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公开(公告)号:US20240075026A1
公开(公告)日:2024-03-07
申请号:US18107243
申请日:2023-02-08
Applicant: AbbVie Inc.
Inventor: Nancy E. Sever , Ulrich Westedt , Ute Lander , Katrin Schneider , Benedikt Steitz , Thomas Mueller , Regina Reul , Constanze Obermiller , Adivaraha Jayasankar , Michael Simon , Yi Gao , Harald Hach , Samuel Kyeremateng , Katharina Asmus , Ping Tong , Donghua Zhu , Marius Naris , Colleen Garrett
IPC: A61K31/498 , A61K9/14 , A61K9/20 , A61K9/24 , A61K31/454 , A61K31/4985
CPC classification number: A61K31/498 , A61K9/146 , A61K9/2027 , A61K9/209 , A61K31/454 , A61K31/4985
Abstract: The present invention features solid pharmaceutical compositions comprising Compound 1 and Compound 2. In one embodiment, the solid pharmaceutical composition includes (1) a first layer which comprises 100 mg Compound 1, as well as a pharmaceutically acceptable hydrophilic polymer and a pharmaceutically acceptable surfactant, all of which are formulated in amorphous solid dispersion; and (2) a second layer which comprises 40 mg Compound 2, as well as a pharmaceutically acceptable hydrophilic polymer and a pharmaceutically acceptable surfactant, all of which are formulated in amorphous solid dispersion.
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公开(公告)号:US11369599B2
公开(公告)日:2022-06-28
申请号:US14340435
申请日:2014-07-24
Applicant: AbbVie Inc. , AbbVie Deutschland GMBH & Co KG
Inventor: Esther Birtalan , Peter Hoelig , David J. Lindley , Yeshwant D. Sanzgiri , Ping Tong
IPC: A61K31/496 , A61K31/5377 , A61K31/541 , A61K47/02 , A61K47/26 , A61K47/32 , A61K9/20 , A61K9/16 , A61K9/00
Abstract: A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises subjecting to elevated temperature the compound of Formula I, the water-soluble polymeric carrier and the surfactant, to provide an extrudable semi-solid mixture; extruding the semi-solid mixture; and cooling the resulting extrudate to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer or an immune or autoimmune disease.
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公开(公告)号:US20220125796A1
公开(公告)日:2022-04-28
申请号:US17341158
申请日:2021-06-07
Applicant: AbbVie Inc.
Inventor: Nathaniel Catron , David Lindley , Jonathan M. Miller , Eric A. Schmitt , Ping Tong
IPC: A61K31/5377 , A61K9/16 , A61K9/14 , A61K31/496 , A61K31/437 , A61K9/48
Abstract: A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises dissolving the compound, the polymeric carrier and the surfactant in a suitable solvent, and removing the solvent to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer.
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公开(公告)号:US20160375087A1
公开(公告)日:2016-12-29
申请号:US15192211
申请日:2016-06-24
Applicant: AbbVie Inc.
Inventor: Nancy E. Sever , Ulrich Westedt , Ute Lander , Katrin Schneider , Benedikt Steitz , Thomas Mueller , Regina Reul , Constanze Obermiller , Adivaraha Jayasankar , Michael Simon , Yi Gao , Harald Hach , Samuel Kyeremateng , Katharina Asmus , Ping Tong , Donghua Zhu , Marius Naris , Colleen Garrett
CPC classification number: A61K38/06 , A61K9/146 , A61K9/1688 , A61K9/2027 , A61K9/2031 , A61K9/2054 , A61K9/209 , A61K9/2866 , A61K31/4184 , A61K31/454 , A61K31/498 , A61K2300/00
Abstract: The present invention features solid pharmaceutical compositions comprising Compound 1 and Compound 2. In one embodiment, the solid pharmaceutical composition includes (1) a first layer which comprises 100 mg Compound 1, as well as a pharmaceutically acceptable hydrophilic polymer and a pharmaceutically acceptable surfactant, all of which are formulated in amorphous solid dispersion; and (2) a second layer which comprises 40 mg Compound 2, as well as a pharmaceutically acceptable hydrophilic polymer and a pharmaceutically acceptable surfactant, all of which are formulated in amorphous solid dispersion.
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15.
公开(公告)号:US20150157639A1
公开(公告)日:2015-06-11
申请号:US14537392
申请日:2014-11-10
Applicant: AbbVie Inc.
Inventor: Nathaniel Catron , David Lindley , Jonathan M. Miller , Eric A. Schmitt , Ping Tong
IPC: A61K31/5377 , A61K31/496
CPC classification number: A61K31/5377 , A61K9/145 , A61K9/146 , A61K9/1617 , A61K9/1635 , A61K9/4866 , A61K31/437 , A61K31/496 , Y02A50/411
Abstract: A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises dissolving the compound, the polymeric carrier and the surfactant in a suitable solvent, and removing the solvent to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer.
Abstract translation: 促凋亡固体分散体以基本上非结晶形式包含分散在固体基质中的如本文定义的式I的Bcl-2家族蛋白质抑制化合物,其包含(a)药学上可接受的水溶性聚合物载体和( b)药学上可接受的表面活性剂。 制备这种固体分散体的方法包括将化合物,聚合物载体和表面活性剂溶解在合适的溶剂中,并除去溶剂以提供包含聚合物载体和表面活性剂的固体基质,并使化合物分散在基本上不结晶 形成。 该固体分散体适合于需要其的受试者口服给药以治疗以一种或多种抗凋亡Bcl-2家族蛋白(例如癌症)过表达为特征的疾病。
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