-19 1999-10-19 Merck & Co., Inc. Method of treating colonic adenomas
JPH11510485A (ja) 1995-07-21 1999-09-14 ニィコメド・オーストリア・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング 酵素のシクロオキシゲナーゼiiの阻害剤としてのベンゼンスルホンアミドの誘導体
JP4422796B2 (ja) 1995-07-21 2010-02-24 タクティカル セラピューティクス インコーポレイテッド アミノイミダゾールカルボキサミドおよび5−アミノ、または置換アミノ1,2,3−トリアゾールの塩による癌の治療および阻止
GB9520584D0 (en) 1995-10-09 1995-12-13 Fujisawa Pharmaceutical Co Pyrazole derivatives,processes for preparation thereof and pharmaceutical composition comprising the same
US6020343A (en) * 1995-10-13 2000-02-01 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
US5981576A (en) 1995-10-13 1999-11-09 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
US6057319A (en) 1995-10-30 2000-05-02 Merck Frosst Canada & Co. 3,4-Diaryl-2-hydroxy-2,5-dihydrofurans as prodrugs to cox-2 inhibitors
CZ293595A3 (cs) 1995-11-09 1999-12-15 Farmak A. S. Deriváty N,N-dimethyl-2-(arylthio)benzylaminu, jejich soli, způsoby jejich přípravy a jejich použití v léčivých přípravcích
US6222048B1 (en) * 1995-12-18 2001-04-24 Merck Frosst Canada & Co. Diaryl-2-(5H)-furanones as Cox-2 inhibitors
AU720628B2 (en) 1996-02-07 2000-06-08 Warner-Lambert Company Novel cyclic amino acids as pharmaceutical agents
US5990114A (en) 1996-02-28 1999-11-23 Recordati, S.A., Chemical And Pharmaceutical Company Use of 5-HT1A receptor antagonists for the treatment of urinary incontinence
NZ331143A (en) 1996-03-14 2001-06-29 Warner Lambert Co Substituted cyclic amino acids as pharmaceutical agents
NZ331142A (en) 1996-03-14 2001-04-27 Warner Lambert Co Bridged cyclic amino acids as pharmaceutical agents
US6180651B1 (en) 1996-04-04 2001-01-30 Bristol-Myers Squibb Diarylmethylidenefuran derivatives, processes for their preparation and their uses in therapeutics
US5908858A (en) 1996-04-05 1999-06-01 Sankyo Company, Limited 1,2-diphenylpyrrole derivatives, their preparation and their therapeutic uses
DE69739003D1 (de) 1996-04-12 2008-10-30 Searle Llc Substituierte Benzensulfonamid-Derivate als Wirkstoff-Vorläufer von COX-2 Inhibitoren
US5883267A (en) 1996-05-31 1999-03-16 Merck & Co., Inc. Process for making phenyl heterocycles useful as cox-2 inhibitors
PL187848B1 (pl) 1996-07-18 2004-10-29 Merck Frosst Canada Inc Podstawione pirydyny, kompozycja farmaceutyczna, podstawione pirydyny jako selektywne inhibitory cyklooksygenazy-2 oraz zastosowanie podstawionych pirydyn
US5861419A (en) 1996-07-18 1999-01-19 Merck Frosst Canad, Inc. Substituted pyridines as selective cyclooxygenase-2 inhibitors
BR9712651A (pt) 1996-10-23 1999-10-26 Warner Lambert Co ‡cidos gama-aminobutìricos substituìdos com agentes farmacêuticos.
ATA16597A (de) 1997-02-03 1998-04-15 Nycomed Austria Gmbh Neue substituierte p-sulfonylaminobenzol- sulfonsäureamide
ATE231504T1 (de) 1997-04-11 2003-02-15 Grelan Pharmaceutical Co Pyrazolderivate und sie enthaltende cox- inhibitoren
US6130334A (en) 1998-04-15 2000-10-10 Merck & Co., Inc. Process for making 2-aryl-3-aryl-5-halo pyridines useful as COX-2 inhibitors
US6127545A (en) 1997-04-18 2000-10-03 Merck & Co., Inc. Process for making 2-aryl-3-aryl-5-halo pyridines useful as COX-2 inhibitors
US6034256A (en) 1997-04-21 2000-03-07 G.D. Searle & Co. Substituted benzopyran derivatives for the treatment of inflammation
US6077850A (en) 1997-04-21 2000-06-20 G.D. Searle & Co. Substituted benzopyran analogs for the treatment of inflammation
US6040320A (en) 1997-06-30 2000-03-21 Ortho-Mcneil Pharmaceutical, Inc. 2-substituted imidazoles useful in the treatment of inflammatory diseases
AP9801302A0 (en) 1997-07-23 2000-01-23 Pfizer Indole compounds as anti-inflammatory/analgesic agents..
US6307047B1 (en) 1997-08-22 2001-10-23 Abbott Laboratories Prostaglandin endoperoxide H synthase biosynthesis inhibitors
ATE311867T1 (de) * 1997-09-08 2005-12-15 Warner Lambert Co Analgetische zusammensetzung enthaltend antiepileptische arzneistoffe und deren verwendungen
US5925769A (en) 1997-09-09 1999-07-20 Ortho Pharmaceutical, Corp. Acetylenic 1,5-diarylpyrazoles as antiinflammatory agents
US6046217A (en) 1997-09-12 2000-04-04 Merck Frosst Canada & Co. 2,3,5-trisubstituted pyridines as inhibitors of cyclooxygenase-2
US6140515A (en) 1997-09-24 2000-10-31 Merck & Co., Inc. Process of making 3-aryloxy, 4-aryl furan-2-ones useful as inhibitors of COX-2
US6040450A (en) 1997-09-25 2000-03-21 Merck & Co., Inc. Process for making diaryl pyridines useful as cox-2-inhibitors
PL199794B1 (pl) 1997-10-27 2008-10-31 Warner Lambert Co Związki pośrednie do wytwarzania pochodnych cyklicznych aminokwasów
US6080876A (en) 1997-10-29 2000-06-27 Merck & Co., Inc. Process for making phenyl heterocycles useful as COX-2 inhibitors
US6133292A (en) 1997-10-30 2000-10-17 Merck Frosst Canada & Co. Diaryl-5-alkyl-5-methyl-2-(5H)-furanones as selective cyclooxygenase-2-inhibitors
PL341291A1 (en) 1997-12-16 2001-04-09 Warner Lambert Co 1-substituted derivatives of 1-aminomethyl-ccycloalkanes (gabapentin analogues), their production and application of them in treating neurological disorders
CN1210268C (zh) 1997-12-16 2005-07-13 沃尼尔·朗伯公司 ((环)烷基取代的)-γ-氨基丁酸衍生物(=GABA类似物),其制备和在治疗神经病中的用途
AU759392B2 (en) 1997-12-16 2003-04-10 Warner-Lambert Company 4(3)substituted-4(3)-aminomethyl-(thio)pyran or -piperidine derivatives (=gabapentin analogues), their preparation and their use in the treatment of neurological disorders
JP3256513B2 (ja) 1998-02-11 2002-02-12 ファイザー製薬株式会社 ベンゾイミダゾールシクロオキシゲナーゼ−2阻害剤
US5994379A (en) 1998-02-13 1999-11-30 Merck Frosst Canada, Inc. Bisaryl COX-2 inhibiting compounds, compositions and methods of use
EP1085845A2 (en) 1998-06-08 2001-03-28 Advanced Medicine, Inc. Multibinding inhibitors of cyclooxygenase-2
KR100295206B1 (ko) 1998-08-22 2001-07-12 서경배 디아릴벤조피란유도체및이를함유하는시클로옥시게네이즈-2저해제조성물
ES2249919T3 (es) 1998-10-27 2006-04-01 Abbott Laboratories Inhibidores de la biosintesis de prostaglandina endoperoxido h sintasa.
US6077869A (en) 1998-10-29 2000-06-20 Ortho-Mcneil Pharmaceutical, Inc. Aryl phenylhydrazides as selective COX-2 inhibitors for treatment of inflammation
US6441156B1 (en) 1998-12-30 2002-08-27 The United States Of America As Represented By The Department Of Health And Human Services Calcium channel compositions and methods of use thereof
NZ512910A (en) 1999-02-23 2003-11-28 Pfizer Prod Inc Monoamine reuptake inhibitors for treatment of CNS disorders
US6451857B1 (en) * 1999-03-10 2002-09-17 Warner-Lambert Company Analgesic compositions comprising anti-epileptic compounds and methods of using same
ES2341059T3 (es) * 1999-04-08 2010-06-14 Warner-Lambert Company Llc Tratamiento de la incontinencia.
US6992109B1 (en) * 1999-04-08 2006-01-31 Segal Catherine A Method for the treatment of incontinence
CN1196671C (zh) 1999-06-10 2005-04-13 沃尼尔·朗伯公司 单和双取代的3-丙基-γ-氨基丁酸
CA2377153A1 (en) 1999-06-16 2000-12-21 Temple University - Of The Commonwealth System Of Higher Education 1-(4-sulfamylaryl)-3-substituted-5-aryl-2-pyrazolines as inhibitors of cyclooxygenase-2
MXPA00006605A (es) 1999-07-02 2004-12-09 Pfizer Compuestos de carbonil-indol biciclicos como agentes antiinflamatorios/analgesicos.
US6077868A (en) 1999-07-20 2000-06-20 Wisconsin Alumni Research Foundation Selective inhibition of cyclooxygenase-2
US6306861B1 (en) * 1999-07-30 2001-10-23 Recordati S.A. Chemical And Pharmaceutical Company Thienopyrancecarboxamide derivatives
US6387909B1 (en) * 1999-07-30 2002-05-14 Recordati S.A. Chemical And Pharmaceutical Company Thienopyranecarboxamide derivatives
US6306890B1 (en) 1999-08-30 2001-10-23 Vanderbilt University Esters derived from indolealkanols and novel amides derived from indolealkylamides that are selective COX-2 inhibitors
PL355289A1 (en) 1999-10-13 2004-04-05 Pfizer Products Inc. Biaryl ether derivatives useful as monoamine reuptake inhibitors
US6365591B1 (en) 1999-10-18 2002-04-02 Recordati, S.A., Chemical And Pharmacueticals Company Isoxazolecarboxamide derivatives
US6403594B1 (en) * 1999-10-18 2002-06-11 Recordati, S.A. Chemical And Pharmaceutical Company Benzopyran derivatives
HN2000000224A (es) 1999-10-20 2001-04-11 Warner Lambert Co Aminoacidos biciclicos como agentes farmaceuticos
US6083969A (en) 1999-10-20 2000-07-04 Ortho-Mcneil Pharaceutical, Inc. 1,3- and 2,3-diarylcycloalkano and cycloalkeno pyrazoles as selective inhibitors of cyclooxygenase-2 and antiinflammatory agents
GB2362646A (en) 2000-05-26 2001-11-28 Warner Lambert Co Cyclic amino acid derivatives useful as pharmaceutical agents
GB2365425A (en) 2000-08-01 2002-02-20 Parke Davis & Co Ltd Alkyl amino acid derivatives useful as pharmaceutical agents
ES2252310T3 (es) 2000-09-14 2006-05-16 Grunenthal Gmbh Beta-tioaminoacidos.
PE20021046A1 (es) 2000-09-30 2002-12-14 Gruenenthal Chemie Sulfonilguanidina que tiene afinidad al punto de fijacion de gabapentina
DE10048715A1 (de) 2000-09-30 2004-05-19 Grünenthal GmbH Verwendung von Aminosäure zur Behandlung von Schmerz
AU2002211863A1 (en) 2000-10-06 2002-04-15 Xenoport, Inc. Bile-acid derived compounds for providing sustained systemic concentrations of drugs after oral administration
GB2367869B (en) 2000-10-14 2004-10-06 Trw Ltd Rear-axle demand for use with front push-through in electrohydraulic (EHB) braking systems
US6359182B1 (en) 2000-10-26 2002-03-19 Duke University C-nitroso compounds and use thereof
GB2368579A (en) 2000-10-31 2002-05-08 Parke Davis & Co Ltd Azole pharmaceutical agents
WO2002042414A2 (en) 2000-11-17 2002-05-30 Xenoport, Inc. Amino acid conjugates providing for sustained systemic concentrations of gaba analogues
ITMI20010733A1 (it) * 2001-04-05 2002-10-05 Recordati Chem Pharm Uso di inibitori dell'isoenzina cox-2 per il trattamento dell'incontinenza urinaria
OA12504A (en) 2001-04-19 2006-05-29 Warner Lambert Co Fused bicyclic or tricyclic amino acids.
MXPA03011566A (es) 2001-06-11 2004-10-28 Xenoport Inc Formas de dosificacion de profarmacos de analogos de gaba administrados oralmente que tienen toxicidad reducida.
ITMI20011308A1 (it) 2001-06-21 2002-12-21 Nicox Sa Farmaci per il dolore cronico
KR20050005410A (ko) * 2002-02-19 2005-01-13 파마시아 코포레이션 요실금 치료용으로서의 시클로옥시게나제 저해제 및항무스카린제의 용도
US20040132826A1 (en) * 2002-10-25 2004-07-08 Collegium Pharmaceutical, Inc. Modified release compositions of milnacipran
ES2341240T3 (es) 2002-12-13 2010-06-17 Warner-Lambert Company Llc Ligando alfa-2-delta para tratar los sintomas del tracto urinario inferior.
AU2003301184A1 (en) 2002-12-20 2004-07-22 Dynogen Pharmaceuticals Inc METHODS OF TREATING NON-PAINFUL BLADDER DISORDERS USING Alpha2Delta SUBUNIT CALCIUM CHANNEL MODULATORS
ATE365554T1 (de) * 2003-04-04 2007-07-15 Dynogen Pharmaceuticals Inc Methode zur behandlung von erkrankungen der unteren harnwege
US20040248979A1 (en) 2003-06-03 2004-12-09 Dynogen Pharmaceuticals, Inc. Method of treating lower urinary tract disorders
NZ545884A (en) 2003-09-11 2010-01-29 Xenoport Inc Treating and/or preventing urinary incontinence using prodrugs of GABA analogs
ES2244326B1 (es) * 2004-04-05 2007-02-16 Laboratorios Del Dr. Esteve, S.A. Combinacion de substancias activas.
WO2006078811A2 (en) 2005-01-21 2006-07-27 Pharmanova Inc. Pharmaceutical formulations and methods of use
WO2006090275A1 (en) * 2005-02-24 2006-08-31 Pfizer Limited Treatment of incontinence
US20080009538A1 (en) * 2005-03-21 2008-01-10 Phil Skolnick Methods and compositions for the treatment of urinary incontinence
GB0509993D0 (en) * 2005-05-17 2005-06-22 Bamford Antony S Load sharing riser tensioning system

Similar Documents

Publication Publication Date Title
JP2010522139A5 (ja)
HRP20110634T1 (hr) KOMBINIRANA TERAPIJA LIGANADA α<SUB>2</SUB>δ I NSAID ZA POREMEĆAJE DONJEG URINARNOG TRAKTA
WO2009067703A3 (en) Tapentadol compositions
Calvo et al. Analgesic and anti-inflammatory dose–response relationship of 7.5 and 15 mg meloxicam after lower third molar removal: a double-blind, randomized, crossover study
WO2008010222A3 (en) Conjugates comprising a gaba- or glycine compound, pharmaceutical compositions and combinations thereof and their use in treating cns disorders
HK1127288A1 (en) Pharmaceutical combination comprising 3- (3-dimethylamino-1-ethyl-2-methyl- propyl) -phenol and an nsaid
WO2010062688A3 (en) Dosage form for insertion into the mouth
RU2013145498A (ru) Способы и композиции для лечения гиперурикемии и метаболических нарушений, связанных с гиперурикемией
JP2009504774A5 (ja)
WO2011100659A3 (en) Ameliorating drug-induced elevations in blood pressure by adjunctive use of antihypertensive drugs
RU2006107552A (ru) Комбинации, содержащие альфа-2-дельта лиганды и ингибиторы обратного захвата серотонина/норадреналина
Sorbera et al. Lumiracoxib
RU2016148182A (ru) (r)-пирлиндол и его фармацевтически приемлемые соли для применения в медицине
RU2015112586A (ru) Фармацевтические композиции, содержащие флурбипрофен
Bannwarth et al. Clinical pharmacology of lumiracoxib, a second-generation cyclooxygenase 2 selective inhibitor
WO2019067768A4 (en) Fixed dose combination formulations for treating pain
JP2011525479A5 (ja)
CA2411960A1 (en) Analgesic and anti-inflammatory compositions containing cox-2 inhibitors
WO2009154944A3 (en) Pharmaceutical formulations and methods of use which combine non-steroidal anti-inflammatory compounds with anti-hypertensive compounds
Choi et al. Update on NSAIDs related peptic ulcers
MX2019008467A (es) Combinacion sinergica de s-ketorolaco y pregabalina en una composicion farmaceutica para el tratamiento del dolor neuropatico.
Hontsariuk Сhronic pancreatitis–how often it is combined with other internal organs diseases
JP2008545616A5 (ja)
RU2006109388A (ru) Композиция для терапии судорожного синдрома
Poulose et al. NSAIDS–What to look out for?