发明名称 PHARMACEUTICAL COMPOSITIONS AND ADMINISTRATIONS THEREOF
摘要 The present invention relates to pharmaceutical compositions comprising a compound of Formula I in combination with one or both of a Compound of Formula II and/or a Compound of Formula III. The invention also relates to solid forms and to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis.;
申请公布号 US2016067239(A9) 申请公布日期 2016.03.10
申请号 US201514603779 申请日期 2015.01.23
申请人 Vertex Pharmaceuticals Incorporated 发明人 Van Goor Fredrick F.;Alargova Rossitza Gueorguieva;Alcacio Tim Edward;Arekar Sneha G.;Johnston Steven C.;Kadiyala Irina Nikolaevna;Keshavarz-Shokri Ali;Krawiec Mariusz;Lee Elaine Chungmin;Medek Ales;Mudunuri Praveen;Sullivan Mark Jeffrey;Zaman Noreen Tasneem;Zhang Beili;Zhang Yuegang;Zlokarnik Gregor
分类号 A61K31/47;A61K31/404;G01N33/50;A61K31/443 主分类号 A61K31/47
代理机构 代理人
主权项 1. A pharmaceutical composition comprising: A. A Compound of Formula I or a pharmaceutically acceptable salt thereof, wherein: Each of WRW2 and WRW4 is independently selected from CN, CF3, halo, C2-6 straight or branched alkyl, C3-12 membered cycloaliphatic, phenyl, a 5-10 membered heteroaryl or 3-7 membered heterocyclic, wherein said heteroaryl or heterocyclic has up to 3 heteroatoms selected from O, S, or N, wherein said WRW2 and WRW4 is independently and optionally substituted with up to three substituents selected from —OR′, —CF3, —OCF3, SR′, S(O)R′, SO2R′, —SCF3, halo, CN, —COOR′, —COR′, —O(CH2)2N(R′)2, —O(CH2)N(R′)2, —CON(R′)2, —(CH2)2OR′, —(CH2)OR′, —CH2CN, optionally substituted phenyl or phenoxy, —N(R′)2, —NR′C(O)OR′, —NR′C(O)R′, —(CH2)2N(R′)2, or —(CH2)N(R′)2; WRW5 is selected from hydrogen, —OCF3, —CF3, —OH, —OCH3, —NH2, —CN, —CHF2, —NHR′, —N(R′)2, —NHC(O)R′, —NHC(O)OR′, —NHSO2R′, —CH2OH, —CH2N(R′)2, —C(O)OR′, —SO2NHR′, —SO2N(R′)2, or —CH2NHC(O)OR′; and Each R′ is independently selected from an optionally substituted group selected from a C1-8 aliphatic group, a 3-8-membered saturated, partially unsaturated, or fully unsaturated monocyclic ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur, or an 8-12 membered saturated, partially unsaturated, or fully unsaturated bicyclic ring system having 0-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or two occurrences of R′are taken together with the atom(s) to which they are bound to form an optionally substituted 3-12 membered saturated, partially unsaturated, or fully unsaturated monocyclic or bicyclic ring having 0-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; provided that: iii) WRW2 and WRW4 are not both —Cl; WRW2, WRW4 and WRW5 are not —OCH2CH2Ph, —OCH2CH2(2-trifluoromethyl-phenyl), —OCH2CH2-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl), or substituted 1H-pyrazol-3-yl; and one or both of the following: B. A Compound of Formula II or pharmaceutically acceptable salts thereof, wherein: T is —CH2—, —CH2CH2—, —CF2—, —C(CH3)2—, or —C(O)—; R1′ is H, C1-6 aliphatic, halo, CF3, CHF2, O(C1-6 aliphatic); and RD1 or RD2 is ZDR9 wherein:ZD is a bond, CONH, SO2NH, SO2N(C1-6 alkyl), CH2NHSO2, CH2N(CH3)SO2, CH2NHCO, COO, SO2, or CO; andR9 is H, C1-6 aliphatic, or aryl; and/or C. A Compound of Formula III or pharmaceutically acceptable salts thereof, wherein: R is H, OH, OCH3 or two R taken together form —OCH2O— or —OCF2O—; R4 is H or alkyl; R5 is H or F; R6 is H or CN; R7 is H, —CH2CH(OH)CH2OH, —CH2CH2N+(CH3)3, or —CH2CH2OH; R8 is H, OH, —CH2CH(OH)CH2OH, —CH2OH, or R7 and R8 taken together form a five membered ring.
地址 Boston MA US