AR077473A2 - Uso de anticuerpos anti-tnf alfa y otro farmaco.metodo de tratamiento. composicion farmaceutica. conjunto de elementos - Google Patents
Uso de anticuerpos anti-tnf alfa y otro farmaco.metodo de tratamiento. composicion farmaceutica. conjunto de elementosInfo
- Publication number
- AR077473A2 AR077473A2 ARP100102558A ARP100102558A AR077473A2 AR 077473 A2 AR077473 A2 AR 077473A2 AR P100102558 A ARP100102558 A AR P100102558A AR P100102558 A ARP100102558 A AR P100102558A AR 077473 A2 AR077473 A2 AR 077473A2
- Authority
- AR
- Argentina
- Prior art keywords
- pharmaceutical composition
- combination
- drug
- clause
- antibodies
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
- C07K16/241—Tumor Necrosis Factors
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- 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
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
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- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
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- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
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- 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
- A61K31/415—1,2-Diazoles
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- 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
- A61K31/45—Non condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- Veterinary Medicine (AREA)
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Abstract
Método de tratamiento de trastornos en los cuales la actividad del TFN es nociva, por medio de una administracion bisemanal, subcutánea de anticuerpos humanos, preferentemente anticuerpos recombinantes humanos, que se unen específicamente al factor de necrosis tumoral humano (hTNF) en combinacion con otro f4rmaco que es de utilidad para el tratamiento de dicho trastorno. El anticuerpo de la solicitud puede ser un anticuerpo de longitud completa o una porcion de union a antígenos del mismo. La solicitud también abarca conjuntos de elementos que contienen una composicion farmacéutica e instrucciones para la dosificacion. Reivindicacion 2: Una composicion farmacéutica, caracterizada porque comprende 40 mg de D2E7, uno o varios fármacos adicionales y un vehículo aceptable para uso farmacéutico. Reivindicacion 3: La composicion farmacéutica de la cláusula 2, caracterizada porque el otro fármaco es un fármaco anti-reumático modificador de la enfermedad (DMARD), un fármaco anti-inflamatorio no esteroide (NSAID), un esteroide o cualquier combinacion de los mismos. Reivindicacion 4: La composicion farmacéutica de la cláusula 2, caracterizada porque el DMARD es hidroxicloroquina, Leflunomida, metotrexato, oro parenteral, oro oral, sulfasalazina o cualquier combinacion de los mismos. Reivindicacion 5: La composicion farmacéutica de la cláusula 2, caracterizada porque el NSAID es prednisona, ácido folico, celecoxib, rofecoxib, paracetamol, naproxeno, ibuprofeno, metilprednisolona, tramadol, Di-gesic, diclofenac, vicodin, triamcinolona, lidocaína o cualquier combinacion de los mismos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/133,715 US20030206898A1 (en) | 2002-04-26 | 2002-04-26 | Use of anti-TNFalpha antibodies and another drug |
Publications (1)
Publication Number | Publication Date |
---|---|
AR077473A2 true AR077473A2 (es) | 2011-08-31 |
Family
ID=29268783
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030101417A AR039656A1 (es) | 2002-04-26 | 2003-04-24 | Uso de anticuerpos anti-tnf alfa y otro farmaco |
ARP100102558A AR077473A2 (es) | 2002-04-26 | 2010-07-14 | Uso de anticuerpos anti-tnf alfa y otro farmaco.metodo de tratamiento. composicion farmaceutica. conjunto de elementos |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030101417A AR039656A1 (es) | 2002-04-26 | 2003-04-24 | Uso de anticuerpos anti-tnf alfa y otro farmaco |
Country Status (18)
Country | Link |
---|---|
US (1) | US20030206898A1 (es) |
EP (3) | EP2347766A1 (es) |
JP (2) | JP2005523946A (es) |
KR (1) | KR20100106631A (es) |
CN (3) | CN1649624A (es) |
AR (2) | AR039656A1 (es) |
AU (2) | AU2003278692B2 (es) |
BR (1) | BR0306444A (es) |
CA (1) | CA2385777A1 (es) |
IL (2) | IL164759A0 (es) |
MX (1) | MXPA04010498A (es) |
NZ (1) | NZ560793A (es) |
PE (1) | PE20040474A1 (es) |
PL (1) | PL373333A1 (es) |
TW (2) | TW201138826A (es) |
UY (1) | UY27780A1 (es) |
WO (1) | WO2004004633A2 (es) |
ZA (1) | ZA200408509B (es) |
Families Citing this family (93)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1501545A2 (en) | 2005-02-02 |
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TW200401647A (en) | 2004-02-01 |
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IL209010A0 (en) | 2011-01-31 |
CA2385777A1 (en) | 2003-10-14 |
EP2196218A3 (en) | 2010-07-07 |
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ZA200408509B (en) | 2006-06-28 |
BR0306444A (pt) | 2004-10-26 |
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