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公开(公告)号:WO2022041664A1
公开(公告)日:2022-03-03
申请号:PCT/CN2021/077412
申请日:2021-02-23
Applicant: 杭州国光药业股份有限公司
Abstract: 一种调色剂、包含该调色剂的溶菌酶含片以及该溶菌酶含片的制备方法。其中,通过将色素加纯化水配制成色素混悬液,再将色素混悬液雾化喷洒至糊精上,充分混合后干燥粉碎可得该调色剂。
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62.
公开(公告)号:WO2022040772A1
公开(公告)日:2022-03-03
申请号:PCT/CA2020/051159
申请日:2020-08-25
Applicant: DU, Wenmin
Inventor: DU, Wenmin
Abstract: A method for preparing, from one or more dried traditional-Chinese-medicine materials in non-powder forms, instant traditional-Chinese-medicine dried powder for decoction. The method has the steps of: adding one or more first edible excipients to the one or more dried traditional-Chinese-medicine materials; and grinding the mixture of the one or more first edible excipients and the one or more dried traditional-Chinese-medicine materials to powder with sizes of a predefined range to obtain the instant traditional-Chinese-medicine dried powder. In this method, the one or more first edible excipients are added to the one or more dried traditional-Chinese-medicine materials before or during said grinding. In various embodiments, the edible excipients may be dextrin, glutinous-rice powder, rice powder, and starch. The instant traditional-Chinese-medicine dried powder may be packaged into sealed tea bags or gauze bags for long-term storage up to five years and for convenient taking.
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公开(公告)号:WO2022028084A1
公开(公告)日:2022-02-10
申请号:PCT/CN2021/098700
申请日:2021-06-07
Applicant: 山东明仁福瑞达制药股份有限公司
IPC: A61K9/14 , A61K9/22 , A61K9/52 , A61K47/38 , A61K47/02 , A61K47/36 , A61K47/69 , A61K36/716 , A61P19/08 , A61P29/00
Abstract: 一种治疗颈椎病的固体分散体及在制备缓释制剂中的应用。颈痛产品作为用于治疗神经根型颈椎病的一线用药具有良好的临床治疗效果,为了进一步降低颈痛产品的用药次数,降低患者用药难度,提供了一种颈痛产品的缓释制剂,所述缓释制剂采用固体分散体技术,有效实现了指标性成分三七总皂苷及人参总皂苷的释放性能,其中三七总皂苷的释放性能接近一级动力学。所述固体分散体可以降低给药次数,将其应用于片剂制备,有望作为现有颈痛产品的替代剂型。
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公开(公告)号:WO2022024979A1
公开(公告)日:2022-02-03
申请号:PCT/JP2021/027505
申请日:2021-07-26
Applicant: 第一三共株式会社
IPC: A61K31/197 , A61K9/16 , A61K9/20 , A61K47/12 , A61K47/22 , A61K47/26 , A61K47/36 , A61K47/38 , A61P25/02 , A61P25/04 , A61P43/00
Abstract: 本発明の課題は、ミロガバリンベシル酸塩を含有する安定性に優れた口腔内崩壊錠を提供することである。 本発明の解決手段は、(A)ミロガバリンベシル酸塩含有顆粒と、(B)結晶セルロースを含有する薬物不含有顆粒、又は、結晶セルロースを含有する薬物不含有混合末とを含有する口腔内崩壊錠である。
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公开(公告)号:WO2022020644A2
公开(公告)日:2022-01-27
申请号:PCT/US2021/042845
申请日:2021-07-22
Inventor: GU, Zhen , HU, Quanyin , LI, Hongjun
IPC: A61K35/17 , A61K39/395 , A61P35/00 , C12N5/0783 , A61K35/00 , A61K38/00 , A61K39/00 , A61K47/12 , A61K47/32 , A61K47/36 , A61K47/42 , A61K47/6901 , A61K9/0019 , A61K9/0024 , A61K9/06 , A61K9/19 , A61K9/5153 , C07K14/00
Abstract: A therapeutic hydrogel material is disclosed for the delivery of CAR-T cells that allows their distribution in the tumor resection recess, cavity, or void in combination with platelets decorated with the anti-programmed death-ligand 1 (PDL1) blocking antibody (aPDL1). The delivered hydrogel material acts as a reservoir for both CAR-T cells and platelet-bound aPDL1. Furthermore, inflammation occurring during the surgical wound healing triggers the release of platelet-derived microparticles containing the aPDL1. Cells delivered by the engineered hydrogel show significant control of local and distant tumor recurrence without causing toxic effects. In some embodiments, nanoparticles containing cytokines are also loaded in the therapeutic hydrogel material to maintain the activity and proliferation ability of CAR-T cells.
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公开(公告)号:WO2022016038A1
公开(公告)日:2022-01-20
申请号:PCT/US2021/041936
申请日:2021-07-16
Applicant: DT IP HOLDINGS I, LLC , FRITZ, Robert
Inventor: GUILFORD, David
Abstract: Provided herein are formulation bases comprising a nanogel comprising a first fraction of hyaluronic acid, or a pharmaceutically acceptable salt thereof, and a second fraction of hyaluronic acid, or a pharmaceutically acceptable salt thereof; and lecithin liposomes within the nanogel, the lecithin liposomes having a d75 of from about 25 nm to about 250 nm, wherein the hyaluronic acid of the first fraction, or a pharmaceutically acceptable salt thereof, has a molecular weight of greater than about 500 kilodaltons, and the hyaluronic acid of the second fraction, or a pharmaceutically acceptable salt thereof, has a molecular weight of less than about 250 kilodaltons. The formulation bases described herein provide for absorption of active substances contained therein into the body, e.g., transdermally, and, therefore, can be used as delivery systems to administer one or more active substances to a subject.
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公开(公告)号:WO2022014695A1
公开(公告)日:2022-01-20
申请号:PCT/JP2021/026729
申请日:2021-07-16
Applicant: 富士フイルム株式会社 , 一般財団法人阪大微生物病研究会 , 国立大学法人北海道大学
Abstract: 本発明は、皮下注射日本脳炎ワクチンの投与量よりも低い投与量、または皮下注射日本脳炎ワクチンの投与回数よりも少ない投与回数であっても、ヒトに対して十分な免疫を付与することができる日本脳炎予防剤及び日本脳炎ワクチン剤を提供することを課題とする。本発明によれば、シート部と、シート部の上面に存在する複数の針部とを有するマイクロニードルアレイであって、上記針部が不活化日本脳炎ウイルスを内包又は担持しているマイクロニードルアレイを含む、日本脳炎予防剤が提供される。
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公开(公告)号:WO2022011040A1
公开(公告)日:2022-01-13
申请号:PCT/US2021/040732
申请日:2021-07-07
Applicant: UNDERDOG PHARMACEUTICALS, INC.
Inventor: O'CONNOR, Matthew, S. , DE LOS ANGELES ESTIARTE-MARTINEZ, Maria , ANDERSON, Ameila, M. , CLEMENS, Daniel, M. , TOM, Christine A.T.M.B. , MALANGA, Milo , KOPE, Michael , SADRERAFI, Keivan
IPC: A61K47/36 , A61K47/40 , C08B7/00 , C08B37/02 , A61K9/0019 , A61K9/0053 , C08B37/0012
Abstract: CD dimers, CD compositions, and uses thereof are disclosed herein. CD dimers, and compositions thereof, that may be useful for various purposes including the targeting of 7KC. The design and testing of CD dimers are described herein. Exemplary CD dimers include heterodimers, homodimers, or asymmetric dimer.
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公开(公告)号:WO2022010444A1
公开(公告)日:2022-01-13
申请号:PCT/TR2021/050689
申请日:2021-07-07
Applicant: IMUNEKS FARMA ILAC SAN. VE TIC. A.S.
Inventor: PISAK, Mehmet Nevzat
IPC: A61K31/167 , A61K47/10 , A61K47/40 , A61P31/14 , A61K47/26 , A61K47/36 , A61K9/0007 , A61K9/0095 , A61K9/08 , A61K9/10 , A61K9/1605
Abstract: The present invention provides pharmaceutical composition comprising niclosamide for use in the therapeutic or prophylactic treatment of viral diseases or conditions. Viral diseases treated or prevented by the compositions of the present invention can be Ebola virus disease, MERS (MERS-CoV), SARS (SARS-CoV), SARS-CoV-2 (COVID-19) virus disease, Rabies, viral diseases caused by Orthomyxoviridae family virus including influenza A, influenza B, influence C, influenza D virus disease, hepatitis A, Rhinovirus, Marburg virus disease, hepatitis C, Yellow fever virus disease, Dengue fever virus disease, West Nile virus disease or ZIKA virus disease.
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公开(公告)号:WO2021261927A1
公开(公告)日:2021-12-30
申请号:PCT/KR2021/007919
申请日:2021-06-23
Applicant: 주식회사태준제약
IPC: A61K9/00 , A61K47/36 , A61K47/32 , A61K47/10 , A61K47/26 , A61K47/14 , A61K31/7072 , A61P27/02 , A61P27/04
Abstract: 본 발명은 디쿠아포솔을 포함하는 점안 조성물에 관한 것으로, 구체적으로 디쿠아포솔, 잔탄검 및 폴리비닐알코올을 포함하는 점안 조성물에 관한 것이다.
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