AR065911A1 - Beta - klotho - Google Patents
Beta - klothoInfo
- Publication number
- AR065911A1 AR065911A1 ARP080101364A ARP080101364A AR065911A1 AR 065911 A1 AR065911 A1 AR 065911A1 AR P080101364 A ARP080101364 A AR P080101364A AR P080101364 A ARP080101364 A AR P080101364A AR 065911 A1 AR065911 A1 AR 065911A1
- Authority
- AR
- Argentina
- Prior art keywords
- klbeta
- fgfr
- antibody
- sample
- disorder
- Prior art date
Links
- 102100020683 Beta-klotho Human genes 0.000 title 1
- 101710104526 Beta-klotho Proteins 0.000 title 1
- 108091008794 FGF receptors Proteins 0.000 abstract 11
- 102000052178 fibroblast growth factor receptor activity proteins Human genes 0.000 abstract 11
- 239000000523 sample Substances 0.000 abstract 8
- 239000000126 substance Substances 0.000 abstract 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 6
- 208000035475 disorder Diseases 0.000 abstract 6
- 230000004071 biological effect Effects 0.000 abstract 5
- 206010028980 Neoplasm Diseases 0.000 abstract 4
- 239000013074 reference sample Substances 0.000 abstract 4
- 208000008589 Obesity Diseases 0.000 abstract 2
- NKANXQFJJICGDU-QPLCGJKRSA-N Tamoxifen Chemical compound C=1C=CC=CC=1C(/CC)=C(C=1C=CC(OCCN(C)C)=CC=1)/C1=CC=CC=C1 NKANXQFJJICGDU-QPLCGJKRSA-N 0.000 abstract 2
- 239000005557 antagonist Substances 0.000 abstract 2
- 201000011510 cancer Diseases 0.000 abstract 2
- 208000035269 cancer or benign tumor Diseases 0.000 abstract 2
- -1 cetuximab Chemical compound 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 231100000433 cytotoxic Toxicity 0.000 abstract 2
- 230000001472 cytotoxic effect Effects 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 235000020824 obesity Nutrition 0.000 abstract 2
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 abstract 1
- BFYIZQONLCFLEV-DAELLWKTSA-N Aromasine Chemical compound O=C1C=C[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CC(=C)C2=C1 BFYIZQONLCFLEV-DAELLWKTSA-N 0.000 abstract 1
- MLDQJTXFUGDVEO-UHFFFAOYSA-N BAY-43-9006 Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3C=C(C(Cl)=CC=3)C(F)(F)F)=CC=2)=C1 MLDQJTXFUGDVEO-UHFFFAOYSA-N 0.000 abstract 1
- 206010006187 Breast cancer Diseases 0.000 abstract 1
- 208000026310 Breast neoplasm Diseases 0.000 abstract 1
- 206010008635 Cholestasis Diseases 0.000 abstract 1
- 206010009944 Colon cancer Diseases 0.000 abstract 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 abstract 1
- 206010016654 Fibrosis Diseases 0.000 abstract 1
- VWUXBMIQPBEWFH-WCCTWKNTSA-N Fulvestrant Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3[C@H](CCCCCCCCCS(=O)CCCC(F)(F)C(F)(F)F)CC2=C1 VWUXBMIQPBEWFH-WCCTWKNTSA-N 0.000 abstract 1
- 208000013016 Hypoglycemia Diseases 0.000 abstract 1
- 239000005517 L01XE01 - Imatinib Substances 0.000 abstract 1
- 239000005551 L01XE03 - Erlotinib Substances 0.000 abstract 1
- 239000005511 L01XE05 - Sorafenib Substances 0.000 abstract 1
- 239000002136 L01XE07 - Lapatinib Substances 0.000 abstract 1
- 230000009824 affinity maturation Effects 0.000 abstract 1
- 230000000202 analgesic effect Effects 0.000 abstract 1
- 229960002932 anastrozole Drugs 0.000 abstract 1
- YBBLVLTVTVSKRW-UHFFFAOYSA-N anastrozole Chemical compound N#CC(C)(C)C1=CC(C(C)(C#N)C)=CC(CN2N=CN=C2)=C1 YBBLVLTVTVSKRW-UHFFFAOYSA-N 0.000 abstract 1
- 230000001772 anti-angiogenic effect Effects 0.000 abstract 1
- 230000003474 anti-emetic effect Effects 0.000 abstract 1
- 239000002111 antiemetic agent Substances 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 229960000397 bevacizumab Drugs 0.000 abstract 1
- 239000003613 bile acid Substances 0.000 abstract 1
- 210000000481 breast Anatomy 0.000 abstract 1
- 201000008275 breast carcinoma Diseases 0.000 abstract 1
- 229940022399 cancer vaccine Drugs 0.000 abstract 1
- 238000009566 cancer vaccine Methods 0.000 abstract 1
- 229960005395 cetuximab Drugs 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000007870 cholestasis Effects 0.000 abstract 1
- 231100000359 cholestasis Toxicity 0.000 abstract 1
- 230000007882 cirrhosis Effects 0.000 abstract 1
- 208000019425 cirrhosis of liver Diseases 0.000 abstract 1
- 201000010989 colorectal carcinoma Diseases 0.000 abstract 1
- 239000003246 corticosteroid Substances 0.000 abstract 1
- 239000000430 cytokine receptor antagonist Substances 0.000 abstract 1
- 229940127089 cytotoxic agent Drugs 0.000 abstract 1
- 230000004064 dysfunction Effects 0.000 abstract 1
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 abstract 1
- 229960001433 erlotinib Drugs 0.000 abstract 1
- 229960000255 exemestane Drugs 0.000 abstract 1
- 229960002258 fulvestrant Drugs 0.000 abstract 1
- 201000001421 hyperglycemia Diseases 0.000 abstract 1
- 230000002218 hypoglycaemic effect Effects 0.000 abstract 1
- 229960002411 imatinib Drugs 0.000 abstract 1
- KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 abstract 1
- 229960003444 immunosuppressant agent Drugs 0.000 abstract 1
- 230000001861 immunosuppressant effect Effects 0.000 abstract 1
- 239000003018 immunosuppressive agent Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229960004768 irinotecan Drugs 0.000 abstract 1
- UWKQSNNFCGGAFS-XIFFEERXSA-N irinotecan Chemical compound C1=C2C(CC)=C3CN(C(C4=C([C@@](C(=O)OC4)(O)CC)C=4)=O)C=4C3=NC2=CC=C1OC(=O)N(CC1)CCC1N1CCCCC1 UWKQSNNFCGGAFS-XIFFEERXSA-N 0.000 abstract 1
- 229960004891 lapatinib Drugs 0.000 abstract 1
- BCFGMOOMADDAQU-UHFFFAOYSA-N lapatinib Chemical compound O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 BCFGMOOMADDAQU-UHFFFAOYSA-N 0.000 abstract 1
- 229960003881 letrozole Drugs 0.000 abstract 1
- HPJKCIUCZWXJDR-UHFFFAOYSA-N letrozole Chemical compound C1=CC(C#N)=CC=C1C(N1N=CN=C1)C1=CC=C(C#N)C=C1 HPJKCIUCZWXJDR-UHFFFAOYSA-N 0.000 abstract 1
- 208000019423 liver disease Diseases 0.000 abstract 1
- 230000004060 metabolic process Effects 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
- 238000001959 radiotherapy Methods 0.000 abstract 1
- 229960003787 sorafenib Drugs 0.000 abstract 1
- 229960001603 tamoxifen Drugs 0.000 abstract 1
- 229960000575 trastuzumab Drugs 0.000 abstract 1
- 229960004528 vincristine Drugs 0.000 abstract 1
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 abstract 1
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 abstract 1
- GBABOYUKABKIAF-GHYRFKGUSA-N vinorelbine Chemical compound C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC GBABOYUKABKIAF-GHYRFKGUSA-N 0.000 abstract 1
- 229960002066 vinorelbine Drugs 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/40—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/138—Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
-
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
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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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/475—Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
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- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/568—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone
- A61K31/5685—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone having an oxo group in position 17, e.g. androsterone
-
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
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- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- 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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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/71—Receptors; Cell surface antigens; Cell surface determinants for growth factors; for growth regulators
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
- G01N33/5032—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects on intercellular interactions
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57407—Specifically defined cancers
- G01N33/57438—Specifically defined cancers of liver, pancreas or kidney
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- G—PHYSICS
- G01—MEASURING; TESTING
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Abstract
Reivindicacion 1: Uso de una cantidad efectiva de un modulador de KLbeta para la manufactura de un medicamento para modular un trastorno asociado a la expresion o actividad de KLbeta a un individuo que necesite tal tratamiento. Reivindicacion 2:Uso de una cantidad efectiva de un antagonista de KLbeta para la manufactura de un medicamento para tratar un trastorno asociado a la expresion o actividad de KLbeta a un individuo que necesite tal tratamiento. Reivindicacion 3: El uso de lareivindicacion 2, donde el trastorno es un tumor, un cáncer o un trastorno de proliferacion celular. Reivindicacion 4: El uso de la reivindicacion 3, donde el tumor, cáncer o trastorno de proliferacion celular es carcinoma hepatocelular, cáncerpancreático, pulmonar de células no pequenas, de mama o colorrectal. Reivindicacion 6: El uso de la reivindicacion 5, donde el trastorno hepático es cirrosis. Reivindicacion 7: El uso de la reivindicacion 2, donde el trastorno es hipoglucemia,colestasis o disfuncion del metabolismo del ácido bílico, Reivindicacion 11: El uso de la reivindicacion 10, donde el segundo compuesto es un anticuerpo, un agente quimioterapéutico, citotoxico, antiangiogénico o inmunosupresor, un profármaco, unacitocina, un antagonista de citocinas, radioterapia citotoxica, un corticoesteroide, un antiemético, una vacuna contra el cáncer, un analgésico o un agente inhibidor del crecimiento. Reivindicacion 12: El uso de la reivindicacion 11, donde elsegundo compuesto es tamoxifeno, letrozol, exemestano, anastrozol, irinotecán, cetuximab, fulvestrant, vinorelbina, erlotinib, bevacizumab, vincristina, imatinib, sorafenib, lapatinib o trastuzumab. Reivindicacion 15: El uso de cualquiera de lasreivindicaciones 2-14, donde el antagonista de Klbeta es un anticuerpo. Reivindicacion 16: El uso de la reivindicacion 15, donde el anticuerpo es un anticuerpo monoclonal. Reivindicacion 17: El anticuerpo de la reivindicacion 15, donde elanticuerpo se selecciona del grupo formado por un anticuerpo quimérico, un anticuerpo humanizado, un anticuerpo con maduracion de afinidad, un anticuerpo humano y un anticuerpo biespecífico. Reivindicacion 25: El uso de la reivindicacion 24, dondeel trastorno es la obesidad o una afeccion relacionada con la obesidad. Reivindicacion 27: El uso de la reivindicacion 25, donde el trastorno es hiperglucemia. Reivindicacion 34: Un método para identificar una sustancia inhibidora candidata queinhiba la union de Klbeta a FGFR que consiste en: (a) poner en contacto una sustancia candidata con una primera muestra que contenga FGFR, FGF y KLbeta, y (b) comparar la cantidad de actividad biologica del FGFR en la muestra con la exhibida en unamuestra de referencia que comprenda cantidades similares de KLbeta, FGF y FGFR a las de la primera muestra pero no haya estado en contacto con dicha sustancia candidata, teniendo en cuenta que un descenso de la cantidad de actividad biologica delFGFR en la primera muestra en comparacion con la exhibida en la muestra de referencia indicaría que la sustancia candidata es capaz de inhibir la union de Klbeta a FGFR. Reivindicacion 35: Un método para determinar si una sustancia candidatapromueve la actividad biologica de la KLbeta que consiste en: (a) poner en contacto una sustancia candidata con una primera muestra que contenga FGFR y KLbeta, y (b) comparar la cantidad de actividad biologica del FGFR en la muestra con la exhibidaen una muestra de referencia que comprenda cantidades similares de KLbeta y FGFR a las de la primera muestra pero no haya estado en contacto con dicha sustancia candidata, teniendo en cuenta que un aumento de la cantidad de actividad biologica delFGFR en la primera muestra en comparacion con la exhibida en la muestra de referencia indicaría que la sustancia candidata es capaz de promover la union de Klbeta a FGFR.
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| US90969907P | 2007-04-02 | 2007-04-02 | |
| US91618707P | 2007-05-04 | 2007-05-04 |
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| ARP080101364A AR065911A1 (es) | 2007-04-02 | 2008-04-01 | Beta - klotho |
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| UA109888C2 (uk) | 2009-12-07 | 2015-10-26 | ІЗОЛЬОВАНЕ АНТИТІЛО АБО ЙОГО ФРАГМЕНТ, ЩО ЗВ'ЯЗУЄТЬСЯ З β-КЛОТО, РЕЦЕПТОРАМИ FGF І ЇХНІМИ КОМПЛЕКСАМИ | |
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- 2008-04-01 EP EP12179244.4A patent/EP2550972B1/en not_active Revoked
- 2008-04-01 AU AU2008275559A patent/AU2008275559B2/en not_active Ceased
- 2008-04-01 TW TW097111903A patent/TWI524898B/zh not_active IP Right Cessation
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2009
- 2009-09-17 ZA ZA2009/06495A patent/ZA200906495B/en unknown
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2014
- 2014-06-12 US US14/302,895 patent/US20140363435A1/en not_active Abandoned
- 2014-12-22 US US14/579,054 patent/US20150132309A1/en not_active Abandoned
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2015
- 2015-03-26 US US14/670,358 patent/US20150368358A1/en not_active Abandoned
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2017
- 2017-09-11 US US15/701,243 patent/US20180208677A1/en not_active Abandoned
- 2017-11-07 CL CL2017002807A patent/CL2017002807A1/es unknown
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2018
- 2018-04-26 HR HRP20180667TT patent/HRP20180667T1/hr unknown
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2020
- 2020-11-10 US US17/094,646 patent/US20210284753A1/en not_active Abandoned
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2021
- 2021-08-25 US US17/411,753 patent/US20220089780A1/en not_active Abandoned
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