Abstract: The present invention relates to the use of cyclin-dependent kinase 9 (CDK9) inhibitors to reduce, inhibit and/or prevent cartilage degradation. CDK9 inhibitors can be used to reduce, inhibit and/or prevent cartilage degradation and loss of cartilage viability during allograft storage. CDK9 inhibitors can be used as a post-injury intervention treatment to reduce, inhibit and/or prevent the acute cellular responses that lead to future cartilage degradation and osteoarthritis.
Type:
Grant
Filed:
November 20, 2018
Date of Patent:
May 5, 2020
Assignee:
THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Inventors:
Dominik Haudenschild, Paul Di Cesare, Jasper Yik, Blaine Christiansen
Abstract: Provided herein are formulations for topical and/or transdermal administration, and methods of using these formulations for the treatment of proliferative diseases related to cancer such as cancers and related conditions, and solid tumors. Also provided are formulations for topical and/or transdermal administration, and methods of using these formulations for melasma, gout, skin disorders, and other diseases and disorders described herein as well as methods for modulating the pH (e.g. raising) of a tissue or microenvironment proximal to a tumor, modulating pH, or improving the effectiveness of know chemotherapeutic agents, immunotherapy and the like for the prevention, treatment of cancers and related conditions described herein.
Abstract: Provided herein are formulations for topical and/or transdermal administration, and methods of using these formulations for the treatment of proliferative diseases related to cancer such as cancers and related conditions, and solid tumors. Also provided are formulations for topical and/or transdermal administration, and methods of using these formulations for melasma, gout, skin disorders, and other diseases and disorders described herein as well as methods for modulating the pH (e.g. raising) of a tissue or microenvironment proximal to a tumor, modulating pH, or improving the effectiveness of know chemotherapeutic agents, immunotherapy and the like for the prevention, treatment of cancers and related conditions described herein.
Abstract: Cosmetic composition comprising a salicylic acid compound The invention relates to a composition in the form of an oil-in-water emulsion comprising: —a fatty acid ester of polyethylene glycol; —a C16-C22 fatty acid ester of glycerol; —a polycondensate of ethylene oxide and of propylene oxide constituted of polyethylene glycol and polypropylene glycol blocks; —an at least partially neutralized acrylic acid homopolymer; —a 2-acrylamido-2-methylpropanesulfonic acid polymer; —a salicylic acid compound. The composition has good stability, in particular after 15 days of storage at 55° C. Use for caring for and making up keratin materials.
Abstract: Valproate is useful as an antifungal agent. The valproate compositions can be used to treat fungal infections. The valproate compositions can be formulated as topical antifungals.
Abstract: The present disclosure relates to antiperspirant and/or deodorizing cosmetic agent agents in the form of emulsions, which contain at least one non-ionic emulsifier a), wherein an ethoxylated, saturated, branched C14-C18 alcohol has an ethoxylation degree of from about 18 to about 22 ethylene oxide units, and at least one further non-ionic emulsifier b), wherein an ethoxylated, linear, mono-unsaturated C16-C20 alcohol has an ethoxylation degree of from about 18 to about 22 ethylene oxide units, wherein the weight ratio of the non-ionic emulsifier a) to the non-ionic emulsifier b) is from about 1.2:1 to about 4.0:1. The cosmetic agents as contemplated herein are optically transparent and have an improved storage stability, even under fluctuating temperatures.
Abstract: Drug combinations and their use are disclosed. A first drug is administered in combination with a second drug. The first drug such as fenfluramine is characterized by the formation of a metabolite including 5-HT2B agonists such as norfenfluramine with known adverse side effects. The second drug is in the form of a CYP inhibitor such as cannabidiol which modulates the formation of metabolite down thereby making the first drug safer.
Abstract: The present disclosure relates to antiperspirant and/or deodorizing cosmetic agents in the form of oil-in-water emulsions, which contain a combination of isopropylisostearate and isopropylmyristate as cosmetic oils and a small total quantity of oils and emulsifiers. The cosmetic agent as contemplated herein surprisingly have extremely low or no stickiness after their application to the skin. They can also be optically transparent and have improved storage stability.
Abstract: A compound containing one mole of a free fatty acid and one mole of the ammonium salt of the fatty acid and represented by the structural formula (I): CH3(CH2)xCOOH.CH3(CH2)xCOO?NH4+??(I) wherein x is 6, 7 or 8. Bacterial contaminated surfaces may be disinfected or bacteria removed from a bacterial contaminated surface by applying onto the surface a bactericidally effective amount of the compound.
Abstract: Generally, the present invention provides novel quinolone compounds and pharmaceutical composition thereof which may inhibit cell proliferation and/or induce cell apoptosis. The present invention also provides methods of preparing such compounds and compositions, and methods of making and using the same.
Abstract: The present invention is directed to methods of treating, preventing, and/or ameliorating fibrosis syndrome, and in particular cardiac fibrosis, by administration of a therapeutically effective amount of ifetroban, or a pharmaceutically acceptable salt thereof.
Type:
Grant
Filed:
April 23, 2019
Date of Patent:
March 10, 2020
Assignees:
CUMBERLAND PHARMACEUTICALS INC., Vanderbilt University
Inventors:
Leo Pavliv, Bryan Voss, James West, Erica Carrier
Abstract: The present invention concerns a composition, in particular in the form of aqueous dispersion for caring for and/or making up keratin materials comprising, in a physiologically acceptable medium, a) one aqueous phase; and b) at least microcapsules comprising:—an inner core comprising at least a dispersion of at least one reflective agent, in particular bismuth oxychloride, in at least one oil, and—at least one outer shell formed of a wall-forming polymeric material surrounding the said core, the said outer shell comprising i) at least one wall-forming polymer, and ii) optionally at least one plasticizer and/or at least one opaque substance and/or at least one fatty acid salt. The present invention concerns also a cosmetic process for caring for and/or making up keratinic materials, comprising application on said keratinic materials in particular on the skin of a composition as above defined.
Abstract: The present invention provides a salt form and compositions thereof, which are useful as an inhibitor of EGFR kinases and which exhibits desirable characteristics for the same.
Type:
Grant
Filed:
June 22, 2018
Date of Patent:
February 25, 2020
Assignee:
Celgene CAR LLC
Inventors:
Mei Lai, Steven Richard Witowski, Richland Wayne Tester, Kwangho Lee
Abstract: The invention relates to a method of treatment and/or prophylaxis of a disease or disorder of the central nervous system comprising administering to a mammal in need thereof an effective amount of a xanthone-rich plant extract, or a compound derived from a xanthone-rich plant extract. The invention also relates to use of a xanthone-rich plant extract, or a compound derived from a xanthone-rich plant extract, in the preparation of a medicament for the treatment and/or prophylaxis of a disease or disorder of the central nervous system and to a xanthone-rich plant extract, or a compound derived from a xanthone-rich plant extract, for use in the treatment and/or prophylaxis of a disease or disorder of the central nervous system.
Abstract: The present invention relates to a composition in the form of a nano- or micro-emulsion, comprising: (a) at least one oil; (b) at least one nonionic surfactant with an HLB value of from 8.0 to 14.0, preferably from 9.0 to 13.5, and more preferably from 10.0 to 13.0; (c) at least one ceramide compound; (d) at least one anionic surfactant; and (e) water. The composition can be used as a cosmetic composition and provides an excellent feeling during use and can be transparent or slightly translucent, and is stable over time, even at an elevated temperature.
Abstract: The present invention relates to a topical preparation for skin tissue protection and reparation. The complex preparation includes the following components: (1) polyethylene glycol; (2) water; and (3) flavonoid compound. The complex preparation may: (1) repair skin injury or promote wound healing; (2) eliminate scars; (3) prevent or treat skin injury caused by radiotherapy; and (4) prevent or treat radiodermatitis.
Type:
Grant
Filed:
June 9, 2017
Date of Patent:
February 18, 2020
Assignee:
NANJING JIANZHUANG BIOTECHNOLOGY LIMITED COMPANY
Abstract: The present invention provides a method for preparing regenerated cellulose fibers having anti-bacteria, anti-mite and anti-mould functions from a fennel extract, a Litsea cubeba extract, and a thyme essential oil. The present invention also relates to the use of the regenerated cellulose fiber prepared by the above method in the field of anti-bacteria, anti-mite and mildew-resistant fabrics. The invention solves the technical defect that regenerated cellulose fibers have a single function and has poor anti-mite and anti-mould effects in the prior art.