IL143870A0 - Method of using a cyclooxygenase-2 inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia - Google Patents
Method of using a cyclooxygenase-2 inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasiaInfo
- Publication number
- IL143870A0 IL143870A0 IL14387099A IL14387099A IL143870A0 IL 143870 A0 IL143870 A0 IL 143870A0 IL 14387099 A IL14387099 A IL 14387099A IL 14387099 A IL14387099 A IL 14387099A IL 143870 A0 IL143870 A0 IL 143870A0
- Authority
- IL
- Israel
- Prior art keywords
- cyclooxygenase
- neoplasia
- inhibitor
- treatment
- combination therapy
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 230000009826 neoplastic cell growth Effects 0.000 title abstract 2
- 229940093444 Cyclooxygenase 2 inhibitor Drugs 0.000 title 1
- 229940034982 antineoplastic agent Drugs 0.000 title 1
- 239000002246 antineoplastic agent Substances 0.000 title 1
- 238000002648 combination therapy Methods 0.000 title 1
- 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 title 1
- 229940123038 Integrin antagonist Drugs 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
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- A61K33/243—Platinum; Compounds thereof
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61K31/47—Quinolines; Isoquinolines
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Inorganic Chemistry (AREA)
- Reproductive Health (AREA)
- Pregnancy & Childbirth (AREA)
- Gynecology & Obstetrics (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyrane Compounds (AREA)
- Radiation-Therapy Devices (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11378698P | 1998-12-23 | 1998-12-23 | |
| PCT/US1999/030693 WO2000038730A2 (en) | 1998-12-23 | 1999-12-22 | Use of a cyclooxygenase-2 inhibitor and one or more antineoplastic agents for combination therapy in neoplasia |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL143870A0 true IL143870A0 (en) | 2002-04-21 |
Family
ID=22351515
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL14387099A IL143870A0 (en) | 1998-12-23 | 1999-12-22 | Method of using a cyclooxygenase-2 inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
| IL14390199A IL143901A0 (en) | 1998-12-23 | 1999-12-22 | Use of cyclooxygenase-2- inhibitor, a matrix metallaproteinase inhibitor, an antineoplastic agent and optionally radiation as a combination treatment of neoplasia |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL14390199A IL143901A0 (en) | 1998-12-23 | 1999-12-22 | Use of cyclooxygenase-2- inhibitor, a matrix metallaproteinase inhibitor, an antineoplastic agent and optionally radiation as a combination treatment of neoplasia |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6689787B1 (de) |
| EP (8) | EP1140194A2 (de) |
| JP (8) | JP2002533405A (de) |
| KR (2) | KR20010110310A (de) |
| CN (3) | CN1346282A (de) |
| AT (1) | ATE322290T1 (de) |
| AU (8) | AU2713500A (de) |
| BR (2) | BR9916536A (de) |
| CA (8) | CA2356302A1 (de) |
| CZ (2) | CZ20012321A3 (de) |
| DE (1) | DE69930764D1 (de) |
| EA (2) | EA006294B1 (de) |
| HU (2) | HUP0104814A3 (de) |
| IL (2) | IL143870A0 (de) |
| MX (1) | MXPA01006499A (de) |
| NO (2) | NO20013156L (de) |
| PL (2) | PL350291A1 (de) |
| TR (1) | TR200102499T2 (de) |
| WO (8) | WO2000038719A1 (de) |
| ZA (2) | ZA200105055B (de) |
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| US6794511B2 (en) | 1997-03-04 | 2004-09-21 | G. D. Searle | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
| US6696449B2 (en) | 1997-03-04 | 2004-02-24 | Pharmacia Corporation | Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors |
| US7115632B1 (en) * | 1999-05-12 | 2006-10-03 | G. D. Searle & Co. | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
| US20040072889A1 (en) * | 1997-04-21 | 2004-04-15 | Pharmacia Corporation | Method of using a COX-2 inhibitor and an alkylating-type antineoplastic agent as a combination therapy in the treatment of neoplasia |
| US6077850A (en) * | 1997-04-21 | 2000-06-20 | G.D. Searle & Co. | Substituted benzopyran analogs for the treatment of inflammation |
| US20030225150A1 (en) * | 1997-04-21 | 2003-12-04 | Pharmacia Corporation | Method of using a COX-2 inhibitor and a topoisomerase II inhibitor as a combination therapy in the treatment of neoplasia |
| US7029652B2 (en) * | 1998-09-16 | 2006-04-18 | The Regents Of The University Of California | Method of treating tumors |
| US20020103141A1 (en) * | 1998-12-23 | 2002-08-01 | Mckearn John P. | Antiangiogenic combination therapy for the treatment of cancer |
| US20040053900A1 (en) * | 1998-12-23 | 2004-03-18 | Pharmacia Corporation | Method of using a COX-2 inhibitor and an aromatase inhibitor as a combination therapy |
| US6800646B1 (en) | 1999-02-08 | 2004-10-05 | Pharmacia Corporation | Sulfamato hydroxamic acid metalloprotease inhibitor |
| HRP20010660A2 (en) | 1999-02-08 | 2005-02-28 | G.D. Searle & Co | Sulfamato hydroxamic acid metalloprotease inhibitor |
| MXPA01011481A (es) * | 1999-05-12 | 2005-06-20 | Searle & Co | Derivados de acido hidroxamico como inhibidores de metaloproteasas de la matriz. |
| CA2373931A1 (en) | 1999-05-17 | 2000-11-23 | Richard Love | Dfmo and celecoxib in combination for cancer chemoprevention and therapy |
| US7141581B2 (en) | 1999-07-02 | 2006-11-28 | Agouron Pharmaceuticals, Inc. | Indazole compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use |
| GB9920548D0 (en) * | 1999-08-31 | 1999-11-03 | Rhone Poulenc Rorer Sa | Treatment of hepatocellular carcinoma |
| US7465754B1 (en) | 1999-09-15 | 2008-12-16 | Wyeth | Method of potentiating chemotherapy and treating solid tumors |
| BR0014001A (pt) * | 1999-09-15 | 2002-05-21 | American Home Prod | Método de potencialização de quimioterapia e tratamento de tumores sólidos |
| AU1767001A (en) * | 1999-11-15 | 2001-05-30 | Advanced Research And Technology Institute, Inc. | Use of nsaids for the treatment of pancreatic cancer |
| JP4039856B2 (ja) | 2000-02-03 | 2008-01-30 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | インテグリン発現阻害剤 |
| WO2001064110A1 (en) * | 2000-02-28 | 2001-09-07 | Zila, Inc. | Method for detecting and killing epithelial cancer cells |
| AR032151A1 (es) | 2000-03-24 | 2003-10-29 | Novartis Ag | Uso de un farmaco anti-angiogenico en conjunto con un agente fotosensible para la preparacion de un medicamento para el tratamiento fotodinamico mejorado de la neovasculatura indeseada |
| EP1138680A1 (de) * | 2000-03-29 | 2001-10-04 | Pfizer Products Inc. | Gem substituierte Sulfonylhydroxamsäuren mit MMP inhibierender Wirkung |
| US6900232B2 (en) | 2000-06-15 | 2005-05-31 | Pharmacia Corporation | Cycloalkyl alkanoic acids as integrin receptor antagonists |
| US6713074B2 (en) | 2000-06-29 | 2004-03-30 | Quick Med Technologies Inc. | Cosmetic composition and method |
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| CN1729002A (zh) * | 2000-09-08 | 2006-02-01 | 法玛西雅意大利公司 | 依西美坦作为化学预防剂 |
| AR034142A1 (es) * | 2000-09-08 | 2004-02-04 | Sloan Kettering Inst Cancer | Una composicion farmaceutica, metodo para fabricar un medicamento en base a dicha composicion y uso de la composicion |
| CA2434611A1 (en) * | 2001-01-26 | 2002-09-19 | Pharmacia Italia Spa | Combined method for treating hormono-dependent disorders |
| CA2440555A1 (en) | 2001-03-14 | 2002-09-19 | Bristol-Myers Squibb Company | Combination of epothilone analogs and chemotherapeutic agents for the treatment of proliferative diseases |
| US20030105144A1 (en) | 2001-04-17 | 2003-06-05 | Ping Gao | Stabilized oral pharmaceutical composition |
| EP1381384B1 (de) | 2001-04-24 | 2011-05-25 | Merck Patent GmbH | KOMBINATIONSTHERAPIE MIT ANTIANGIOGENEN MITTELN UND TNFalpha |
| US6872730B2 (en) | 2001-04-27 | 2005-03-29 | 3-Dimensional Pharmaceuticals, Inc. | Substituted benzofurans and benzothiophenes, methods of making and methods of use as integrin antagonists |
| JP2004527568A (ja) * | 2001-05-03 | 2004-09-09 | エフ.ホフマン−ラ ロシュ アーゲー | ゼラチナーゼインヒビターと抗腫瘍剤との組み合わせ、およびその使用 |
| AU2002345792A1 (en) | 2001-06-21 | 2003-01-08 | Pfizer Inc. | Thienopyridine and thienopyrimidine anticancer agents |
| US6683078B2 (en) | 2001-07-19 | 2004-01-27 | Pharmacia Corporation | Use of sulfonyl aryl or heteroaryl hydroxamic acids and derivatives thereof as aggrecanase inhibitors |
| AU2002328952A1 (en) * | 2001-07-23 | 2003-02-24 | Epidauros Biotechnologie Ag | Irinotecan for treatment of cancer |
| KR20040066103A (ko) * | 2001-10-19 | 2004-07-23 | 노파르티스 아게 | 조합제제내에 비스포스포네이트, cox-2 저해제 및탁솔을 포함하는, 악성 종양의 치료에 사용하기 위한 약학조성물 |
| US20050043409A1 (en) * | 2001-10-25 | 2005-02-24 | Chen Ying-Nan Pan | Combinations comprising a selective cyclooxygenase-2 inhibitor |
| EP1769795B1 (de) * | 2001-12-03 | 2013-07-24 | Bayer HealthCare LLC | Arylharnstoffverbindungen in Kombination mit anderen zytostatischen oder zytotoxischen Substanzen zur Behandlung von Krebs beim Menschen |
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| CA2478050A1 (en) | 2002-03-01 | 2003-09-12 | Pfizer Inc. | Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents |
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| JP3835763B2 (ja) * | 2002-08-19 | 2006-10-18 | ファイザー・プロダクツ・インク | 増殖亢進疾患のための組み合わせ治療 |
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| BR0317548A (pt) | 2002-12-19 | 2005-11-22 | Pfizer | Compostos de indazole e composições farmacêuticas para a inibição de proteìnas-cinases e métodos para o seu uso |
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| IL138677A0 (en) * | 1998-04-10 | 2001-10-31 | Searle & Co | Heterocyclic glycyl beta-alanine derivatives as vitronectin antagonists |
| AU747784B2 (en) * | 1998-07-29 | 2002-05-23 | Merck & Co., Inc. | Integrin receptor antagonists |
| US6277878B1 (en) * | 1998-09-07 | 2001-08-21 | Pfizer Inc | Substituted indole compounds as anti-inflammatory and analgesic agents |
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1999
- 1999-12-22 EP EP99968540A patent/EP1140194A2/de not_active Withdrawn
- 1999-12-22 EP EP99966587A patent/EP1140178A2/de not_active Ceased
- 1999-12-22 CZ CZ20012321A patent/CZ20012321A3/cs unknown
- 1999-12-22 DE DE69930764T patent/DE69930764D1/de not_active Expired - Lifetime
- 1999-12-22 AU AU27135/00A patent/AU2713500A/en not_active Abandoned
- 1999-12-22 BR BR9916536-8A patent/BR9916536A/pt not_active IP Right Cessation
- 1999-12-22 JP JP2000590668A patent/JP2002533405A/ja active Pending
- 1999-12-22 EP EP99966594A patent/EP1140179A2/de not_active Withdrawn
- 1999-12-22 EP EP99968941A patent/EP1140182A2/de not_active Withdrawn
- 1999-12-22 AU AU25926/00A patent/AU2592600A/en not_active Abandoned
- 1999-12-22 JP JP2000590670A patent/JP2002533407A/ja active Pending
- 1999-12-22 AT AT99967543T patent/ATE322290T1/de not_active IP Right Cessation
- 1999-12-22 JP JP2000590734A patent/JP2002533422A/ja active Pending
- 1999-12-22 AU AU22104/00A patent/AU2210400A/en not_active Abandoned
- 1999-12-22 AU AU22070/00A patent/AU2207000A/en not_active Abandoned
- 1999-12-22 CA CA002356302A patent/CA2356302A1/en not_active Abandoned
- 1999-12-22 CN CN99816332A patent/CN1346282A/zh active Pending
- 1999-12-22 WO PCT/US1999/030700 patent/WO2000038719A1/en not_active Ceased
- 1999-12-22 EA EA200100572A patent/EA006294B1/ru not_active IP Right Cessation
- 1999-12-22 WO PCT/US1999/030699 patent/WO2000038718A2/en not_active Ceased
- 1999-12-22 MX MXPA01006499A patent/MXPA01006499A/es unknown
- 1999-12-22 KR KR1020017008112A patent/KR20010110310A/ko not_active Ceased
- 1999-12-22 EP EP99968529A patent/EP1140193A2/de not_active Withdrawn
- 1999-12-22 CA CA002356929A patent/CA2356929A1/en not_active Abandoned
- 1999-12-22 AU AU22098/00A patent/AU2209800A/en not_active Abandoned
- 1999-12-22 CA CA002356426A patent/CA2356426A1/en not_active Abandoned
- 1999-12-22 CA CA002356462A patent/CA2356462A1/en not_active Abandoned
- 1999-12-22 PL PL99350291A patent/PL350291A1/xx not_active Application Discontinuation
- 1999-12-22 TR TR2001/02499T patent/TR200102499T2/xx unknown
- 1999-12-22 KR KR1020017008113A patent/KR20010109275A/ko not_active Ceased
- 1999-12-22 WO PCT/US1999/030670 patent/WO2000038665A2/en not_active Ceased
- 1999-12-22 PL PL99349216A patent/PL349216A1/xx not_active Application Discontinuation
- 1999-12-22 JP JP2000590666A patent/JP2002533404A/ja active Pending
- 1999-12-22 CA CA002356402A patent/CA2356402A1/en not_active Abandoned
- 1999-12-22 HU HU0104814A patent/HUP0104814A3/hu unknown
- 1999-12-22 CA CA002356606A patent/CA2356606A1/en not_active Abandoned
- 1999-12-22 JP JP2000590669A patent/JP2002533406A/ja active Pending
- 1999-12-22 CZ CZ20012320A patent/CZ20012320A3/cs unknown
- 1999-12-22 WO PCT/US1999/030693 patent/WO2000038730A2/en not_active Ceased
- 1999-12-22 JP JP2000590619A patent/JP2002533387A/ja active Pending
- 1999-12-22 CA CA002356748A patent/CA2356748A1/en not_active Abandoned
- 1999-12-22 AU AU25936/00A patent/AU2593600A/en not_active Abandoned
- 1999-12-22 EA EA200100573A patent/EA200100573A1/ru unknown
- 1999-12-22 JP JP2000590681A patent/JP2002533416A/ja active Pending
- 1999-12-22 CN CN99816333A patent/CN1371286A/zh active Pending
- 1999-12-22 IL IL14387099A patent/IL143870A0/xx unknown
- 1999-12-22 EP EP99967543A patent/EP1140192B1/de not_active Expired - Lifetime
- 1999-12-22 CN CN99816063A patent/CN1398189A/zh active Pending
- 1999-12-22 AU AU27136/00A patent/AU2713600A/en not_active Abandoned
- 1999-12-22 CA CA002356459A patent/CA2356459A1/en not_active Abandoned
- 1999-12-22 AU AU23805/00A patent/AU783992B2/en not_active Ceased
- 1999-12-22 HU HU0104747A patent/HUP0104747A3/hu unknown
- 1999-12-22 IL IL14390199A patent/IL143901A0/xx unknown
- 1999-12-22 WO PCT/US1999/030676 patent/WO2000038717A2/en not_active Ceased
- 1999-12-22 EP EP99968942A patent/EP1140183A1/de not_active Ceased
- 1999-12-22 US US09/857,871 patent/US6689787B1/en not_active Expired - Fee Related
- 1999-12-22 EP EP99966558A patent/EP1140177A2/de not_active Withdrawn
- 1999-12-22 WO PCT/US1999/030776 patent/WO2000037107A2/en not_active Ceased
- 1999-12-22 JP JP2000589217A patent/JP2002532563A/ja active Pending
- 1999-12-22 WO PCT/US1999/030621 patent/WO2000038715A2/en not_active Ceased
- 1999-12-22 WO PCT/US1999/030692 patent/WO2000038786A2/en not_active Ceased
- 1999-12-22 BR BR9916518-0A patent/BR9916518A/pt not_active IP Right Cessation
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2001
- 2001-06-20 ZA ZA200105055A patent/ZA200105055B/en unknown
- 2001-06-21 ZA ZA200105120A patent/ZA200105120B/en unknown
- 2001-06-22 NO NO20013156A patent/NO20013156L/no not_active Application Discontinuation
- 2001-06-22 NO NO20013155A patent/NO20013155L/no not_active Application Discontinuation
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