FR15C0046I1 - Medicaments pour le traitement ou la prevention de maladies fibrotiques - Google Patents
Medicaments pour le traitement ou la prevention de maladies fibrotiquesInfo
- Publication number
- FR15C0046I1 FR15C0046I1 FR15C0046C FR15C0046I1 FR 15C0046 I1 FR15C0046 I1 FR 15C0046I1 FR 15C0046 C FR15C0046 C FR 15C0046C FR 15C0046 I1 FR15C0046 I1 FR 15C0046I1
- Authority
- FR
- France
- Prior art keywords
- drugs
- prevention
- treatment
- fibrotic diseases
- fibrotic
- 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.)
- Active
Links
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 230000003176 fibrotic effect Effects 0.000 title 1
- 230000002265 prevention Effects 0.000 title 1
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
- A61K31/403—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
-
- 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
-
- 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
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/495—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
-
- 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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0031—Rectum, anus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
- A61K9/0075—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
- A61K9/0078—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/02—Suppositories; Bougies; Bases therefor; Ovules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/08—Solutions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/155—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pulmonology (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Dispersion Chemistry (AREA)
- Otolaryngology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Window Of Vehicle (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04030770 | 2004-12-24 | ||
PCT/EP2005/057002 WO2006067165A2 (fr) | 2004-12-24 | 2005-12-21 | Medicaments pour le traitement ou la prevention de maladies fibrotiques |
EP05823930A EP1830843B1 (fr) | 2004-12-24 | 2005-12-21 | Medicaments pour le traitement ou la prevention de maladies fibrotiques |
Publications (2)
Publication Number | Publication Date |
---|---|
FR15C0046I1 true FR15C0046I1 (fr) | 2015-08-28 |
FR15C0046I2 FR15C0046I2 (fr) | 2018-01-26 |
Family
ID=36602118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR15C0046C Active FR15C0046I2 (fr) | 2004-12-24 | 2015-07-03 | Medicaments pour le traitement ou la prevention de maladies fibrotiques |
Country Status (32)
Country | Link |
---|---|
US (7) | US20060142373A1 (fr) |
EP (4) | EP2384751B1 (fr) |
JP (1) | JP5122976B2 (fr) |
KR (1) | KR101235094B1 (fr) |
CN (1) | CN101087605B (fr) |
AR (1) | AR052177A1 (fr) |
AU (1) | AU2005318126B2 (fr) |
BE (1) | BE2015C038I2 (fr) |
CA (1) | CA2591083C (fr) |
CY (3) | CY1113766T1 (fr) |
DK (2) | DK2878297T3 (fr) |
EA (1) | EA015011B1 (fr) |
ES (2) | ES2399270T3 (fr) |
FR (1) | FR15C0046I2 (fr) |
HR (1) | HRP20130059T1 (fr) |
HU (2) | HUE050998T2 (fr) |
IL (1) | IL184125A (fr) |
LT (2) | LT2878297T (fr) |
LU (1) | LU92762I2 (fr) |
ME (1) | ME01493B (fr) |
MY (1) | MY148108A (fr) |
NO (4) | NO339784B1 (fr) |
NZ (1) | NZ556681A (fr) |
PE (1) | PE20060777A1 (fr) |
PL (2) | PL2878297T3 (fr) |
PT (2) | PT2878297T (fr) |
RS (1) | RS52653B (fr) |
SI (2) | SI1830843T1 (fr) |
TW (1) | TWI418351B (fr) |
UA (1) | UA94390C2 (fr) |
WO (1) | WO2006067165A2 (fr) |
ZA (1) | ZA200703601B (fr) |
Families Citing this family (66)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060154939A1 (en) * | 2004-12-24 | 2006-07-13 | Boehringer Ingelheim International Gmbh | Medicaments for the Treatment or Prevention of Fibrotic Diseases |
PE20060777A1 (es) | 2004-12-24 | 2006-10-06 | Boehringer Ingelheim Int | Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas |
EP2167465A1 (fr) * | 2007-06-12 | 2010-03-31 | Boehringer Ingelheim International GmbH | Dérivés d'indolinone et leur utilisation dans le traitement d'états pathologiques tels que le cancer |
WO2008155421A2 (fr) | 2007-06-21 | 2008-12-24 | Janssen Pharmaceutica Nv | Indolin-2-ones et aza-indolin-2-ones |
EA029996B1 (ru) * | 2008-06-06 | 2018-06-29 | Бёрингер Ингельхайм Интернациональ Гмбх | Капсулярная лекарственная форма, содержащая суспензионную композицию производного индолинона |
ES2662824T3 (es) * | 2008-06-06 | 2018-04-09 | Boehringer Ingelheim International Gmbh | Combinación farmacéutica |
US20170065529A1 (en) | 2015-09-09 | 2017-03-09 | Boehringer Ingelheim International Gmbh | Pharmaceutical dosage form for immediate release of an indolinone derivative |
UA107560C2 (uk) * | 2008-06-06 | 2015-01-26 | Фармацевтична лікарська форма для негайного вивільнення похідної індолінону | |
AU2015227503B2 (en) * | 2008-06-06 | 2017-02-23 | Boehringer Ingelheim International Gmbh | Capsule pharmaceutical dosage form comprising a suspension formulation of an indolinone derivative |
TW201011002A (en) * | 2008-07-29 | 2010-03-16 | Boehringer Ingelheim Int | New compounds |
US8802384B2 (en) * | 2009-03-12 | 2014-08-12 | Boehringer Ingelheim International Gmbh | Method or system using biomarkers for the monitoring of a treatment |
JP2012526766A (ja) * | 2009-05-14 | 2012-11-01 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 腫瘍性及び線維性疾患の処置における新規な併用療法 |
EP2429527A1 (fr) * | 2009-05-14 | 2012-03-21 | Boehringer Ingelheim International GmbH | Nouvelle thérapie en combinaison dans le traitement du cancer et de maladies fibreuses |
US20120107304A1 (en) | 2010-04-27 | 2012-05-03 | Boehringer Ingelheim International Gmbh | Combination therapy in treatment of oncological and fibrotic diseases |
US8381108B2 (en) | 2010-06-21 | 2013-02-19 | Microsoft Corporation | Natural user input for driving interactive stories |
WO2012021974A1 (fr) | 2010-08-20 | 2012-02-23 | The Hospital For Sick Children | Compositions et procédés de traitement d'une fibrose kystique et maladies associées à une transformation cellulaire des protéines aberrantes |
CN103102352B (zh) * | 2011-11-15 | 2015-08-12 | 山东亨利医药科技有限责任公司 | 酪氨酸激酶抑制剂吲哚满酮衍生物 |
CN103130775B (zh) * | 2011-11-22 | 2015-09-30 | 山东亨利医药科技有限责任公司 | 作为酪氨酸激酶抑制剂的吲哚满酮衍生物 |
AU2013211888B2 (en) * | 2012-01-26 | 2017-08-31 | Angion Biomedica Corp. | Antifibrotic compounds and uses thereof |
CN103848814B (zh) * | 2012-12-06 | 2016-08-17 | 山东亨利医药科技有限责任公司 | 作为酪氨酸激酶抑制剂的取代吲哚满酮衍生物 |
US20140350022A1 (en) | 2013-05-10 | 2014-11-27 | Boehringer Ingelheim International Gmbh | Efficacious treatment of NSCLC and predictive clinical marker of the responsiveness of a tumour to a treatment |
CN104003925B (zh) * | 2013-06-05 | 2016-03-30 | 四川大学 | 吲哚酮化合物或其衍生物及其用途 |
WO2015009889A1 (fr) * | 2013-07-18 | 2015-01-22 | Concert Pharmaceuticals, Inc. | Dérivés deutériés d'intédanib et leur utilisation pour le traitement de troubles prolifératifs |
US20150044288A1 (en) * | 2013-07-31 | 2015-02-12 | Windward Pharma, Inc. | Aerosol tyrosine kinase inhibitor compounds and uses thereof |
US10450295B2 (en) * | 2013-08-09 | 2019-10-22 | Acclaim BioMed USA LLC | Method of using an indolinone molecule and derivatives for inhibiting liver fibrosis and hepatitis |
CA2938244A1 (fr) | 2014-02-07 | 2015-08-13 | Auspex Pharamaceuticals, Inc. | Nouvelles formulations pharmaceutiques |
CN106432042A (zh) * | 2015-08-13 | 2017-02-22 | 南京华威医药科技开发有限公司 | 尼达尼布乙磺酸水合物的药物新晶型 |
KR102317700B1 (ko) * | 2015-10-07 | 2021-10-26 | 아이비바 바이오파마, 인크. | 피부 섬유성 장애를 치료하는 조성물 및 방법 |
PT3722291T (pt) * | 2015-12-24 | 2023-09-22 | Respivert Ltd | Compostos de indolinona e sua utilização no tratamento de doenças fibróticas |
CN107019697A (zh) * | 2016-02-02 | 2017-08-08 | 瑞阳(苏州)生物科技有限公司 | 预防或治疗纤维化疾病的药物组合物及其应用 |
AU2017231860C1 (en) | 2016-03-08 | 2022-01-20 | Respivert Limited | Indole derivatives and their use as protein kinase inhibitors |
EP3442534A1 (fr) | 2016-04-13 | 2019-02-20 | Boehringer Ingelheim International GmbH | Combinaison pharmaceutique de nintédanib, de trifluridine et de tipiracil pour le traitement du cancer colorectal |
EP3246029A1 (fr) | 2016-05-19 | 2017-11-22 | Boehringer Ingelheim International Gmbh | Combinaison pharmaceutique de nintedanib et de capécitabine dans le traitement du cancer colorectal |
EP3464240A1 (fr) | 2016-05-27 | 2019-04-10 | Boehringer Ingelheim International GmbH | Utilisation de biomarqueurs de matrice extracellulaire pour déterminer le moment d'instauration d'un traitement sous nintédanib et pirfénidone |
JP2019523225A (ja) | 2016-06-01 | 2019-08-22 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ニンテダニブおよびピルフェニドンによる治療開始を決定するためのecmバイオマーカーの使用 |
US10654802B2 (en) | 2016-07-08 | 2020-05-19 | Arizona Board Of Regents On Behalf Of The Unversit | Indoline derivatives and method for using and producing the same |
CN108066343A (zh) * | 2016-11-08 | 2018-05-25 | 瑞阳(苏州)生物科技有限公司 | 一种预防或治疗肾纤维化疾病的药物 |
EP3551187B1 (fr) * | 2016-12-12 | 2021-02-17 | Boehringer Ingelheim International GmbH | Nintédanib destiné à être utilisé dans des méthodes de traitement de maladies pulmonaires interstitielles par co-administration d'olodatérol |
CN106692150B (zh) * | 2016-12-21 | 2019-08-20 | 中国人民解放军第三〇二医院 | 尼达尼布在制备预防和治疗肝纤维化与肝硬化的药物中的用途 |
US20190388407A1 (en) * | 2017-02-12 | 2019-12-26 | Aiviva Biopharma, Inc. | Multikinase inhibitors of vegf and tfg beta and uses thereof |
WO2018177893A1 (fr) | 2017-03-28 | 2018-10-04 | Boehringer Ingelheim International Gmbh | Nintedanib destiné à être utilisé dans des procédés de traitement de dystrophie musculaire |
US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
SG10202110259QA (en) | 2017-10-05 | 2021-10-28 | Fulcrum Therapeutics Inc | Use of p38 inhibitors to reduce expression of dux4 |
WO2019081235A1 (fr) * | 2017-10-23 | 2019-05-02 | Boehringer Ingelheim International Gmbh | Nouvelle association d'agents actifs pour le traitement de pneumopathies interstitielles fibrosantes progressives (pf-ild) |
HUE065887T2 (hu) | 2018-03-07 | 2024-06-28 | Pliant Therapeutics Inc | Aminosav vegyületek és alkalmazási eljárások |
JP7061310B2 (ja) * | 2018-04-05 | 2022-04-28 | 国立大学法人 大分大学 | 慢性脂肪性疾患の予防および治療用医薬 |
CA3101102A1 (fr) | 2018-04-23 | 2019-10-31 | Tlc Biopharmaceuticals, Inc. | Composition liposomale inhalable a liberation prolongee destinee a etre utilisee dans le traitement de maladies pulmonaires |
CN108358827A (zh) * | 2018-05-07 | 2018-08-03 | 日照市普达医药科技有限公司 | 一种治疗牛皮癣的2-氧代-吲哚类衍生物及其制备方法 |
CN115192540A (zh) | 2018-06-15 | 2022-10-18 | 汉达癌症医药责任有限公司 | 激酶抑制剂的盐类及其组合物 |
CN109134431B (zh) * | 2018-10-10 | 2021-06-04 | 成都理工大学 | 作为囊性纤维化跨膜传导调节因子抑制剂的氨基咪唑偶联吡啶酮衍生物 |
GB201905371D0 (en) | 2019-04-16 | 2019-05-29 | Mission Therapeutics Ltd | Novel compounds |
GB201905375D0 (en) | 2019-04-16 | 2019-05-29 | Mission Therapeutics Ltd | Novel compounds |
GB201912674D0 (en) | 2019-09-04 | 2019-10-16 | Mission Therapeutics Ltd | Novel compounds |
BR112022010891A2 (pt) | 2019-12-04 | 2022-08-16 | Idorsia Pharmaceuticals Ltd | Combinação de um antagonista do receptor lpa1 de azetidina com agentes antifibróticos |
US20230135671A1 (en) | 2020-04-01 | 2023-05-04 | Boehringer Ingelheim International Gmbh | Use of biomarkers in the treatment of fibrotic conditions |
KR20230006487A (ko) | 2020-04-08 | 2023-01-10 | 미션 테라퓨틱스 엘티디 | Usp30 억제제로서의 활성을 갖는 n-시아노피롤리딘 |
GB202006079D0 (en) | 2020-04-24 | 2020-06-10 | Vicore Pharma Ab | New composition |
GB202006074D0 (en) | 2020-04-24 | 2020-06-10 | Vicore Pharma Ab | New composition |
EP4157834B1 (fr) | 2020-05-28 | 2024-07-03 | Mission Therapeutics Limited | Dérivés de n-(1-cyano-pyrrolidin-3-yl)-5-(3-(trifluorométhyl)phényl)oxazole-2-carboxamide et les dérivés de oxadiazole correspondants en tant qu'inhibiteurs d'usp30 pour le traitement de dysfonctionnement mitochondrial |
KR20230019198A (ko) | 2020-06-04 | 2023-02-07 | 미션 테라퓨틱스 엘티디 | Usp30 억제제로서의 활성을 갖는 n-시아노피롤리딘 |
BR112022024794A2 (pt) | 2020-06-08 | 2022-12-27 | Mission Therapeutics Ltd | Hexahidropirrolo[3,4-b]pirrolo-5(1h)-carbonitrilas com atividade como inibidores de usp30 para uso no tratamento de disfunção mitocondrial, câncer e fibrose |
GB202016800D0 (en) | 2020-10-22 | 2020-12-09 | Mission Therapeutics Ltd | Novel compounds |
US20250034122A1 (en) | 2021-12-01 | 2025-01-30 | Mission Therapeutics Limited | Substituted n-cyanopyrrolidines with activity as usp30 inhibitors |
AU2022443590A1 (en) | 2022-02-28 | 2024-10-17 | Nuformix Technologies Limited | Compositions and methods for treatment of idiopathic pulmonary fibrosis |
WO2024037982A1 (fr) | 2022-08-16 | 2024-02-22 | Boehringer Ingelheim International Gmbh | Formulations pharmaceutiques de nintédanib pour utilisation intraoculaire |
CN118772038A (zh) * | 2023-01-03 | 2024-10-15 | 天津征程医药科技有限公司 | 2-吲哚酮衍生物及其用途 |
Family Cites Families (178)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4460581A (en) | 1982-10-12 | 1984-07-17 | Boehringer Ingelheim Kg | (1-Hydroxy-2-amino-alkyl)-substituted benzoxazinones and benzoxazolinones |
WO1992012154A1 (fr) | 1990-12-31 | 1992-07-23 | Fujisawa Pharmaceutical Co., Ltd. | Derive d'immidazotriazine |
GB9816837D0 (en) | 1998-08-04 | 1998-09-30 | Zeneca Ltd | Amide derivatives |
US5656644A (en) | 1994-07-20 | 1997-08-12 | Smithkline Beecham Corporation | Pyridyl imidazoles |
MX9300141A (es) | 1992-01-13 | 1994-07-29 | Smithkline Beecham Corp | Compuestos de imidazol novedosos, procedimiento para su preparacion y composiciones farmaceuticas que lo contienen. |
US5716972A (en) | 1993-01-13 | 1998-02-10 | Smithkline Beecham Corporation | Pyridyl substituted imidazoles |
GB9303993D0 (en) | 1993-02-26 | 1993-04-14 | Fujisawa Pharmaceutical Co | New heterocyclic derivatives |
US5593992A (en) | 1993-07-16 | 1997-01-14 | Smithkline Beecham Corporation | Compounds |
US5670527A (en) | 1993-07-16 | 1997-09-23 | Smithkline Beecham Corporation | Pyridyl imidazole compounds and compositions |
US5593991A (en) | 1993-07-16 | 1997-01-14 | Adams; Jerry L. | Imidazole compounds, use and process of making |
US5543520A (en) | 1993-10-01 | 1996-08-06 | Ciba-Geigy Corporation | Pyrimidine derivatives |
ATE208772T1 (de) | 1993-10-01 | 2001-11-15 | Novartis Erfind Verwalt Gmbh | Pharmacologisch wirksame pyridinderivate und verfahren zu deren herstellung |
DE69434721T2 (de) | 1993-10-01 | 2006-11-09 | Novartis Ag | Pharmacologisch wirksame pyrimidinderivate und verfahren zu deren herstellung |
EP0672035A1 (fr) | 1993-10-01 | 1995-09-20 | Novartis AG | Derives pyrimidineamine et leurs procedes de preparation |
GB9401182D0 (en) | 1994-01-21 | 1994-03-16 | Inst Of Cancer The Research | Antibodies to EGF receptor and their antitumour effect |
US5559137A (en) | 1994-05-16 | 1996-09-24 | Smithkline Beecham Corp. | Compounds |
ES2161290T3 (es) | 1995-03-30 | 2001-12-01 | Pfizer | Derivados de quinazolina. |
TW449590B (en) | 1995-04-14 | 2001-08-11 | Boehringer Ingelheim Kg | New arylglycinamide derivatives, processes for the manufacture thereof and pharmaceutical compositions containing these compounds |
US5739143A (en) | 1995-06-07 | 1998-04-14 | Smithkline Beecham Corporation | Imidazole compounds and compositions |
IL118544A (en) | 1995-06-07 | 2001-08-08 | Smithkline Beecham Corp | History of imidazole, the process for their preparation and the pharmaceutical preparations containing them |
US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
ATE212993T1 (de) | 1995-07-06 | 2002-02-15 | Novartis Erfind Verwalt Gmbh | Pyrolopyrimidine und verfahren zu ihrer herstellung |
DE69637948D1 (de) | 1995-10-06 | 2009-07-23 | Merck & Co Inc | Substituierte imidazole mit krebsremmender und cytokininhibierender wirkung |
EP0859771A4 (fr) | 1995-10-31 | 2000-03-15 | Merck & Co Inc | Pyrroles de pyridyle substitues, compositions contenant de tels composes et mode d'utilisation |
WO1997016441A1 (fr) | 1995-10-31 | 1997-05-09 | Merck & Co., Inc. | Pyrroles aryliques de substitution, compositions renfermant de telles composes et methodes d'utilisation de ces substances |
AP9700912A0 (en) | 1996-01-11 | 1997-01-31 | Smithkline Beecham Corp | Novel cycloalkyl substituted imidazoles |
ZA97175B (en) | 1996-01-11 | 1997-11-04 | Smithkline Beecham Corp | Novel substituted imidazole compounds. |
JP2001508395A (ja) | 1996-01-11 | 2001-06-26 | スミスクライン・ビーチャム・コーポレイション | 新規シクロアルキル置換イミダゾール |
CN1213306A (zh) | 1996-01-11 | 1999-04-07 | 史密丝克莱恩比彻姆公司 | 新的取代咪唑化合物 |
DE19608665A1 (de) | 1996-03-06 | 1997-09-11 | Boehringer Ingelheim Kg | Neue Arylglycinamidderivate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Zusammensetzungen |
JP2000506532A (ja) | 1996-03-13 | 2000-05-30 | スミスクライン・ビーチャム・コーポレイション | サイトカイン介在疾患の治療にて有用な新規ピリミジン化合物 |
US6235760B1 (en) | 1996-03-25 | 2001-05-22 | Smithkline Beecham Corporation | Treatment for CNS injuries |
EP0889888A4 (fr) | 1996-03-25 | 2003-01-08 | Smithkline Beecham Corp | Nouveau traitement des lesions du systeme nerveux central |
CA2250232A1 (fr) | 1996-04-03 | 1997-10-09 | Allen I. Oliff | Methode de traitement du cancer |
WO1997047618A1 (fr) | 1996-06-10 | 1997-12-18 | Merck & Co., Inc. | Imidazoles substitues inhibant la cytokine |
JP2001506230A (ja) | 1996-08-09 | 2001-05-15 | スミスクライン・ビーチャム・コーポレイション | 新規ピペラジン含有化合物 |
DE19633640C2 (de) | 1996-08-21 | 1999-05-06 | Ford Global Tech Inc | Vorrichtung zur Winkelverstellung einer Welle gegenüber einem Antriebsrad |
EP0956018A4 (fr) | 1996-08-21 | 2000-01-12 | Smithkline Beecham Corp | Composes d'imidazole, compositions les contenant et leur utilisation |
KR20000057137A (ko) | 1996-11-19 | 2000-09-15 | 스티븐 엠. 오드레 | 아릴 및 헤테로아릴로 치환된 융합 피롤 항염증제 |
AU730295B2 (en) | 1996-11-20 | 2001-03-01 | Merck & Co., Inc. | Triaryl substituted imidazoles as glucagon antagonists |
BR9713863A (pt) | 1996-12-05 | 2000-03-14 | Amgen Inc | Composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, processos de profilaxia ou tratamento, para abaixar as concentrações no plasma, para diminuir a produção de prostaglandinas, e, para diminuir a atividade de enzima ciclooxigenase |
TW520362B (en) | 1996-12-05 | 2003-02-11 | Amgen Inc | Substituted pyrimidine compounds and pharmaceutical composition comprising same |
ZA9711092B (en) | 1996-12-11 | 1999-07-22 | Smithkline Beecham Corp | Novel compounds. |
US6147080A (en) | 1996-12-18 | 2000-11-14 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
AU723895B2 (en) | 1997-01-29 | 2000-09-07 | Pfizer Inc. | Sulfonyl urea derivatives and their use in the control of interleukin-1 activity |
RU2222534C2 (ru) | 1997-04-24 | 2004-01-27 | Орто-Макнейл Фармасьютикал, Инк. | Замещенные имидазолы, способ их получения, фармацевтическая композиция на их основе, способы лечения цитокин-опосредованных заболеваний |
WO1998047899A1 (fr) | 1997-04-24 | 1998-10-29 | Ortho-Mcneil Corporation, Inc. | Pyrrolopyridines substituees utilisees dans le traitement des maladies inflammatoires |
US6235883B1 (en) | 1997-05-05 | 2001-05-22 | Abgenix, Inc. | Human monoclonal antibodies to epidermal growth factor receptor |
ES2239393T3 (es) | 1997-05-07 | 2005-09-16 | Sugen, Inc. | Derivados de 2-indolinona utilizados como moduladores de la actividad de la proteina-quinasa. |
US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
AU7726898A (en) | 1997-05-22 | 1998-12-11 | G.D. Searle & Co. | Pyrazole derivatives as p38 kinase inhibitors |
EE9900527A (et) | 1997-05-22 | 2000-06-15 | G.D. Searle & Co. | Substitueeritud pürasoolid kui p38 kinaasi inhibiitorid |
EP0983260A2 (fr) | 1997-05-22 | 2000-03-08 | G.D. Searle & Co. | PYRAZOLES 3(5)-HETEROARYL SUBSTITUEES UTILISEES COMME INHIBITEURS DE KINASE p38 |
JP2002500650A (ja) | 1997-05-23 | 2002-01-08 | バイエル、コーポレイション | Rafキナーゼ阻害剤 |
WO1998052558A1 (fr) | 1997-05-23 | 1998-11-26 | Bayer Corporation | INHIBITION DE L'ACTIVITE DE LA p38 KINASE PAR DES ARYL-UREES |
ES2270520T3 (es) | 1997-06-12 | 2007-04-01 | Aventis Pharma Limited | Imidazolil-acetales ciclicos. |
EP1023066A4 (fr) | 1997-06-13 | 2001-05-23 | Smithkline Beecham Corp | Nouveaux composes de pyrazole et de pyrazoline substitues |
US6093742A (en) | 1997-06-27 | 2000-07-25 | Vertex Pharmaceuticals, Inc. | Inhibitors of p38 |
GB9713726D0 (en) | 1997-06-30 | 1997-09-03 | Ciba Geigy Ag | Organic compounds |
CA2295021A1 (fr) | 1997-06-30 | 1999-01-28 | Ortho-Mcneil Pharmaceutical, Inc. | Imidazoles substituees en 2 utilisables pour le traitement de maladies inflammatoires |
US5939421A (en) | 1997-07-01 | 1999-08-17 | Signal Pharmaceuticals, Inc. | Quinazoline analogs and related compounds and methods for treating inflammatory conditions |
WO1999001452A1 (fr) | 1997-07-02 | 1999-01-14 | Smithkline Beecham Corporation | Nouveaux imidazoles cycloalkyle-substitues |
AR016294A1 (es) | 1997-07-02 | 2001-07-04 | Smithkline Beecham Corp | Compuesto de imidazol sustituido, composicion farmaceutica que la contiene, su uso en la fabricacion de un medicamento y procedimiento para supreparacion |
TW517055B (en) | 1997-07-02 | 2003-01-11 | Smithkline Beecham Corp | Novel substituted imidazole compounds |
US5981710A (en) | 1997-07-21 | 1999-11-09 | Baxter International, Inc. | Therapeutic hemoglobin composition having isotropically increased size |
GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
WO1999015164A1 (fr) | 1997-09-23 | 1999-04-01 | Zeneca Limited | Derives amide pour le traitement de maladies induites par les cytokines |
US5975738A (en) | 1997-09-30 | 1999-11-02 | Lsi Logic Corporation | Method for detecting failure in redundant controllers using a private LUN |
CA2306077A1 (fr) | 1997-10-08 | 1999-04-15 | Smithkline Beecham Corporation | Nouveaux composes substitues de cycloalcenyle |
IL136045A0 (en) | 1997-11-14 | 2001-05-20 | Sankyo Co | Pyridylpyrrole derivatives and pharmaceutical compositions containing the same |
EP1037639A4 (fr) | 1997-12-19 | 2002-04-17 | Smithkline Beecham Corp | .0mposes d'imidazole heteroaryle substitues, leurs compositions et usages pharmaceutiques |
JP2002515891A (ja) | 1997-12-19 | 2002-05-28 | スミスクライン・ビーチャム・コーポレイション | 新規なピペリジン含有化合物 |
ES2154253T3 (es) | 1997-12-22 | 2012-01-27 | Bayer Healthcare Llc | Inhibición de la actividad de p38 cinasa usando ureas heterocíclicas sustituidas. |
IL136737A0 (en) | 1997-12-22 | 2001-06-14 | Bayer Ag | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
DE1043995T1 (de) | 1997-12-22 | 2001-06-07 | Bayer Corp., Pittsburgh | INHIBIERUNG DER p38 KINASE-AKTIVITÄT DURCH DIE VERWENDUNG VON ARYL- UND HETEROARYLSUBSTITUIERTEN HARNSTOFFEN |
GB9800569D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
US6147096A (en) | 1998-02-26 | 2000-11-14 | Ortho Mcneil Pharmaceutical, Inc. | Substituted pyrrolobenzimidazoles for treating inflammatory diseases |
EP1072591A4 (fr) | 1998-03-26 | 2005-01-05 | Santen Pharmaceutical Co Ltd | Nouveaux derives d'uree |
DE19815020A1 (de) | 1998-04-03 | 1999-10-07 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
DE19816624A1 (de) | 1998-04-15 | 1999-10-21 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
CA2329065A1 (fr) | 1998-05-05 | 1999-11-11 | Francisco Xavier Talamas | Derives de pyrazole tenant lieu d'inhibiteurs de p-38 map kinase |
US6316466B1 (en) | 1998-05-05 | 2001-11-13 | Syntex (U.S.A.) Llc | Pyrazole derivatives P-38 MAP kinase inhibitors |
MY132496A (en) | 1998-05-11 | 2007-10-31 | Vertex Pharma | Inhibitors of p38 |
WO1999058523A1 (fr) | 1998-05-14 | 1999-11-18 | G.D. Searle & Co. | PYRAZOLES A SUBSTITUTION 1,5-DIARYLE COMME INHIBITEURS DE LA PROTEINE p38 KINASE |
WO1999059959A1 (fr) | 1998-05-15 | 1999-11-25 | Astrazeneca Ab | Derives de benzamide pour le traitement de maladies dont la mediation est assuree par les cytokines |
EP1077930B1 (fr) | 1998-05-15 | 2004-11-10 | AstraZeneca AB | Derives de benzamide servant a traiter des maladies provoquees par des cytokines |
DE69929689T2 (de) | 1998-05-22 | 2006-11-02 | Scios Inc., Fremont | Heterocyclische Verbindungen und Verfahren zur Behandlung von Herzversagen und anderer Erkrankungen |
US6589954B1 (en) | 1998-05-22 | 2003-07-08 | Scios, Inc. | Compounds and methods to treat cardiac failure and other disorders |
EP1080087A4 (fr) | 1998-05-22 | 2001-11-21 | Smithkline Beecham Corp | Nouveaux composes d'imidazole a substitution alkyle en position 2 |
US6340685B1 (en) | 1998-05-22 | 2002-01-22 | Scios, Inc. | Compounds and methods to treat cardiac failure and other disorders |
JP2002516325A (ja) | 1998-05-26 | 2002-06-04 | スミスクライン・ビーチャム・コーポレイション | 新規な置換イミダゾール化合物 |
DE19824922A1 (de) * | 1998-06-04 | 1999-12-09 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
AU4429799A (en) | 1998-06-12 | 1999-12-30 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
AU4395399A (en) | 1998-07-02 | 2000-01-24 | Sankyo Company Limited | Five-membered heteroaryl compounds |
US6207687B1 (en) | 1998-07-31 | 2001-03-27 | Merck & Co., Inc. | Substituted imidazoles having cytokine inhibitory activity |
SK1762001A3 (en) | 1998-08-04 | 2001-07-10 | Astrazeneca Ab | Amide derivatives useful as inhibitors of the production of cytokines |
KR100663143B1 (ko) | 1998-08-05 | 2007-01-02 | 산텐 세이야꾸 가부시키가이샤 | 질소 포함 방향족 헤테로고리를 갖는 신규 우레아 유도체 |
JP2003525201A (ja) | 1998-08-20 | 2003-08-26 | スミスクライン・ビーチャム・コーポレイション | 新規な置換トリアゾール化合物 |
US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
EP1107758A2 (fr) | 1998-08-28 | 2001-06-20 | Scios Inc. | INHIBITEURS DE p38-APLHA KINASE |
JP4191825B2 (ja) | 1998-09-10 | 2008-12-03 | あすか製薬株式会社 | 5−アミノイソキサゾール誘導体 |
AR023659A1 (es) | 1998-09-18 | 2002-09-04 | Vertex Pharma | Un compuesto inhibidor de p38, una composicion farmaceutica que lo comprende y el uso de dicha composicion en el tratamiento y prevencion de estados patologicos |
DE19842833B4 (de) | 1998-09-18 | 2005-04-14 | Merckle Gmbh | 2-Arylalkylthio-imidazole, 2-Arylalkenylthio-imidazole und 2-Arylalkinylthio-imidazole als Entzündungs-Hemmstoffe und Hemmstoffe der Cytokin-Freisetzung |
CA2337755C (fr) | 1998-09-18 | 2008-07-29 | Vertex Pharmaceuticals Incorporated | Inhibiteurs de p38 |
EE200100184A (et) | 1998-09-25 | 2002-08-15 | Boehringer Ingelheim Pharma Kg | Uudsed asendatud indolinoonid inhibeeriva toimegamitmesugustele kinaasidele ja tsükliin/CDK kompleksidele |
EP1115707B1 (fr) | 1998-09-25 | 2003-11-12 | AstraZeneca AB | Derives de benzamide et leur utilisation en tant qu'inhibiteurs de cytokines |
BR9914162A (pt) | 1998-10-01 | 2001-06-26 | Astrazeneca Ab | Derivado de amida, processo para preparar um derivado de amida, ou um sal farmaceuticamente aceitável ou éster clivável in vivo do mesmo, composição farmacêutica e uso de um derivado de amida, ou um sal farmaceuticamente aceitável ou éster clivável in vivo do mesmo |
EP1261334A1 (fr) | 1998-10-20 | 2002-12-04 | Omeros Corporation | Solution d'irrigation contenant des inhibiteurs de mapk et son utilisation pour traiter la douleur et l'inflammation |
AU6476599A (en) | 1998-11-03 | 2000-05-22 | Novartis Ag | Anti-inflammatory 4-phenyl-5-pyrimidinyl-imidazoles |
DE69914357T2 (de) | 1998-11-04 | 2004-11-11 | Smithkline Beecham Corp. | Pyridin-4-yl oder pyrimidin-4-yl substituierte pyrazine |
PL347717A1 (en) | 1998-11-19 | 2002-04-22 | Warner Lambert Co | N-[4-(3-chloro-4-fluoro-phenylamino)-7-(3-morpholin-4-yl-propoxy)-quinazolin-6-yl]-acrylamide, an irreversible inhibitor of tyrosine kinases |
US6350744B1 (en) | 1998-11-20 | 2002-02-26 | Merck & Co., Inc. | Compounds having cytokine inhibitory activity |
AU758811B2 (en) | 1998-11-20 | 2003-04-03 | G.D. Searle & Co. | Process for making 5-substituted pyrazoles using dithietanes |
WO2000036096A1 (fr) | 1998-12-16 | 2000-06-22 | Vertex Pharmaceuticals Incorporated | Complexes p38 cristallises |
JP4634613B2 (ja) | 1998-12-16 | 2011-02-16 | アベンティス・フアーマ・リミテッド | ヘテロアリール環状アセタール類 |
DE69926542T2 (de) | 1998-12-25 | 2006-04-27 | Teikoku Hormone Mfg. Co., Ltd. | Aminopyrazolderivate |
WO2000041698A1 (fr) | 1999-01-13 | 2000-07-20 | Bayer Corporation | DIPHENYLE UREES A SUBSTITUTION φ-CARBOXY ARYLE EN TANT QU'INHIBITEURS DE LA KINASE p38 |
UA73492C2 (en) | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
GB9904933D0 (en) * | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
CN1511830A (zh) | 1999-03-12 | 2004-07-14 | ���ָ��.Ӣ��ķҩ�﹫˾ | 作为消炎剂的化合物 |
ES2251360T3 (es) | 1999-03-12 | 2006-05-01 | Boehringer Ingelheim Pharmaceuticals Inc. | Compuestos heterociclicos aromaticos en calidad de agentes antiinflamatorios. |
NZ513726A (en) | 1999-03-17 | 2001-09-28 | Astrazeneca Ab | Amide derivatives |
HUP0105114A3 (en) | 1999-03-17 | 2002-09-30 | Astrazeneca Ab | Quinazolinone derivatives, pharmaceutical compositions containing them, their use and process for their preparation |
GB9906566D0 (en) | 1999-03-23 | 1999-05-19 | Zeneca Ltd | Chemical compounds |
CO5170501A1 (es) | 1999-04-14 | 2002-06-27 | Novartis Ag | AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO |
US6492516B1 (en) | 1999-05-14 | 2002-12-10 | Merck & Co., Inc. | Compounds having cytokine inhibitory activity |
HUP0201261A3 (en) | 1999-05-21 | 2003-12-29 | Scios Inc Sunnyvale | Indole-type derivatives as inhibitors of p38 kinase and pharmaceutical compositions containing them |
DE19924401A1 (de) | 1999-05-27 | 2000-11-30 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
PT1731511E (pt) | 1999-06-21 | 2015-11-13 | Boehringer Ingelheim Pharma | Heterociclos bicíclicos, medicamentos contendo estes compostos, a sua utilização e processos para a sua preparação |
US6403596B1 (en) | 1999-06-28 | 2002-06-11 | Merck & Co., Inc. | Substituted pyridones having cytokine inhibitory activity |
NZ516824A (en) | 1999-07-16 | 2004-03-26 | Leo Pharm Prod Ltd | Novel aminobenzophenones |
PL353646A1 (en) | 1999-07-16 | 2003-12-01 | Leo Pharmaceutical Products Ltd.A/S (Lovens Kemiskleo Pharmaceutical Products Ltd.A/S (Lovens Kemiske Fabrik Produktionsaktieselskab)E Fabrik Produktionsaktieselskab) | Aminobenzophenones as inhibitors of il-1beta and tnf-alpha |
DE60014393T2 (de) | 1999-07-16 | 2006-02-16 | Leo Pharma A/S | Aminobenzophenone als inhibitoren von il-1beta und tnf-alpha |
CN1249025C (zh) | 1999-07-16 | 2006-04-05 | 里奥药物制品有限公司 | 作为IL-1β和TNF-α的抑制剂的氨基二苯酮 |
EP1210320B1 (fr) | 1999-07-16 | 2004-09-29 | Leo Pharma A/S | Aminobenzophenones en tant qu'inhibiteurs de il-1beta et tnf-alpha |
EP1212318B1 (fr) | 1999-08-27 | 2006-01-25 | Boehringer Ingelheim Pharma GmbH & Co.KG | Indolinones substituees utilisees comme inhibiteurs de la tyrosine kinase |
DE19949209A1 (de) | 1999-10-13 | 2001-04-19 | Boehringer Ingelheim Pharma | In 5-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
GB9924092D0 (en) | 1999-10-13 | 1999-12-15 | Zeneca Ltd | Pyrimidine derivatives |
EP1224321A2 (fr) | 1999-10-13 | 2002-07-24 | Leo Pharmaceutical Products Ltd. A/S (Lovens Kemiske Fabrik Produktionsaktieselskab) | Procede de criblage de substances agissant sur la kinase msk1 |
UA75054C2 (uk) * | 1999-10-13 | 2006-03-15 | Бьорінгер Інгельхайм Фарма Гмбх & Ко. Кг | Заміщені в положенні 6 індолінони, їх одержання та їх застосування як лікарського засобу |
US6762180B1 (en) * | 1999-10-13 | 2004-07-13 | Boehringer Ingelheim Pharma Kg | Substituted indolines which inhibit receptor tyrosine kinases |
CN1171889C (zh) | 1999-10-21 | 2004-10-20 | 霍夫曼-拉罗奇有限公司 | 作为p38蛋白激酶的抑制剂的杂烷基氨基-取代的双环氮杂环类化合物 |
ES2277858T3 (es) | 1999-10-21 | 2007-08-01 | F. Hoffmann-La Roche Ag | Heterociclos de nitrogeno biciclicos alquilamino sustituidos como inhibidores de proteina kinasa p38. |
MXPA01007019A (es) | 1999-11-10 | 2002-09-18 | Johnson & Johnson | 2-aril-3-(heteroaril)-imidazo[1,2-a]pirimidinas, sustituidas y composiciones farmaceuticas relacionados y metodos. |
UA74803C2 (uk) | 1999-11-11 | 2006-02-15 | Осі Фармасьютікалз, Інк. | Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування |
ATE375334T1 (de) | 1999-11-16 | 2007-10-15 | Boehringer Ingelheim Pharma | Harnstoff derivate als entzündungshemmende mittel |
ES2241675T3 (es) | 1999-11-23 | 2005-11-01 | Smithkline Beecham Corporation | Compuestos de 3,4-dihidro-(1h)quinazolin-2-ona como inhibidores de cspb/p38 quinasa. |
EP1233950B1 (fr) | 1999-11-23 | 2005-10-05 | Smithkline Beecham Corporation | 3,4-dihydro-(1h)quinazolin-2-ones comme inhibiteurs de csbp/p38 kinase |
JP2003517471A (ja) | 1999-11-23 | 2003-05-27 | スミスクライン・ビーチャム・コーポレイション | 3,4−ジヒドロ−(1H)−キナゾリン−2−オンおよびそのCSBP/p38キナーゼ阻害剤としての使用 |
WO2001038312A1 (fr) | 1999-11-23 | 2001-05-31 | Smithkline Beecham Corporation | COMPOSES DE 3,4-DIHYDRO-(1H)QUINAZOLINE-2-ONE UTILISES COMME INHIBITEURS DE LA KINASE CSBP/p38 |
OA12097A (en) | 1999-11-30 | 2006-05-04 | Pfizer Prod Inc | 2,4-Diaminopyrimidine compounds useful as immunosuppressants. |
EP1237845B1 (fr) | 1999-12-06 | 2007-05-23 | Leo Pharma A/S | Aminobenzophenones inhibiteurs de l'il-1beta et du tnf-alpha |
US6602872B1 (en) | 1999-12-13 | 2003-08-05 | Merck & Co., Inc. | Substituted pyridazines having cytokine inhibitory activity |
EP1242385B1 (fr) | 1999-12-28 | 2009-11-25 | Pharmacopeia, Inc. | Inhibiteurs de la cytokine, en particulier de tnf-alpha |
DE20002820U1 (de) | 2000-02-16 | 2000-05-25 | Igus Spritzgußteile für die Industrie GmbH, 51147 Köln | Energieführungskette |
EP1259486A1 (fr) | 2000-02-23 | 2002-11-27 | Iconix Pharmaceuticals, Inc. | Pyridine-amidines comme modulateurs de la p38 map kinase |
WO2001064676A2 (fr) | 2000-02-28 | 2001-09-07 | Scios, Inc. | INHIBITEURS DE LA P38-α KINASE |
AR035851A1 (es) | 2000-03-28 | 2004-07-21 | Wyeth Corp | 3-cianoquinolinas, 3-ciano-1,6-naftiridinas y 3-ciano-1,7-naftiridinas como inhibidoras de proteina quinasas |
EP1280798B1 (fr) | 2000-04-08 | 2007-01-03 | Boehringer Ingelheim Pharma GmbH & Co.KG | Heterocycles bicycliques, medicaments contenant ces composes, leur utilisation et leur procede de production |
DE10042058A1 (de) | 2000-08-26 | 2002-03-07 | Boehringer Ingelheim Pharma | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung |
DE10042062A1 (de) | 2000-08-26 | 2002-03-07 | Boehringer Ingelheim Pharma | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Hertellung |
DE10042060A1 (de) | 2000-08-26 | 2002-03-07 | Boehringer Ingelheim Pharma | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung |
DE10042059A1 (de) | 2000-08-26 | 2002-03-07 | Boehringer Ingelheim Pharma | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung |
DE10051320A1 (de) | 2000-10-17 | 2002-04-25 | Boehringer Ingelheim Pharma | Neue Neurokininantagonisten, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Zusammensetzungen |
US6638965B2 (en) | 2000-11-01 | 2003-10-28 | Boehringer Ingelheim Pharma Kg | Substituted indolinones, preparation thereof and their use as pharmaceutical compositions |
DE10054019A1 (de) | 2000-11-01 | 2002-05-23 | Boehringer Ingelheim Pharma | Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
DE10063435A1 (de) | 2000-12-20 | 2002-07-04 | Boehringer Ingelheim Pharma | Chinazolinderviate,diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung |
DE10117204A1 (de) | 2001-04-06 | 2002-10-10 | Boehringer Ingelheim Pharma | In 6-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel |
CA2476008C (fr) | 2002-03-30 | 2011-12-13 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Composes heterocyclique bicyclique, compositions pharmaceutiques contenat ces composes, leur utilisation et procede de preparation |
DE10233500A1 (de) * | 2002-07-24 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 3-Z-[1-(4-(N-((4-Methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylen]-6-methoxycarbonyl-2-indolinon-Monoethansulfonat und dessen Verwendung als Arzneimittel |
US20040204458A1 (en) | 2002-08-16 | 2004-10-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Use of Lck inhibitors for treatment of immunologic diseases |
DE10237423A1 (de) * | 2002-08-16 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verwendung von LCK-Inhibitoren für die Behandlung von immunologischen Erkrankungen |
US7148249B2 (en) | 2002-09-12 | 2006-12-12 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinones substituted by heterocycles, the preparation thereof and their use as medicaments |
US20050043233A1 (en) * | 2003-04-29 | 2005-02-24 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis |
US20060154939A1 (en) | 2004-12-24 | 2006-07-13 | Boehringer Ingelheim International Gmbh | Medicaments for the Treatment or Prevention of Fibrotic Diseases |
PE20061155A1 (es) | 2004-12-24 | 2006-12-16 | Boehringer Ingelheim Int | Derivados de indolinona como agentes para el tratamiento o la prevencion de enfermedades fibroticas |
PE20060777A1 (es) | 2004-12-24 | 2006-10-06 | Boehringer Ingelheim Int | Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas |
ES2662824T3 (es) | 2008-06-06 | 2018-04-09 | Boehringer Ingelheim International Gmbh | Combinación farmacéutica |
-
2005
- 2005-12-16 PE PE2005001476A patent/PE20060777A1/es not_active Application Discontinuation
- 2005-12-20 US US11/275,223 patent/US20060142373A1/en not_active Abandoned
- 2005-12-21 EP EP10184949.5A patent/EP2384751B1/fr active Active
- 2005-12-21 ES ES05823930T patent/ES2399270T3/es active Active
- 2005-12-21 AU AU2005318126A patent/AU2005318126B2/en active Active
- 2005-12-21 HR HRP20130059TT patent/HRP20130059T1/hr unknown
- 2005-12-21 PT PT141903989T patent/PT2878297T/pt unknown
- 2005-12-21 KR KR1020077017058A patent/KR101235094B1/ko active Active
- 2005-12-21 EA EA200701175A patent/EA015011B1/ru not_active IP Right Cessation
- 2005-12-21 JP JP2007547503A patent/JP5122976B2/ja active Active
- 2005-12-21 HU HUE14190398A patent/HUE050998T2/hu unknown
- 2005-12-21 SI SI200531656T patent/SI1830843T1/sl unknown
- 2005-12-21 CA CA2591083A patent/CA2591083C/fr active Active
- 2005-12-21 ES ES14190398T patent/ES2797546T3/es active Active
- 2005-12-21 EP EP14190398.9A patent/EP2878297B1/fr active Active
- 2005-12-21 WO PCT/EP2005/057002 patent/WO2006067165A2/fr active Application Filing
- 2005-12-21 DK DK14190398.9T patent/DK2878297T3/da active
- 2005-12-21 PT PT58239302T patent/PT1830843E/pt unknown
- 2005-12-21 DK DK05823930.2T patent/DK1830843T3/da active
- 2005-12-21 ME MEP-2013-13A patent/ME01493B/me unknown
- 2005-12-21 EP EP05823930A patent/EP1830843B1/fr active Active
- 2005-12-21 PL PL14190398T patent/PL2878297T3/pl unknown
- 2005-12-21 RS RS20130037A patent/RS52653B/en unknown
- 2005-12-21 EP EP19209457.1A patent/EP3643309A1/fr active Pending
- 2005-12-21 CN CN2005800447033A patent/CN101087605B/zh active Active
- 2005-12-21 UA UAA200708383A patent/UA94390C2/ru unknown
- 2005-12-21 LT LTEP14190398.9T patent/LT2878297T/lt unknown
- 2005-12-21 PL PL05823930T patent/PL1830843T3/pl unknown
- 2005-12-21 NZ NZ556681A patent/NZ556681A/en unknown
- 2005-12-21 SI SI200532279T patent/SI2878297T1/sl unknown
- 2005-12-22 AR ARP050105468A patent/AR052177A1/es unknown
- 2005-12-22 MY MYPI20056170A patent/MY148108A/en unknown
- 2005-12-23 TW TW094146425A patent/TWI418351B/zh not_active IP Right Cessation
-
2007
- 2007-05-04 ZA ZA200703601A patent/ZA200703601B/xx unknown
- 2007-06-21 IL IL184125A patent/IL184125A/en active IP Right Grant
- 2007-07-23 NO NO20073831A patent/NO339784B1/no active Protection Beyond IP Right Term
-
2009
- 2009-12-22 US US12/645,151 patent/US20100204211A1/en not_active Abandoned
-
2013
- 2013-01-30 CY CY20131100088T patent/CY1113766T1/el unknown
-
2014
- 2014-02-20 US US14/184,821 patent/US20140296217A1/en not_active Abandoned
-
2015
- 2015-06-29 BE BE2015C038C patent/BE2015C038I2/fr unknown
- 2015-06-30 CY CY2015024C patent/CY2015024I1/el unknown
- 2015-06-30 HU HUS1500034C patent/HUS1500034I1/hu unknown
- 2015-06-30 LT LTPA2015025C patent/LTC1830843I2/lt unknown
- 2015-07-02 LU LU92762C patent/LU92762I2/fr unknown
- 2015-07-03 FR FR15C0046C patent/FR15C0046I2/fr active Active
- 2015-12-29 US US14/982,179 patent/US10154990B2/en active Active
-
2016
- 2016-10-12 NO NO20161634A patent/NO341591B1/no unknown
-
2017
- 2017-06-12 NO NO20170945A patent/NO342914B1/no unknown
- 2017-07-28 NO NO2017035C patent/NO2017035I2/no unknown
-
2018
- 2018-10-23 US US16/167,567 patent/US20190038600A1/en not_active Abandoned
-
2020
- 2020-06-16 CY CY20201100551T patent/CY1123050T1/el unknown
- 2020-07-06 US US16/921,043 patent/US20200330435A1/en not_active Abandoned
-
2023
- 2023-08-02 US US18/363,779 patent/US20230372297A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR15C0046I2 (fr) | Medicaments pour le traitement ou la prevention de maladies fibrotiques | |
AP2037A (en) | Use of substituted quinoline derivatives for the treatment of drug resistant mycobacterial diseases | |
EP1838320A4 (fr) | Antagonistes de cxcr4 pour le traitement de troubles medicaux | |
FR16C0029I2 (fr) | Combinaisons medicamenteuses contenant de la benzoxazine pour traiter des maladies des voies respiratoires | |
FR13C0060I2 (fr) | Omega-carboxyaryldiphenyluree fluoro-subtituee pour le traitement et la prevention de maladies et d'etats pathologiques | |
IL184124A0 (en) | Medicaments for the treatment or prevention of fibrotic diseases | |
EP1809369A4 (fr) | Dispositif medicaux pour la detection, la prevention et/ou le traitement de troubles neurologiques, et procedes associes | |
EP1711197A4 (fr) | Methodes et compositions pour la prevention et le traitement de maladies ou de troubles inflammatoires | |
MA29085B1 (fr) | Agent prophylactique ou thérapeutique pour le traitement des troubles du sommeil | |
FR2882654B1 (fr) | Utilisation de derives de la diosmetine pour le traitement et la prevention des pathologies thrombotiques | |
FR2860154B1 (fr) | Composition pour le traitement de la mauvaise haleine | |
FR2919187B1 (fr) | Utilisation d'ecorces de levure pour le traitement et/ou la prevention de l'hyperinsulinemie. | |
DE602005014141D1 (de) | Medikamente zur behandlung oder prävention fibrotischer krankheiten | |
EP1895996A4 (fr) | Preparation pour le traitement des maladies de la cavite buccale | |
EP1726313A4 (fr) | Medicament pour la prevention et le traitement de l'arteriosclerose | |
EP1637162A4 (fr) | Composition medicinale de prevention ou de traitement de maladies immunologiques de type th1 | |
EP2174666A4 (fr) | Agent médicamenteux pour la prévention ou le traitement de la maladie d'alzheimer | |
EP1799849A4 (fr) | Agents pour le traitement ou la prevention d'une affection allergique | |
EP1644483A4 (fr) | Utilisation de la pleiotrophine pour le diagnostic, le traitement et la prevention de maladies | |
FR2908892B1 (fr) | Procede pour le dosage chromogenique de l'activite du facteur viii:c et necessaire de dosage chromogenique de l'activite du facteur viii:c,dans les plasmas ou les fractions therapeutiques | |
FR2862875B1 (fr) | Preparation pharmaceutique pour le traitement des acouphenes | |
MA28482B1 (fr) | Composés pour le traitement de maladies | |
FR2848573B1 (fr) | Compositions et methodes pour la detection et le traitement de pathologies neurodegeneratives | |
MA28475B1 (fr) | Composés utiles pour le traitement de maladies | |
MA28894B1 (fr) | Composition pharmaceutique pour traitement des maladies de la population aviaire |