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公开(公告)号:US20220202962A1
公开(公告)日:2022-06-30
申请号:US17389674
申请日:2021-07-30
IPC分类号: A61K49/20 , A61K31/4709 , A61K31/4015 , C07D207/20 , A61K31/4178 , C07D491/052 , C07D207/273 , C07D207/14 , A61K31/015 , A61K31/05 , A61K31/353 , A61K31/4184 , A61K31/423 , A61K31/428 , A61K31/4439 , A61K31/53
摘要: The present invention provides methods of using nitroxide spin-labeled amyloid beta-binding compounds to image amyloid. The present invention also provides nitroxide spin-labeled amyloid beta-binding compounds.
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公开(公告)号:US20220202833A1
公开(公告)日:2022-06-30
申请号:US17399015
申请日:2021-08-10
申请人: Scynexis, Inc.
IPC分类号: A61K31/58 , A61K31/4439 , A61P31/10 , A61K31/4196 , A61K45/06 , A61K31/496 , A61K31/506 , A61K31/7048
摘要: The present invention relates to the use of enfumafungin derivative triterpenoid antifungal compounds in combination with other antifungal agents such azoles, polyenes, lipopeptides, and allylamides to treat fungal diseases. More particularly, the invention relates to antifungal combinations of enfumafungin derivative triterpenoids which are inhibitors of (1,3)-β-D-glucan synthesis, in combination with other antifungal agents such as mold-active agents that have activity against molds, including but not limited to voriconazole, isavuconazole, posaconazole, itraconazole and amphotericin B, for the treatment and/or prevention of infections caused by molds.
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公开(公告)号:US20220202795A1
公开(公告)日:2022-06-30
申请号:US17600639
申请日:2020-04-01
发明人: Hyuk Jun CHO , Taek KWON , Ho Taek IM , Yong ll KIM , Jin A JUNG , Han Kil SON , Sung Hee HONG
IPC分类号: A61K31/4439 , A61K9/28
摘要: The present disclosure relates to a pharmaceutical composition containing esomeprazole or a pharmaceutically acceptable salt thereof and with a dual release profile, and particularly to a pharmaceutical composition which exhibits a dual release profile of immediate release and sustained release so that long-term efficacy can be sustained. The pharmaceutical composition containing esomeprazole or a pharmaceutically acceptable salt thereof and with a dual release profile, according to the present disclosure, can secure bioavailability equivalent to that of existing esomeprazole immediate-release/enteric-release formulations, and can maintain long-term efficacy due to the dual release profile thereof even when administered once a day, thus preventing the occurrence of nocturnal acid breakthrough, and accordingly, can be effectively used as a therapeutic agent for nocturnal acid breakthrough.
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公开(公告)号:US20220202783A1
公开(公告)日:2022-06-30
申请号:US17605857
申请日:2020-04-24
发明人: Yuh-Pyng Sher , Juan-Cheng Yang , Jing-Pei Liu , Yu-Kai Huang
IPC分类号: A61K31/427 , A61K39/395 , A61P35/00 , A61K31/4709 , A61K31/4439 , A61K31/454
摘要: The present disclosure relates to a use of an ADAM9 inhibitor in manufacture of an immunomodulator. The immunomodulator can change the distribution of immune cells in a tumor and increase the infiltration of the immune cells, thereby increasing the efficacy of cancer immunotherapy. Furthermore, the immunomodulator can be used to enhance an effectiveness of a cancer immunotherapy, and the ADAM9 inhibitor can be a compound of Formula (I), or a pharmaceutically acceptable salt or stereoisomer thereof.
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公开(公告)号:US20220202779A1
公开(公告)日:2022-06-30
申请号:US17584951
申请日:2022-01-26
发明人: Li Chen , Yongguo Li , Gaosen Wang
IPC分类号: A61K31/4155 , A61K9/20 , A61K31/426 , A61K31/427 , A61K31/437 , A61K31/4439 , A61K31/444 , A61K31/497
摘要: Disclosed is a solid dispersion and a preparation method therefor. The solid dispersion contains a glucokinase activator, an isotopic label thereof, or a medicinal salt thereof and a polymer support. Further disclosed is a solid dispersion composition containing the solid dispersion and an excipient. Also disclosed is an oral preparation of the glucokinase activator, containing the solid dispersion or the solid dispersion composition. Also disclosed is a tablet and a capsule of the glucokinase activator and a preparation method therefor. In addition, also disclosed is the uses of the solid dispersion, the solid dispersion composition and the oral preparations comprising the tablet and the capsule, which can be used for treating and/or preventing selected diseases or medical conditions and especially one or more diseases selected from type I diabetes mellitus, type II diabetes mellitus, impaired glucose tolerance, impaired fasting glucose and hyperglycemia.
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公开(公告)号:US11370786B2
公开(公告)日:2022-06-28
申请号:US16925974
申请日:2020-07-10
发明人: Maria Emilia Di Francesco , Philip Jones , Timothy Heffernan , Matthew M. Hamilton , Zhijun Kang , Michael J. Soth , Jason P. Burke , Kang Le , Christopher Lawrence Carroll , Wylie S. Palmer , Richard Lewis , Timothy McAfoos , Barbara Czako , Gang Liu , Jay Theroff , Zachary Herrera , Anne Yau
IPC分类号: C07D417/14 , A61K31/4439 , A61K45/06 , C07D417/06 , A61K31/433 , C07D403/06 , A61K31/501 , C07D401/14 , A61K31/454 , A61K31/4192 , C07D405/14 , C07D403/14 , A61K31/444 , C07D493/08 , A61K31/497
摘要: Disclosed herein are compounds of structural Formula VIIa or VIIb: or a pharmaceutically acceptable salt thereof, and compositions thereof useful in the treatment of GLS1 mediated diseases, such as cancer. Methods of inhibition GLS1 activity in a human or animal subject are also provided.
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公开(公告)号:US20220193079A1
公开(公告)日:2022-06-23
申请号:US17504177
申请日:2021-10-18
申请人: Novartis AG
发明人: Yan CHEN , Xizhong HUANG , Sunkyu KIM
IPC分类号: A61K31/519 , A61K45/06 , A61K31/4439 , A61K31/5377 , A61K31/5513 , A61K31/138 , A61K31/4196 , A61K31/436 , A61K31/551 , A61K31/565 , A61K31/5685
摘要: The present disclosure relates to a pharmaceutical combination comprising (1) a first agent which is a CDK inhibitor or a pharmaceutically acceptable salt thereof and (2) a second agent which is an anti-hormonal agent or a pharmaceutically acceptable salt thereof. The present disclosure also relates to a pharmaceutical combination comprising (1) a first agent which is a CDK inhibitor or a pharmaceutically acceptable salt thereof, (2) a second agent which is an anti-hormonal agent or a pharmaceutically acceptable salt thereof, and (3) a third agent which is an agent that regulates the PI3K/Akt/mTOR pathway or a pharmaceutically acceptable salt thereof.
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公开(公告)号:US11358711B2
公开(公告)日:2022-06-14
申请号:US17025371
申请日:2020-09-18
发明人: Thomas H. Graham , Tao Yu , Yonglian Zhang , John A. McCauley
IPC分类号: A61K31/5365 , B64C27/48 , B64C11/08 , A61P31/18 , A61K31/18 , A61K31/407 , A61K31/4188 , A61K31/4439 , A61K31/4985 , A61K31/519 , A61K31/553 , A61K31/7076 , C07D498/16 , C07D498/22 , C12N15/113
摘要: The present invention relates to Tetracyclic Heterocycle Compounds of Formula and pharmaceutically acceptable salts or prodrug thereof, wherein A, X, R1, R2, R3 and Ware as defined herein. The present invention also relates to compositions comprising at least one Tetracyclic Heterocycle Compound, and methods of using the Tetracyclic Heterocycle Compounds for treating or preventing HIV infection in a subject.
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公开(公告)号:US20220175927A1
公开(公告)日:2022-06-09
申请号:US17678495
申请日:2022-02-23
发明人: Herriot Tabuteau
IPC分类号: A61K47/02 , A61K31/5415 , A61K31/4439 , A61K9/00 , A61K47/69 , A61K47/40 , A61K9/20 , C08B37/16 , A61K45/06
摘要: Disclosed herein are compositions comprising an NSAID such as meloxicam and/or rizatriptan in combination with a cyclodextrin and/or a carbonate or a bicarbonate. These compositions may be orally administered, for example, to improve the bioavailability or pharmacokinetics of the NSAID for the treatment of pain such as migraine, arthritis, and other conditions. Also disclosed herein are methods of treating pain, such as migraine, comprising administering meloxicam and rizatriptan to a human being suffering from pain, such as migraine. For migraine, these methods may be particularly useful when the meloxicam and rizatriptan are administered while the human being is suffering from an acute attack of migraine pain or migraine aura. In some embodiments, the combination of meloxicam and rizatriptan may be administered in a manner that results in a Tmax of meloxicam of 3 hours or less.
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公开(公告)号:US20220175758A1
公开(公告)日:2022-06-09
申请号:US17600194
申请日:2019-12-27
发明人: Christos Mantzoros , Glenn D. Rosen
IPC分类号: A61K31/473 , A61K31/437 , A61K31/4439 , A61K31/501 , A61K31/444 , A61K45/06 , A61P1/16
摘要: Provided herein are methods and combination therapies useful for the treatment of non-alcoholic fatty liver diseases (NAFLD). In particular, provided herein are methods and combination therapies for treating NAFLD by administering a combination therapy comprising (a) the compound of Formula (I), or a pharmaceutically acceptable salt thereof, and (b) an additional therapeutic agent, or a pharmaceutically acceptable salt thereof. Also provided are pharmaceutical compositions and pharmaceutical combinations comprising the compound of Formula (I), or a pharmaceutically acceptable salt thereof, and an additional therapeutic agent, or a pharmaceutically acceptable salt thereof.
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