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公开(公告)号:US11524077B2
公开(公告)日:2022-12-13
申请号:US16878325
申请日:2020-05-19
申请人: Vascular BioSciences
发明人: David Mann
IPC分类号: A61K47/42 , A61K47/62 , A61K45/06 , C07K7/06 , A61K9/00 , A61K31/506 , A61K31/519 , A61K38/00
摘要: Disclosed are compositions and methods useful for oral delivery of targeted therapies for pulmonary diseases, fibrotic disorders and cancer. The compositions and methods are based on peptide sequences that selectively bind to and home to diseased tissue and enable targeted therapies to affect a beneficial therapeutic result. The disclosed targeting is useful for oral delivery of therapeutic and detectable agents to diseased tissue in an animal.
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公开(公告)号:US11524072B2
公开(公告)日:2022-12-13
申请号:US17061696
申请日:2020-10-02
IPC分类号: A61K39/39 , A61K39/00 , A61K39/104 , A61K39/12 , A61K9/00 , A61K9/06 , A61K39/02 , A61K39/145 , A61K39/29 , A61K47/42 , A61K39/012 , A61K39/108 , A61K39/112 , A61K39/04 , A61K39/05 , A61K39/08 , A61K39/085 , A61K39/09 , A61K39/102 , A61K39/15 , A61K39/155 , A61K39/17 , A61K39/215 , A61K39/255 , A61K39/265
摘要: A vaccine delivery method is presented that includes a composition including as one component a slurry matrix that is a liquid at room temperature and a gel at physiological pH, physiological salt concentrations and/or physiological temperatures and as a second component one or more antigens. Also included are methods of inducing an immune response in a subject and vaccinating a subject by administering such compositions.
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公开(公告)号:US20220370573A1
公开(公告)日:2022-11-24
申请号:US17541546
申请日:2021-12-03
申请人: Allergan, Inc.
发明人: Ahmet Tezel , Wendy M. Blanda , Patrick M. Hughes , Scott M. Whitcup , James N. Chang , Michael R. Robinson
IPC分类号: A61K38/48 , A61K47/36 , A61L27/20 , A61L27/54 , A61K8/64 , C12N9/64 , A61K8/66 , A61K8/73 , A61Q19/08 , A61K47/32 , A61K47/38 , A61K47/42
摘要: Improved dermal filler formulation comprising a hyaluronic acid and a botulinum toxin.
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公开(公告)号:US20220362205A1
公开(公告)日:2022-11-17
申请号:US17873800
申请日:2022-07-26
发明人: Qun Sun
IPC分类号: A61K31/337 , A61K47/64 , A61K9/08 , A61K47/42
摘要: This document relates to non-covalently bound complexes including Docetaxel and human serum albumin, and to compositions comprising such complexes. This document also relates to compositions comprising Docetaxel and human serum albumin, wherein the composition is a clear aqueous solution when the composition is dissolved in an aqueous solution, and wherein the composition has a solubility in an aqueous solution of at least 10 mg/ml. This document also relates to compositions comprising Docetaxel and human serum albumin, wherein the Docetaxel and the human serum albumin in the composition have a weight ratio from about 1:50 to about 1:1000. This document also relates to compositions consisting essentially of Docetaxel and human serum albumin, wherein the Docetaxel and the human serum albumin in the composition have a weight ratio from about 1:50 to about 1:1000. The pH of the docetaxel compositions of the present disclosure is from about 5 to about 8.
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公开(公告)号:US20220354790A1
公开(公告)日:2022-11-10
申请号:US17621587
申请日:2020-06-11
发明人: Kwang Dae HONG , Jihun SEO , Joon Bum LEE
摘要: The present invention relates to an in-vivo bulking agent which can be used as a medicinal agent for prevention or treatment of at least one disease selected from the group consisting of urinary incontinence, fecal incontinence, and gastroesophageal reflux or as a filler for use in a plastic surgery procedure, and to a preparation method therefor. The in-vivo bulking agent can exhibit a bulking effect when injected into the body and particularly, is highly biocompatible because a first composition in which silicone particles are coated with a zwitterionic polymer having a surfactant property is introduced into a second composition, whereby the bulking agent can inhibit inflammatory reactions in vivo.
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86.
公开(公告)号:US11491216B2
公开(公告)日:2022-11-08
申请号:US16645048
申请日:2018-09-04
申请人: Merck Sharp & Dohme Corp. , Richard J. Porambo , Chitrananda Abeygunawardana , Luwy Kavuka Musey , Michael J. Kosinski , Yadong Adam Cui , Julie Marie Skinner
发明人: Richard J. Porambo , Chitrananda Abeygunawardana , Luwy Kavuka Musey , Michael J. Kosinski , Yadong Adam Cui , Julie Marie Skinner
摘要: The present invention provides capsular polysaccharides from Streptococcus pneumoniae serotypes identified using NMR. The present invention further provides polysaccharide-protein conjugates in which capsular polysaccharides from one or more of these serotypes are conjugated to a carrier protein such as CRM197. Polysaccharide-protein conjugates from one or more of these serotypes may be included in multivalent pneumococcal conjugate vaccines having polysaccharides from multiple additional Streptococcus pneumoniae serotypes.
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公开(公告)号:US11484595B2
公开(公告)日:2022-11-01
申请号:US15841059
申请日:2017-12-13
发明人: Siak-Khim Tan , Janifer Yeo-Tan
IPC分类号: A61K38/10 , A61K38/16 , A61K38/00 , C07K14/575 , A61P23/00 , A61P17/00 , A61P29/00 , C07K5/00 , C07K7/00 , C07K16/00 , C07K17/00 , A61K39/02 , A61K39/08 , A61K9/127 , A61K47/42 , A61K31/60 , A61K38/48 , A61K9/00 , A61K9/107 , A61K38/08 , C07K14/33 , C07K7/08 , A61P25/00 , A61K39/00
摘要: A carrier molecule composition. Specific implementations may include: a carrier molecule including at least one cell penetrating peptide (CPP) where the carrier molecule may include at least one hydrophobic domain and where the carrier is non-covalently associated with a biologically active molecule in one of a micelle and a liposome.
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公开(公告)号:US20220305089A1
公开(公告)日:2022-09-29
申请号:US17633836
申请日:2020-08-14
申请人: OCTAPHARMA AG
发明人: Ronny SCHMIDT , Tilo SCHWIENTEK
摘要: The invention relates to a pharmaceutical composition comprising an isolated Factor VIII protein and/or an isolated VWF protein in a stabilizing buffer composition, wherein said pharmaceutical composition is free of albumin and said stabilizing buffer 5 composition comprises cryoprotectants and bulking agents in a weight ratio of more than 0.65:1. The invention relates further relates to the use of a stabilizing buffer formulating an FVIII protein and/or a VWF protein to the use of a VWF protein for stabilizing a FVIII protein in vitro.
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公开(公告)号:US20220305013A1
公开(公告)日:2022-09-29
申请号:US17619837
申请日:2020-06-18
申请人: THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO , THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
IPC分类号: A61K31/506 , A61K9/10 , A61K47/42 , A61K31/4174 , A61K31/438 , A61K47/28 , A61K47/34 , A61K31/566 , A61K31/44
摘要: The present application provides a colloid drug aggregate composition and methods of use and manufacture thereof. While the formation of colloidal aggregates leads to artifacts in early drug discovery, their composition makes them attractive as nanoparticle formulations for targeted drug delivery. The present application provides an acid-responsive composition comprising: a colloidal aggregate of one or more drugs and a stabilizing agent, wherein the colloidal aggregate disrupts, dissolves or disassembles when the acid-responsive composition is in an acid environment having a pH of less than 7.4. The colloidal aggregate of the composition will disassemble upon contact with acid or upon introduction to an acidic environment, such as is found in the endosomes of cells. This approach makes this composition an attractive vehicle for drug delivery to a target site in a subject or to cells.
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公开(公告)号:US11452688B2
公开(公告)日:2022-09-27
申请号:US16554015
申请日:2019-08-28
IPC分类号: A61K9/00 , A61K47/10 , A61K47/12 , A61K47/42 , A61K47/18 , A61K47/26 , A61Q19/00 , A61K9/06 , A61K38/28 , A61K31/728 , A61K8/02 , A61K8/34 , A61K8/36 , A61K8/60 , A61K8/64
摘要: A transdermally absorbable base material including: a lipid peptide compound including at least one of compound of Formula (1) below and the similar compounds or pharmaceutically usable salts thereof; a surfactant; a specific polyhydric alcohol; a fatty acid; and water, wherein R1 is a C9-23 aliphatic group; R2 is a hydrogen atom or a C1-4 alkyl group that optionally has a branched chain having a carbon atom number of 1 or 2; R3 is a —(CH2)n—X group; n is a number of 1 to 4; and X is amino group, guanidino group, —CONH2 group, or a 5-membered cyclic group optionally having 1 to 3 nitrogen atoms, a 6-membered cyclic group optionally having 1 to 3 nitrogen atoms, or a condensed heterocyclic group constituted by a 5-membered cyclic group and a 6-membered cyclic group which optionally have 1 to 3 nitrogen atoms.
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