SI2081571T1 - Mešani ORL 1/u agonisti za zdravljenje bolečine - Google Patents
Mešani ORL 1/u agonisti za zdravljenje bolečineInfo
- Publication number
- SI2081571T1 SI2081571T1 SI200730414T SI200730414T SI2081571T1 SI 2081571 T1 SI2081571 T1 SI 2081571T1 SI 200730414 T SI200730414 T SI 200730414T SI 200730414 T SI200730414 T SI 200730414T SI 2081571 T1 SI2081571 T1 SI 2081571T1
- Authority
- SI
- Slovenia
- Prior art keywords
- orl1
- receptor
- agonist
- pain
- agonists
- Prior art date
Links
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
- A61K31/407—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 other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
- A61P23/02—Local anaesthetics
-
- 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
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Anesthesiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102006046745A DE102006046745A1 (de) | 2006-09-29 | 2006-09-29 | Gemischte ORL1/µ-Agonisten zur Behandlung von Schmerz |
EP07818462A EP2081571B1 (de) | 2006-09-29 | 2007-09-26 | GEMISCHTE ORL1/µ -AGONISTEN ZUR BEHANDLUNG VON SCHMERZ |
PCT/EP2007/008379 WO2008040481A1 (de) | 2006-09-29 | 2007-09-26 | GEMISCHTE ORL1/μ-AGONISTEN ZUR BEHANDLUNG VON SCHMERZ |
Publications (1)
Publication Number | Publication Date |
---|---|
SI2081571T1 true SI2081571T1 (sl) | 2010-12-31 |
Family
ID=38982475
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI200730414T SI2081571T1 (sl) | 2006-09-29 | 2007-09-26 | Mešani ORL 1/u agonisti za zdravljenje bolečine |
SI200730850T SI2206498T1 (sl) | 2006-09-29 | 2007-09-26 | Mešani ORL mu agonisti za zdravljenje bolečine |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI200730850T SI2206498T1 (sl) | 2006-09-29 | 2007-09-26 | Mešani ORL mu agonisti za zdravljenje bolečine |
Country Status (13)
Country | Link |
---|---|
US (3) | US20080125475A1 (sl) |
EP (2) | EP2081571B1 (sl) |
JP (2) | JP5203373B2 (sl) |
AT (2) | ATE478667T1 (sl) |
CA (1) | CA2664702C (sl) |
CY (2) | CY1110879T1 (sl) |
DE (2) | DE102006046745A1 (sl) |
DK (2) | DK2206498T3 (sl) |
ES (2) | ES2377482T3 (sl) |
PL (2) | PL2081571T3 (sl) |
PT (2) | PT2206498E (sl) |
SI (2) | SI2081571T1 (sl) |
WO (1) | WO2008040481A1 (sl) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10252667A1 (de) | 2002-11-11 | 2004-05-27 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
DE102006046745A1 (de) * | 2006-09-29 | 2008-04-03 | Grünenthal GmbH | Gemischte ORL1/µ-Agonisten zur Behandlung von Schmerz |
DE102007009319A1 (de) * | 2007-02-22 | 2008-08-28 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
DE102007009235A1 (de) * | 2007-02-22 | 2008-09-18 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
ES2523580T3 (es) | 2008-01-11 | 2014-11-27 | Albany Molecular Research, Inc. | Piridoindoles substituidos con (1-Azinona) |
CN102046633B (zh) | 2008-03-27 | 2015-03-25 | 格吕伦塔尔有限公司 | 取代的螺环状环己烷衍生物 |
CN102046591B (zh) | 2008-03-27 | 2014-12-03 | 格吕伦塔尔有限公司 | 羟甲基环己胺 |
WO2009118174A1 (de) | 2008-03-27 | 2009-10-01 | Grünenthal GmbH | Substituierte cyclohexyldiamine |
BR122013017393A2 (pt) | 2008-03-27 | 2019-10-15 | Grünenthal GmbH | Compostos derivados substituídos de 4-aminociclohexano, medicamentos contendo pelo menos um composto e uso dos referidos compostos |
JP5542119B2 (ja) | 2008-03-27 | 2014-07-09 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | スピロ(5.5)ウンデカン誘導体 |
WO2011003021A1 (en) * | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
WO2011003012A1 (en) * | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle mch-1 antagonists, methods of making, and use thereof |
WO2011003007A1 (en) * | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
JP2012532144A (ja) * | 2009-07-01 | 2012-12-13 | アルバニー モレキュラー リサーチ, インコーポレイテッド | アジノン置換アゼピノ[b]インドールおよびピリド−ピロロ−アゼピンmch−1拮抗薬、ならびにその作製方法および使用 |
DE102009041581B4 (de) | 2009-09-15 | 2011-09-29 | Airbus Operations Gmbh | Vorrichtung zur Abgrenzung eines Crew-Ruhebereichs und Verfahren zur Inbetriebnahme einer derartigen Vorrichtung |
TWI582092B (zh) * | 2010-07-28 | 2017-05-11 | 歌林達股份有限公司 | 順式-四氫-螺旋(環己烷-1,1’-吡啶[3,4-b]吲哚)-4-胺-衍生物 |
BR112013002696A2 (pt) * | 2010-08-04 | 2016-05-31 | Gruenenthal Gmbh | forma de dosagem farmacêutica compreendendo 6'-fluor-(n-metil- ou n,n-dimetil-)4-fenil-4',9'-diidro-3'h-espiro[cicloexano-1,-1'-pirano[3,4-b]indol]-4 amina 13'' |
WO2012016703A2 (en) | 2010-08-04 | 2012-02-09 | Grünenthal GmbH | Pharmaceutical dosage form comprising 6'-fluoro-(n-methyl- or n,n-dimethyl-)-4-phenyl-4',9'-dihydro-3'h-spiro[cyclohexane-1,1'-pyrano[3,4,b]indol]-4-amine |
HUE039328T2 (hu) * | 2010-08-04 | 2018-12-28 | Gruenenthal Gmbh | 6'-Fluor-(N-metil- vagy N,N-dimetil-)-4-fenil-4',9'-dihidro-3'H-spiro[ciklohexán-1,1'pirano[3,4,B]indol]-4-amin összetételû gyógyszerészeti adagolási forma a neuropátiás fájdalom kezelésére |
KR101828768B1 (ko) | 2010-08-04 | 2018-02-13 | 그뤼넨탈 게엠베하 | 6’플루오로(N메틸 또는 N,N디메틸)4페닐4’,9’디하이드로3’H스피로[사이클로헥산1,1’피라노[3,4,b]인돌]4아민을 포함하는 약제학적 투여형 |
US8993765B2 (en) | 2010-12-21 | 2015-03-31 | Albany Molecular Research, Inc. | Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof |
US8697700B2 (en) | 2010-12-21 | 2014-04-15 | Albany Molecular Research, Inc. | Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof |
US8614245B2 (en) | 2011-07-08 | 2013-12-24 | Gruenenthal Gmbh | Crystalline (1r,4r)-6′-fluoro-N,N-dimethyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano[3,4,b]indol]-4-amine |
US8618156B2 (en) | 2011-07-08 | 2013-12-31 | Gruenenthal Gmbh | Crystalline (1r,4r)-6'-fluoro-N,N-dimethyl-4-phenyl-4',9'-dihydro-3'H-spiro[cyclohexane-1,1'-pyrano[3,4,b]indol]-4-amine |
PL2797925T3 (pl) | 2011-12-12 | 2016-07-29 | Gruenenthal Gmbh | Sposób wytwarzania (1R,4R)-6'-fluoro-(N,N-dimetylo- i n-metylo)-4-fenylo-4',9'-dihydro-3'H-spiro[cykloheksano-1,1-pirano-[3,4,b]indolo]-4-aminy |
ES2605786T3 (es) | 2011-12-12 | 2017-03-16 | Grünenthal GmbH | Formas sólidas de clorhidrato de (1R,4R)-6'-fluor-N,N-dimetil-4-fenil-4',9'-dihidro-3'H-espiro[ciclohexano-1,1'-pirano[3,4b]indol]-4-amina |
SI2797924T1 (sl) | 2011-12-12 | 2016-08-31 | Gruenenthal Gmbh | Trdne oblike (1r,4r)-6'-fluoro-N,N-dimetil-4-fenil-4',9'-dihidro-3'H-spiro (ciklo-heksan-1,1'-pirano(3,4,b)indol)-4-amina in žveplove kisline |
EP2809307B1 (en) | 2012-01-31 | 2017-12-20 | Grünenthal GmbH | Pharmaceutical patch for transdermal administration of (1r,4r)-6'-fluoro-n,n-dimethyl-4-phenyl-4',9'-dihydro-3'h-spiro[cyclohexane-1,1'-pyrano[3,4-b]indol]-4-amine |
SI2809320T1 (sl) * | 2012-02-03 | 2017-07-31 | Gruenenthal Gmbh | (1r,4r)-6'-fluoro-(N-metil- ali N,N-dimetil-)-4-fenil-4',9'-dihidro-3'H -spiro(cikloheksan-1,1'-pirano(3,4,b)indol)-4-amin za zdravljenje fibromialgije in sindroma kronične utrujenosti |
US9320729B2 (en) | 2012-05-18 | 2016-04-26 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r)-6′-flouro-N,N-dimethyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano-[3,4,b]indol]-4-amine and a propionic acid derivative |
US20130310385A1 (en) * | 2012-05-18 | 2013-11-21 | Gruenenthal Gmbh | Pharmaceutical Composition Comprising (1r,4r)-6'-fluoro-N,N-dimethyl-4-phenyl-4',9'-dihydro-3'H-spiro[cyclohexane-1,1'-pyrano[3,4,b]indol]-4-amine and Antidepressants |
US9345689B2 (en) * | 2012-05-18 | 2016-05-24 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r)-6′-fluoro-N, N-dimethyl-4-phenyl-4,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano[3,4,b]indol]-4-amine and an anticonvulsant |
US9855286B2 (en) | 2012-05-18 | 2018-01-02 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r)-6′-fluoro-N,N-di methyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano-[3,4,b]indol]-4-amine and a salicylic acid component |
US9320725B2 (en) | 2012-05-18 | 2016-04-26 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r)-6′-fluoro-N,N-dimethyl-4-phenyl-4′9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano[3,4,b]indol]-4-amine and a gabapentinoid |
US20130310435A1 (en) | 2012-05-18 | 2013-11-21 | Gruenenthal Gmbh | Pharmaceutical Composition Comprising (1r,4r)-6'-fluoro-N, N-dimethyl-4-phenyl-4,9' -dihydro-3'H-spiro[cyclohexane-1,1' -pyrano[3,4,b]indol]-4-amine and Paracetamol or Propacetamol |
US9308196B2 (en) * | 2012-05-18 | 2016-04-12 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1 r,4r) -6'-fluoro-N ,N-dimethyl-4-phenyl-4',9'-d ihydro-3'H-spiro[cyclohexane-1,1'-pyrano-[3,4,b]indol]-4-amine and an oxicam |
US8912226B2 (en) | 2012-05-18 | 2014-12-16 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r) -6′-fluoro-N,N-dimethyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano[3,4,b]indol]-4-amine and a NSAR |
US9358022B2 (en) | 2012-05-21 | 2016-06-07 | Noha, Llc | Clot removal device and method of using same |
PL3110797T3 (pl) | 2014-02-27 | 2019-11-29 | Gruenenthal Gmbh | Proces otrzymywania 5-fluorotryptofolu |
TW201642853A (zh) | 2015-01-23 | 2016-12-16 | 歌林達有限公司 | 用於治療肝功能之損傷及/或腎功能之損傷個體疼痛之西博帕多(Cebranopadol) |
BR112018017167A2 (pt) | 2016-02-29 | 2019-01-02 | Gruenenthal Gmbh | titulação de cebranopadol |
WO2024129782A1 (en) | 2022-12-12 | 2024-06-20 | Park Therapeutics, Inc. | Regimens and compositions useful for alleviating pain |
WO2024173714A1 (en) | 2023-02-15 | 2024-08-22 | Park Therapeutics, Inc. | Regimens and compositions useful for alleviating pain |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2226058C (en) * | 1997-01-30 | 2008-01-29 | F. Hoffmann-La Roche Ag | 8-substituted-1,3,8-triaza-spiro[4.5]decan-4-one derivatives |
CA2335339A1 (en) * | 1998-06-12 | 1999-12-16 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R | .beta.-carboline compounds |
US20040038970A1 (en) * | 1998-06-12 | 2004-02-26 | Societe De Conseils De Recherches Etd' Application Scientifiques, S.A.S. A Paris, France Corp. | Beta-carboline compounds |
ID29137A (id) * | 1998-07-27 | 2001-08-02 | Schering Corp | Ligan-ligan afinitas tinggi untuk reseptor nosiseptin orl-1 |
ES2237047T3 (es) * | 1998-10-23 | 2005-07-16 | Pfizer Inc. | Compuestos de 1,3,8-triazaespiro(4,5)decanona como agonistas del receptor orl1. |
DE60022226D1 (de) * | 1999-12-06 | 2005-09-29 | Euro Celtique Sa | Benzimidazolverbindungen die nociceptinrezeptoraffinität haben |
JP3989247B2 (ja) * | 1999-12-06 | 2007-10-10 | ユーロ−セルティーク エス.エイ. | ノシセプチン受容体親和性を有するトリアゾスピロ化合物 |
RU2003129531A (ru) * | 2001-03-02 | 2005-04-10 | ЕВРО-КЕЛТИК Эс. Эй. (LU) | N-бут-3-енил-норбупренорфин и способы его применения |
PE20030719A1 (es) * | 2001-11-07 | 2003-08-28 | Schering Corp | Derivados de 8-[bis(2-halofenil)metil]-3-heteroaril-8-azabiciclo[3.2.1] octan-3-ol como agonistas del receptor de nociceptina orl-1 |
DE10252667A1 (de) * | 2002-11-11 | 2004-05-27 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
DE10252666A1 (de) * | 2002-11-11 | 2004-08-05 | Grünenthal GmbH | N-Piperidyl-cyclohexan-Derivate |
DE10252665A1 (de) * | 2002-11-11 | 2004-06-03 | Grünenthal GmbH | 4-Aminomethyl-1-aryl-cyclohexylamin-Derivate |
DE50306277D1 (de) * | 2002-11-12 | 2007-02-22 | Gruenenthal Gmbh | 4-alkyl-/4-alkenyl-/4-alkinylmethyl/-1-arylcyclohexylamin-derivate |
WO2005016913A1 (en) * | 2003-08-19 | 2005-02-24 | Pfizer Japan, Inc. | Tetrahydroisoquinoline or isochroman compounds as orl-1 receptor ligands for the treatment of pain and cns disorders |
US7314886B2 (en) * | 2003-10-02 | 2008-01-01 | Cephalon, Inc. | Tetrahydropyrano-indole derivatives |
DE10360792A1 (de) * | 2003-12-23 | 2005-07-28 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
DE10360793A1 (de) * | 2003-12-23 | 2005-07-28 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
JP2005314347A (ja) * | 2004-04-30 | 2005-11-10 | Japan Tobacco Inc | 疼痛抑制剤 |
DE102004023635A1 (de) * | 2004-05-10 | 2006-04-13 | Grünenthal GmbH | Heteroarylsubstituierte Cyclohexyl-1,4-diamin-Derivate |
DE102006046745A1 (de) * | 2006-09-29 | 2008-04-03 | Grünenthal GmbH | Gemischte ORL1/µ-Agonisten zur Behandlung von Schmerz |
-
2006
- 2006-09-29 DE DE102006046745A patent/DE102006046745A1/de not_active Withdrawn
-
2007
- 2007-09-26 ES ES10003202T patent/ES2377482T3/es active Active
- 2007-09-26 JP JP2009529599A patent/JP5203373B2/ja not_active Expired - Fee Related
- 2007-09-26 DE DE502007004875T patent/DE502007004875D1/de active Active
- 2007-09-26 DK DK10003202.8T patent/DK2206498T3/da active
- 2007-09-26 AT AT07818462T patent/ATE478667T1/de active
- 2007-09-26 PL PL07818462T patent/PL2081571T3/pl unknown
- 2007-09-26 WO PCT/EP2007/008379 patent/WO2008040481A1/de active Application Filing
- 2007-09-26 AT AT10003202T patent/ATE542532T1/de active
- 2007-09-26 DK DK07818462.9T patent/DK2081571T3/da active
- 2007-09-26 SI SI200730414T patent/SI2081571T1/sl unknown
- 2007-09-26 SI SI200730850T patent/SI2206498T1/sl unknown
- 2007-09-26 ES ES07818462T patent/ES2351528T3/es active Active
- 2007-09-26 PL PL10003202T patent/PL2206498T3/pl unknown
- 2007-09-26 EP EP07818462A patent/EP2081571B1/de active Active
- 2007-09-26 CA CA2664702A patent/CA2664702C/en not_active Expired - Fee Related
- 2007-09-26 PT PT10003202T patent/PT2206498E/pt unknown
- 2007-09-26 PT PT07818462T patent/PT2081571E/pt unknown
- 2007-09-26 EP EP10003202A patent/EP2206498B9/de active Active
- 2007-09-28 US US11/864,080 patent/US20080125475A1/en not_active Abandoned
-
2010
- 2010-09-21 US US12/887,102 patent/US20110015220A1/en not_active Abandoned
- 2010-11-03 CY CY20101100993T patent/CY1110879T1/el unknown
-
2012
- 2012-03-12 CY CY20121100252T patent/CY1112471T1/el unknown
-
2013
- 2013-02-12 JP JP2013024900A patent/JP5698282B2/ja not_active Expired - Fee Related
-
2015
- 2015-06-05 US US14/732,451 patent/US20150342929A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2008040481A1 (de) | 2008-04-10 |
CY1110879T1 (el) | 2015-06-10 |
DE102006046745A1 (de) | 2008-04-03 |
JP5203373B2 (ja) | 2013-06-05 |
PL2081571T3 (pl) | 2011-02-28 |
EP2206498B9 (de) | 2012-04-18 |
JP2013116907A (ja) | 2013-06-13 |
PL2206498T3 (pl) | 2012-04-30 |
CA2664702C (en) | 2016-08-09 |
PT2206498E (pt) | 2012-02-15 |
ATE542532T1 (de) | 2012-02-15 |
ATE478667T1 (de) | 2010-09-15 |
PT2081571E (pt) | 2010-11-29 |
CY1112471T1 (el) | 2015-12-09 |
US20150342929A1 (en) | 2015-12-03 |
DK2206498T3 (da) | 2012-03-19 |
JP5698282B2 (ja) | 2015-04-08 |
US20080125475A1 (en) | 2008-05-29 |
EP2206498B1 (de) | 2012-01-25 |
DE502007004875D1 (de) | 2010-10-07 |
ES2351528T3 (es) | 2011-02-07 |
EP2206498A1 (de) | 2010-07-14 |
US20110015220A1 (en) | 2011-01-20 |
EP2081571B1 (de) | 2010-08-25 |
SI2206498T1 (sl) | 2012-03-30 |
DK2081571T3 (da) | 2010-11-08 |
CA2664702A1 (en) | 2008-04-10 |
EP2081571A1 (de) | 2009-07-29 |
JP2010504926A (ja) | 2010-02-18 |
ES2377482T3 (es) | 2012-03-28 |
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