HRP20110349T1 - Nova kombinacijska upotreba spoja sulfonamida u liječenju karcinoma - Google Patents
Nova kombinacijska upotreba spoja sulfonamida u liječenju karcinoma Download PDFInfo
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- HRP20110349T1 HRP20110349T1 HR20110349T HRP20110349T HRP20110349T1 HR P20110349 T1 HRP20110349 T1 HR P20110349T1 HR 20110349 T HR20110349 T HR 20110349T HR P20110349 T HRP20110349 T HR P20110349T HR P20110349 T1 HRP20110349 T1 HR P20110349T1
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- Prior art keywords
- sulfonamide compound
- cancer
- treatment
- substance
- inhibitory effect
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- 229940124530 sulfonamide Drugs 0.000 title claims abstract 12
- -1 sulfonamide compound Chemical class 0.000 title claims abstract 12
- 206010028980 Neoplasm Diseases 0.000 title claims 9
- 201000011510 cancer Diseases 0.000 title claims 9
- 230000002401 inhibitory effect Effects 0.000 claims abstract 11
- 239000000126 substance Substances 0.000 claims abstract 11
- LWGUASZLXHYWIV-UHFFFAOYSA-N 3-cyano-n-(3-cyano-4-methyl-1h-indol-7-yl)benzenesulfonamide Chemical compound C1=2NC=C(C#N)C=2C(C)=CC=C1NS(=O)(=O)C1=CC=CC(C#N)=C1 LWGUASZLXHYWIV-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000005411 L01XE02 - Gefitinib Substances 0.000 claims abstract 2
- 239000005551 L01XE03 - Erlotinib Substances 0.000 claims abstract 2
- 229960005395 cetuximab Drugs 0.000 claims abstract 2
- 229960001433 erlotinib Drugs 0.000 claims abstract 2
- 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 claims abstract 2
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical group C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 claims abstract 2
- 229960002584 gefitinib Drugs 0.000 claims abstract 2
- SETFNECMODOHTO-UHFFFAOYSA-N indisulam Chemical compound C1=CC(S(=O)(=O)N)=CC=C1S(=O)(=O)NC1=CC=CC2=C1NC=C2Cl SETFNECMODOHTO-UHFFFAOYSA-N 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 239000012453 solvate Substances 0.000 claims abstract 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims 7
- 238000009472 formulation Methods 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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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
- A61K31/64—Sulfonylureas, e.g. glibenclamide, tolbutamide, chlorpropamide
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- 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
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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
- A61K31/33—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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39541—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against normal tissues, cells
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Mycology (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)
Abstract
Farmaceutski pripravak obuhvaća spoj sulfonamida u kombinaciji sa supstancom koja ima inhibicijsko djelovanje EGF, naznačen time, što spoj sulfonamida je: N-(3-klor-1H-indol-7-il)-4-sulfamoilbenzensulfonamid,N-(3-cijano-4-metil-1H-indol-7-il)-3-cijanobenzensulfonamid, ili njegova farmakološki prihvatljiva sol ili njegov solvat, i pri čemu supstanca koja ima inhibicijsko djelovanje EGF je gefitinib, erlotinib ili cetuksimab. Patent sadrži još 9 patentnih zahtjeva.
Claims (10)
1. Farmaceutski pripravak obuhvaća spoj sulfonamida u kombinaciji sa supstancom koja ima inhibicijsko djelovanje EGF, naznačen time, što spoj sulfonamida je:
N-(3-klor-1H-indol-7-il)-4-sulfamoilbenzensulfonamid,N-(3-cijano-4-metil-1H-indol-7-il)-3-cijanobenzensulfonamid, ili njegova farmakološki prihvatljiva sol ili njegov solvat,
i pri čemu supstanca koja ima inhibicijsko djelovanje EGF je gefitinib, erlotinib ili cetuksimab.
2. Farmaceutski pripravak prema zahtjevu 1, naznačen time, što se farmaceutski pripravak koristi za liječenje karcinoma.
3. Pribor, naznačen time, što obuhvaća skup formulacije koja sadrži spoj sulfonamida definiran u zahtjevu 1 i formulacije koja sadrži supstancu koja ima inhibicijsko djelovanje EGF definiranu u zahtjevu 1.
4. Pribor prema zahtjevu 4, naznačen time, što je za uporabu u liječenju karcinoma.
5. Upotreba spoja sulfonamida definiranog u zahtjevu 1 naznačena time, što za proizvodnju farmaceutskog pripravka za upotrebu u kombinaciji sa supstancom koja ima inhibicijsko djelovanje EGF definiranom u zahtjevu 1 za liječenje karcinoma.
6. Upotreba supstance koja ima inhibicijsko djelovanje EGF definirano u zahtjevu 1 naznačena time, što za proizvodnju farmaceutskog pripravka za upotrebu u kombinaciji sa spojem sulfonamida definirano u zahtjevu 1 za liječenje karcinoma.
7. Spoj sulfonamida definiran u zahtjevu 1 naznačen time, što za upotrebu u kombinaciji sa supstancom koja ima inhibicijsko djelovanje EGF definiranom u zahtjevu 1 za liječenje karcinoma.
8. Supstanca koja ima inhibicijsko djelovanje EGF definirana u zahtjevu 1 naznačena time, što za upotrebu u kombinaciji sa spojem sulfonamida definiranim u zahtjevu 1 za liječenje karcinoma.
9. Farmaceutski pripravak obuhvaća spoj sulfonamida definiran u zahtjevu 1 naznačen time, što za upotrebu u kombinaciji sa supstancom koja ima inhibicijsko djelovanje EGF definiranom u zahtjevu 1 za liječenje karcinoma.
10. Farmaceutski pripravak obuhvaća supstancu koja ima inhibicijsko djelovanje EGF definiranu u zahtjevu 1 naznačen time, što za upotrebu u kombinaciji sa spojem sulfonamida definiranim u zahtjevu 1 za liječenje karcinoma.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005054111 | 2005-02-28 | ||
PCT/JP2006/304218 WO2006090930A1 (ja) | 2005-02-28 | 2006-02-28 | スルホンアミド化合物の新規併用 |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20110349T1 true HRP20110349T1 (hr) | 2011-07-31 |
Family
ID=36927547
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20110349T HRP20110349T1 (hr) | 2005-02-28 | 2011-05-11 | Nova kombinacijska upotreba spoja sulfonamida u liječenju karcinoma |
Country Status (18)
Country | Link |
---|---|
US (1) | US20090047278A1 (hr) |
EP (1) | EP1859793B1 (hr) |
JP (1) | JPWO2006090930A1 (hr) |
KR (1) | KR20070108270A (hr) |
CN (1) | CN101163468A (hr) |
AU (1) | AU2006217692A1 (hr) |
CA (1) | CA2599115A1 (hr) |
CY (1) | CY1111579T1 (hr) |
DE (1) | DE602006021401D1 (hr) |
DK (1) | DK1859793T3 (hr) |
ES (1) | ES2362898T3 (hr) |
HR (1) | HRP20110349T1 (hr) |
ME (1) | ME01222B (hr) |
PL (1) | PL1859793T3 (hr) |
PT (1) | PT1859793E (hr) |
RS (1) | RS51821B (hr) |
SI (1) | SI1859793T1 (hr) |
WO (1) | WO2006090930A1 (hr) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU9598601A (en) * | 2000-10-20 | 2002-04-29 | Eisai Co Ltd | Nitrogenous aromatic ring compounds |
JPWO2004080462A1 (ja) * | 2003-03-10 | 2006-06-08 | エーザイ株式会社 | c−Kitキナーゼ阻害剤 |
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 |
WO2006030826A1 (ja) | 2004-09-17 | 2006-03-23 | Eisai R & D Management Co., Ltd. | 医薬組成物 |
MX2007009317A (es) | 2005-02-03 | 2008-01-30 | Gen Hospital Corp | Metodo para tratar cancer resistente a gefitinib. |
EP1859804B1 (en) * | 2005-02-10 | 2016-12-07 | Oncolys BioPharma, Inc. | Anticancer agent combination therapy |
JP5106098B2 (ja) * | 2005-02-28 | 2012-12-26 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | スルホンアミド化合物の抗癌剤との新規併用 |
JP4989476B2 (ja) | 2005-08-02 | 2012-08-01 | 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検定する方法 |
AU2006285673B2 (en) * | 2005-09-01 | 2010-12-02 | Eisai R&D Management Co., Ltd. | Method for preparation of pharmaceutical composition having improved disintegratability |
RU2451524C2 (ru) | 2005-11-04 | 2012-05-27 | Вайет | Противоопухолевые комбинации с ингибиторами mtor, герцептином и/или hki-272 |
WO2007052850A1 (ja) | 2005-11-07 | 2007-05-10 | Eisai R & D Management Co., Ltd. | 血管新生阻害物質とc-kitキナーゼ阻害物質との併用 |
WO2007061127A1 (ja) * | 2005-11-22 | 2007-05-31 | Eisai R & D Management Co., Ltd. | 多発性骨髄腫に対する抗腫瘍剤 |
RU2448708C3 (ru) * | 2006-05-18 | 2017-09-28 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Противоопухолевое средство против рака щитовидной железы |
EP2044939A1 (en) * | 2006-06-29 | 2009-04-08 | Eisai R&D Management Co., Ltd. | Therapeutic agent for liver fibrosis |
EP2065372B1 (en) * | 2006-08-28 | 2012-11-28 | Eisai R&D Management Co., Ltd. | Antitumor agent for undifferentiated gastric cancer |
CA2675736A1 (en) * | 2007-01-19 | 2008-07-24 | Eisai R&D Management Co., Ltd. | Composition for treatment of pancreatic cancer |
WO2008093855A1 (ja) | 2007-01-29 | 2008-08-07 | Eisai R & D Management Co., Ltd. | 未分化型胃癌治療用組成物 |
US8022216B2 (en) | 2007-10-17 | 2011-09-20 | Wyeth Llc | Maleate salts of (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide and crystalline forms thereof |
WO2009060945A1 (ja) | 2007-11-09 | 2009-05-14 | Eisai R & D Management Co., Ltd. | 血管新生阻害物質と抗腫瘍性白金錯体との併用 |
AU2009210098B2 (en) * | 2008-01-29 | 2013-06-13 | Eisai R & D Management Co., Ltd. | Combined use of angiogenesis inhibitor and taxane |
PL2656844T3 (pl) | 2008-06-17 | 2015-05-29 | Wyeth Llc | Kombinacje przeciwnowotworowe zawierające HKI-272 i winorelbinę |
NZ590464A (en) | 2008-08-04 | 2012-10-26 | Wyeth Llc | Antineoplastic combinations of the 4-anilino-3-cyanoquinoline neratinib and capecitabine |
MX356593B (es) | 2009-04-06 | 2018-06-05 | Wyeth Llc | Régimen de tratamiento que utiliza neratinib para cáncer de mama. |
EP2586443B1 (en) | 2010-06-25 | 2016-03-16 | 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 |
JP6038128B2 (ja) | 2011-06-03 | 2016-12-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | レンバチニブ化合物に対する甲状腺癌対象及び腎臓癌対象の反応性を予測及び評価するためのバイオマーカー |
CN104755463A (zh) | 2012-12-21 | 2015-07-01 | 卫材R&D管理有限公司 | 非晶态形式的喹啉衍生物及其生产方法 |
MX368099B (es) | 2013-05-14 | 2019-09-19 | Eisai R&D Man Co Ltd | Biomarcadores para predecir y evaluar el grado de respuesta de sujetos con cancer de endometrio a compuestos de tipo lenvatinib. |
US10259791B2 (en) | 2014-08-28 | 2019-04-16 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
MX2017010474A (es) | 2015-02-25 | 2017-11-28 | Eisai R&D Man Co Ltd | Metodo para suprimir el amargor de un derivado de quinoleina. |
KR102662228B1 (ko) | 2015-03-04 | 2024-05-02 | 머크 샤프 앤드 돔 코포레이션 | 암을 치료하기 위한 pd-1 길항제 및 vegfr/fgfr/ret 티로신 키나제 억제제의 조합 |
RU2729936C2 (ru) | 2015-06-16 | 2020-08-13 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Противораковое средство |
CU24558B1 (es) * | 2017-11-28 | 2021-12-08 | Ct Inmunologia Molecular | Anticuerpos monoclonales que reconocen al receptor del factor de crecimiento epidérmico y sus fragmentos derivados |
WO2019147783A1 (en) * | 2018-01-25 | 2019-08-01 | Dana-Farber Cancer Institute, Inc. | Sulfonamide derivatives for protein degradation |
AU2019255310B2 (en) | 2018-04-18 | 2022-11-24 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
US11919912B2 (en) | 2018-05-21 | 2024-03-05 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
WO2021151974A1 (en) | 2020-01-28 | 2021-08-05 | Stichting Het Nederlands Kanker Instituut - Antoni Van Leeuwenhoek Ziekenhuis | Interfering with mrna splicing to enhance response to checkpoint immunotherapies. |
US20230190707A1 (en) * | 2020-05-15 | 2023-06-22 | Fred Hutchinson Cancer Center | Compositions and methods for enhancing cancer immunotherapy |
CN113679720B (zh) * | 2020-05-19 | 2024-09-27 | 苏中药业集团股份有限公司 | 一种取代丁烯酰胺联合铂类化合物的药物组合物及其用途 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CU22545A1 (es) * | 1994-11-18 | 1999-03-31 | Centro Inmunologia Molecular | Obtención de un anticuerpo quimérico y humanizado contra el receptor del factor de crecimiento epidérmico para uso diagnóstico y terapéutico |
JPS5857710A (ja) | 1981-09-30 | 1983-04-06 | Matsushita Electric Works Ltd | コイル |
DE3474040D1 (en) * | 1984-11-22 | 1988-10-20 | Holsten Brauerei Ag | Beer and process for its preparation |
IL80032A (en) * | 1985-09-23 | 1992-07-15 | Lilly Co Eli | Anti-tumor phenyl-aminocarbonylsulfonamides,their preparation and pharmaceutical compositions containing them |
AU4128089A (en) * | 1988-09-15 | 1990-03-22 | Rorer International (Overseas) Inc. | Monoclonal antibodies specific to human epidermal growth factor receptor and therapeutic methods employing same |
RU2139351C1 (ru) * | 1991-04-25 | 1999-10-10 | Чугаи Сейяку Кабусики Кайся | Н- и l-цепи моноклонального антитела рм1 (монат) к рецептору il-6r человека и их v-области, модифицированная монат, его н- и l-цепи и их v-области, cdr- последовательности, днк-последовательности |
DK0673937T3 (da) | 1993-09-10 | 2004-03-22 | Eisai Co Ltd | Bicyclisk heterocyclisk sulfonamid og sulfonsyreesterderivater |
JP3545461B2 (ja) | 1993-09-10 | 2004-07-21 | エーザイ株式会社 | 二環式ヘテロ環含有スルホンアミド誘導体 |
EP3103799B1 (en) | 1995-03-30 | 2018-06-06 | OSI Pharmaceuticals, LLC | Quinazoline derivatives |
GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
JP2000247949A (ja) | 1999-02-26 | 2000-09-12 | Eisai Co Ltd | スルホンアミド含有インドール化合物 |
RS49836B (sr) * | 1999-03-31 | 2008-08-07 | Pfizer Products Inc., | Postupci i intermedijeri za dobijanje anti-kancernih jedinjenja |
CA2410371C (en) * | 2000-06-22 | 2015-11-17 | University Of Iowa Research Foundation | Methods for enhancing antibody-induced cell lysis and treating cancer |
PL367188A1 (en) | 2001-06-06 | 2005-02-21 | Eli Lilly And Company | Benzoylsulfonamides and sulfonylbenzamidines for use as antitumour agents |
DE10133394A1 (de) * | 2001-07-13 | 2003-01-30 | Merck Patent Gmbh | Flüssige Formulierung enthaltend Cetuximab |
TWI281916B (en) * | 2001-10-25 | 2007-06-01 | Lilly Co Eli | Antitumor compounds and methods |
EP1481678A4 (en) * | 2002-03-05 | 2009-12-30 | Eisai R&D Man Co Ltd | ANTITUMORAL AGENT CONTAINING A SULFONAMIDE-CONTAINING HETEROCYCLIC COMPOUND AND AN ANGIOGENESIS INHIBITOR |
AU2003270846B2 (en) * | 2002-09-19 | 2006-11-23 | Merck Sharp & Dohme Corp. | Pyrazolopyridines as cyclin dependent kinase inhibitors |
JP3785390B2 (ja) | 2002-09-24 | 2006-06-14 | 平野整機工業株式会社 | 自転車後輪駆動装置及び自転車 |
US20040209930A1 (en) * | 2002-10-02 | 2004-10-21 | Carboni Joan M. | Synergistic methods and compositions for treating cancer |
US7378423B2 (en) * | 2004-06-11 | 2008-05-27 | Japan Tobacco Inc. | Pyrimidine compound and medical use thereof |
WO2006030941A1 (ja) * | 2004-09-13 | 2006-03-23 | Eisai R & D Management Co., Ltd. | スルホンアミド含有化合物の血管新生阻害物質との併用 |
-
2006
- 2006-02-28 ME MEP-2011-128A patent/ME01222B/me unknown
- 2006-02-28 DK DK06715261.1T patent/DK1859793T3/da active
- 2006-02-28 DE DE602006021401T patent/DE602006021401D1/de active Active
- 2006-02-28 US US11/885,081 patent/US20090047278A1/en not_active Abandoned
- 2006-02-28 AU AU2006217692A patent/AU2006217692A1/en not_active Abandoned
- 2006-02-28 WO PCT/JP2006/304218 patent/WO2006090930A1/ja active Application Filing
- 2006-02-28 PL PL06715261T patent/PL1859793T3/pl unknown
- 2006-02-28 PT PT06715261T patent/PT1859793E/pt unknown
- 2006-02-28 JP JP2007504857A patent/JPWO2006090930A1/ja active Pending
- 2006-02-28 SI SI200631061T patent/SI1859793T1/sl unknown
- 2006-02-28 RS RS20110308A patent/RS51821B/en unknown
- 2006-02-28 CA CA002599115A patent/CA2599115A1/en not_active Abandoned
- 2006-02-28 ES ES06715261T patent/ES2362898T3/es active Active
- 2006-02-28 KR KR1020077022300A patent/KR20070108270A/ko not_active Application Discontinuation
- 2006-02-28 EP EP06715261A patent/EP1859793B1/en active Active
- 2006-02-28 CN CNA2006800137614A patent/CN101163468A/zh active Pending
-
2011
- 2011-05-11 HR HR20110349T patent/HRP20110349T1/hr unknown
- 2011-06-17 CY CY20111100583T patent/CY1111579T1/el unknown
Also Published As
Publication number | Publication date |
---|---|
SI1859793T1 (sl) | 2011-08-31 |
CA2599115A1 (en) | 2006-08-31 |
US20090047278A1 (en) | 2009-02-19 |
WO2006090930A1 (ja) | 2006-08-31 |
CY1111579T1 (el) | 2015-10-07 |
DE602006021401D1 (de) | 2011-06-01 |
KR20070108270A (ko) | 2007-11-08 |
ME01222B (me) | 2013-06-20 |
PL1859793T3 (pl) | 2011-09-30 |
RS51821B (en) | 2012-02-29 |
EP1859793A1 (en) | 2007-11-28 |
EP1859793B1 (en) | 2011-04-20 |
JPWO2006090930A1 (ja) | 2008-07-24 |
PT1859793E (pt) | 2011-07-05 |
AU2006217692A1 (en) | 2006-08-31 |
EP1859793A4 (en) | 2008-07-23 |
ES2362898T3 (es) | 2011-07-14 |
DK1859793T3 (da) | 2011-08-01 |
CN101163468A (zh) | 2008-04-16 |
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