HUE027443T2 - Stat3 útvonal gátlók újszerû csoportja és tumor-õssejt útvonal gátlók - Google Patents
Stat3 útvonal gátlók újszerû csoportja és tumor-õssejt útvonal gátlók Download PDFInfo
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- HUE027443T2 HUE027443T2 HUE08830619A HUE08830619A HUE027443T2 HU E027443 T2 HUE027443 T2 HU E027443T2 HU E08830619 A HUE08830619 A HU E08830619A HU E08830619 A HUE08830619 A HU E08830619A HU E027443 T2 HUE027443 T2 HU E027443T2
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Claims (4)
- készítmény, amely a következőkbe! -áll: f| vegyidet a következő csoportból választva: 2-acetik7-k!ór-n3ftöl2i3-blfurán-4,9'd$en; |-acet!í7-toí--na^ £«eetlHMrfto[23~ bjfurán-mg.-díon, :Μ^^12.3^Ιΐ0^η·»4^^#: löszförsav mm4H#&&oxa~n$MM~ tetrahidra'nafto[23-b]furá«^ői)-vWi| észter és foszförsav l-|4j-3fe5(ö-3%493a-tetrablcirx>-nafto[2,3-b]furán->2-i{}-vÍnÍífeter-ditr\ettlészter és ennek egy gyógyászatiiag elfogadható sója vagy szóivá^ és fii) egy kötőanyag, hordozó vagy oldószer, tumor-dsséif gátiásápan való felhasználásra olyan rak kezelésének esetén, amelynek ismerten vannak tumor-őssejtjei Is aberrált Stat3 útyönsImktMíása, olyan betegeknél., akiknek erre szükségük van, .ahol a kötőanyag, hordozó vagy oldószer a következőket tartalmazza:: lipkl a következő csoportból választva: tozfoiipid, szintetikus foszfefidii-koítn, tefmészétés foszfatidii-kolin, szfingomielin, semmid, foszfatidÜ-etanolemin, fosrfaüdil-glicerin, foszfadósav, koleszterin, koleszterin-szulfát, valamint haptén és poíietüeg-glikol (PEG) által konjogát fpdek intravénás adagoláshoz; vagy viaszos anyag a következő csoporfbél választve:: hiono-, dl- vágy fn-'gllééridóló 8 PEi mono- és di-zslrsa vészterel, PEéhgei: konjugáít g-vItatni « is ©eldcire: orális: adagoláshoz;: vagy a kötőanyag, hordozó vagy oldószer formája a kővetkező csoportból választott: miceíiáris emulzió,: szüszpenzié és nanorészecskés szuszpeozsé, továbbá tartalmaz még humán albumint Intravénás adagoláshoz, óz 1. igénypont szerinti felhasználású készítmény, ahol a készítmény a tumor-őssejt önmegújulását gátolja;. Az i. Igénypont szerinti felhasználású készítmény,: áhoka készítmény megöli éi tomon-össesiaket. Az 1, igénypont szerinti; felhasználásó vegyöfet ahol a rák fajtája a; kővetkező: csopcríhöi választott: emlődaganat, feji és nyak! daganat, tüdőrák, petefészefedaganat, hasnyálmirigy-daganat, kolorektális ksrcmőma, prosztatarák, melanoma, szarkoma, májdagaoat agydaganatok, myeloma multiplex és leukémia. Az l, Igénypont szerinti: felhasználású készítmény,. ahol; a rák metásztatskos. kemoterápiára vagy radfeterápiára: nem reagáló vagy a kezdeti kezelés után visszaeső. Az 1. igénypont szerinti felhasználású készítmény, alpi a rák a; következő csoportból; választott;: májdapnaí. feji és nyak! daganat, hasnyátalrlgy-tíagángt,: gypmorrék. yssérál, m*Mm, pfeelóma multiplex, metasztatikus emiőőageoat, ieakémla, limfóma, hyeíőcsőrafe agydaganat, giiőrna, hugyhólyagrák, endometriáiis daganat pajzsmlógyrák, epevezeíék-daganat, csontrák. skémrák IrétirmMasltbmal epeboíysgrék, ihifölskíspga^si;, -vastagbéldaganai, komrektáiis ^lamat, ^liiíri|^rá%: öír-garSí daganat, emlőrák, tüdőrák, prosztatarák, pet.##«^|k, risébnyffcráfc, melanoma és bőrrák:. ^ &&igénypont sxeríníí ifelhasanálásu késkftmány, ahol a rak kolöíéktiks rák, & & 6. igénypont szerinti ftelhasknálású készítmény, ahol a tik gyomorrak.: A $, Igé rsy:pí>nt »ÉI fáiba sznáiásct ü^ltmé hy, ahol a rák; nyéiocsősá k.
- 10. Az 1-S. igénypont bármelyike szsrmíi félhasznáiásó készítmény; aboí » M$ziímé«y· orális adagolasó ás napi négyszeri adagolásnál\-mm gyakoribb CQ.ID).
- 31. Az 1--6. Igénypont bármelyike szerinti felhasználású készítmény, ahol a készítményt l-'big/ro2 és kérölbélul 50 SÖÖ mg/mM^l közötti dózisban alkalmazzék.
- 12. Az 3 igénypont bármelyiké szerinti feidesználésu shot a Ms?ftm#nyl íö mg/nv és kör bibéiül §0 0(50 ?r5gymí £P0f közötti dózisban alkalmazzuk, 13 Az x, sgéeyppnt szerinti feihssznáíásó készítmény, ahol a vegyuiei 2meetrina0af2f3-b)fu;rán-á3· dión.
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US97114407P | 2007-09-10 | 2007-09-10 | |
US1337207P | 2007-12-13 | 2007-12-13 |
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HUE027443T2 true HUE027443T2 (hu) | 2016-10-28 |
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Application Number | Title | Priority Date | Filing Date |
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HUE08830619A HUE027443T2 (hu) | 2007-09-10 | 2008-09-10 | Stat3 útvonal gátlók újszerû csoportja és tumor-õssejt útvonal gátlók |
HUE08830633A HUE029111T2 (hu) | 2007-09-10 | 2008-09-10 | Rák kezelését célzó új készítmények és módszerek |
HUE08830471A HUE027657T2 (hu) | 2007-09-10 | 2008-09-10 | Új STAT3 útvonal inhibitorok és rák-õssejt inhibitorok |
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HUE08830633A HUE029111T2 (hu) | 2007-09-10 | 2008-09-10 | Rák kezelését célzó új készítmények és módszerek |
HUE08830471A HUE027657T2 (hu) | 2007-09-10 | 2008-09-10 | Új STAT3 útvonal inhibitorok és rák-õssejt inhibitorok |
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US (12) | US9732055B2 (hu) |
EP (6) | EP3058941B1 (hu) |
JP (16) | JP5688840B2 (hu) |
CN (6) | CN104586832B (hu) |
CA (4) | CA2736532C (hu) |
CY (3) | CY1117604T1 (hu) |
DK (4) | DK2190429T3 (hu) |
ES (3) | ES2584904T3 (hu) |
HK (3) | HK1148906A1 (hu) |
HR (3) | HRP20160430T1 (hu) |
HU (3) | HUE027443T2 (hu) |
PL (4) | PL2200431T3 (hu) |
PT (2) | PT2194987T (hu) |
SI (3) | SI2194987T1 (hu) |
WO (3) | WO2009036059A2 (hu) |
Families Citing this family (130)
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CN101155579B (zh) | 2005-02-03 | 2012-10-31 | 综合医院公司 | 治疗吉非替尼耐药性癌症的方法 |
CN103110948A (zh) | 2005-11-04 | 2013-05-22 | 惠氏公司 | mTOR抑制剂、赫赛汀和/或HKI-272的抗肿瘤组合 |
US9732055B2 (en) * | 2007-09-10 | 2017-08-15 | Boston Biomedical, Inc. | Compositions and methods for cancer treatment |
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 |
US20130331294A1 (en) | 2007-11-09 | 2013-12-12 | Fox Chase Cancer Center | Egfr/nedd9/tgf-beta interactome and methods of use thereof for the identification of agents having efficacy in the treatment of hyperproliferative disorders |
WO2009062199A1 (en) * | 2007-11-09 | 2009-05-14 | Fox Chase Cancer Center | EGFR/NEDD9/TGF-β LNTERACTOME AND METHODS OF USE THEREOF FOR THE IDENTIFICATION OF AGENTS HAVING EFFICACY IN THE TREATMENT OF HYPERPROLIFERATIVE DISORDERS |
UY31800A (es) * | 2008-05-05 | 2009-11-10 | Smithkline Beckman Corp | Metodo de tratamiento de cancer usando un inhibidor de cmet y axl y un inhibidor de erbb |
KR20130088908A (ko) | 2008-06-17 | 2013-08-08 | 와이어쓰 엘엘씨 | Hki-272 및 비노렐빈을 함유하는 항신생물성 조합물 |
EA020766B1 (ru) | 2008-07-08 | 2015-01-30 | Борд Оф Риджентс, Дзе Юниверсити Оф Техас Систем | Ингибиторы пролиферации и активации переносчика сигнала и активатора транскрипции (stats) |
CN109464445A (zh) | 2008-08-04 | 2019-03-15 | 惠氏有限责任公司 | 4-苯胺基-3-氰基喹啉和卡培他滨的抗肿瘤组合 |
EP2370082A4 (en) * | 2008-12-01 | 2012-05-30 | Univ Central Florida Res Found | FOR BELLY CANCER CELLS CYTOTOXIC DRUG COMPOSITION |
ES2941894T3 (es) | 2009-04-06 | 2023-05-26 | Wyeth Llc | Régimen de tratamiento que utiliza neratinib contra el cáncer de mama |
CN101897979B (zh) * | 2009-05-27 | 2012-08-22 | 上海市计划生育科学研究所 | 治疗前列腺疾病的靶向药物 |
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