ME00152B - Nove farmaceutske kompozicije 4-(4-(3-(4-hlor0 -3-trifluorometil-fenil)-ureid0)-3-fluoro-fenoksi)piridin-2-karbonska kiseline za lečenje hiper-prolifera tivnih poremećaja - Google Patents
Nove farmaceutske kompozicije 4-(4-(3-(4-hlor0 -3-trifluorometil-fenil)-ureid0)-3-fluoro-fenoksi)piridin-2-karbonska kiseline za lečenje hiper-prolifera tivnih poremećajaInfo
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- ME00152B ME00152B MEP-2008-358A MEP2008358A ME00152B ME 00152 B ME00152 B ME 00152B ME P2008358 A MEP2008358 A ME P2008358A ME 00152 B ME00152 B ME 00152B
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- 238000011282 treatment Methods 0.000 title claims abstract 4
- 230000003463 hyperproliferative effect Effects 0.000 title claims abstract 3
- BZESFMLUNMTDFR-UHFFFAOYSA-N 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]-3-fluorophenoxy]pyridine-2-carboxylic acid Chemical compound C1=NC(C(=O)O)=CC(OC=2C=C(F)C(NC(=O)NC=3C=C(C(Cl)=CC=3)C(F)(F)F)=CC=2)=C1 BZESFMLUNMTDFR-UHFFFAOYSA-N 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract 16
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- 150000001875 compounds Chemical class 0.000 claims abstract 12
- 206010028980 Neoplasm Diseases 0.000 claims abstract 5
- 201000011510 cancer Diseases 0.000 claims abstract 5
- 238000002560 therapeutic procedure Methods 0.000 claims abstract 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims 25
- 239000011159 matrix material Substances 0.000 claims 10
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 5
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- 229920002785 Croscarmellose sodium Polymers 0.000 claims 4
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims 4
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- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 2
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
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- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims 1
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- YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 claims 1
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- 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
- A61K31/435—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
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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
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- A61K31/4415—Pyridoxine, i.e. Vitamin B6
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Abstract
Ovaj pronalazak se odnosi na nove farmaceutske kompozicije koje se sastoje od čvrste disperzije jedinjenja Formule (I), napostupke za pripremanje ovih novih farmaceutskih kompozicija i na njihovu upotrebu za lečenje hiper-proliferativnih poremećaja, kao što je kancer, bilo kao samostalno sredstvo ili u kombinaciji sa drugim terapijama.
Claims (35)
1.Kompozicija, naznačena time , što sadrži 4{4-[3-(4-hloro-3- trifluorometilfenil) -ureido]-3-fluorofenoksi}-piridin-2-karbonska kiselina metil amid i/ili njegove soli, hidrate. solvate u obliku čvrste disperzije.
2.Kompozicija, naznačena time , što se sastoji od čvrste suspenzije koja sadrži bar jedno jedinjenje Formule l i farmaceutski prihvatljivu matricu.
3.Kompozicija prema zahtevu 2, naznačena time , što se matrica sastoji od polimernih vezivnih sredstava ili ne-polimernih vezivnih sredstava koja su sposobna da rastvore ili disperguju jedinjenje Formule l.
4.Kompozicija prema zahtevu 2, naznačena time, što se matrica sastoji od kombinacije polimernih vezivnih sredstava i ne-polimernih vezivnih sredstava koja su sposobna da rastvore ili disperguju jedinjenje Formule l.
5.Kompozicija prema zahtevu 2, naznačena time , što se matrica sastoji od u vodi rastvorljivog polimera.
6.Kompozicija prema zahtevu 5, naznačena time, što se matrica sastoji od bar jednog polimera iz grupe koja sadrži polivinilpirolidon, copovidon, hidroksipropil celulozu, hidroksipropil metil celulozu, polietilen glikol ili polietilen oksid.
7.Kompozicija prema zahtevu 6, naznačena time, što se upotrebljava polivinilpirolidon kao sredstvo matrice.
8.Kompozicija prema zahtevu 7, naznačena time, što je maseni odnos jedinjenja Formule l izračunat kao rastvarač-slobodna baza prema polivinilpirolidonu između 1:0,5 i 1:20.
9.Kompozicija prema zahtevu 6, naznačena time , što se upotrebljava hidroksipropil celuloza kao sredstvo matrice.
10.Kompozicija prema zahtevu 9, naznačena time , što je maseni odnos jedinjenja Formule l izračunat kao rastvarač-slobodna baza prema hidroksipropil celulozi između 1:0,5 i 1:20.
11.Kompozicija prema bilo kom od prethodnih zahteva, naznačena time , što se čvrsta disperzija sastoji od kroskarmeloza natrijuma, natrijum skrob glikolata, krospovidona, nisko supstituisane hidroksipropil celuloze, skroba, mikrokristalne celuloze ili njihovih kombinacija.
12.Kompozicija prema zahtevu 8, naznačena time , što čvrsta disperzija sadrži polivinilpirolidon i kroskarmeloza natrijum.
13.Kompozicija prema zahtevu 8, naznačena time , što čvrsta disper zija sadrži polivinilpirolidon i natrijum skrob glikolat.
14.Kompozicija prema zahtevu 8, naz načena time , što čvrsta disperzija sadrži polivinilpirolidon, kroskarmeloza natrijum i mikrokristalnu celulozu.
15.Kompozicija prema zahtevu 1 O, naznačena time , što čvrsta disperzija sadrži hidroksipropil celulozu i kroskarmeloza natrijum.
16.Kompozicija prema zahtevu 1O, naznačena time, što čvrsta dispeizija sadrži hidroksipropil celulozu i bar jedno vezivno sredstvo koje je šećer, šećerni alkohol, ciklodekstrin.
17.Kompozicija prema bilo kom od prethodnih zahteva, na značena time, što je čvrsta disperzija suštinski homogena.
18.Kompozicija prema bilo kom od prethodnih zahteva, na značena time , što sadrži jedinjenje Formule l u suštinski amorfnom obliku.
19.Kompozicija kako je zatražena zaštita prema bilo kom od prethodnih zahteva, naznačena time , što predstavlja farmaceutsku kompoziciju za oralnu davanje.
20.Kompozicija kako je zatražena zaštita prema bilo kom od prethodnih zahteva, naznačena time , što predstavlja farmaceutsku kompoziciju u obliku tablete.
21.Kompozicija kako je zatražena zaštita prema bilo kom od prethodnih zahteva, naznačena time , što predstavlja farmaceutsku kompoziciju u obliku kapsule.
22.Kompozicija kako je zatražena zaštita prema bilo kom od prethodnih zahteva, naznačena time , što predstavlja farmaceutsku kompoziciju u obliku pudera, granulata ili kesice.
23.Postupak za pripremanje čvrste disperzije jedinjenja Formule l ,naznačen time, što se sastoji od simultanog izlaganja jedinjenja Formule l i bar jednog sredstva matrice istiskivanju vrele otopine, oblaganju vrelom otopinom, očvršćivanja rasprskavanjem, zamrzavanjem, tehnikama isparavanja rastvarača ili njihovim kombinacijama.
24.Postupak prema zahtevu 23, naznačen time , što se čvrsta disperzija priprema izlaganjem jedinjenja Formule l i bar jednog sredstva matrice istiskivanju vrele otopine.
25.Postupak prema zahtevu 23, naznačen time , što se čvrsta disperzija priprema izlaganjem jedinjenja Formule l i bar jednog sredstva matrice tehnikama isparavanja rastvarača.
26.Postupak prema zahtevu 25, naznačen time , što se rastvarač sastoji od jednog ili više rastvarač odabranih od grupe koja sadrži metanol, etanol, n-propanol, izopropanol i aceton.
27.Postupak prema zahtevu 26, naznačen time , što se kao rastvarač upotrebljava smeša etanola i acetona.
28.Postupak kako je zatražena zaštita u zahtevima 23 do 27, naznačen time, što se čvrsta disperzija dalje tretira bar sa još jednim korakom u postupku, kao što je mlevenje, prosejavanje, valjanje radi postizanja kompaktnosti, drobljenje, sejanje, smešanje ili njihova kombinacija.
29.Postupak kako je zatražena zaštita u zahtevima 23 do 28, naznačen time , što se sastoji od dodatnog koraka stvaranja jedinjenja čvrste disperzije sa jednim ili više farmaceutski prihvatljivih vezivnih sredstava da se formira smeša i oblikovanja ove smeše u tablete, punjene kapsule i kesice.
30.Farmaceutska kompozicija, naznačena time , što se uvek proizvodi postupkom bilo kog od zahteva 23 do 29.
31.Postupak za lečenje hiper-proliferativnih poremećaja, naznačen time , što se sastoji od davanja farmaceutske kompozicije prema bilo kom od zahteva 1 do 22 i 30 sisaru, uključujući čoveka, bilo kao jedino sredstvo ili u kombinaciji sa drugim terapijama.
32.Postupak za lečenje kancera, naznačen time, što se sastoji od davanja farmaceutske kompozicije prema bilo kom od zahteva 1 do 22 i 30 sisaru, uključujući čoveka, bilo kao jedino sredstvo ili u kombinaciji sa drugim terapijama.
33.Postupak za lečenje kancera, naznačen time, što se sastoji od davanja farmaceutske kompozicije prema bilo kom od zahteva 1 do 22 i 30 sisaru, uključujući čoveka, bilo kao jedino sredstvo ili u kombinaciji sa radioaktivnom terapijom.
34.Postupak za lečenje kancera, naznačen time, što se sastoji od davanja farmaceutske kompozicije prema bilo kom od zahteva 1 do 22 i 30 sisaru, uključujući čoveka, u kombinaciji sa citotoksičnom terapijom.
35.Postupak za lečenje kancera, naznačen time , što se sastoji od davanja farmaceutske kompozicije prema bilo kom od zahteva 1 do 22 i 30 sisaru, uključujući čoveka, u kombinaciji sa nekom drugom anti-kancer terapijom koja cilja bilo VEGFR, PDGFR, src, abi flt-3, EGFR, HER-2, aurora, raf, MEK, ERK, Pl-3 kinazu, AKT, mTOR, ili HDAC.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60475204P | 2004-08-27 | 2004-08-27 | |
| PCT/US2005/030541 WO2006026500A1 (en) | 2004-08-27 | 2005-08-29 | New pharmaceutical compositions comprising 4-(4-(3-(4-chloro-3-trifluoromethyl-phenyl)-ureido)-3-fluoro-phenoxy)-pyridine-2-carboxylic acid for the treatment of hyper-proliferative disorders |
Publications (1)
| Publication Number | Publication Date |
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| ME00152B true ME00152B (me) | 2010-10-10 |
Family
ID=35517032
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2008-358A ME00152B (me) | 2004-08-27 | 2005-08-29 | Nove farmaceutske kompozicije 4-(4-(3-(4-hlor0 -3-trifluorometil-fenil)-ureid0)-3-fluoro-fenoksi)piridin-2-karbonska kiseline za lečenje hiper-prolifera tivnih poremećaja |
| MEP-358/08A MEP35808A (en) | 2004-08-27 | 2005-08-29 | New pharmaceutical compositions comprising 4-(4-(3-(4-chloro-3-trifluoromethyl-phenyl)-ureido)-3-fluoro-phenoxy)-pyridine-2-carboxylic acid for the treatment of hyper-proliferative disorders |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-358/08A MEP35808A (en) | 2004-08-27 | 2005-08-29 | New pharmaceutical compositions comprising 4-(4-(3-(4-chloro-3-trifluoromethyl-phenyl)-ureido)-3-fluoro-phenoxy)-pyridine-2-carboxylic acid for the treatment of hyper-proliferative disorders |
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| EP (2) | EP2589384A1 (me) |
| JP (1) | JP5017115B2 (me) |
| KR (1) | KR101336737B1 (me) |
| CN (2) | CN102885813A (me) |
| AR (1) | AR050616A1 (me) |
| AU (1) | AU2005279996A1 (me) |
| BR (1) | BRPI0514715B1 (me) |
| CA (1) | CA2578438C (me) |
| CL (1) | CL2010001484A1 (me) |
| CR (1) | CR8980A (me) |
| CY (1) | CY2017038I2 (me) |
| DK (1) | DK1793824T3 (me) |
| EA (1) | EA010832B1 (me) |
| EC (1) | ECSP077299A (me) |
| ES (1) | ES2561618T3 (me) |
| GT (1) | GT200500230A (me) |
| HN (1) | HN2005000484A (me) |
| HR (1) | HRP20160156T1 (me) |
| HU (2) | HUE026654T2 (me) |
| IL (1) | IL181590A (me) |
| LT (1) | LTC1793824I2 (me) |
| LU (1) | LUC00047I2 (me) |
| MA (1) | MA28911B1 (me) |
| ME (2) | ME00152B (me) |
| MX (1) | MX2007002397A (me) |
| MY (1) | MY191349A (me) |
| NI (1) | NI200700064A (me) |
| NO (2) | NO343937B1 (me) |
| NZ (1) | NZ553557A (me) |
| PE (2) | PE20100432A1 (me) |
| PL (1) | PL1793824T3 (me) |
| PT (1) | PT1793824E (me) |
| RS (1) | RS54580B1 (me) |
| SI (1) | SI1793824T1 (me) |
| TN (1) | TNSN07076A1 (me) |
| TW (1) | TWI369987B (me) |
| UA (1) | UA92472C2 (me) |
| UY (1) | UY29086A1 (me) |
| WO (1) | WO2006026500A1 (me) |
| ZA (1) | ZA200702392B (me) |
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- 2005-08-25 MY MYPI20054000A patent/MY191349A/en unknown
- 2005-08-26 US US11/212,109 patent/US20060058358A1/en not_active Abandoned
- 2005-08-26 AR ARP050103568A patent/AR050616A1/es not_active Application Discontinuation
- 2005-08-26 HN HN2005000484A patent/HN2005000484A/es unknown
- 2005-08-26 UY UY29086A patent/UY29086A1/es not_active Application Discontinuation
- 2005-08-26 PE PE2010000029A patent/PE20100432A1/es active IP Right Grant
- 2005-08-26 TW TW094129395A patent/TWI369987B/zh not_active IP Right Cessation
- 2005-08-26 PE PE2005000984A patent/PE20060505A1/es active IP Right Grant
- 2005-08-26 GT GT200500230A patent/GT200500230A/es unknown
- 2005-08-29 EP EP13151040.6A patent/EP2589384A1/en not_active Withdrawn
- 2005-08-29 ME MEP-2008-358A patent/ME00152B/me unknown
- 2005-08-29 DK DK05792486.2T patent/DK1793824T3/en active
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- 2005-08-29 BR BRPI0514715-8A patent/BRPI0514715B1/pt active IP Right Grant
- 2005-08-29 ES ES05792486.2T patent/ES2561618T3/es not_active Expired - Lifetime
- 2005-08-29 EP EP05792486.2A patent/EP1793824B1/en not_active Revoked
- 2005-08-29 ME MEP-358/08A patent/MEP35808A/xx unknown
- 2005-08-29 KR KR1020077006801A patent/KR101336737B1/ko not_active Expired - Lifetime
- 2005-08-29 RS RS20160039A patent/RS54580B1/sr unknown
- 2005-08-29 CA CA2578438A patent/CA2578438C/en not_active Expired - Lifetime
- 2005-08-29 HR HRP20160156TT patent/HRP20160156T1/hr unknown
- 2005-08-29 HU HUE05792486A patent/HUE026654T2/en unknown
- 2005-08-29 AU AU2005279996A patent/AU2005279996A1/en not_active Abandoned
- 2005-08-29 MX MX2007002397A patent/MX2007002397A/es active IP Right Grant
- 2005-08-29 CN CNA2005800371513A patent/CN101287463A/zh active Pending
- 2005-08-29 JP JP2007533489A patent/JP5017115B2/ja not_active Expired - Lifetime
- 2005-08-29 WO PCT/US2005/030541 patent/WO2006026500A1/en not_active Ceased
- 2005-08-29 SI SI200532037T patent/SI1793824T1/sl unknown
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2007
- 2007-02-26 TN TNP2007000076A patent/TNSN07076A1/en unknown
- 2007-02-27 IL IL181590A patent/IL181590A/en active IP Right Grant
- 2007-02-27 NI NI200700064A patent/NI200700064A/es unknown
- 2007-03-05 EC EC2007007299A patent/ECSP077299A/es unknown
- 2007-03-07 CR CR8980A patent/CR8980A/es unknown
- 2007-03-22 ZA ZA200702392A patent/ZA200702392B/xx unknown
- 2007-03-22 MA MA29767A patent/MA28911B1/fr unknown
- 2007-03-26 NO NO20071584A patent/NO343937B1/no active Protection Beyond IP Right Term
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2010
- 2010-12-20 CL CL2010001484A patent/CL2010001484A1/es unknown
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2016
- 2016-03-22 LT LTPA2016008C patent/LTC1793824I2/lt unknown
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2017
- 2017-01-27 US US15/417,469 patent/US20170165243A1/en not_active Abandoned
- 2017-11-08 LU LU00047C patent/LUC00047I2/fr unknown
- 2017-11-09 CY CY2017038C patent/CY2017038I2/el unknown
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2019
- 2019-08-05 NO NO2019033C patent/NO2019033I1/no unknown
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