CO5540315A2 - Combinacion que comprende n-{5-[4-(4-metil-piperazino-metil) benzoilamido]-2-metilfenil}-4-(3-piridil)-2-pirimidin-amina, y un agente quimioterapeutico - Google Patents
Combinacion que comprende n-{5-[4-(4-metil-piperazino-metil) benzoilamido]-2-metilfenil}-4-(3-piridil)-2-pirimidin-amina, y un agente quimioterapeuticoInfo
- Publication number
- CO5540315A2 CO5540315A2 CO03098325A CO03098325A CO5540315A2 CO 5540315 A2 CO5540315 A2 CO 5540315A2 CO 03098325 A CO03098325 A CO 03098325A CO 03098325 A CO03098325 A CO 03098325A CO 5540315 A2 CO5540315 A2 CO 5540315A2
- Authority
- CO
- Colombia
- Prior art keywords
- group
- compounds
- methyl
- chemotherapeutic agent
- acute
- Prior art date
Links
- 239000002246 antineoplastic agent Substances 0.000 title abstract 4
- 229940127089 cytotoxic agent Drugs 0.000 title abstract 3
- -1 4-METHYL-PIPERAZINO-METHYL Chemical class 0.000 title abstract 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 206010052779 Transplant rejections Diseases 0.000 abstract 3
- 230000001154 acute effect Effects 0.000 abstract 3
- 230000001684 chronic effect Effects 0.000 abstract 3
- 230000000694 effects Effects 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- 229930012538 Paclitaxel Natural products 0.000 abstract 2
- 108010038512 Platelet-Derived Growth Factor Proteins 0.000 abstract 2
- 102000010780 Platelet-Derived Growth Factor Human genes 0.000 abstract 2
- 102000001253 Protein Kinase Human genes 0.000 abstract 2
- 108010073929 Vascular Endothelial Growth Factor A Proteins 0.000 abstract 2
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 abstract 2
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 abstract 2
- 230000001772 anti-angiogenic effect Effects 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 229960001592 paclitaxel Drugs 0.000 abstract 2
- 230000002062 proliferating effect Effects 0.000 abstract 2
- 108060006633 protein kinase Proteins 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 abstract 2
- AADVCYNFEREWOS-UHFFFAOYSA-N (+)-DDM Natural products C=CC=CC(C)C(OC(N)=O)C(C)C(O)C(C)CC(C)=CC(C)C(O)C(C)C=CC(O)CC1OC(=O)C(C)C(O)C1C AADVCYNFEREWOS-UHFFFAOYSA-N 0.000 abstract 1
- AOJJSUZBOXZQNB-VTZDEGQISA-N 4'-epidoxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-VTZDEGQISA-N 0.000 abstract 1
- GAGWJHPBXLXJQN-UORFTKCHSA-N Capecitabine Chemical compound C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1[C@H]1[C@H](O)[C@H](O)[C@@H](C)O1 GAGWJHPBXLXJQN-UORFTKCHSA-N 0.000 abstract 1
- GAGWJHPBXLXJQN-UHFFFAOYSA-N Capecitabine Natural products C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1C1C(O)C(O)C(C)O1 GAGWJHPBXLXJQN-UHFFFAOYSA-N 0.000 abstract 1
- 229940123780 DNA topoisomerase I inhibitor Drugs 0.000 abstract 1
- 229940124087 DNA topoisomerase II inhibitor Drugs 0.000 abstract 1
- AADVCYNFEREWOS-OBRABYBLSA-N Discodermolide Chemical compound C=C\C=C/[C@H](C)[C@H](OC(N)=O)[C@@H](C)[C@H](O)[C@@H](C)C\C(C)=C/[C@H](C)[C@@H](O)[C@@H](C)\C=C/[C@@H](O)C[C@@H]1OC(=O)[C@H](C)[C@@H](O)[C@H]1C AADVCYNFEREWOS-OBRABYBLSA-N 0.000 abstract 1
- HTIJFSOGRVMCQR-UHFFFAOYSA-N Epirubicin Natural products COc1cccc2C(=O)c3c(O)c4CC(O)(CC(OC5CC(N)C(=O)C(C)O5)c4c(O)c3C(=O)c12)C(=O)CO HTIJFSOGRVMCQR-UHFFFAOYSA-N 0.000 abstract 1
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 abstract 1
- XDXDZDZNSLXDNA-TZNDIEGXSA-N Idarubicin Chemical compound C1[C@H](N)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XDXDZDZNSLXDNA-TZNDIEGXSA-N 0.000 abstract 1
- XDXDZDZNSLXDNA-UHFFFAOYSA-N Idarubicin Natural products C1C(N)C(O)C(C)OC1OC1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2CC(O)(C(C)=O)C1 XDXDZDZNSLXDNA-UHFFFAOYSA-N 0.000 abstract 1
- 102000029749 Microtubule Human genes 0.000 abstract 1
- 108091022875 Microtubule Proteins 0.000 abstract 1
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 abstract 1
- 102000003923 Protein Kinase C Human genes 0.000 abstract 1
- 108090000315 Protein Kinase C Proteins 0.000 abstract 1
- 239000000365 Topoisomerase I Inhibitor Substances 0.000 abstract 1
- 239000000317 Topoisomerase II Inhibitor Substances 0.000 abstract 1
- JXLYSJRDGCGARV-WWYNWVTFSA-N Vinblastine Natural products O=C(O[C@H]1[C@](O)(C(=O)OC)[C@@H]2N(C)c3c(cc(c(OC)c3)[C@]3(C(=O)OC)c4[nH]c5c(c4CCN4C[C@](O)(CC)C[C@H](C3)C4)cccc5)[C@@]32[C@H]2[C@@]1(CC)C=CCN2CC3)C JXLYSJRDGCGARV-WWYNWVTFSA-N 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 239000002168 alkylating agent Substances 0.000 abstract 1
- 150000004056 anthraquinones Chemical class 0.000 abstract 1
- 230000002280 anti-androgenic effect Effects 0.000 abstract 1
- 229940046836 anti-estrogen Drugs 0.000 abstract 1
- 230000001833 anti-estrogenic effect Effects 0.000 abstract 1
- 239000000051 antiandrogen Substances 0.000 abstract 1
- 229940030495 antiandrogen sex hormone and modulator of the genital system Drugs 0.000 abstract 1
- 229940034982 antineoplastic agent Drugs 0.000 abstract 1
- 239000002814 antineoplastic antimetabolite Substances 0.000 abstract 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 abstract 1
- 239000003886 aromatase inhibitor Substances 0.000 abstract 1
- 229940046844 aromatase inhibitors Drugs 0.000 abstract 1
- 229960004117 capecitabine Drugs 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229960003668 docetaxel Drugs 0.000 abstract 1
- 229950006700 edatrexate Drugs 0.000 abstract 1
- FSIRXIHZBIXHKT-MHTVFEQDSA-N edatrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CC(CC)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FSIRXIHZBIXHKT-MHTVFEQDSA-N 0.000 abstract 1
- 229960001904 epirubicin Drugs 0.000 abstract 1
- 239000000328 estrogen antagonist Substances 0.000 abstract 1
- 229960002949 fluorouracil Drugs 0.000 abstract 1
- SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 abstract 1
- 229960005277 gemcitabine Drugs 0.000 abstract 1
- 229960000908 idarubicin Drugs 0.000 abstract 1
- 229960001101 ifosfamide Drugs 0.000 abstract 1
- HOMGKSMUEGBAAB-UHFFFAOYSA-N ifosfamide Chemical compound ClCCNP1(=O)OCCCN1CCCl HOMGKSMUEGBAAB-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
- YROQEQPFUCPDCP-UHFFFAOYSA-N losoxantrone Chemical compound OCCNCCN1N=C2C3=CC=CC(O)=C3C(=O)C3=C2C1=CC=C3NCCNCCO YROQEQPFUCPDCP-UHFFFAOYSA-N 0.000 abstract 1
- 229950008745 losoxantrone Drugs 0.000 abstract 1
- 229960001924 melphalan Drugs 0.000 abstract 1
- SGDBTWWWUNNDEQ-LBPRGKRZSA-N melphalan Chemical compound OC(=O)[C@@H](N)CC1=CC=C(N(CCCl)CCCl)C=C1 SGDBTWWWUNNDEQ-LBPRGKRZSA-N 0.000 abstract 1
- 210000004688 microtubule Anatomy 0.000 abstract 1
- KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 abstract 1
- 229960001156 mitoxantrone Drugs 0.000 abstract 1
- CTMCWCONSULRHO-UHQPFXKFSA-N nemorubicin Chemical compound C1CO[C@H](OC)CN1[C@@H]1[C@H](O)[C@H](C)O[C@@H](O[C@@H]2C3=C(O)C=4C(=O)C5=C(OC)C=CC=C5C(=O)C=4C(O)=C3C[C@](O)(C2)C(=O)CO)C1 CTMCWCONSULRHO-UHQPFXKFSA-N 0.000 abstract 1
- 229950010159 nemorubicin Drugs 0.000 abstract 1
- 150000003058 platinum compounds Chemical class 0.000 abstract 1
- NRUKOCRGYNPUPR-QBPJDGROSA-N teniposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@@H](OC[C@H]4O3)C=3SC=CC=3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 NRUKOCRGYNPUPR-QBPJDGROSA-N 0.000 abstract 1
- 229960001278 teniposide Drugs 0.000 abstract 1
- 229960000575 trastuzumab Drugs 0.000 abstract 1
- 229960003048 vinblastine Drugs 0.000 abstract 1
- JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-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
- XRASPMIURGNCCH-UHFFFAOYSA-N zoledronic acid Chemical compound OP(=O)(O)C(P(O)(O)=O)(O)CN1C=CN=C1 XRASPMIURGNCCH-UHFFFAOYSA-N 0.000 abstract 1
- 229960004276 zoledronic acid Drugs 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Abstract
1.- Un método para el tratamiento de un animal de sangre caliente que tiene una enfermedad proliferativa o rechazo de trasplante agudo o crónico, el cual comprende administrar al animal una combinación que comprende: (a) N-{5-[4-(4-metil-piperazino-metil)-benzoilamido]-2-metilfenil}-4-(3-piridil)-2-pirimidin-amina, y (b) un agente quimioterapéutico seleccionado a partir de agentes antineoplásticos, seleccionados a partir del grupo que consiste en inhibidores de aromatasa, antiestrógenos, inhibidores de topoisomerasa I, inhibidores de topoisomerasa II seleccionados a partir del grupo que consiste en epirrubicina, idarrubicina, nemorrubicina, las antraquinonas mitoxantrona y losoxantrona, y teniposida, agentes activos en microtúbulos seleccionados a partir del grupo que consiste en paclitaxel, vinblastina, vinorelbina, y discodermolida, agentes alquilantes seleccionados a partir del grupo que consiste en ifosfamida y melfalano, antimetabolitos antineoplásticos seleccionados a partir del grupo que consiste en 5-fluorouracilo, capecitabina, gemcitabina, y edatrexato, compuestos de platina y compuestos que reducen la actividad de cinasa de proteína, y otros compuestos anti-angiogénicos seleccionados a partir del grupo que consiste en compuestos que reducen la actividad del factor de crecimiento endotelial vascular (VEGF), del factor de crecimiento derivado de plaquetas (PDGF), y la cinasa de proteína, y de la cinasa C de proteína, y compuestos anti-angiogénicos que tienen otro mecanismo para su actividad, agonistas de gonadorrelina, anti-andrógenos y trastuzumab, y agentes efectivos en el tratamiento de rechazo de trasplante agudo o crónico, en una cantidad que es conjuntamente efectiva terapéuticamente contra una enfermedad proliferativa o rechazo de trasplante agudo o crónico, y en donde los compuestos mencionados en (a) y (b) también pueden estar presentes en la forma de sus sales farmacéuticamente aceptables, o cualquier hidrato de los mismos.2.- El método de acuerdo con la reivindicación 1, en donde el compuesto (a) se utiliza en la forma de su sal de monometansulfonato.3.- El método de acuerdo con la reivindicación 1 ó con la reivindicación 2, en donde el agente quimioterapéutico se selecciona a partir de paclitaxel, docetaxel, letrozol, o ácido zoledrónico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29142701P | 2001-05-16 | 2001-05-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5540315A2 true CO5540315A2 (es) | 2005-07-29 |
Family
ID=23120246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO03098325A CO5540315A2 (es) | 2001-05-16 | 2003-11-06 | Combinacion que comprende n-{5-[4-(4-metil-piperazino-metil) benzoilamido]-2-metilfenil}-4-(3-piridil)-2-pirimidin-amina, y un agente quimioterapeutico |
Country Status (28)
| Country | Link |
|---|---|
| US (3) | US20040167134A1 (es) |
| EP (2) | EP1392313B1 (es) |
| JP (2) | JP4477303B2 (es) |
| KR (2) | KR20030094415A (es) |
| CN (1) | CN1700917B (es) |
| AT (1) | ATE359790T1 (es) |
| AU (1) | AU2002342335B2 (es) |
| BR (1) | BR0209647A (es) |
| CA (1) | CA2444867C (es) |
| CO (1) | CO5540315A2 (es) |
| CZ (1) | CZ299756B6 (es) |
| DE (1) | DE60219617T2 (es) |
| DK (1) | DK1392313T3 (es) |
| EC (1) | ECSP034823A (es) |
| ES (1) | ES2283570T3 (es) |
| HK (1) | HK1062895A1 (es) |
| HU (1) | HUP0400038A3 (es) |
| IL (1) | IL158274A0 (es) |
| MX (1) | MXPA03010401A (es) |
| NO (2) | NO325453B1 (es) |
| NZ (1) | NZ529145A (es) |
| PL (2) | PL392652A1 (es) |
| PT (1) | PT1392313E (es) |
| RU (1) | RU2318517C2 (es) |
| SI (1) | SI1392313T1 (es) |
| SK (1) | SK14042003A3 (es) |
| WO (1) | WO2002092091A1 (es) |
| ZA (1) | ZA200307665B (es) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60134679D1 (de) | 2000-10-20 | 2008-08-14 | Eisai R&D Man Co Ltd | Stickstoff enthaltende aromatische Heterozyklen |
| GB0201882D0 (en) * | 2002-01-28 | 2002-03-13 | Novartis Ag | Organic compounds |
| AU2007201056B2 (en) * | 2002-01-28 | 2010-06-10 | Hyks-Instituutti Oy | Treatment of rheumatoid arthritis using imatinib |
| GB0202874D0 (en) * | 2002-02-07 | 2002-03-27 | Novartis Ag | Organic compounds |
| WO2004004644A2 (en) * | 2002-07-05 | 2004-01-15 | Beth Israel Deaconess Medical Center | Combination of mtor inhibitor and a tyrosine kinase inhibitor for the treatment of neoplasms |
| US7994159B2 (en) | 2003-03-10 | 2011-08-09 | Eisai R&D Management Co., Ltd. | c-Kit kinase inhibitor |
| 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 |
| GB0311971D0 (en) * | 2003-05-23 | 2003-06-25 | Novartis Ag | Organic compounds |
| JP4303726B2 (ja) | 2003-11-11 | 2009-07-29 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ウレア誘導体およびその製造方法 |
| US8969379B2 (en) | 2004-09-17 | 2015-03-03 | Eisai R&D Management Co., Ltd. | Pharmaceutical compositions of 4-(3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7=methoxy-6-quinolinecarboxide |
| US20060235006A1 (en) * | 2005-04-13 | 2006-10-19 | Lee Francis Y | Combinations, methods and compositions for treating cancer |
| JP5066446B2 (ja) * | 2005-08-01 | 2012-11-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 血管新生阻害物質の効果を予測する方法 |
| EP1925676A4 (en) | 2005-08-02 | 2010-11-10 | Eisai R&D Man Co Ltd | TEST METHOD FOR THE EFFECT OF A VASCULARIZATION INHIBITOR |
| BRPI0614090A2 (pt) * | 2005-08-03 | 2011-03-09 | Novartis Ag | uso de inibidores da hdac para o tratamento do mieloma |
| WO2007056118A1 (en) * | 2005-11-04 | 2007-05-18 | Wyeth | Antineoplastic combinations with mtor inhibitor, herceptin, and/or hki-272 |
| CN101316590B (zh) * | 2005-11-07 | 2011-08-03 | 卫材R&D管理有限公司 | 血管生成抑制剂和c-kit激酶抑制剂的组合使用 |
| ES2556173T3 (es) | 2006-05-18 | 2016-01-13 | Eisai R&D Management Co., Ltd. | Agente antitumoral para un cáncer de tiroides |
| CN1899616A (zh) * | 2006-07-20 | 2007-01-24 | 中国人民解放军军事医学科学院生物工程研究所 | 非受体酪氨酸激酶c－Abl特异性抑制剂的新用途 |
| US8865737B2 (en) * | 2006-08-28 | 2014-10-21 | Eisai R&D Management Co., Ltd. | Antitumor agent for undifferentiated gastric cancer |
| EP2119707B1 (en) | 2007-01-29 | 2015-01-14 | Eisai R&D Management Co., Ltd. | Composition for treatment of undifferentiated-type of gastric cancer |
| CN101848895B (zh) * | 2007-11-09 | 2013-10-23 | 卫材R&D管理有限公司 | 血管新生抑制物质和抗肿瘤性铂络合物的组合使用 |
| AU2009210098B2 (en) * | 2008-01-29 | 2013-06-13 | Eisai R & D Management Co., Ltd. | Combined use of angiogenesis inhibitor and taxane |
| EP2915532B1 (en) * | 2008-06-17 | 2016-10-19 | Wyeth LLC | Antineoplastic combinations containing hki-272 and vinorelbine |
| US9012458B2 (en) | 2010-06-25 | 2015-04-21 | Eisai R&D Management Co., Ltd. | Antitumor agent using compounds having kinase inhibitory effect in combination |
| WO2012144463A1 (ja) | 2011-04-18 | 2012-10-26 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 腫瘍治療剤 |
| WO2012166899A2 (en) | 2011-06-03 | 2012-12-06 | Eisai R&D Management Co., Ltd. | Biomarkers for predicting and assessing responsiveness of thyroid and kidney cancer subjects to lenvatinib compounds |
| KR20150098605A (ko) | 2012-12-21 | 2015-08-28 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 퀴놀린 유도체의 비정질 형태 및 그의 제조방법 |
| KR102204279B1 (ko) | 2013-05-14 | 2021-01-15 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 자궁내막암 대상의 렌바티닙 화합물에 대한 반응성을 예측 및 평가하기 위한 생체표지 |
| RS63559B1 (sr) | 2014-08-28 | 2022-10-31 | Eisai R&D Man Co Ltd | Derivat hinolina velike čistoće i postupak za njegovu proizvodnju |
| PL3263106T3 (pl) | 2015-02-25 | 2024-04-02 | Eisai R&D Management Co., Ltd. | Sposób tłumienia goryczy pochodnej chinoliny |
| AU2015384801B2 (en) | 2015-03-04 | 2022-01-06 | Eisai R&D Management Co., Ltd. | Combination of a PD-1 antagonist and a VEGFR/FGFR/RET tyrosine kinase inhibitor for treating cancer |
| BR112017027227B1 (pt) | 2015-06-16 | 2023-12-12 | Eisai R&D Management Co., Ltd | Agente anti-câncer |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1524747A (en) | 1976-05-11 | 1978-09-13 | Ici Ltd | Polypeptide |
| EP0100172B1 (en) | 1982-07-23 | 1987-08-12 | Imperial Chemical Industries Plc | Amide derivatives |
| GB8327256D0 (en) | 1983-10-12 | 1983-11-16 | Ici Plc | Steroid derivatives |
| GB8517360D0 (en) | 1985-07-09 | 1985-08-14 | Erba Farmitalia | Substituted androsta-1,4-diene-3,17-diones |
| US4749713A (en) | 1986-03-07 | 1988-06-07 | Ciba-Geigy Corporation | Alpha-heterocycle substituted tolunitriles |
| US4978672A (en) | 1986-03-07 | 1990-12-18 | Ciba-Geigy Corporation | Alpha-heterocyclc substituted tolunitriles |
| IL84497A (en) | 1986-11-21 | 1994-10-21 | Ciba Geigy Ag | History 2-) Imidazol-1-yl (ethane-1,1-diphosphonic acid, their preparation and pharmaceutical preparations containing them |
| IL86632A0 (en) | 1987-06-15 | 1988-11-30 | Ciba Geigy Ag | Derivatives substituted at methyl-amino nitrogen |
| US5010099A (en) | 1989-08-11 | 1991-04-23 | Harbor Branch Oceanographic Institution, Inc. | Discodermolide compounds, compositions containing same and method of preparation and use |
| NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| TW225528B (es) | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
| DK1167384T3 (da) | 1992-10-28 | 2007-04-10 | Genentech Inc | Vaskular endotheliel cellevækstfaktor antagonister |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| US5843901A (en) | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
| JP4146514B2 (ja) | 1995-07-06 | 2008-09-10 | ノバルティス アクチエンゲゼルシャフト | ピロロピリミジン類およびその製造方法 |
| US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
| GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| AU2195297A (en) * | 1996-02-20 | 1997-09-02 | Sloan-Kettering Institute For Cancer Research | Combinations of pkc inhibitors and therapeutic agents for treating cancers |
| SI0892789T2 (sl) | 1996-04-12 | 2010-03-31 | Warner Lambert Co | Ireverzibilni inhibitorji tirozin kinaz |
| AU2557097A (en) * | 1996-04-17 | 1997-11-07 | Board Of Regents, The University Of Texas System | Enhanced expression of transgenes |
| CA2258548C (en) | 1996-06-24 | 2005-07-26 | Pfizer Inc. | Phenylamino-substituted tricyclic derivatives for treatment of hyperproliferative diseases |
| DE19638745C2 (de) | 1996-09-11 | 2001-05-10 | Schering Ag | Monoklonale Antikörper gegen die extrazelluläre Domäne des menschlichen VEGF - Rezeptorproteins (KDR) |
| AU4342997A (en) | 1996-09-13 | 1998-04-02 | Sugen, Inc. | Use of quinazoline derivatives for the manufacture of a medicament in the reatment of hyperproliferative skin disorders |
| EP0837063A1 (en) | 1996-10-17 | 1998-04-22 | Pfizer Inc. | 4-Aminoquinazoline derivatives |
| US20020128240A1 (en) * | 1996-12-30 | 2002-09-12 | Bone Care International, Inc. | Treatment of hyperproliferative diseases using active vitamin D analogues |
| CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| CO4940418A1 (es) * | 1997-07-18 | 2000-07-24 | Novartis Ag | Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso |
| GB9721069D0 (en) | 1997-10-03 | 1997-12-03 | Pharmacia & Upjohn Spa | Polymeric derivatives of camptothecin |
| US20010051628A1 (en) * | 1998-05-04 | 2001-12-13 | H.-J. Su Huang | Methods to modulate the resistance of cells to apoptosis mediated by mutant epidermal growth factor receptors |
| JP4516690B2 (ja) | 1998-08-11 | 2010-08-04 | ノバルティス アーゲー | 血管形成阻害活性を有するイソキノリン誘導体 |
| UA71587C2 (uk) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
| GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
| JP4731016B2 (ja) | 1998-12-22 | 2011-07-20 | ジェネンテック， インコーポレイテッド | 血管内皮細胞増殖因子アンタゴニストとその用途 |
| US6833373B1 (en) * | 1998-12-23 | 2004-12-21 | G.D. Searle & Co. | Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
| GB9903547D0 (en) | 1999-02-16 | 1999-04-07 | Novartis Ag | Organic compounds |
| ES2265929T3 (es) | 1999-03-30 | 2007-03-01 | Novartis Ag | Derivados de ftalazina para el tratamiento de enfermedades inflamatorias. |
| GB9907908D0 (en) * | 1999-04-07 | 1999-06-02 | Bataille Regis | Organic compounds |
| GB9911582D0 (en) * | 1999-05-18 | 1999-07-21 | Pharmacia & Upjohn Spa | Combined method of treatment comprising an aromatase inhibitor and a further biologically active compound |
| BR0014001A (pt) * | 1999-09-15 | 2002-05-21 | American Home Prod | Método de potencialização de quimioterapia e tratamento de tumores sólidos |
| AU775373B2 (en) * | 1999-10-01 | 2004-07-29 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
| JP2003512353A (ja) * | 1999-10-19 | 2003-04-02 | メルク エンド カムパニー インコーポレーテッド | チロシンキナーゼ阻害剤 |
| TWI310684B (en) * | 2000-03-27 | 2009-06-11 | Bristol Myers Squibb Co | Synergistic pharmaceutical kits for treating cancer |
| US7238525B2 (en) * | 2000-06-30 | 2007-07-03 | The Regents Of The University Of California | Strategy for leukemia therapy |
| WO2002028409A2 (en) * | 2000-10-05 | 2002-04-11 | Whitehead Institute For Biomedical Research | Effects of combined administration of farnesyl transferase inhibitors and signal transduction inhibitors |
| BR0114655A (pt) * | 2000-10-06 | 2004-02-10 | Biomedicines Inc | Método para a identificação de uma combinação de drogas para tratamento de câncer de mama em um animal, método para o tratamento de câncer de mama em um animal, método para a identificação de uma combinação de drogas para a prevenção de câncer de mama em um animal predisposto ao referido câncer, método de prevenção de câncer de mama em um animal predisposto ao referido câncer, método para a otimização de tratamento de um paciente com câncer de mama, método para a otimização de um regime de prevenção de câncer em um animal, conjunto útil para o tratamento de câncer de mama em um paciente em necessidade de tratamento e composição farmacêutica para tratamento ou prevenção de câncer de mama |
| PL209733B1 (pl) * | 2000-10-27 | 2011-10-31 | Novartis Ag | Zastosowanie 4-(4-metylopiperazyno-1-ylometylo)-N-[4-metylo-3-(4-pirydyn-3-ylo)pirymidyn-2-yloamino)fenylo]benzamidu w leczeniu żołądkowo-jelitowych guzów podścieliskowych |
| JP4499359B2 (ja) * | 2001-02-27 | 2010-07-07 | ノバルティス アーゲー | シグナル変換阻害剤とエポチロン誘導体とを含有してなる組合せ剤 |
| JP4942297B2 (ja) * | 2002-10-25 | 2012-05-30 | ジ アドミニストレイターズ オブ ザ チューレン エデュケイショナル ファンド | 肺高血圧症の処置を目的としたｎ−｛５−［４−（４−メチルピペラジノメチル）−ベンゾイルアミド］−２−メチルフェニル｝−４−（３−ピリジル）−２−ピリジン−アミンの使用 |
| US8168621B2 (en) * | 2005-09-30 | 2012-05-01 | Endece, Llc | 6-substituted estradiol derivatives and methods of use |
| TW200740776A (en) * | 2006-02-06 | 2007-11-01 | Osi Pharm Inc | N-phenylbenzotriazolyl c-kit inhibitors |
| WO2009140554A1 (en) * | 2008-05-15 | 2009-11-19 | University Of Southern California | Ercc-1 expression predicts chemotherapy outcome |
-
2002
- 2002-05-15 SK SK1404-2003A patent/SK14042003A3/sk not_active Application Discontinuation
- 2002-05-15 HU HU0400038A patent/HUP0400038A3/hu unknown
- 2002-05-15 RU RU2003135786/14A patent/RU2318517C2/ru not_active IP Right Cessation
- 2002-05-15 WO PCT/EP2002/005362 patent/WO2002092091A1/en active Application Filing
- 2002-05-15 BR BR0209647-1A patent/BR0209647A/pt not_active IP Right Cessation
- 2002-05-15 ES ES02743024T patent/ES2283570T3/es not_active Expired - Lifetime
- 2002-05-15 DE DE60219617T patent/DE60219617T2/de not_active Expired - Fee Related
- 2002-05-15 PL PL392652A patent/PL392652A1/pl unknown
- 2002-05-15 AU AU2002342335A patent/AU2002342335B2/en not_active Ceased
- 2002-05-15 SI SI200230560T patent/SI1392313T1/sl unknown
- 2002-05-15 CA CA2444867A patent/CA2444867C/en not_active Expired - Fee Related
- 2002-05-15 PL PL02368068A patent/PL368068A1/xx unknown
- 2002-05-15 DK DK02743024T patent/DK1392313T3/da active
- 2002-05-15 EP EP02743024A patent/EP1392313B1/en not_active Expired - Lifetime
- 2002-05-15 CN CN028093623A patent/CN1700917B/zh not_active Expired - Fee Related
- 2002-05-15 NZ NZ529145A patent/NZ529145A/en unknown
- 2002-05-15 KR KR10-2003-7014844A patent/KR20030094415A/ko active Search and Examination
- 2002-05-15 AT AT02743024T patent/ATE359790T1/de not_active IP Right Cessation
- 2002-05-15 MX MXPA03010401A patent/MXPA03010401A/es active IP Right Grant
- 2002-05-15 PT PT02743024T patent/PT1392313E/pt unknown
- 2002-05-15 CZ CZ20033098A patent/CZ299756B6/cs not_active IP Right Cessation
- 2002-05-15 JP JP2002589008A patent/JP4477303B2/ja not_active Expired - Lifetime
- 2002-05-15 IL IL15827402A patent/IL158274A0/xx unknown
- 2002-05-15 EP EP10173158A patent/EP2253319A1/en not_active Withdrawn
- 2002-05-15 US US10/476,817 patent/US20040167134A1/en not_active Abandoned
- 2002-05-15 KR KR1020087023228A patent/KR20080091866A/ko not_active Application Discontinuation
-
2003
- 2003-10-01 ZA ZA200307665A patent/ZA200307665B/en unknown
- 2003-10-21 NO NO20034713A patent/NO325453B1/no not_active IP Right Cessation
- 2003-10-29 EC EC2003004823A patent/ECSP034823A/es unknown
- 2003-11-06 CO CO03098325A patent/CO5540315A2/es not_active Application Discontinuation
-
2004
- 2004-08-05 HK HK04105830A patent/HK1062895A1/xx not_active IP Right Cessation
-
2007
- 2007-12-07 NO NO20076323A patent/NO20076323L/no not_active Application Discontinuation
-
2009
- 2009-04-14 US US12/423,079 patent/US20090202541A1/en not_active Abandoned
- 2009-12-11 JP JP2009281667A patent/JP2010059202A/ja not_active Ceased
-
2012
- 2012-07-17 US US13/551,079 patent/US20120283206A1/en not_active Abandoned
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CO5540315A2 (es) | Combinacion que comprende n-{5-[4-(4-metil-piperazino-metil) benzoilamido]-2-metilfenil}-4-(3-piridil)-2-pirimidin-amina, y un agente quimioterapeutico | |
| Edmunds Jr | Thrombotic and bleeding complications of prosthetic heart valves | |
| AR112118A2 (es) | Inhibidores de pi-3 quinasa | |
| ES2366132T3 (es) | Derivados del ácido escuárico como inhibidores de la histona desacetilasa. | |
| ECSP066752A (es) | Formas de sal de 4-(4-metilpiperazin-1-ilmetil)-n-[4-metil-3-(4-piridin-3-il)pirimidin-2-ilamino)fenil]-benzamida | |
| PE20070806A1 (es) | Composicion farmaceutica que comprende un derivado de diarilurea | |
| JP2008523055A (ja) | 熱ショックタンパク質（ｈｓｐ）および上室性不整脈 | |
| BRPI0511065A (pt) | método para tratar crescimento de célula anormal | |
| PE20071337A1 (es) | Nanoparticulas que comprenden imatinib, composiciones farmaceuticas y dispositivos que comprenden dichas nanoparticulas y uso farmaceutico de las mismas | |
| Hale et al. | Dabigatran treatment: effects on infarct size and the no-reflow phenomenon in a model of acute myocardial ischemia/reperfusion | |
| Gifre-Renom et al. | Vessel enlargement in development and pathophysiology | |
| PE20230165A1 (es) | Inhibidores de sarm1 | |
| JP2024040421A5 (es) | ||
| MX2007013741A (es) | Uso de derivados de pirimidilaminobenzamida para el tratamiento de mastocitosis sistemica. | |
| Misztal et al. | Peroxynitrite–altered platelet mitochondria—A new link between inflammation and hemostasis | |
| Borrelli et al. | Reduction of levels of nuclear-associated protein in heated cells by cycloheximide, D2 O, and thermotolerance | |
| PE20230405A1 (es) | Profarmacos de itaconato e itaconato de metilo desarrollo o investigacion patrocinados por el gobierno | |
| RU2015103985A (ru) | Ингибиторы коррозии меди и медьсодержащих сплавов | |
| Oury et al. | ERK2 activation in arteriolar and venular murine thrombosis: platelet receptor GPIb vs. P2X1 | |
| Xu et al. | Impact of Na+ permeation on collective migration of pulmonary arterial endothelial cells | |
| Jugdutt | Extracellular matrix and cardiac remodeling | |
| Layland et al. | Myofilament‐based relaxant effect of isoprenaline revealed during work‐loop contractions in rat cardiac trabeculae | |
| Smith et al. | The influence of endocardial endothelium on myocardial contraction | |
| Ernst et al. | Hemorheology, thrombogenesis, and atherosclerosis | |
| Nishida et al. | L-cis diltiazem attenuates intracellular Ca2+ overload by metabolic inhibition in guinea pig myocytes |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Application refused |