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公开(公告)号:AU2020239751B2
公开(公告)日:2022-10-27
申请号:AU2020239751
申请日:2020-09-24
Applicant: PHARMACYCLICS LLC
Inventor: SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D , PURRO NORBERT
Abstract: CRYSTALLINE FORMS OF A BRUTON'S TYROSINE KINASE INHIBITOR Described herein is the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4 phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one, including crystalline forms, solvates and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the Btk inhibitor, as well as methods of using the Btk in hibitor, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
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公开(公告)号:AU2018211201A1
公开(公告)日:2018-08-16
申请号:AU2018211201
申请日:2018-07-31
Applicant: PHARMACYCLICS LLC
Inventor: SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D , PURRO NORBERT
Abstract: CRYSTALLINE FORMS OF A BRUTON'S TYROSINE KINASE INHIBITOR Described herein is the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4 phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin- 1 -yl)piperidin- 1 -yl)prop-2-en- 1-one, including crystalline forms, solvates and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the Btk inhibitor, as well as methods of using the Btk inhibitor, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions. (20992107_1):GGG
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公开(公告)号:AU2013271918C1
公开(公告)日:2017-02-09
申请号:AU2013271918
申请日:2013-06-03
Applicant: PHARMACYCLICS LLC
Inventor: SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D , PURRO NORBERT
Abstract: Described herein is the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one, including crystalline forms, solvates and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the Btk inhibitor, as well as methods of using the Btk inhibitor, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
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公开(公告)号:NZ621221A
公开(公告)日:2016-07-29
申请号:NZ62122111
申请日:2011-09-13
Applicant: PHARMACYCLICS LLC
Inventor: BUGGY JOSEPH J , MODY TARAK D , VERNER ERIK J , PURRO NORBERT , BALASUBRAMANIAN SRIRAM , KLOOS IOANA , DEPIL STÉPHANE , LOURY DAVID J
IPC: A61K31/343 , A61K9/14 , A61K9/28 , A61K31/4184 , A61P35/00
Abstract: Provided are combinations and pharmaceutical compositions comprising bendamustine and a HDAC inhibitor. A preferred HDAC inhibitor is N-hydroxy-4-{ 2-[3-(N,N-dimethylaminomethyl)benzofuran-2-ylcarbonylamino]ethoxy} -benzamide. The combinations and pharmaceutical compositions are useful in the treatment of cancer.
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公开(公告)号:ZA202105175B
公开(公告)日:2022-07-27
申请号:ZA202105175
申请日:2021-07-22
Applicant: PHARMACYCLICS LLC
Inventor: PURRO NORBERT , SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D
Abstract: Described herein is the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one, including crystalline forms, solvates and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the Btk inhibitor, as well as methods of using the Btk inhibitor, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
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公开(公告)号:AR118108A2
公开(公告)日:2021-09-15
申请号:ARP200100425
申请日:2020-02-14
Applicant: PHARMACYCLICS LLC
Inventor: WIRTH DAVID D , GOLDMAN ERICK , SMYTH MARK , PURRO NORBERT
IPC: A61K31/519 , A61K9/48 , A61K47/30 , A61K47/38 , A61P29/00 , A61P35/00 , A61P37/00 , C07D487/04
Abstract: Se describe aquí al inhibidor de tirosina quinasa (Btk) de Bruton 1-((R)-3-(4-amino-3-(4-fenoxifenil)-1H-pirazolo[3,4-d]pirimidin-1-il)piperidin-1-il)prop-2-en-1-ona, incluyendo las formas cristalinas, solvatos y sus sales aceptables en el campo farmacéutico. Se describe también composiciones farmacéuticas que incluyen al inhibidor Btk, así como métodos para usar a dicho inhibidor solo o en combinación con otros agentes terapéuticos, para el tratamiento de enfermedades o condiciones autoinmunes, enfermedades o condiciones heteroinmunes, cáncer, incluyendo linfoma, así como enfermedades o condiciones inflamatorias. Reivindicación 1: Una preparación farmacéutica para administración oral caracterizada porque comprende: (a) más o menos 40 a más o menos 200 mgs de 1-((R)-3-(4-amino-3-(4-fenoxifenil)-1H-pirazolo[3,4-d]pirimidin-1-il)piperidin-1-il)prop-2-en-1-ona; (b) más o menos 40% en peso a más o menos 50% en peso de un diluyente; (c) más o menos 3% en peso a más o menos 10% en peso de un agente desintegrador; (d) más o menos 2% en peso a más o menos 7% en peso de un agente de actividad superficial; y (e) más o menos 0,2% en peso a más o menos 1,0% en peso de un lubricante. Reivindicación 2: La preparación farmacéutica, de acuerdo con la reivindicación 1, caracterizada porque el diluyente está seleccionado a partir del grupo que consiste de lactosa, sucrosa, dextrosa, dextratos, maltodextrin, manitol, xilitol, sorbitol, ciclodextrinas, fosfato de calcio, sulfato de calcio, almidones, almidones modificados, celulosa microcristalina, microcelulosa, etc. Reivindicación 3: La preparación farmacéutica, de acuerdo con la reivindicación 2, caracterizada porque el diluyente es una celulosa microcristalina. Reivindicación 11: La preparación farmacéutica, de acuerdo con cualesquiera reivindicaciones 1 - 10, caracterizada porque la forma de dosificación es una cápsula de gelatina dura.
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公开(公告)号:ECSP19015794A
公开(公告)日:2019-03-29
申请号:ECDI201915794
申请日:2019-03-06
Applicant: PHARMACYCLICS LLC
Inventor: WIRTH DAVID , PURRO NORBERT , GOLDMAN ERICK , SMYTH MARK
Abstract: Se describe aquí al inhibidor de tirosina quinasa (Btk) de Bruton 1-((R)-3-(4-amino-3-(4-fenoxifenil)-1H-pirazolo[3,4-d] pirimidin-1-il)piperidin-1-il)prop-2-en-1-ona, incluyendo las formas cristalinas, solvatos y sus sales aceptables en el campo farmacéutico. Se describe también composiciones farmacéuticas que incluyen al inhibidor Btk, así como métodos para usar a dicho inhibidor solo o en combinación con otros agentes terapéuticos, para el tratamiento de enfermedades o condiciones autoinmunes, enfermedades o condiciones heteroinmunes, cáncer, incluyendo linfoma, así como enfermedades o condiciones inflamatorias.
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公开(公告)号:AU2018211216A1
公开(公告)日:2018-08-16
申请号:AU2018211216
申请日:2018-07-31
Applicant: PHARMACYCLICS LLC
Inventor: SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D , PURRO NORBERT
Abstract: CRYSTALLINE FORMS OF A BRUTON'S TYROSINE KINASE INHIBITOR Described herein is the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4 phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin- 1 -yl)piperidin- 1 -yl)prop-2-en- 1-one, including crystalline forms, solvates and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the Btk inhibitor, as well as methods of using the Btk inhibitor, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions. (20992107_1):GGG
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公开(公告)号:UA114421C2
公开(公告)日:2017-06-12
申请号:UAA201414091
申请日:2013-06-03
Applicant: PHARMACYCLICS LLC
Inventor: SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D , PURRO NORBERT
Abstract: УданійзаявцірозкриваєтьсяінгібітортирозинкіназиБрутона (Btk) 1-((R)-3-(4-аміно-3-(4-феноксифеніл)-1H-піразоло[3,4-d]піримідин-1-іл)піпередин-1-іл)проп-2-ен-1-он, включаючийогокристалічніформи, сольватитафармацевтичноприйнятнісолі. Такожрозкриваютьсяфармацевтичнікомпозиції, яківключаютьінгібітор Btk, іспособизастосуванняінгібітору Btk, самостійноабов комбінаціїз іншимитерапевтичнимиагентами, длялікуванняаутоімуннихзахворюваньабопатологічнихстанів, гетероімуннихзахворюваньабопатологічнихстанів, раку, включаючилімфомутазапальнізахворюванняабопатологічністани.
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公开(公告)号:AU2016250445A1
公开(公告)日:2016-11-17
申请号:AU2016250445
申请日:2016-10-28
Applicant: PHARMACYCLICS LLC
Inventor: SMYTH MARK , GOLDMAN ERICK , WIRTH DAVID D , PURRO NORBERT
Abstract: CRYSTALLINE FORMS OF A BRUTON'S TYROSINE KINASE INHIBITOR Described herein is the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4 phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1 -yl)piperidin-1-yl)prop-2-en-1-one, including crystalline forms, solvates and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the Btk inhibitor, as well as methods of using the Btk in hibitor, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
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