PE20010389A1 - Combinacion de un agonista del receptor 5ht1, cafeina, un inhibidor de la cox-2 y su uso para el tratamiento de la migrana - Google Patents
Combinacion de un agonista del receptor 5ht1, cafeina, un inhibidor de la cox-2 y su uso para el tratamiento de la migranaInfo
- Publication number
- PE20010389A1 PE20010389A1 PE2000000644A PE0006442000A PE20010389A1 PE 20010389 A1 PE20010389 A1 PE 20010389A1 PE 2000000644 A PE2000000644 A PE 2000000644A PE 0006442000 A PE0006442000 A PE 0006442000A PE 20010389 A1 PE20010389 A1 PE 20010389A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- day
- migrana
- caffeine
- inhibitor
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- 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
-
- 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
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- 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
- A61K31/41—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
- A61K31/4196—1,2,4-Triazoles
-
- 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
- A61K31/41—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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4465—Non condensed piperidines, e.g. piperocaine only substituted in position 4
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (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)
Abstract
SE REFIERE A UNA COMBINACION FARMACEUTICA QUE COMPRENDE a)UN AGONISTA DEL RECEPTOR 5HT1 TAL COMO ELETRIPTAN, RIZATRIPTAN, ZOLMITRIPTAN, SUMATRIPTAN, NARATRIPTAN UTILIZANDOSE 0,05 mg/DIA A 100 mg/DIA; b)CAFEINA UTILIZANDOSE 15 mg/DIA A 200 mg/DIA; c)UN INHIBIDOR DE CICLOOXIGENASA 2 TAL COMO i)UN DERIVADO DE INDOL DE FORMULA I; DONDE R1 ES H, ALQUILO C1-C4; R2 ES C(=L`)R3, SO2R4; Y ES UN ENLACE, ALQUILENO C1-C4; L Y L' SON O, S; Q ES ALQUILO C1-C6, CICLOALQUILO C3-C7, FENILO, NAFTILO, MONOCICLO AROMATICO DE 5-6 MIEMBROS; R3 ES OR6, NR7R8, N(OR1)R7, GRUPO a; Z ES UN ENLACE, O, S, NR5; R4 ES ALQUILO C1-C6, ENTRE OTROS; R5 ES ALQUILO C1-C4; R6 ES ALQUILO C1-C4, CICLOALQUILO C3-C7, ENTRE OTROS; R7 Y R8 SON H, ALQUILO C1-C6, CICLOALQUILO C3-C7, ENTRE OTROS; X ES HALO, ALQUILO C1-C4, ENTRE OTROS; n ES 0-3; r ES 1-3; ii)UN COMPUESTO XX; DONDE A ES UN HETEROCICLO DE 5 MIEMBROS, CARBOCICLO DE 5 MIEMBROS; R1 ES ARILO, HETEROARILO; R2 ES ALQUILO C1-4; R3, R4, R5 SON H, HALO, ALQUILO C1-C4; R6 Y R7 SON H, HALO, ALQUILO, ENTRE OTROS, DE PREFERENCIA (2-BENZOIL-6-CLORO-1H-3-IL)-ACETICO, ACIDO 6-CLORO-2-(2-METILBENZOIL)-1H-1H-INDOL-3-IL]ACETICO, ENTRE OTROS; UTILIZANDOSE DE 10/DIA mg A 300 mg/DIA. LA COMBINACION PUEDE SER UTIL PARA EL TRATAMIENTO DE LA MIGRANA
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14171599P | 1999-06-30 | 1999-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20010389A1 true PE20010389A1 (es) | 2001-04-07 |
Family
ID=22496903
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2000000644A PE20010389A1 (es) | 1999-06-30 | 2000-06-27 | Combinacion de un agonista del receptor 5ht1, cafeina, un inhibidor de la cox-2 y su uso para el tratamiento de la migrana |
Country Status (11)
Country | Link |
---|---|
US (1) | US6476042B1 (es) |
EP (1) | EP1064966A3 (es) |
JP (1) | JP2001039870A (es) |
KR (1) | KR20010049684A (es) |
AU (1) | AU4373600A (es) |
CA (1) | CA2312989A1 (es) |
CO (1) | CO5190664A1 (es) |
HU (1) | HUP0002509A3 (es) |
IL (1) | IL136960A0 (es) |
PE (1) | PE20010389A1 (es) |
ZA (1) | ZA200003236B (es) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8022095B2 (en) | 1996-08-16 | 2011-09-20 | Pozen, Inc. | Methods of treating headaches using 5-HT agonists in combination with long-acting NSAIDs |
AP869A (en) * | 1998-01-05 | 2000-09-04 | Pfizer | 2,3-Substituted indole compounds as anti-inflammatory and analgesic agents. |
US8680081B2 (en) | 2000-08-29 | 2014-03-25 | Peter Van Patten | Prophylactic treatment of migraine |
JP2004537526A (ja) * | 2001-06-12 | 2004-12-16 | メルク エンド カムパニー インコーポレーテッド | 片頭痛の治療又は予防用nr2b受容体拮抗薬 |
US7335779B2 (en) * | 2002-03-08 | 2008-02-26 | Quonova, Llc | Modulation of pathogenicity |
US7338969B2 (en) * | 2002-03-08 | 2008-03-04 | Quonova, Llc | Modulation of pathogenicity |
US6855332B2 (en) * | 2002-07-03 | 2005-02-15 | Lyfjathroun Hf. | Absorption promoting agent |
EP1575566B1 (en) | 2002-12-26 | 2012-02-22 | Pozen, Inc. | Multilayer dosage forms containing naproxen and triptans |
US20080213363A1 (en) * | 2003-01-23 | 2008-09-04 | Singh Nikhilesh N | Methods and compositions for delivering 5-HT3 antagonists across the oral mucosa |
US20040214861A1 (en) * | 2003-03-28 | 2004-10-28 | Pharmacia Corporation | Compositions of a cyclooxygenase-2 selective inhibitors and 5-HT1B1D antagonists for the treatment and prevention of migraine |
US20040204475A1 (en) * | 2003-04-11 | 2004-10-14 | Humphrey Michael John | Pharmaceutical combination |
US20070196340A1 (en) * | 2003-05-06 | 2007-08-23 | Aldo Ammendola | Modulation of Pathogenicity |
CA2545771A1 (en) * | 2003-11-12 | 2005-05-26 | Nps Pharmaceuticals, Inc. | Migraine treatments including isovaleramide compounds and serotonin agonists |
WO2005123043A2 (en) * | 2004-06-10 | 2005-12-29 | Duramed Pharmaceuticals, Inc. | Formulations of sumatriptan for absorption across biological membranes, and methods of making and using the same |
US20050282879A1 (en) * | 2004-06-17 | 2005-12-22 | Foad Salehani | Methods and composition for treatment of migraine and symptoms thereof |
US20080139510A1 (en) * | 2006-12-07 | 2008-06-12 | Abe Rose | Treatment of migraine headaches with sublingual amino acids |
CN102088966B (zh) | 2008-06-20 | 2015-06-10 | 阿尔法制药有限公司 | 药物制剂 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ283018B6 (cs) * | 1991-02-01 | 1997-12-17 | Merck Sharp And Dohme Limited | Deriváty imidazolu, triazolu a tetrazolu a farmaceutické přípravky na jejich bázi |
GB9108362D0 (en) | 1991-04-18 | 1991-06-05 | Radoslavov Alexander | A pharmaceutical composition suitable for alleviation of headaches,migraine and other painful conditions |
US5474995A (en) | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
KR100229343B1 (ko) | 1993-11-30 | 1999-11-01 | 윌리암스 로저 에이 | 염증치료용 치환 피라졸일벤젠술폰아미드 |
US5466823A (en) | 1993-11-30 | 1995-11-14 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides |
DE4342568A1 (de) * | 1993-12-14 | 1994-06-01 | Paul Ralf Peter | Coffeinhaltige Kaugummiware |
CA2182950A1 (en) | 1994-02-10 | 1995-08-17 | David B. Reitz | Substituted spiro compounds for the treatment of inflammation |
US5691374A (en) | 1995-05-18 | 1997-11-25 | Merck Frosst Canada Inc. | Diaryl-5-oxygenated-2-(5H) -furanones as COX-2 inhibitors |
KR100373622B1 (ko) | 1996-05-17 | 2003-07-12 | 머크 앤드 캄파니 인코포레이티드 | 사이클로옥시게나제-2로매개된질환의1일1회치료용조성물 |
US5861419A (en) | 1996-07-18 | 1999-01-19 | Merck Frosst Canad, Inc. | Substituted pyridines as selective cyclooxygenase-2 inhibitors |
US5872145A (en) | 1996-08-16 | 1999-02-16 | Pozen, Inc. | Formulation of 5-HT agonist and NSAID for treatment of migraine |
US5891885A (en) * | 1996-10-09 | 1999-04-06 | Algos Pharmaceutical Corporation | Method for treating migraine |
DK1007067T3 (da) | 1996-10-21 | 2002-05-06 | Eurovita As | Farmaceutiske præparater indeholdende Parthenium integrifolium eller dele deraf eller en ekstrakt bestanddel deraf, anvendelsen af et sådant plantemateriale til fremstilling af ... |
EP0863134A1 (en) | 1997-03-07 | 1998-09-09 | Merck Frosst Canada Inc. | 2-(3,5-difluorophenyl)-3-(4-(methyl-sulfonyl)phenyl)-2-cyclopenten-1-one useful as an inhibitor of cyclooxygenase-2 |
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 |
ATE206921T1 (de) * | 1997-07-03 | 2001-11-15 | Pfizer | Eletriptanhemisulfat und kaffein enthaltende pharmazeutische zusammenstellungen |
US5994379A (en) | 1998-02-13 | 1999-11-30 | Merck Frosst Canada, Inc. | Bisaryl COX-2 inhibiting compounds, compositions and methods of use |
DE69922688T2 (de) | 1998-11-02 | 2005-12-01 | Merck & Co. Inc. | Zusammensetzungen aus einem 5ht1b/1d agonisten und einem selektiven cox-2 hemmer zur behandlung von migräne |
WO2000026216A1 (en) | 1998-11-03 | 2000-05-11 | Glaxo Group Limited | Pyrazolopyridine derivatives as selective cox-2 inhibitors |
-
2000
- 2000-05-26 CO CO00039187A patent/CO5190664A1/es unknown
- 2000-06-22 IL IL13696000A patent/IL136960A0/xx unknown
- 2000-06-23 EP EP00305312A patent/EP1064966A3/en not_active Withdrawn
- 2000-06-26 US US09/603,630 patent/US6476042B1/en not_active Expired - Fee Related
- 2000-06-27 PE PE2000000644A patent/PE20010389A1/es not_active Application Discontinuation
- 2000-06-28 ZA ZA200003236A patent/ZA200003236B/xx unknown
- 2000-06-29 HU HU0002509A patent/HUP0002509A3/hu unknown
- 2000-06-29 CA CA002312989A patent/CA2312989A1/en not_active Abandoned
- 2000-06-29 AU AU43736/00A patent/AU4373600A/en not_active Abandoned
- 2000-06-30 JP JP2000197928A patent/JP2001039870A/ja active Pending
- 2000-06-30 KR KR1020000037111A patent/KR20010049684A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CO5190664A1 (es) | 2002-08-29 |
AU4373600A (en) | 2001-01-04 |
HU0002509D0 (en) | 2000-08-28 |
EP1064966A3 (en) | 2003-01-08 |
EP1064966A2 (en) | 2001-01-03 |
ZA200003236B (en) | 2002-01-02 |
HUP0002509A3 (en) | 2003-12-29 |
HUP0002509A2 (en) | 2001-03-28 |
US6476042B1 (en) | 2002-11-05 |
CA2312989A1 (en) | 2000-12-30 |
IL136960A0 (en) | 2001-06-14 |
KR20010049684A (ko) | 2001-06-15 |
JP2001039870A (ja) | 2001-02-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20010389A1 (es) | Combinacion de un agonista del receptor 5ht1, cafeina, un inhibidor de la cox-2 y su uso para el tratamiento de la migrana | |
EA200200708A1 (ru) | Производные бензазола и их применение в качестве модуляторов jnk | |
PE20081658A1 (es) | Derivados indolicos con anillo unido en las posiciones 5,6 y sus metodos de uso | |
ES2096639T3 (es) | Derivados de benzofurano, benzotiofeno, indol o indolizina, su procedimiento de preparacion, asi como las composiciones que los contienen. | |
EA200600348A1 (ru) | Новые соединения | |
NO166129C (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive tetrahydro-9h-pyrido (3,4-b)indoler. | |
TW346485B (en) | Substituted N-(indole-2-carbonyl)-glycinamides and derivatives as antidiabetic agents | |
PE20040512A1 (es) | Compuesto de pirazol-pirimidina anilina | |
HUP0102563A2 (hu) | Indolszármazékok és alkalmazásuk rosszindulatú és egyéb, patológiás sejtproliferáción alapuló megbetegedések kezelésére | |
AR037222A1 (es) | Un derivado de indol, su uso, un procedimiento para su preparacion, una composicion farmaceutica que lo comprende, y un procedimiento para preparar dicha composicion | |
ATE168102T1 (de) | 1,4-benzodiazepinderivate und ihre verwendung als cck-modulatoren | |
CA2271085A1 (fr) | Nouveaux composes de la famille des indole-carboxyliques et leur utilisation | |
BR9710230A (pt) | Derivados de indol para o tratamento de osteoporose | |
ES2178451T3 (es) | Derivados de benzoxadiazoles, benzotiadiazoles, benzotriazoles y quinoxalinas. | |
KR900016196A (ko) | 테트라하이드로벤즈[c, d]인돌 세로토닌 효능제 | |
DK1189900T3 (da) | Heterocykliske aminopyrrolidinderivater som melatonerge lægemidler | |
DE10199016I2 (de) | Indol derivate zur Behandlung von Migraene | |
PE20090112A1 (es) | Derivados de indol como agonistas del receptor de canabinoides cb1 | |
PE20021018A1 (es) | DERIVADOS DE ß - CARBOLINA | |
RS20060502A (en) | (indol-3-yl)-heterocycle derivatives as agonists of the cannabinoid cb1 receptor | |
NZ505060A (en) | 2-Aryl or heterocyclyl substituted indole derivatives useful for the treatment of osteoporosis | |
AR054329A1 (es) | Compuestos no esteroideos moduladores de los receptores de glucocorticoides | |
PE20010128A1 (es) | Composicion de un agonista del receptor 5ht1 y un inhibidor de la cox-2 para el tratamiento de la migrana | |
PE20040160A1 (es) | 1,2-dihidropirazol-3-onas que controlan citoquinas inflamatorias | |
PE20010134A1 (es) | Uso de agonistas de receptores 5ht1 y un inhibidor de la cox-2 para el tratamiento de la migrana |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |