JP6687248B2 - 回腸−空腸薬物送達用組成物 - Google Patents
回腸−空腸薬物送達用組成物 Download PDFInfo
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- JP6687248B2 JP6687248B2 JP2017533932A JP2017533932A JP6687248B2 JP 6687248 B2 JP6687248 B2 JP 6687248B2 JP 2017533932 A JP2017533932 A JP 2017533932A JP 2017533932 A JP2017533932 A JP 2017533932A JP 6687248 B2 JP6687248 B2 JP 6687248B2
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- oral preparation
- cellulose
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- 125000001544 thienyl group Chemical group 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229960004906 thiomersal Drugs 0.000 description 1
- 125000005505 thiomorpholino group Chemical group 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 210000003371 toe Anatomy 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical class CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- JEJAMASKDTUEBZ-UHFFFAOYSA-N tris(1,1,3-tribromo-2,2-dimethylpropyl) phosphate Chemical compound BrCC(C)(C)C(Br)(Br)OP(=O)(OC(Br)(Br)C(C)(C)CBr)OC(Br)(Br)C(C)(C)CBr JEJAMASKDTUEBZ-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
- 229920001664 tyloxapol Polymers 0.000 description 1
- MDYZKJNTKZIUSK-UHFFFAOYSA-N tyloxapol Chemical compound O=C.C1CO1.CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 MDYZKJNTKZIUSK-UHFFFAOYSA-N 0.000 description 1
- 229960004224 tyloxapol Drugs 0.000 description 1
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 description 1
- 229950001544 verdinexor Drugs 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
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Description
本出願は、参照によりその内容が本明細書に援用される2014年12月24日に出願された米国仮特許出願第62/096,812号明細書に対する優先権の利益を主張するものである。
本開示は、胃では活性成分を放出せず、小腸の回腸及び空腸で薬物分子を実質的に放出する、可逆的又は非可逆的な共有結合性薬物分子を含有する経口医薬製剤、ならびに例えば癌及び自己免疫疾患などの、かかる化合物での治療が可能な疾患の治療のためのこれら製剤の使用を提供する。
結合性マイケル受容体含有薬剤の低い経口生体利用効率の原因となっている可能性もある(例えば、Johnson D. S., et. al., Future Med Chem. 2010 June 1; 2(6):949-964、及び Potashman M. H. et al. J. Med. Chem., Vol 52, No. 5. Pgs. 1231-1246を参照のこと)。 例えば、システインプロテアーゼ、ペプシンなどの消化酵素、輸送体、及び例えば胃粘膜中のCYP酵素などの代謝酵素の組み合わせによって、低いpHでの可逆的及び不可逆的な共有結合性マイケル受容体の化学的及び/又は代謝的な高い転換が生じる場合がある。したがって、低pH、及び消化酵素又は代謝酵素の組み合わせ、ならびに他のチオール源が生じる胃に対する可逆的及び不可逆的な共有結合性薬剤の曝露を回避することにより、これら薬剤の全身曝露の大幅な上昇を獲得し得る。したがって、胃に対する曝露の回避は、例えば下痢、及び俗に嘔吐と言われる悪心などのこれら薬剤の有害な副作用の可能性が低下又は完全に排除され得る。
ングにより覆われたコアを含有する固形経口製剤が提供される。
結合を通り引かれた直線「
識される患者に本明細書に開示される固形経口医薬製剤を投与することを含む。1つの実施形態において、チロシンキナーゼはBTKである。
J. Exp. Med. 2000 192:1611)。
Ar1は、置換アリール又は置換ヘテロアリールであり、
Zは、結合、アルキレン、シクロアルキレン、O、−アルキレン−O−、NRa、−(アルキレン)−NRa−(各Raは水素、アルキル、又はシクロアルキルである)、又は式IIに相当する断片であり、
Rbは、シアノ、ニトロ、ハロ、ハロアルキル、ハロアルコキシ、アルキルチオ、又はアルキルスルホニルであり、
Rcは、アルキル、ハロアルコキシ、置換アルキル、シクロアルキル、シクロアルキレンNRdReもしくはシクロアルキレン(アルキレン)NRdRe(Rd及びReは独立して水素、アルキル、又はシクロアルキルである)、又はN、O及びSから選択される1つまたは2つのヘテロ原子を含有する3〜6員の飽和単環ヘテロシクリルであり、任意選択的にヒドロキシ、アルキル及びフルオロから独立して選択される1つまたは2つの置換基で置換されている。
ミノイミダゾ[1,2−a]ピラジニル、8−アミノイミダゾ[1,2−a]ピリジニル、8−アミノ−[1,2,4]トリアゾロ[1,5−a]ピリジニル、又は本明細書に定義されるように置換されたベンズイミダゾリルである。
(R)−4−(8−アミノ−3−(1−(ブタ−2−イノイル)ピロリジン−2−イル)イミダゾ[1,5−a]ピラジン−1−イル)−N−(ピリジン−2−イル)ベンズアミド、
(S)−7−(1−アクリロイルピペリジン−4−イル)−2−(4−フェノキシフェニル)−4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピリミジン−3−カルボキサミド、
(S)−7−(1−(ブタ−2−イノイル)ピペリジン−4−イル)−2−(4−フェノキシフェニル)−4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピリミジン−3−カルボキサミド、
N−(3−((2−((2−メトキシ−4−(4−メチルピペラジン−1−イル)フェニル)アミノ)チエノ[3,2−d]ピリミジン−4−イル)オキシ)フェニル)アクリルアミド、
1−(3−((2−((4−(4−メチルピペラジン−1−イル)フェニル)アミノ)−[1,2,4]トリアゾロ[1,5−a]ピリジン−8−イル)オキシ)フェニル)プロパ−2−エン−1−オン、
(R)−6−アミノ−9−(1−(ブタ−2−イノイル)ピロリジン−3−イル)−7−(4−フェノキシフェニル)−7H−プリン−8(9H)−オン、
N−(2−((6−((5−(5−フルオロ−2−(ヒドロキシメチル)−3−(4−オキソ−6,7,8,9−テトラヒドロベンゾ[4,5]チエノ[2,3−d]ピリダジン−3(4H)−イル)フェニル)−1−メチル−2−オキソ−1,2−ジヒドロピリジン−3−イル)アミノ)ピリジン−2−イル)アミノ)エチル)アクリルアミド、
N−(3−((5−フルオロ−2−((4−(2−メトキシエトキシ)フェニル)アミノ)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(S)−5−アミノ−1−(1−シアノピペリジン−3−イル)−3−(4−(2,4−ジフルオロフェノキシ)フェニル)−1H−ピラゾール−4−カルボキサミド、
6−(1−アクリロイルピペリジン−4−イル)−2−(4−フェノキシフェニル)ニコチンアミド、
(R)−1−(1−アクリロイルピペリジン−3−イル)−4−アミノ−N−(5−クロロベンゾ[d]オキサゾール−2−イル)−1H−ピラゾロ[3,4−d]ピリミジン−3−カルボキサミド、
(S,E)−N−(4−((3−クロロ−4−フルオロフェニル)アミノ)−7−((テトラヒドロフラン−3−イル)オキシ)キナゾリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(R)−1−(3−(4−アミノ−3−(4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−イル)プロパ−2−エン−1−オン、
N−(2−((2−(ジメチルアミノ)エチル)(メチル)アミノ)−4−メトキシ−5−((4−(1−メチル−1H−インドール−3−イル)ピリミジン−2−イル)アミノ)フェニル)アクリルアミド、
N−(3−((2−((4−(4−アセチルピペラジン−1−イル)−2−メトキシフェニル)アミノ)−5−(トリフルオロメチル)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(E)−N−(4−((3−クロロ−4−(ピリジン−2−イルメトキシ)フェニル)アミノ)−3−シアノ−7−エトキシキノリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(E)−N−(4−((3−クロロ−4−フルオロフェニル)アミノ)−7−メトキシキナゾリン−6−イル)−4−(ピペリジン−1−イル)ブタ−2−エナミド、
1−(4−((4−((3,4−ジクロロ−2−フルオロフェニル)アミノ)−7−メトキシキナゾリン−6−イル)オキシ)ピペリジン−1−イル)プロパ−2−エン−1−オン、
N−(3−((5−フルオロ−2−((4−(2−メトキシエトキシ)フェニル)アミノ)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(E)−4−((4−((3−ブロモ−4−クロロフェニル)アミノ)ピリド[3,4−d]ピリミジン−6−イル)アミノ)−N,N−ジメチル−N−((1−メチル−4−ニトロ−1H−イミダゾール−5−イル)メチル)−4−オキソブタ−2−エン−1−アミニウムブロミド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−(ピラジン−2−イル)アクリロヒドラジド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,
4−トリアゾール−1−イル)−N’−(ピリジン−2−イル)アクリロヒドラジド、
N−((3R,4R)−4−フルオロ−1−(6−((3−メトキシ−1−メチル−1H−ピラゾール−4−イル)アミノ)−9−メチル−9H−プリン−2−イル)ピロリジン−3−イル)アクリルアミド、
N−((3S,4S)−3−((6−(2,6−ジクロロ−3,5−ジメトキシフェニル)キナゾリン−2−イル)アミノ)テトラヒドロ−2H−ピラン−4−イル)アクリルアミド、
(3E,5E)−1−アクリロイル−3,5−ビス(4−ニトロベンジリデン)ピペリジン−4−オン、
(E)−N−(7−((1R,5S,6s)−3−オキサビシクロ[3.1.0]ヘキサン−6−イルエチニル)−4−((3−クロロ−4−フルオロフェニル)アミノ)キナゾリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(3E,5E)−1−アクリロイル−3,5−ビス(4−フルオロ−3−ニトロベンジリデン)アゼパン−4−オン、
N−(2−((6−(2,6−ジクロロ−3,5−ジメトキシフェニル)キナゾリン−2−イル)アミノ)−3−メチルフェニル)アクリルアミド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−ピバロイルアクリロヒドラジド、及び
N−(2−((2−((テトラヒドロ−2H−ピラン−4−イル)アミノ)−5−(トリフルオロメチル)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド。
くはR及びR’が上述に定義される−CONRR’から独立して選択される1つ又は2つの基で任意選択的に置換されたヘテロシクリル(例えばヘテロシクロアミノ)から独立して選択される1つ、2つ、又は3つの置換基で置換された、本明細書に定義されるアルキル基を意味する。
本明細書において用いられる場合、「アルキルアミノ」とは、−NHR基を意味し、Rは上記に定義されるアルキルであり、例えばメチルアミノ、エチルアミノ、プロピルアミノ、又は2−プロピルアミノなどがある。
アルキルアミノカルボニルから独立して選択される1つ、2つ、又は3つの置換基で置換されており、例えば−CONH2、メチルアミノカルボニル、2−ジメチルアミノカルボニルなどがある。−CONRR’において、Rが水素であり、R’がアルキルである場合、この基は本明細書においてアルキルアミノカルボニルとも呼称され、−CONRR’においてR及びR’の両方がアルキルである場合、この基は本明細書においてジアルキルアミノカルボニルとも呼称される。−CONRR’において、Rが水素であり、R’が置換アルキルである場合、この基は本明細書において置換アルキルアミノカルボニルとも呼称される。
本明細書において用いられる場合、「シクロアルキル」とは、3〜10個の炭素原子の環状飽和一価炭化水素基を意味し、この場合において1個又は2個の炭素原子がオキソ基により置換されていてもよく、例えばシクロプロピル、シクロブチル、シクロペンチル、又はシクロヘキシルなどがある。
ある。
「二置換アミノ」とは、−NRR’基を意味し、R及びR’は独立して、各々本明細書に定義されるアルキル、シクロアルキル、シクロアルキルアルキル、アシル、アリール、アラルキル、ヘテロアリール、ヘテロアラルキル、ヘテロシクリル、ヘテロシクリルアルキル、又は置換アルキルであり、この場合において、単独、又は例えばアラルキルなどの他の基の一部のいずれかのアリール、ヘテロアリール又はヘテロシクリルの環は、任意選択的に、アルキル、ヒドロキシ、アルコキシ、ハロ、ハロアルキル、ハロアルコキシ、カルボキシ、アルコキシカルボニル、アルキルカルボニル、シアノ、−CONH2、アルキルアミノカルボニル、ジアルキルアミノカルボニル、又は置換アルキルアミノカルボニルから独立して選択される1つ、2つ、又は3つの置換基で置換されており、例えばジメチルアミノ、フェニルメチルアミノなどがある。R基及びR’基がアルキルである場合、二置換アミノ基は本明細書においてジアルキルアミノとも呼称され得る。
本明細書において用いられる場合、「ヘテロシクロアミノ」とは、1個又は2個の環原子が、N、O又はS(O)nから選択されるヘテロ原子である4〜8個の環原子の飽和又は不飽和の一価単環基を意味し、nは0〜2の整数であり、残りの環原子は、この環原子のうちの少なくとも1つがNである場合には、Cである。さらに、このヘテロシクロアミノ環中の1個又は2個の環炭素原子は、任意選択的に−CO−基により置換されていてもよい。このヘテロシクロアミノ環が不飽和であるとき、環が芳香族でなければ、環は1個又は2個の環二重結合を含有してもよい。
ロシクロアミノから付着されている窒素原子と共にあり;3つの置換基のうちの少なくとも1つが水素ではなく、さらには式中、上述の基のいずれかのアリール(「置換アリール」の場合を除き)、ヘテロアリール(「置換アリール」の場合を除き)、シクロアルキル、ヘテロシクロアミノ、及びヘテロシクリルの環の各々は、任意選択的に以下で置換されている:
を指し、この場合において単糖反復単位上のヒドロキシルの少なくとも一部が反応し、エーテル結合又はエステル結合を形成している。例としては、限定されないが、ヒドロキシアルキルセルロース、ヒドロキシアルキルアルキルセルロース、及びカルボキシアルキルセルロースのエステルが挙げられ、例えばヒドロキシプロピルメチルセルロース(ヒプロメロース又はHPMC)、ヒドロキシプロピルセルロース(HPC)などがある。
Co.から入手可能な商標名Methocel(商標)で販売されているものがある。低粘性グレードのヒドロキシプロピルメチルセルロースの例としては、Methocel
E5、Methocel E−15 LV、Methocel E50 LV、Methocel K100 LV、及びMethocel F50 LVの商標名で市販されているものが挙げられ、その2重量%の水溶液はそれぞれ5cP、15cP、50cP、100cP、及び50cPの粘度を有している。中粘性を有するヒドロキシプロピルメチルセルロースの例としては、Methocel E4M及びMethocel K4Mの商標名で市販されているものが挙げられ、その2重量%の水溶液は両方とも4000cpの粘度を有している。高粘性を有するヒドロキシプロピルメチルセルロースポリマーの例としては、Methocel K15M及びMethocel K100Mの商標名で販売されているものが挙げられ、その2重量%の水溶液はそれぞれ15,000cP、及び100,000cPの粘度を有している。ヒドロキシプロピルメチルセルロースポリマーは、約0.1重量%〜50重量%の量で本開示の医薬組成物中に存在していてもよい。
、セチルエステルワックス、パルミトステアリン酸グリセリン、ベヘン酸グリセリン、水素添加ヒマシ油、綿実油、脂肪酸グリセリド(モノ−、ジ−、及びトリ−グリセリド)、水素化脂肪、炭化水素、通常のワックス、ステアリン酸、ステアリルアルコール、炭化水素主鎖を有する物質、及び上述の物質の1つ以上を含有する組み合わせである。適切なワックスとしては、限定されないが、蜜ろう、Glycowax(登録商標)(N,N’−ジステアロイルエチレンジアミン、Lonza社)、キャスターワックス、カルナバワックス、及びワックス様物質が挙げられる。
であることを示す。
(Shin Etsu社))が挙げられる。 性能は、置換の程度及びタイプによって変化し得る。例えばHP−50、HP−55、HP−55S、HP−55FグレードのHPMCPなどが適切である。適切なグレードの酢酸コハク酸ヒドロキシプロピルメチルセルロースとしては、限定されないが、pH5で溶解するAS−LG(LF)、pH5.5で溶解するAS−MG(MF)、及び高いpHで溶解するAS−HG(HF)が挙げられる。これらのポリマーは顆粒として、又は水分散液用の微粉末として販売されている。
。
又は約7000〜5400の分子量を有していてもよい)、カルボキシメチルセルロースナトリウム、メチルセルロース、ポリソルベート−80、アルギン酸ナトリウム、例えばトラガカントゴム及びアカシアゴムなどのゴム、グアーガム、キサンタンガムをはじめとするキサンタン、糖類、例えばカルボキシメチルセルロースナトリウム、メチルセルロース、カルボキシメチルセルロースナトリウムなどのセルロース誘導体、ポリソルベート−80、アルギン酸ナトリウム、ポリエトキシ化ソルビタンモノラウレート、ポリエトキシ化ソルビタンモノラウレート、ポビドン、カルボマー、ポリビニルアルコール(PVA)、アルギン酸塩、キトサン類、及びそれらの組み合わせなどの、例えば親水性ポリマー、電解質、Tween(登録商標)20、60又は80、PEG、ポリビニルピロリドン(PVP、Plasdone(登録商標)として市販)、及び炭水化物ベースの分散剤が挙げられる。
イモデンプンなどの天然デンプン、例えばNational1551などのアルファデンプン、又は例えばPromogel(登録商標)もしくはExplotab(登録商標)などのデンプングリコール酸ナトリウムなどのデンプン、例えば木製品などのセルロース、例えばAvicel(登録商標)、Avicel(登録商標)PH101、Avicel(登録商標)PH 102、Avicel(登録商標)PH105、Elceme(登録商標)P100、Emcocel(登録商標)、Vivacel(登録商標)、及びSolka−Floc(登録商標)などの微晶質セルロースメチル、メチルセルロース、クロスカルメロース、又は例えば架橋カルボキシメチルセルロースナトリウム(Ac−di−sol(登録商標))などの架橋セルロース、架橋カルボキシメチルセルロース、又は架橋クロスカルメロース、例えばデンプングリコール酸ナトリウムなどの架橋デンプン、例えばクロスポビドンなどの架橋ポリマー、架橋ポリビニルピロリドン、例えばアルギン酸などのアルギン酸塩、例えばアルギン酸ナトリウムなどのアルギン酸の塩、例えばVeegum(登録商標)HVなどの粘土(ケイ酸アルミニウムマグネシウム)、例えばアガー、グアー、イナゴマメ、Karaya、ペクチンもしくはトラガカントなどのゴム、デンプングリコール酸ナトリウム、ベントナイト、海綿、界面活性剤、例えばカチオン交換樹脂などの樹脂、柑橘ジュース粕、ラウリル硫酸ナトリウム、デンプンと組み合わせたラウリル硫酸ナトリウムなどが挙げられる。
ゼ阻害剤、及び/又はその薬学的に受容可能な塩、(b)空腸及び回腸から選択される1つ以上の哺乳動物の腸管部位における、この化合物及び/又はその薬学的に受容可能な塩の放出のための手段、及び(c)薬学的に受容可能な賦形剤、を含有する固形経口製剤が提供される。
(R)−1−(3−(4−アミノ−3−(4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−イル)プロパ−2−エン−1−オン、
(R)−4−(8−アミノ−3−(1−(ブタ−2−イノイル)ピロリジン−2−イル)イミダゾ[1,5−a]ピラジン−1−イル)−N−(ピリジン−2−イル)ベンズアミド、
(S)−7−(1−アクリロイルピペリジン−4−イル)−2−(4−フェノキシフェニル)−4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピリミジン−3−カルボキサミド、
(S)−7−(1−(ブタ−2−イノイル)ピペリジン−4−イル)−2−(4−フェノキシフェニル)−4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピリミジン−3−カルボキサミド、
N−(3−((2−((2−メトキシ−4−(4−メチルピペラジン−1−イル)フェニル)アミノ)チエノ[3,2−d]ピリミジン−4−イル)オキシ)フェニル)アクリルアミド、
1−(3−((2−((4−(4−メチルピペラジン−1−イル)フェニル)アミノ)−[1,2,4]トリアゾロ[1,5−a]ピリジン−8−イル)オキシ)フェニル)プロパ−2−エン−1−オン、
(R)−6−アミノ−9−(1−(ブタ−2−イノイル)ピロリジン−3−イル)−7−(4−フェノキシフェニル)−7H−プリン−8(9H)−オン、
N−(2−((6−((5−(5−フルオロ−2−(ヒドロキシメチル)−3−(4−オキソ−6,7,8,9−テトラヒドロベンゾ[4,5]チエノ[2,3−d]ピリダジン−3(4H)−イル)フェニル)−1−メチル−2−オキソ−1,2−ジヒドロピリジン−3−イル)アミノ)ピリジン−2−イル)アミノ)エチル)アクリルアミド、
N−(3−((5−フルオロ−2−((4−(2−メトキシエトキシ)フェニル)アミノ)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(S)−5−アミノ−1−(1−シアノピペリジン−3−イル)−3−(4−(2,4−ジフルオロフェノキシ)フェニル)−1H−ピラゾール−4−カルボキサミド、
6−(1−アクリロイルピペリジン−4−イル)−2−(4−フェノキシフェニル)ニコチンアミド、
(R)−1−(1−アクリロイルピペリジン−3−イル)−4−アミノ−N−(5−クロロベンゾ[d]オキサゾール−2−イル)−1H−ピラゾロ[3,4−d]ピリミジン−3−カルボキサミド、
(S,E)−N−(4−((3−クロロ−4−フルオロフェニル)アミノ)−7−((テトラヒドロフラン−3−イル)オキシ)キナゾリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(R)−1−(3−(4−アミノ−3−(4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−イル)プロパ−2−エン−1−オン、
N−(2−((2−(ジメチルアミノ)エチル)(メチル)アミノ)−4−メトキシ−5−((4−(1−メチル−1H−インドール−3−イル)ピリミジン−2−イル)アミノ)フェニル)アクリルアミド、
N−(3−((2−((4−(4−アセチルピペラジン−1−イル)−2−メトキシフェニル)アミノ)−5−(トリフルオロメチル)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(E)−N−(4−((3−クロロ−4−(ピリジン−2−イルメトキシ)フェニル)アミノ)−3−シアノ−7−エトキシキノリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(E)−N−(4−((3−クロロ−4−フルオロフェニル)アミノ)−7−メトキシキナゾリン−6−イル)−4−(ピペリジン−1−イル)ブタ−2−エナミド、
1−(4−((4−((3,4−ジクロロ−2−フルオロフェニル)アミノ)−7−メトキシキナゾリン−6−イル)オキシ)ピペリジン−1−イル)プロパ−2−エン−1−オン、
N−(3−((5−フルオロ−2−((4−(2−メトキシエトキシ)フェニル)アミノ)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(E)−4−((4−((3−ブロモ−4−クロロフェニル)アミノ)ピリド[3,4−d]ピリミジン−6−イル)アミノ)−N,N−ジメチル−N−((1−メチル−4−ニトロ−1H−イミダゾール−5−イル)メチル)−4−オキソブタ−2−エン−1−アミニウムブロミド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−(ピラジン−2−イル)アクリロヒドラジド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−(ピリジン−2−イル)アクリロヒドラジド、
N−((3R,4R)−4−フルオロ−1−(6−((3−メトキシ−1−メチル−1H−ピラゾール−4−イル)アミノ)−9−メチル−9H−プリン−2−イル)ピロリジン−3−イル)アクリルアミド、
N−((3S,4S)−3−((6−(2,6−ジクロロ−3,5−ジメトキシフェニル)キナゾリン−2−イル)アミノ)テトラヒドロ−2H−ピラン−4−イル)アクリルアミド、
(3E,5E)−1−アクリロイル−3,5−ビス(4−ニトロベンジリデン)ピペリジン−4−オン、
(E)−N−(7−((1R,5S,6s)−3−オキサビシクロ[3.1.0]ヘキサン−6−イルエチニル)−4−((3−クロロ−4−フルオロフェニル)アミノ)キナゾリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(3E,5E)−1−アクリロイル−3,5−ビス(4−フルオロ−3−ニトロベンジリデン)アゼパン−4−オン、
N−(2−((6−(2,6−ジクロロ−3,5−ジメトキシフェニル)キナゾリン−2−イル)アミノ)−3−メチルフェニル)アクリルアミド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−ピバロイルアクリロヒドラジド、及び
N−(2−((2−((テトラヒドロ−2H−ピラン−4−イル)アミノ)−5−(トリフルオロメチル)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド。
ファチニブ、メレレチニブ、オシメルチニブ、ロシレチニブ、ネラチニブ、ダコミチニブ、ポジオチニブ、スペブルチニブ、タルロキソチニブ、セリネキソール、ベルジネキソール、PF−06747775、BLU−554、NSC−687852、VLX−1500、KU−113、NT−113、BLU−9931、KPT−350、及びAZ−13767370から選択される化合物を備えている。
(R)−1−(3−(4−アミノ−3−(4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−イル)プロパ−2−エン−1−オン、
(R)−4−(8−アミノ−3−(1−(ブタ−2−イノイル)ピロリジン−2−イル)イミダゾ[1,5−a]ピラジン−1−イル)−N−(ピリジン−2−イル)ベンズアミド、
(S)−7−(1−アクリロイルピペリジン−4−イル)−2−(4−フェノキシフェニル)−4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピリミジン−3−カルボキサミド、
(S)−7−(1−(ブタ−2−イノイル)ピペリジン−4−イル)−2−(4−フェノキシフェニル)−4,5,6,7−テトラヒドロピラゾロ[1,5−a]ピリミジン−3−カルボキサミド、
N−(3−((2−((2−メトキシ−4−(4−メチルピペラジン−1−イル)フェニル)アミノ)チエノ[3,2−d]ピリミジン−4−イル)オキシ)フェニル)アクリルアミド、
1−(3−((2−((4−(4−メチルピペラジン−1−イル)フェニル)アミノ)−[1,2,4]トリアゾロ[1,5−a]ピリジン−8−イル)オキシ)フェニル)プロパ−2−エン−1−オン、
(R)−6−アミノ−9−(1−(ブタ−2−イノイル)ピロリジン−3−イル)−7−(4−フェノキシフェニル)−7H−プリン−8(9H)−オン、
N−(2−((6−((5−(5−フルオロ−2−(ヒドロキシメチル)−3−(4−オキソ−6,7,8,9−テトラヒドロベンゾ[4,5]チエノ[2,3−d]ピリダジン−3(4H)−イル)フェニル)−1−メチル−2−オキソ−1,2−ジヒドロピリジン−3−イル)アミノ)ピリジン−2−イル)アミノ)エチル)アクリルアミド、
N−(3−((5−フルオロ−2−((4−(2−メトキシエトキシ)フェニル)アミノ)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(S)−5−アミノ−1−(1−シアノピペリジン−3−イル)−3−(4−(2,4−ジフルオロフェノキシ)フェニル)−1H−ピラゾール−4−カルボキサミド、
6−(1−アクリロイルピペリジン−4−イル)−2−(4−フェノキシフェニル)ニコチンアミド、
(R)−1−(1−アクリロイルピペリジン−3−イル)−4−アミノ−N−(5−クロロベンゾ[d]オキサゾール−2−イル)−1H−ピラゾロ[3,4−d]ピリミジン−3−カルボキサミド、
(S,E)−N−(4−((3−クロロ−4−フルオロフェニル)アミノ)−7−((テトラヒドロフラン−3−イル)オキシ)キナゾリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(R)−1−(3−(4−アミノ−3−(4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−イル)プロパ−2−エン−1−オン、
N−(2−((2−(ジメチルアミノ)エチル)(メチル)アミノ)−4−メトキシ−5−((4−(1−メチル−1H−インドール−3−イル)ピリミジン−2−イル)アミノ)フェニル)アクリルアミド、
N−(3−((2−((4−(4−アセチルピペラジン−1−イル)−2−メトキシフェ
ニル)アミノ)−5−(トリフルオロメチル)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(E)−N−(4−((3−クロロ−4−(ピリジン−2−イルメトキシ)フェニル)アミノ)−3−シアノ−7−エトキシキノリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(E)−N−(4−((3−クロロ−4−フルオロフェニル)アミノ)−7−メトキシキナゾリン−6−イル)−4−(ピペリジン−1−イル)ブタ−2−エナミド、
1−(4−((4−((3,4−ジクロロ−2−フルオロフェニル)アミノ)−7−メトキシキナゾリン−6−イル)オキシ)ピペリジン−1−イル)プロパ−2−エン−1−オン、
N−(3−((5−フルオロ−2−((4−(2−メトキシエトキシ)フェニル)アミノ)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド、
(E)−4−((4−((3−ブロモ−4−クロロフェニル)アミノ)ピリド[3,4−d]ピリミジン−6−イル)アミノ)−N,N−ジメチル−N−((1−メチル−4−ニトロ−1H−イミダゾール−5−イル)メチル)−4−オキソブタ−2−エン−1−アミニウムブロミド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−(ピラジン−2−イル)アクリロヒドラジド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−(ピリジン−2−イル)アクリロヒドラジド、
N−((3R,4R)−4−フルオロ−1−(6−((3−メトキシ−1−メチル−1H−ピラゾール−4−イル)アミノ)−9−メチル−9H−プリン−2−イル)ピロリジン−3−イル)アクリルアミド、
N−((3S,4S)−3−((6−(2,6−ジクロロ−3,5−ジメトキシフェニル)キナゾリン−2−イル)アミノ)テトラヒドロ−2H−ピラン−4−イル)アクリルアミド、
(3E,5E)−1−アクリロイル−3,5−ビス(4−ニトロベンジリデン)ピペリジン−4−オン、
(E)−N−(7−((1R,5S,6s)−3−オキサビシクロ[3.1.0]ヘキサン−6−イルエチニル)−4−((3−クロロ−4−フルオロフェニル)アミノ)キナゾリン−6−イル)−4−(ジメチルアミノ)ブタ−2−エナミド、
(3E,5E)−1−アクリロイル−3,5−ビス(4−フルオロ−3−ニトロベンジリデン)アゼパン−4−オン、
N−(2−((6−(2,6−ジクロロ−3,5−ジメトキシフェニル)キナゾリン−2−イル)アミノ)−3−メチルフェニル)アクリルアミド、
(Z)−3−(3−(3,5−ビス(トリフルオロメチル)フェニル)−1H−1,2,4−トリアゾール−1−イル)−N’−ピバロイルアクリロヒドラジド、及び
N−(2−((2−((テトラヒドロ−2H−ピラン−4−イル)アミノ)−5−(トリフルオロメチル)ピリミジン−4−イル)アミノ)フェニル)アクリルアミド。
グを何も有していない製剤を指す。
物理的性質を改善する場合がある。
らかの予想がされる位置で薬剤の放出が達成される送達を指す。一部の実施形態では、放出遅延の方法は、設定された期間の後に、透過性となる、溶解する、破壊される、及び/又は元の形を保たなくなるコーティングを行うことである。
ものである。それらは本発明の範囲を限定するものとみなされるべきではなく、本発明の単なる解説及び代表例である。
回腸−空腸の浸透活性化製剤
以下の成分を用いて、BTK阻害剤、(R)−2−(3−(4−アミノ−3−(2−フルオロ−4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−カルボニル)−4−メチル−4−(4−(オキセタン−3−イル)ピペラジン−1−イル)ペンタ−2−エンニトリルの回腸−空腸製剤を調製する。
回腸−空腸送達用の腸溶コート化錠剤
各コート化錠剤に対し、200mgの活性成分を最初に計測し、次いで7mgのクロスカルメロースナトリウム(Ac−Disol(登録商標))及び143mgの微晶質セルロース(Avicel(登録商標)PH101)と共にV−ブレンダー中で20〜30分間、乾式混合する。このフマル酸ステアリルナトリウム5mgを潤滑剤として加えた後、4〜5分間、混合する。この混合物は、回転式打錠機上で、5/16”の標準的な凹穴を用
いて錠剤化される。コーティング混合物は、250mgのEudragit(登録商標)L−30 D−55、7.5gのクエン酸トリエチル、37.5gの滑石、及び205gの脱イオン水から調製される。錠剤のコアは、40℃、15rpmで回転する穴の開いたパン塗工機内に置かれる。この混合物は、44〜48℃の流入空気温度、29〜32℃の排気温度、26℃の製造温度、30〜32rpmの回転、20psiのスプレー圧、及び30〜32CFMの気流でスプレーされる。60℃の流入空気温度、及び15rpmの回転で30分間硬化させた後、加熱器を止め、回転させながら錠剤を室温まで冷却する。コーティング後の重量増加量は、約5〜15%、典型的には約10%である。pH6.8での腸溶コーティングの溶解時間は、1時間で80%超を目的とした。
腸溶コーティング顆粒
300〜500ミクロンのサイズ範囲の腸溶コーティング顆粒を、ゼラチンカプセルもしくはヒプロメロースカプセル、サッシェもしくはスティックパック、又は経口懸濁液のいずれかの含有物に組み込む。活性成分及び低粘性ヒプロメロース(約2%)を計測し、Vブレンダー中で混合し、次いで流動床造粒機に加える。希釈ポリビニルピロリドン水溶液を粉末にスプレーするし、次いで45℃の流動床で顆粒を乾燥させることにより顆粒を形成する。次いで流動床でこれら乾燥顆粒をOpadry(登録商標)clear水溶液でコートし、密封コーティングし、乾燥させる。30%ポリマー、0.7%ラウリル硫酸ナトリウム、及び2.3%Tween(登録商標)20の水性分散液としてEudragit(登録商標)L−30 D−55を、可塑剤、クエン酸トリエチル、及びモノステアリン酸グリセリンと混合し、流動層において粉末にコーティングする。乾燥後、腸溶コーティング顆粒の最終組成は、約81.8%の活性成分、約1.5%のヒプロメロース、約0.5%のOpadryClear、約14.5%のメタクリル酸コポリマー、1.45%のクエン酸トリエチル、及び0.25%のモノステアリン酸グリセリンである。乾燥させた顆粒をサイズ0のヒプロメロースカプセル内に充てんする。pH2でのカプセルの溶解は、2時間で2%未満の放出を示し、このカプセルは理論上の薬剤量の80%超を約45分で放出する。
ラットにおける(R)−2−(3−(4−アミノ−3−(2−フルオロ−4−フェノキシフェニル)−1H−ピラゾロ[3,4−d]ピリミジン−1−イル)ピペリジン−1−カルボニル)−4−メチル−4−(4−(オキセタン−3−イル)ピペラジン−1−イル)ペンタ−2−エンニトリルの回腸−空腸投与
)ピペラジン−1−イル)ペンタ−2−エンニトリルのAUC及びCmaxが増加したこと、及び両実験においてIJ投与は、PO投与と比較し、AUC及びCmaxを大幅に増加させたことが示されている。
Ussingチャンバーにおける、ラットの異なる腸管領域を介したIn vitro透過
試薬:10X Krebs−Ringer緩衝液(KRB)は、結晶化を防ぐために個々に調製及び保存された1.26M NaCl(Promega社、マジソン、WI)、25mM KCl、250mM NaHCO3、12mM NaH2PO4、12mM MgCl2、25mM CaCl2、及び18g/L D−Glucose(すべてSigma Aldrich社、セントルイス、MOから購入)で構成された。使用前に1Xのワーキング濃度に希釈し、20分間、カルボゲンかん流でpH7.4(酸素化KRB)、又は1M HCl(Alfar Aesar社、Ward Hill、MA)でpH3.5、6.5もしくは7.4のいずれかにpH調整を行った。0.1%のフェノールレッド、アンチピリン、及びアテノロールは、Sigma Aldrich社、セントルイス、MOから購入した。
ャンバーアセンブリの各々を、37℃に維持されたサーモサーキュレートヒートブロック上に連続して載せ、3〜5泡/秒の速度でカルボゲンガスを連続して通気させたガス連結管に取り付けた。フェノールレッド(10μL 0.1%)を各粘膜チャンバーに加え、pH平衡を確認し、組織中の微細な破れ形跡を確認した。
溶解度の検証
溶解度の検証は、シンカー代替2Aを備えた装置2(75rpmでの混合)を用いたUnited States Pharmacopeia(http://www.pharmacopeia.cn/v29240/usp29nf24s0_c711h.html) のセクション711に従い行われる。両方の酸(pH2及び3)及びpH6.8に対し、900mLを含有する槽を37℃(±0.5℃)の温度で検証する。
れかの参照文献と、本明細書の具体的な教示の間に何らかの矛盾がある場合、後者を基準として解決されるものとする。同様に、当分野に理解される文言又は表現の定義と、本明細書に具体的に教示される文言又は表現の定義の間に何らかの矛盾がある場合、後者を基準として解決されるものとする。
Claims (20)
- (A)下記から選ばれる化合物、
(B)腸溶コーティング、
(C)前記腸溶コーティングと前記コアとの間のサブコートであって、
(1)ヒドロキシメチルセルロース(HPMC)、ヒドロキシエチルセルロース、ヒドロキシメチルセルロース、ヒドロキシプロピルセルロース、微晶質セルロース、ポリビニルピロリドン、多糖(又は多糖誘導体)、ポリビニルアルコール、ポリエチレングリコール(PEG)、ポリプロピレングリコール(PPG)、及びPEG−PPGブロックコポリマーから選択される低分子量ポリマーである、水溶性又は親水性浸食可能ポリマー、又は、
(2)水不溶性組成物であって、(i)前記水不溶性組成物中にチャンネルを形成することができる水溶性化合物の粒子、若しくは(ii)水性媒体と接触した際に前記サブコートに膨潤を生じさせる水不溶性の親水性粒子、を含有する前記水不溶性組成物
である前記サブコート、並びに、
(D)薬学的に受容可能な賦形剤
を含有する固形経口製剤であって、
前記固形経口製剤は、前記コア(A)の前記化合物及び/又は前記その薬学的に受容可能な塩を、哺乳動物による前記製剤の経口摂取後、前記哺乳動物の小腸の回腸−空腸部分に放出でき、かつ前記固形経口製剤は、前記化合物及び/又は前記その薬学的に受容可能な塩の80重量%以上を、6.4〜7.4のpHの水性溶液を含有する溶解容器において、120分間、放出できる、前記固形経口製剤。 - 前記固形経口製剤は、前記コア(A)の前記化合物及び/又は前記その薬学的に受容可能な塩の10重量%未満を、3未満のpH若しくは4.5〜5.5のpHの水性溶液を含有する溶解容器において1.5時間で放出でき、かつ、前記固形経口製剤は、前記化合物及び/又は前記その薬学的に受容可能な塩の80重量%以上を、6.4〜7.4のpHの水性溶液を含有する溶解容器において、20分〜2時間、放出できる、請求項1記載の固形経口製剤。
- 前記サブコート(C)が、水溶性化合物の粒子を含有する、請求項1〜3のいずれか1項に記載の固形経口製剤。
- 前記サブコート(C)が、水性媒体と接触した際に前記サブコートに膨潤を生じさせる水不溶性の親水性粒子を含有する、請求項1〜3のいずれか1項に記載の固形経口製剤。
- 前記サブコート(C)が、前記固形経口製剤への水の流入と、前記化合物及び/又はその薬学的に受容可能な塩の腸管への拡散を可能とするチャンネルを形成する水溶性化合物の粒子を含有する水不溶性の組成物である、請求項1〜3のいずれか1項に記載の固形経口製剤。
- 前記サブコート(C)が、前記化合物及び/又はその薬学的に受容可能な塩に対して不浸透性であるが、水の流入は許容するチャンネルを形成することができ、前記サブコートを膨潤及び破裂させることができ、前記化合物及び/又はその薬学的に受容可能な塩の放出を生じさせることができる水溶性化合物の粒子を含有する水不溶性組成物である、請求項1〜3のいずれか1項に記載の固形経口製剤。
- 前記水性溶液が、6.4〜7.4のpHの擬似腸管液である、請求項1〜7のいずれか1項に記載の固形経口製剤。
- 前記固形経口製剤が、前記化合物の薬学的に受容可能な塩を含有する、請求項1〜8のいずれか1項に記載の固形経口製剤。
- 前記コア(A)が、
(a)前記化合物及び/又は前記その薬学的に受容可能な塩の、前記固形経口製剤からの放出の前に、前記固形経口製剤内に酸性水溶液を生じさせるために十分な量の薬学的に受容可能な酸、及び/又は
(b)50mlの水性媒体中での分解時、その臨界ミセル濃度を超える濃度で存在する界面活性剤
をさらに含有する、請求項1〜9のいずれか1項に記載の固形経口製剤。 - 前記化合物及び/又は前記その薬学的に受容可能な塩の平均粒子サイズが、0.3ミク
ロン〜100ミクロンである、請求項1〜10のいずれか1項に記載の固形経口製剤。 - 前記腸溶コーティング(B)が、
(a)前記コアの重量の10%〜150%であり、
(b)5〜500ミクロンの厚さであり、
(c)重合ゼラチン、シェラック、メタクリル酸コポリマー型CNF、ブチル化フタル酸セルロース、フタル酸水素セルロース、フタル酸プロプリオネートセルロース、フタル酸ポリ酢酸ビニル(PVAP)、酢酸フタル酸セルロース(CAP)、酢酸トリメリット酸セルロース(CAT)、フタル酸ヒドロキシプロピルメチルセルロース、酢酸ヒドロキシプロピルメチルセルロース、コハク酸ジオキシプロピルメチルセルロース、カルボキシメチルエチルセルロース(CMEC)、酢酸コハク酸ヒドロキシプロピルメチルセルロース(HPMCAS)、並びに(メタ)アクリル酸ポリマー及びコポリマーから選択され、前記ポリマーは1種のモノマーから作られており、前記コポリマーは2種以上のモノマーから作られており、前記モノマーは、アクリル酸メチル、アクリル酸エチル、メタクリル酸メチル、及びメタクリル酸エチルから選択され、
(d)セルロース誘導体を含有し、及び/又は
(e)フタル酸ポリ酢酸ビニル(PVAP)ポリマーを含有する、
請求項1〜11のいずれか1項に記載の固形経口製剤。 - 前記腸溶コーティングが、ポリ(メタ)アクリル酸ポリマーを含有する、請求項12に記載の固形経口製剤。
- 前記腸溶コーティングが、Eudragit(登録商標)L又はSのシリーズである、請求項12又は13に記載の固形経口製剤。
- 前記腸溶コーティングが、Eudragit(登録商標)L100、L12.5、S100、S12.5、又はFS30Dである、請求項12〜14のいずれか1項に記載の固形経口製剤。
- 前記セルロース誘導体が、メチルセルロース、酢酸フタル酸セルロース、フタル酸ヒドロキシメチルセルロース(HPMCP)、コハク酸ヒドロキシプロピルメチルセルロース(HPMCS)、及び酢酸コハク酸ヒドロキシメチルセルロース(HPMCAS)から選択される、請求項12〜15のいずれか1項に記載の固形経口製剤。
- 前記薬学的に受容可能な賦形剤(D)が、結合剤、界面活性剤、希釈剤、緩衝剤、抗付着剤、流動促進剤、崩壊剤、抗酸化剤、消泡剤、充てん剤、香味剤、着色剤、潤滑剤、吸着剤、保存剤、可塑剤、及び甘味料から独立して選択される、請求項1〜16のいずれか1項に記載の固形経口製剤。
- 前記固形経口製剤が、錠剤又はカプセルである、請求項1〜17のいずれか1項に記載の固形経口製剤。
- BTKの阻害により治療可能な疾患の治療用である、請求項1〜18のいずれか1項に記載の固形経口製剤。
- 前記疾患が、自己免疫疾患、癌、及び炎症性疾患から選択される、請求項19に記載の固形経口製剤。
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PCT/US2015/000515 WO2016105582A1 (en) | 2014-12-24 | 2015-12-23 | Compositions for ileo-jejunal drug delivery |
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PT2989106T (pt) | 2013-04-25 | 2017-03-15 | Beigene Ltd | Compostos heterocíclicos fundidos como inibidores da proteína quinase |
ES2927567T3 (es) | 2013-09-13 | 2022-11-08 | Beigene Switzerland Gmbh | Anticuerpos anti-PD1 y su uso como productos terapéuticos y de diagnóstico |
JP6504548B2 (ja) | 2014-02-21 | 2019-04-24 | プリンシピア バイオファーマ インコーポレイテッド | Btk阻害剤の塩および固体形態 |
KR102003754B1 (ko) | 2014-07-03 | 2019-07-25 | 베이진 엘티디 | Pd-l1 항체와 이를 이용한 치료 및 진단 |
EA036269B1 (ru) | 2014-12-18 | 2020-10-21 | Принсипиа Биофарма Инк. | Лечение пузырчатки |
TW201718572A (zh) | 2015-06-24 | 2017-06-01 | 普林斯匹亞生物製藥公司 | 酪胺酸激酶抑制劑 |
EP3464275B1 (en) | 2016-05-26 | 2024-05-08 | Recurium IP Holdings, LLC | Egfr inhibitor compounds |
KR102391693B1 (ko) | 2016-06-29 | 2022-04-29 | 프린시피아 바이오파마, 인코퍼레이티드 | 2-[3-[4-아미노-3-(2-플루오로-4-페녹시-페닐)피라졸로[3,4-d]피리미딘-1-일]피페리딘-1-카르보닐]-4-메틸-4-[4-(옥세탄-3-일)피페라진-1-일]펜트-2-엔니트릴의 변형 방출 제제 |
JP6993056B2 (ja) | 2016-07-05 | 2022-02-15 | ベイジーン リミテッド | 癌治療のためのpd-1アンタゴニスト及びraf阻害剤の組合せ |
MX2019001900A (es) | 2016-08-16 | 2019-07-01 | Beigene Ltd | Forma cristalina de (s)-7-(1-acriloilpiperidin-4-il)-2-(4-fenoxife nil)-4,5,6,7-tetra-hidropirazolo[1,5-a]pirimidin-3-carboxamida, preparacion y usos de la misma. |
CN118252927A (zh) | 2016-08-19 | 2024-06-28 | 百济神州有限公司 | 使用包含btk抑制剂的组合产品治疗癌症 |
CN106588937B (zh) | 2017-01-16 | 2018-09-21 | 东莞市真兴贝特医药技术有限公司 | 咪唑并吡嗪类化合物及其制备方法和应用 |
US11555038B2 (en) | 2017-01-25 | 2023-01-17 | Beigene, Ltd. | Crystalline forms of (S)-7-(1-(but-2-ynoyl)piperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide, preparation, and uses thereof |
AU2018290532A1 (en) | 2017-06-26 | 2019-11-21 | Beigene, Ltd. | Immunotherapy for hepatocellular carcinoma |
WO2019034009A1 (en) | 2017-08-12 | 2019-02-21 | Beigene, Ltd. | BTK INHIBITOR WITH ENHANCED DOUBLE SELECTIVITY |
AU2018342342B2 (en) * | 2017-09-28 | 2021-01-07 | Shanghai Haiyan Pharmaceutical Technology Co., Ltd. | 4,6,7-trisubstituted 1,2-dihydropyrrol(3,4-c)pyridin/pyrimidin-3-one derivative and use |
WO2019108795A1 (en) | 2017-11-29 | 2019-06-06 | Beigene Switzerland Gmbh | Treatment of indolent or aggressive b-cell lymphomas using a combination comprising btk inhibitors |
WO2019142207A1 (en) | 2018-01-20 | 2019-07-25 | Natco Pharma Limited | Pharmaceutical compositions comprising ibrutinib |
AU2019341284B2 (en) * | 2018-09-18 | 2024-09-05 | Beijing Innocare Pharma Tech Co., Ltd. | Crystalline forms of 6- (1-acryloylpiperidin-4-yl) -2- (4-phenoxyphenyl) nicotinamide |
SG11202103861YA (en) * | 2018-11-06 | 2021-05-28 | Beijing Innocare Pharma Tech Co Ltd | Amorphous solid dispersion comprising 6- (1-acryloylpiperidin-4-yl) -2- (4-phenoxyphenyl) nicotinamide |
WO2020102304A1 (en) * | 2018-11-13 | 2020-05-22 | Rain Therapeutics Inc. | Combination of a kinase inhibitor and an electrolyte, compositions and methods comprising the same |
CN109851725A (zh) * | 2018-12-29 | 2019-06-07 | 华南理工大学 | 纳米纤维素-聚丙烯酰胺-明胶复合水凝胶、其制备方法及应用 |
JP2023548055A (ja) * | 2020-11-02 | 2023-11-15 | ブラック ダイアモンド セラピューティクス,インコーポレイティド | 癌をアルキン置換キナゾリン誘導体で治療する方法 |
CN113855695B (zh) * | 2021-11-01 | 2023-06-06 | 上海理工大学 | 一种结肠释药口服复方药物组合物及其制备方法 |
CN114181159B (zh) * | 2021-12-28 | 2024-02-20 | 南通大学 | 含2,4,5-三取代嘧啶酰肼衍生物及其制备方法与应用 |
US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
CN116473923B (zh) * | 2023-05-29 | 2024-05-14 | 杭州剂泰医药科技有限责任公司 | 一种奈拉替尼固体分散体组合物及其制备方法和应用 |
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CA2851808C (en) * | 2011-10-19 | 2021-04-13 | Pharmacyclics, Inc. | Use of inhibitors of bruton's tyrosine kinase (btk) |
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US20150140085A1 (en) * | 2012-06-29 | 2015-05-21 | Principia Biopharma Inc. | Formulations comprising ibrutinib |
US9266895B2 (en) * | 2012-09-10 | 2016-02-23 | Principia Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidines as kinase inhibitors |
MX2020011594A (es) * | 2013-01-05 | 2022-01-13 | Anji Pharma Us Llc | Composición de liberación demorada que comprende biguanida. |
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SI3236943T1 (sl) | 2023-06-30 |
HK1245071A1 (zh) | 2018-08-24 |
US20180193274A1 (en) | 2018-07-12 |
HUE061809T2 (hu) | 2023-08-28 |
JP2018500353A (ja) | 2018-01-11 |
PL3236943T3 (pl) | 2023-05-29 |
EP3236943B1 (en) | 2023-01-25 |
ES2942642T3 (es) | 2023-06-05 |
PT3236943T (pt) | 2023-04-20 |
LT3236943T (lt) | 2023-04-11 |
EP3236943A1 (en) | 2017-11-01 |
MA41265B1 (fr) | 2023-05-31 |
FI3236943T3 (fi) | 2023-04-27 |
DK3236943T3 (da) | 2023-04-11 |
WO2016105582A1 (en) | 2016-06-30 |
HRP20230305T1 (hr) | 2023-05-26 |
RS64139B1 (sr) | 2023-05-31 |
MA41265A (fr) | 2017-10-31 |
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