WO2004039321A2 - Therapie associee agoniste nicotinique/agoniste d1 pour le traitement de la maladie d'alzheimer - Google Patents
Therapie associee agoniste nicotinique/agoniste d1 pour le traitement de la maladie d'alzheimer Download PDFInfo
- Publication number
- WO2004039321A2 WO2004039321A2 PCT/US2003/033729 US0333729W WO2004039321A2 WO 2004039321 A2 WO2004039321 A2 WO 2004039321A2 US 0333729 W US0333729 W US 0333729W WO 2004039321 A2 WO2004039321 A2 WO 2004039321A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alpha
- nicotinic
- agonist
- disease
- subject
- 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.)
- Ceased
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
- 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
Definitions
- Another embodiment of the invention provides a method of treating Alzheimer's disease in a subject comprising administration to the subject a combination comprising an alpha-7-nicotinic agonist and a Dl receptor agonist, wherein the alpha-7-nicotinic agonist and the Dl receptor agonist together comprise a therapeutically effective amount of the alpha-7-nicotinic agonist and the Dl receptor agonist.
- the administration of each of the alpha-7-nicotinic agonist and the Dl receptor agonist can occur sequentially within about 24 hours, about 12 hours, about 6 hours, about 3 hours, and about 1 hour.
- the administration of each of the alpha-7-nicotinic agonist and the Dl receptor agonist can occur substantially concomitantly.
- compositions of the invention can be delivered to a subject by systemic administration.
- Systemic administration is in vivo systemic absorption or accumulation of drugs in the blood stream followed by distribution throughout the entire body. Administration routes that can lead to systemic absorption include, without limitation: intravenous, subcutaneous, intraperitoneal, inhalation, transdermal, oral, intrapulmonary and intramuscular.
- Formulations for oral use can also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil.
- an inert solid diluent for example, calcium carbonate, calcium phosphate or kaolin
- water or an oil medium for example peanut oil, liquid paraffin or olive oil.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2003284898A AU2003284898A1 (en) | 2002-10-29 | 2003-10-24 | Combinative nicotinic/d1 agonism therapy for the treatment of alzheimer's disease |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42204702P | 2002-10-29 | 2002-10-29 | |
| US60/422,047 | 2002-10-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2004039321A2 true WO2004039321A2 (fr) | 2004-05-13 |
| WO2004039321A8 WO2004039321A8 (fr) | 2005-05-26 |
Family
ID=32230314
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2003/033729 Ceased WO2004039321A2 (fr) | 2002-10-29 | 2003-10-24 | Therapie associee agoniste nicotinique/agoniste d1 pour le traitement de la maladie d'alzheimer |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU2003284898A1 (fr) |
| WO (1) | WO2004039321A2 (fr) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006048294A1 (fr) * | 2004-11-05 | 2006-05-11 | Novartis Ag | Combinaisons d'agonistes du recepteur nicotinique alpha 7 de l'acetylcholine |
| US7713976B2 (en) | 2005-12-16 | 2010-05-11 | Novartis Ag | [(1H-indol-5-yl)-heteroaryloxy]-1-aza-bicylco[3.3.1]nonanes as cholinergic ligands of the n-AChR for the treatment of psychotic and neurodegenerative disorders |
| US7713977B2 (en) | 2005-12-16 | 2010-05-11 | Novartis Ag | (1-aza-bicyclo[3.3.1]non-4-yl)-[5-(1H-indol-5-yl)-heteroaryl]-amines as cholinergic ligands of the n-achr for the treatment of psychotic and neurodegenerative disorders |
| US8173667B2 (en) | 2005-10-21 | 2012-05-08 | Novartis Ag | 1-aza-bicycloalkyl derivatives |
| US8236803B2 (en) | 2002-09-04 | 2012-08-07 | Novartis Ag | Aza-bicycloalkyl ethers and their use as alpha7-nAChR agonists |
| US8609662B2 (en) | 2004-07-14 | 2013-12-17 | Novartis Ag | 3-(heteroaryl-oxy)-2-alkyl-1-aza-bicycloalkyl derivatives as alpha. 7-nachr ligands for the treatment of CNS diseases |
| US8884017B2 (en) | 2001-12-27 | 2014-11-11 | Bayer Intellectual Property Gmbh | 2-heteroarylcarboxylic acid amides |
| US8933090B2 (en) | 2004-06-18 | 2015-01-13 | Novartis Ag | 1-aza-bicyclo[3.3.1]nonanes |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101698250B1 (ko) | 2010-05-17 | 2017-01-19 | 포럼 파마슈티칼즈 인크. | (R)-7-클로로-N-(퀴누클리딘-3-일)벤조[b]티오펜-2-카르복사미드 히드로클로리드 모노히드레이트의 결정질 형태 |
| RU2635522C2 (ru) | 2012-05-08 | 2017-11-13 | Форум Фармасьютикалз, Инк. | Способы поддержания, лечения или улучшения когнитивной функции |
-
2003
- 2003-10-24 WO PCT/US2003/033729 patent/WO2004039321A2/fr not_active Ceased
- 2003-10-24 AU AU2003284898A patent/AU2003284898A1/en not_active Abandoned
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8884017B2 (en) | 2001-12-27 | 2014-11-11 | Bayer Intellectual Property Gmbh | 2-heteroarylcarboxylic acid amides |
| US9567343B2 (en) | 2002-09-04 | 2017-02-14 | Novartis Ag | Aza-bicyloalkyl ethers and their use as alpha7-nachr agonists |
| US9849117B2 (en) | 2002-09-04 | 2017-12-26 | Novartis Ag | Aza-bicycloalkyl ethers and their use as alpha7-nachr agonists |
| US9012451B2 (en) | 2002-09-04 | 2015-04-21 | Novartis Ag | Aza-bicycloalkyl ethers and their use as ALPHA7-nachr agonists |
| US8236803B2 (en) | 2002-09-04 | 2012-08-07 | Novartis Ag | Aza-bicycloalkyl ethers and their use as alpha7-nAChR agonists |
| US9475811B2 (en) | 2004-06-18 | 2016-10-25 | Novartis Ag | 1-aza-bicyclo[3.3.1]nonanes |
| US8933090B2 (en) | 2004-06-18 | 2015-01-13 | Novartis Ag | 1-aza-bicyclo[3.3.1]nonanes |
| US9657010B2 (en) | 2004-07-14 | 2017-05-23 | Novartis Ag | Substituted quinuclidines as alpha 7-nicotinic acetylcholine receptor activity modulators |
| US8609662B2 (en) | 2004-07-14 | 2013-12-17 | Novartis Ag | 3-(heteroaryl-oxy)-2-alkyl-1-aza-bicycloalkyl derivatives as alpha. 7-nachr ligands for the treatment of CNS diseases |
| EP2135609A1 (fr) * | 2004-11-05 | 2009-12-23 | Novartis AG | Combinaisons d'agonistes du recepteur nicotine-acetylcholine-alpha-7 |
| EP2332537A1 (fr) * | 2004-11-05 | 2011-06-15 | Novartis AG | Combinaisons d'agonistes du recepteur nicotine-acetylcholine-alpha-7 |
| WO2006048294A1 (fr) * | 2004-11-05 | 2006-05-11 | Novartis Ag | Combinaisons d'agonistes du recepteur nicotinique alpha 7 de l'acetylcholine |
| JP2008518896A (ja) * | 2004-11-05 | 2008-06-05 | ノバルティス アクチエンゲゼルシャフト | ニコチン性アセチルコリンα7受容体アンタゴニストの組合せ剤 |
| US8173667B2 (en) | 2005-10-21 | 2012-05-08 | Novartis Ag | 1-aza-bicycloalkyl derivatives |
| US8637517B2 (en) | 2005-12-16 | 2014-01-28 | Novartis Ag | Organic compounds |
| US9206181B2 (en) | 2005-12-16 | 2015-12-08 | Novartis Ag | 1-aza-bicyclo[3.3.1] non-4-yl)-[5-(1H-indol-5-yl)-heteroaryl]-amines as cholinergic ligands of the n-AChR for the treatment of psychotic and neurodegenerative disorders |
| US8759346B2 (en) | 2005-12-16 | 2014-06-24 | Novartis Ag | Organic compounds |
| US8048885B2 (en) | 2005-12-16 | 2011-11-01 | Novartis Ag | Organic compounds |
| US7713977B2 (en) | 2005-12-16 | 2010-05-11 | Novartis Ag | (1-aza-bicyclo[3.3.1]non-4-yl)-[5-(1H-indol-5-yl)-heteroaryl]-amines as cholinergic ligands of the n-achr for the treatment of psychotic and neurodegenerative disorders |
| US7713976B2 (en) | 2005-12-16 | 2010-05-11 | Novartis Ag | [(1H-indol-5-yl)-heteroaryloxy]-1-aza-bicylco[3.3.1]nonanes as cholinergic ligands of the n-AChR for the treatment of psychotic and neurodegenerative disorders |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003284898A1 (en) | 2004-05-25 |
| WO2004039321A8 (fr) | 2005-05-26 |
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