Abstract: Disclosed herein is a physically stable solid dispersion comprising Compound 1, i.e., the B-RAF kinase dimer inhibitor 1-((1S, 1aS, 6bS)-5-((7-oxo-5, 6, 7, 8-tetrahydro-1, 8-naphthyridin-4-yl)oxy)-1a,6b-dihydro-1H-cyclopropa [b] benzofuran-1-yl)-3-(2, 4, 5-trifluorophenyl) urea and a specific stabilizing polymer, the method for preparing the same, and the uses of the solid dispersion. Also disclosed herein is the crystalline form of Compound 1.
Type:
Grant
Filed:
January 23, 2020
Date of Patent:
March 24, 2026
Assignee:
BeiGene, Ltd.
Inventors:
Guoliang Zhang, Changyou Zhou, Huangbin Sun
Abstract: Disclosed herein are cyclic di-nucleotide compounds and derivatives thereof that may be useful as STING agonists, and a pharmaceutical composition comprising the same. Also disclosed herein is the process for synthesis and to uses of such cyclic di-nucleotide compounds in various diseases including cancer, HIV infection and HBV infection.
Abstract: Disclosed herein is a compound of Formula (I) for inhibiting both Bcl-2 wild type and mutated Bcl-2, in particular, Bcl-2 G101V and D103Y, and a method of using the compound disclosed herein for treating dysregulated apoptotic diseases.
Abstract: Disclosed herein is 3-[(1H-pyrazol-4-yl)oxy]pyrazin-2-amine compounds of Formula (I), or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions comprising thereof. Also disclosed is a method of modulating, e.g.
Abstract: Provided herein are compounds having the following structure: wherein the substituents are as defined herein, compositions comprising an effective amount of a compound, and methods for modulating activity of KRAS G12D.
Type:
Application
Filed:
January 6, 2025
Publication date:
July 10, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Ce WANG, Chao YU, Hao YUAN, Xiaoyu LI, Zhiwei WANG, Hanzi SUN
Abstract: Anti-FGFR2b antibodies and antigen-binding fragments thereof are provided herein, as are immunoconjugates comprising the same, and compositions comprising the antibodies and immunoconjugates. Also provided are methods of making and using the antibodies and immunoconjugates, such as to treat an FGFR2b-related disease or disorder. The antibodies of the disclosure bind to human FGFR2b and can block the interaction between the KGF ligand and FGFR2b.
Abstract: Disclosed herein are novel bifunctional compounds formed by conjugating IRAK4 inhibitor moieties with E3 ligase ligand moieties, which function to recruit targeted proteins to E3 ubiquitin ligase for degradation, and methods of preparation and uses thereof.
Abstract: Provided herein are compounds having the following structure: wherein the substituents are as defined herein, compositions comprising an effective amount of a compound, and methods for modulating activity of an immune cell.
Type:
Application
Filed:
August 7, 2024
Publication date:
May 22, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Guoliang Zhang, Jianzhuang Miao, Hanzi Sun, Zhikun Ni, Zhi Zhang, Ce Wang
Abstract: Disclosed herein are fused bi-cyclic compounds used as Small Molecule IL-17A Modulators. Disclosed herein is the use of these Small Molecule IL-17A Modulators for the use of decreasing IL-17 activity by inhibition, and the use of such compounds for the use in the treatment of autoimmune diseases or inflammatory diseases.
Type:
Application
Filed:
October 17, 2024
Publication date:
May 15, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Hai Xue, Yunhang Guo, Si Chen, Zhiwei Wang
Abstract: The present disclosure provides for the antibodies or antigen-binding fragment thereof that specifically binds human CD137, multispecific antibodies and antigen-binding fragments thereof that specifically bind to human GPC3 and CD137, a pharmaceutical composition comprising said antibody, and use of the antibody, multispecific antibody or the composition for treating a disease, such as cancer.
Type:
Application
Filed:
November 20, 2024
Publication date:
May 15, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Liang QU, Liu XUE, Ruyue JI, Xi YUAN, Zhuo LI, Jie LI, Jian SUN
Abstract: This disclosure provides compounds containing 7-(pyrimidin-4-yl)quinolin-4(1H)-one structure, the use thereof for selectively inhibiting the activity of CDK4, and pharmaceutical compositions comprising the compounds as treatment of various diseases including cancer.
Abstract: Disclosed herein is a compound of Formula (I) for inhibiting both Bcl-2 wild type and mutated Bcl-2, in particular, Bcl-2 G101V and D103Y, and a method of using the compound disclosed herein for treating dysregulated apoptotic diseases.
Abstract: Disclosed herein is an imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivative or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof useful as a TLR7 agonist, and a pharmaceutical composition comprising the same. Also disclosed herein is a method of treating cancer using the imidazo [2, 1-f] [1, 2, 4] triazin-4-amine derivative or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof as TLR7 agonist.
Type:
Grant
Filed:
February 6, 2020
Date of Patent:
April 22, 2025
Assignee:
BEIGENE, LTD.
Inventors:
Guoliang Zhang, Jianzhuang Miao, Changyou Zhou, Gang Chen, Jing Li
Abstract: The present disclosure provides antibodies and antigen-binding fragments thereof that bind to human CCR8, a pharmaceutical composition comprising said antibody, and use of the antibody or the composition for treating a disease, such as cancer.
Type:
Application
Filed:
October 29, 2024
Publication date:
April 10, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Ming FANG, Liu XUE, Hanzi SUN, Xiaoyan TANG, Ming JIANG, Xitao WANG, Yun CHEN, Chichi HUANG, Wenjie WANG, Jing ZHANG, Wenbo JIANG
Abstract: Provided herein are compounds having the following structure: wherein the substituents are as defined herein, compositions comprising an effective amount of a compound, and methods for modulating activity of KRAS G12D and/or G12V.
Type:
Application
Filed:
September 19, 2024
Publication date:
March 27, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Chao YU, Jie CHEN, Hanzi SUN, Huaqing LIU, Ce WANG, Zhiwei WANG
Abstract: Provided herein are compounds having the following structure: or a pharmaceutically acceptable salt, tautomer, stereoisomer, or enantiomer thereof, wherein the substituents are as defined herein compositions comprising an effective amount of a compound, and methods for inhibiting activity of cyclin-dependent kinases.
Type:
Application
Filed:
November 1, 2024
Publication date:
February 27, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Chao YU, Hanzi SUN, Ce WANG, Zhiwei WANG
Abstract: The present invention relates to salts of a HPK1 inhibitor (referred to as “Compound A” hereinafter), preferably citrate, and the crystalline forms thereof. The present invention also relates to the process of preparation and uses of the salts and crystalline forms of Compound A.
Type:
Application
Filed:
October 23, 2024
Publication date:
February 6, 2025
Applicant:
BeiGene, Ltd.
Inventors:
Hui Chen, Sanjia Xu, Jing Li, Zhengming Du, Zhiwei Wang
Abstract: Disclosed herein is a compound of Formula (I) for inhibiting Bcl-xL and treating a disease associated with the undesirable Bcl-xL activity (Bcl-xL related diseases), a method of using the compounds disclosed herein for treating tumor or cancer, and a pharmaceutical composition comprising the same.
Abstract: The present invention relates to compounds containing thiazolopyridyl amide structure, the process for their synthesis, as well as the use of such compounds for inhibiting DNA Polymerase Theta (Pol Theta), and in the treatment of various diseases including cancers.