Patents Issued in June 6, 2013
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Publication number: 20130142837Abstract: The present invention is directed to cellulosic gel compositions having improved viscosity stability through the exclusion of particular antioxidants and/or the exclusion of chemical entities that tend to produce free radicals. Preferably, the composition is an ophthalmic cellulosic gel composition that is suitable as a multi-dose composition.Type: ApplicationFiled: November 28, 2012Publication date: June 6, 2013Applicant: ALCON RESEARCH, LTD.Inventor: Alcon Research, Ltd.
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Publication number: 20130142838Abstract: Compositions, preferably pharmaceutical compositions, containing micronized tanaproget, or pharmaceutically acceptable salt thereof, microcrystalline cellulose, croscarmellose sodium, sodium lauryl sulfate, butylated hydroxyanisole, povidone, and magnesium stearate, are provided. The compositions are useful in contraception and hormone replacement therapy and in the treatment and/or prevention of uterine myometrial fibroids, benign prostatic hypertrophy, benign and malignant neoplastic to disease, dysfunctional bleeding, uterine leiomyomata, endometriosis, polycystic ovary syndrome, and carcinomas and adenocarcinomas of the pituitary, endometrium, kidney, ovary, breast, colon, and prostate and other hormone-dependent tumors, and in the preparation of medicaments useful therefor. Additional uses include stimulation of food intake.Type: ApplicationFiled: November 29, 2012Publication date: June 6, 2013Applicant: Wyeth LLCInventor: Wyeth LLC
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Publication number: 20130142839Abstract: A method and system for administering pharmaceutical agents to a subject is provided. The system includes a course of treatment regimen, which includes a prescribed order of medicine amounts for periodic administration to the subject in the prescribed order. The amount of medicine includes a dose of at least one active pharmacological agent (APA) and an amount of at least one non-active pharmacological agent (NPA). The NPA provides at least one non-visual sensory cue. The dosage amounts of the APA contained within the amounts of medicine periodically administered in the prescribed order are varied within the course of treatment regimen, and the amount of the NPA contained within the amounts of medicine periodically administered in the prescribed order are held constant within the course of treatment regimen.Type: ApplicationFiled: November 30, 2012Publication date: June 6, 2013Inventors: Joshua D. Levine, Robert A. Levine
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Publication number: 20130142840Abstract: Method for preparing a homogeneous collagen-based material by concentration of a collagen solution, includes bringing a collagen solution into contact by way of continuous injection and use of the material for tissue repair.Type: ApplicationFiled: May 30, 2011Publication date: June 6, 2013Applicants: UNIVERSITE PIERRE ET MARIE CURIE (PARIS 6), UNIVERSITE DE VERSAILLES SAINT QUENTIN EN YVELINES, CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUEInventors: Marie-Madeleine Giraud-Guille, Nadine Nassif, Yan Wang, Christophe Helary, Anne Pelle
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Publication number: 20130142841Abstract: Highly compactable granulations and methods for preparing highly compactable granulations are disclosed. More particularly, highly compactable calcium carbonate granulations are disclosed. The granulations comprise powdered materials such as calcium carbonate that have small median particle sizes. The disclosed granulations are useful in pharmaceutical and nutraceutical tableting and provide smaller tablet sizes upon compression than previously available.Type: ApplicationFiled: January 30, 2013Publication date: June 6, 2013Applicant: DELAVAU L.L.C.Inventor: DELAVAU L.L.C.
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Publication number: 20130142842Abstract: Highly compactable granulations and methods for preparing highly compactable granulations are disclosed. More particularly, highly compactable calcium carbonate granulations are disclosed. The granulations comprise powdered materials such as calcium carbonate that have small median particle sizes. The disclosed granulations are useful in pharmaceutical and nutraceutical tableting and provide smaller tablet sizes upon compression than previously available.Type: ApplicationFiled: January 30, 2013Publication date: June 6, 2013Applicant: DELAVAU L.L.C.Inventor: Delavau L.L.C.
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Publication number: 20130142843Abstract: Highly compactable granulations and methods for preparing highly compactable granulations are disclosed. More particularly, highly compactable calcium carbonate granulations are disclosed. The granulations comprise powdered materials such as calcium carbonate that have small median particle sizes. The disclosed granulations are useful in pharmaceutical and nutraceutical tableting and provide smaller tablet sizes upon compression than previously available.Type: ApplicationFiled: January 30, 2013Publication date: June 6, 2013Applicant: DELAVAU L.L.C.Inventor: DELAVAU L.L.C.
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Publication number: 20130142844Abstract: A method is provided for preparing a tissue implant for implantation. The method includes harvesting a tissue material from a human or an animal donor, treating the tissue material in a nuclease-containing solution, and thereafter treating the tissue material with an alkaline alcohol solution. The nuclease-containing solution includes an antimicrobial. The alkaline alcohol solution comprises sodium hydroxide and ethanol.Type: ApplicationFiled: January 30, 2013Publication date: June 6, 2013Applicant: CRYOLIFE, INC.Inventor: CRYOLIFE, INC.
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Publication number: 20130142845Abstract: The present invention is concerned with the use of combinations of opioid agonists and antagonists for treating Crohn's disease.Type: ApplicationFiled: January 30, 2013Publication date: June 6, 2013Applicant: Euro-Celtique S.A.Inventor: Euro-Celtique S.A.
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Publication number: 20130142846Abstract: A pharmaceutical dosage form comprising non-steroidal-anti-inflammatory drugs, in particular propionic acid derivatives such as ibuprofen, along with a second active ingredient having a shorter therapeutically effective plasma concentration duration, such as phenylephrine, and methods of administering the same are provided. This method provides improved therapeutic effect, in particular pain relief along with decongestant relief, over extended time periods.Type: ApplicationFiled: January 31, 2013Publication date: June 6, 2013Applicant: MCNEIL-PPC, INCInventor: MCNEIL-PPC, INC
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Publication number: 20130142847Abstract: Provided herein are compositions and methods to enhance the absorption of S-adenosylmethionine (SAMe) and methods of treating various disorders or diseases using non-parenteral SAMe formulations with enhanced-absorption and improved bioavailability. In certain embodiments, the enhanced bioavailability formulations provided herein may be used to treat a variety of diseases or disorders, such as for example, psychiatric disorders including, generalized anxiety disorder, obsessive compulsive disorder, post traumatic stress disorder, panic disorder, depressive disorders (e.g. major clinical depression) and dysthymia; as well as treating liver disorders, cancer, autoimmune disorders, inflammatory disorders, joint disorders, gastrointestinal disorders and cardiovascular disease.Type: ApplicationFiled: July 27, 2011Publication date: June 6, 2013Applicant: Methylation Sciences, Inc.Inventors: I. David MacDonald, Nancy Harrison, Aniko Takacs-Cox, Admir Purac, Almira Blazek-Welsh
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Publication number: 20130142848Abstract: The present invention is a solid sustained-release formulation comprising an agent for inhibiting semaphorin 3A as an active ingredient, which comprises an agent for inhibiting semaphorin 3A and pharmaceutically acceptable hardly water-soluble solid substance, in which the carrier is silicone.Type: ApplicationFiled: August 4, 2011Publication date: June 6, 2013Inventors: Miho Maeda, Akiyoshi Kishino, Akihiko Sano, Hideyuki Okano, Masaya Nakamura, Liang Zhang
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Publication number: 20130142849Abstract: The present invention relates to controlled release formulation of dronedarone or pharmaceutically acceptable salts, esters, metabolites, prodrugs or enantiomers thereof and controlled release polymers. The use of controlled release formulations of Dronedarone would improve the bioavailability and the patient compliance with reduction in number of dosages to be taken per day.Type: ApplicationFiled: August 13, 2011Publication date: June 6, 2013Applicant: LUPIN LIMITEDInventors: Ashish Ashokrao Deshmukh, Pravin Meghrajji Bhutada, Sajeev Chandran, Shirish Kulkarni
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Publication number: 20130142850Abstract: A composition comprising an alloplastic injectable suspension for use as a dermal filler comprising a biocompatible and pliable material and a physiologically acceptable suspending agent is provided. A method of making a composition comprising an alloplastic injectable suspension for use as a dermal filler comprising a biocompatible and pliable material and a physiologically acceptable suspending agent, said method comprising admixing a biocompatible and pliable material with a physiologically acceptable suspending agent, is also provided. A method of augmenting soft tissue to provide long-term reduction of a skin defect, said method comprising stimulating collagen beneath the skin defect is further provided.Type: ApplicationFiled: January 14, 2013Publication date: June 6, 2013Inventor: Ayman Boutros
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Publication number: 20130142851Abstract: The present invention relates to medically efficacious agents coated with substance that forms a liquid impermeable but gas permeable layer, the treatment of medical conditions therewith, and particularly medical conditions at least partially characterised by blockage or other malfunction of ducts of exocrine glands and especially ducts of sweat glands.Type: ApplicationFiled: January 25, 2013Publication date: June 6, 2013Inventor: Warren Ward
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Publication number: 20130142852Abstract: A nanofiber laminate sheet including a layer of a nanofiber of a water insoluble polymer and a layer of a water soluble polymer containing a cosmetic component or a medicinal component. The nanofiber is preferably colored. The layer of a water soluble polymer is preferably a layer of a nanofiber of the water soluble polymer containing the cosmetic component or the medicinal component. The nanofiber laminate sheet is suited for use as a cosmetic sheet for makeup.Type: ApplicationFiled: June 28, 2011Publication date: June 6, 2013Applicant: KAO CORPORATIONInventors: Takehiko Tojo, Masataka Ishikawa, Ritsuko Yamazaki, Yuko Yago, Motoaki Ito, Yoshimi Yamashita
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Publication number: 20130142853Abstract: The present invention is a skin cosmetic comprising agar hydrogel particles having an average particle size of 0.2-5 mm obtained by stirring and cooling, in an oil based solvent, an agar aqueous solution prepared such that the breaking stress after the cooling/solidification is 0.005-0.1 MPa and an oil based gel prepared by mixing fine particles of silicone that are three-dimensionally cross-linked chemically and silicone oil and/or hydrocarbon oil. The object of the present invention is to provide a cosmetic that gives a moderate massaging sensation at the time of use.Type: ApplicationFiled: July 14, 2011Publication date: June 6, 2013Applicant: SHISEIDO COMPANY, LTD.Inventors: Akira Matsuo, Tomomi Furukawara
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Publication number: 20130142854Abstract: Provided is a manicure composition of a French nail type which has less disturbance of the lines brought about by a base color and a topcoat and is quickly dried, which does not cause dew condensation on the coating film under a moist environment for coating and has less leveling and less irregular color and which is excellent in a drying property, an adhesive property, flexibility, a masking property, a finished property, a discharge performance and a restirring property. The above manicure composition comprises at least ethanol and propylene glycol monomethyl ether as a solvent, titanium oxide A having an average primary particle diameter of 200 to 400 nm, titanium oxide B having an average primary particle diameter of 10 to 80 nm, an acrylic resin, polyether-modified polydimethylsiloxane and a plasticizer.Type: ApplicationFiled: August 30, 2011Publication date: June 6, 2013Inventors: Takayuki Hayakawa, Masaaki Morita
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Publication number: 20130142855Abstract: A method to control, inhibit, and kill pathogens and normal microbial strains that includes, but not limited to plant, animal and human pathogens, biofilm forming microbes, biofouling microbes, algae, fungi, bacteria, virus and protozoa using natural SL, MSL derivative and combinations thereof encompassed by the combination invention.Type: ApplicationFiled: February 2, 2013Publication date: June 6, 2013Applicant: Polytechnic Institute of New York UniversityInventor: Polytechnic Institute of New York University
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Publication number: 20130142856Abstract: The present invention provides an antiseptic composition comprising a germinant and an antimicrobial agent, wherein the germinant increases a pathogen's susceptibility to attack from the antimicrobial agent and wherein the antimicrobial agent does not inhibit the germinant. The present invention also provides an antiseptic wipe, handwash or paint comprising such antiseptic composition and a method of sterilizing a surface using such a composition.Type: ApplicationFiled: February 15, 2011Publication date: June 6, 2013Applicant: INSIGHT HEALTH LIMITEDInventors: Tony Worthington, Laura Wheeldon
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Publication number: 20130142857Abstract: The invention relates to toilet paper which can be used to satisfy human sanitary and hygiene requirements and makes it possible to reduce toilet paper consumption because the central sector of a sheet of the toilet paper has a higher average density and/or a higher average elasticity than the outer sector of said sheet of toilet paper, wherein the outer sector of the sheet of toilet paper completely or partially surrounds the central sector.Type: ApplicationFiled: July 21, 2011Publication date: June 6, 2013Inventors: Vladimir Vitalievich Miroshnichenko, Vitaly Evgenievich Pilkin
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Publication number: 20130142858Abstract: Drug delivery devices comprising a non-bioabsorbable polymer structure configured to support a composition comprising an active agent. The devices include a plurality of portions fused together and a recess configured to support the composition. At least one of the portions includes an impermeable polymer and at least one other portion includes a rate-limiting water-permeable polymer. The rate-limiting water-permeable polymer allows for transportation of the active agent to an exterior of the device.Type: ApplicationFiled: May 17, 2011Publication date: June 6, 2013Applicant: Aerie Pharmaceuticals, Inc.Inventors: Casey Kopczynski, Cheng-Wen Lin, Chris Sutay
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Publication number: 20130142859Abstract: Methods and compositions are provided for increasing the anaerobic working capacity of muscle and other tissues. Also provided are compositions formulated for the sustained release of free beta-alanine. Also provided is a dietary supplement formulated, for example, as a solid food product, an edible suspension, liquid or semi-liquid as described herein.Type: ApplicationFiled: January 31, 2013Publication date: June 6, 2013Applicant: NATURAL ALTERNATIVES INTERNATIONAL, INC.Inventors: NATURAL ALTERNATIVES INTERNATIONAL, INC., Ken Wolf
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Publication number: 20130142860Abstract: The invention relates to material compositions comprising adult stem cells obtained from exocrine gland tissue and a supporting matrix having the shape of a thread structure and/or of a net. The supporting matrix preferably consists of a plastic material which is physiologically acceptable and degradable in the body. The material compositions of the invention are in particular suited for use in regenerative medicine, e.g. for regeneration of injured or damaged myocard tissue.Type: ApplicationFiled: November 13, 2012Publication date: June 6, 2013Applicant: FRAUNHOFER-GESELLSCHAFT ZUR FORDERUNG ANGEWANDTEN FORSCHUNG E.V.Inventor: FRAUNHOFER-GESELLSCHAFT ZUR FORDERUNG DER ANGEWANDTEN FORSCHUNG E.V.
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Publication number: 20130142861Abstract: Novel compositions and methods for detecting and preventing and/or treating abnormal liver homeostasis and hepatocarcinoma as well as conditions that may be regulated by microRNA-122 are provided. A transgenic knockout non-human animal comprising a disruption in the endogenous mir-122 gene is also provided.Type: ApplicationFiled: November 29, 2012Publication date: June 6, 2013Applicant: NATIONAL YANG MING UNIVERSITYInventor: National Yang Ming University
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Publication number: 20130142862Abstract: Clostridium novyi is an obligate anaerobe that can infect hypoxic regions within experimental tumors. We found that mice bearing large, established tumors were often cured when treated with C. novyi plus a single dose of liposomal doxorubicin. The secreted factor responsible for this phenomenon was identified and, surprisingly, proved to be a member of the lipase family. The gene encoding this protein, called liposomase, has the potential to be incorporated into diverse therapeutic methods to deliver specifically a variety of chemotherapeutic agents to tumors.Type: ApplicationFiled: December 3, 2012Publication date: June 6, 2013Applicant: JOHNS HOPKINS UNIVERSITYInventor: Johns Hopkins University
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Publication number: 20130142863Abstract: The invention provides a method for lubricating one or more surfaces, comprising applying gel-phase liposomes onto said one or more surfaces, wherein the temperature of said surface(s) at the time of lubrication is below the phase transition temperature Tm of said liposomes. The method can be used for lubricating non-biological surfaces, and also for lubricating the surfaces of a biological tissue in a mammalian subject, e.g., for treating joint dysfunction.Type: ApplicationFiled: June 16, 2011Publication date: June 6, 2013Applicants: YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM, LTD., YEDA RESEARCH AND DEVELOPMENT CO., LTD.Inventors: Jacob Klein, Ronit Goldberg, Yechezkel Barenholtz, Avi Schroeder
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Publication number: 20130142864Abstract: The invention provides a composition for modulating immunity by the in vivo targeting of an antigen to dendritic cells. The composition comprises: a preparation of antigen-containing membrane vesicles or antigen-containing liposomes which have on their surfaces a plurality of metal chelating groups; and, a ligand for a receptor on the dendritic cells, the ligand being linked to a metal chelating group via a metal affinity tag on the ligand. The composition further includes an immunomodulatory factor. A process for preparing the composition is also provided. The invention further provides a method of modulating an immune disorder, and methods of treating tumours and infections.Type: ApplicationFiled: December 28, 2012Publication date: June 6, 2013Applicant: Lipotek Pty Ltd.Inventors: Joseph Altin, Christopher Richard Parish
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Publication number: 20130142865Abstract: The present invention concerns fixed dosing of HER antibodies, such as Pertuzumab.Type: ApplicationFiled: January 18, 2013Publication date: June 6, 2013Applicant: GENENTECH, INC.Inventor: Genentech, Inc.
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Publication number: 20130142866Abstract: The invention provides a novel aqueous composition for the storage and preservation of transplants, such as organ or tissue allografts. The composition comprises the compound N-octanoyl dopamine in solubilised form. The composition may also be administered as a pre-treatment of transplant donors. Moreover, it may be used in transplant recipients, optionally in combination with immunosuppressants.Type: ApplicationFiled: August 16, 2011Publication date: June 6, 2013Applicant: NOVALIQ GMBHInventors: Bastian Theisinger, Sonja Theisinger, Bernhard Günther
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Publication number: 20130142867Abstract: Cancer-targeting peptides having a PX1LX2 motif, in which X1 is His or an amino acid residue with a hydrophobic side chain and X2 is Pro, Phe, or Trp. Also disclosed herein are conjugates containing the cancer-targeting peptides and uses thereof in cancer treatment and diagnosis.Type: ApplicationFiled: October 25, 2011Publication date: June 6, 2013Applicant: Academia SinicaInventors: John Yu, Alice L. Yu, H.C. Wu, I-Ju Chen, Sheng-Hung Wang
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Publication number: 20130142868Abstract: Methods of delivering a pharmaceutical compounds directly to the olfactory epithelium of a mammal by providing a pharmaceutical aerosol suspension comprising an aerosol and the pharmaceutical compound; aerosolizing the suspension to generate a stream of droplets, the stream having a rotational component, and, delivering the droplets directly to the olfactory epithelium, wherein at least 15% of the droplets are delivered directly to the olfactory deposition. The pharmaceutical compound may be encapsulated within a liposome nanoparticle.Type: ApplicationFiled: August 19, 2011Publication date: June 6, 2013Applicant: UNIVERSITY OF WASHINGTONInventors: John D. Hoekman, Rodney J.Y. Ho
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Publication number: 20130142869Abstract: The invention provides analgesic, antipyretic and anti-inflammatory compositions containing epilactose in combination with non-steroidal anti-inflammatory drugs and pharmaceutically acceptable zinc compounds. This invention relates to the use of these novel compositions for significantly improved and synergistic safety and therapeutic profiles.Type: ApplicationFiled: December 5, 2012Publication date: June 6, 2013Inventors: Phillip Alex, Ben Johns
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Publication number: 20130142870Abstract: Unit comprising neramexane, a pharmaceutically acceptable salt, solvate, conjugate, prodrug, polymorphic form, isomer, or derivative thereof; and a release-controlling excipient; wherein said unit has a diameter of from 0.1 to less than 6 mm.Type: ApplicationFiled: June 22, 2011Publication date: June 6, 2013Applicant: MERZ PHARMA GmbH & CO. KGaAInventors: Bernhard Hauptmeier, Brigitte Purmann
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Publication number: 20130142871Abstract: The invention relates to an oral dosage form containing deferasirox, binder, disintegrant and optionally wicking agent, wherein the introduction of the dosage form into water leads to a suspension wherein the suspended particles have an average particle size (D50) of 20 ?m to 120 ?m, and also to a method of producing it.Type: ApplicationFiled: July 7, 2011Publication date: June 6, 2013Applicant: Ratiopharm GmbHInventors: Jana Paetz, Katrin Rimkus
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Publication number: 20130142872Abstract: The invention is a novel series of compounds represented by general formula, its analogs, tautomeric forms, stereoisomers, pharmaceutically acceptable salts and polymorphs wherein said compound described is a group of antisense molecules possessing immediate global cellular penetration due to their molecular structure and lipophilicity. The molecules are combinations of ethyl and methyl pyruvates. They induce riboswitch activity and reduce target RNA and nucleic acids such as HbA1c. They reduce inflammation and enhance energy production. These features improve therapeutic outcomes of diabetes, neuropathy and cellular aging.Type: ApplicationFiled: August 9, 2012Publication date: June 6, 2013Inventors: John James Fitzgerald, JR., Ranya Ludwig Alexander, Anthony Joseph Meduri
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Publication number: 20130142873Abstract: Provided herein are compositions of 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one, solid forms, isotopologues and metabolites thereof, and methods of their use for the treatment of a disease, disorder, or condition.Type: ApplicationFiled: November 30, 2012Publication date: June 6, 2013Applicant: SIGNAL PHARMACEUTICALS, LLCInventor: Signal Pharmaceuticals, LLC
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Publication number: 20130142874Abstract: New pharmaceutical compositions for oral use containing Diclofenac together with alkali metal bicarbonates in amounts of from 20 to 80 by weight with respect to Diclofenac are described. These compositions are entirely palatable and free from any unpleasant taste or other side effects; in particular, these formulations permit to obtain in human patients higher Cmax of the active principle and shorter Tmax together with a lower coefficient of variation.Type: ApplicationFiled: May 25, 2012Publication date: June 6, 2013Applicant: APR Applied Pharma Research SAInventors: Alberto Reiner, Giorgio Reiner
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Publication number: 20130142875Abstract: Treatment of prostate cancer by regional and prolonged release of one or more nucleotide-based RNAi agents is provided.Type: ApplicationFiled: November 14, 2012Publication date: June 6, 2013Applicant: SILENSEED LTD.Inventor: SILENSEED LTD.
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Publication number: 20130142876Abstract: Chewable sustained release compositions and their methods of production are provided. The sustained release compositions contain amphipathic lipids, which are used to encapsulate various drugs and active ingredients.Type: ApplicationFiled: November 30, 2012Publication date: June 6, 2013Applicant: PEGASUS LABORATORIES, INC.Inventor: Pegasus Laboratories, Inc.
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Publication number: 20130142877Abstract: The invention relates to a pharmaceutical dosage form comprising one or more antiretroviral active ingredients in the form of a solid dispersion or solid solution in a matrix, wherein said matrix comprises an amino(meth)acrylate copolymer, characterized in that the matrix does not contain any essential amounts of pharmaceutically acceptable surfactants with an HLB value from 12 to 18 and in that the matrix comprises a mono carboxylic acid or an alcohol with 12 to 22 carbon atoms or both.Type: ApplicationFiled: March 3, 2011Publication date: June 6, 2013Applicant: EVONIK ROEHM GmbHInventors: Pravin Nalawade, Smitha Shetty, Hema Ravishankar, Shripad Gadhinglajkar, Andreas Gryczke, Hans-Ulrich Petereit, Kathrin Nollenberger
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Publication number: 20130142878Abstract: A composition as disclosed is comprised of a plurality of groups of particles. The particles are comprised of a biocompatible polymer which may be a co-polymer such as PLGA combined with a peptide of a sequence of interest, e.g. a sequence which corresponds to a sequence presented on a surface of a cell infected with a virus. A plurality of different groups of particles are provided in the formulation wherein the particles within any single group include peptides of identical amino acid sequence. The particles are sized such that they are sufficiently large so as to prevent more than the contents of a single particle from being presented to a single immune system cell.Type: ApplicationFiled: November 30, 2012Publication date: June 6, 2013Applicant: FLOW PHARMA, INC.Inventor: FLOW PHARMA, INC
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Publication number: 20130142879Abstract: The present invention relates to suspension formulations, especially those for delivering a pharmaceutically active agent in aerosol form using a spray or aerosol device, such as a pressurised metered dose inhaler (pMDI). The formulations may be for pulmonary, nasal, buccal or topical administration, but are preferably for pulmonary inhalation.Type: ApplicationFiled: January 29, 2013Publication date: June 6, 2013Applicants: INNOVATA BIOMED LIMITED, VECTURA LIMITEDInventors: VECTURA LIMITED, INNOVATA BIOMED LIMITED
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Publication number: 20130142880Abstract: The present invention refers to pharmaceutical beclomethasone dipropionate compositions in modified-release gastro-resistant microspheres and to their oral use in the treatment of inflammatory pathologies of the intestinal tract. Said compositions in microspheres comprise: a) a core consisting of a microsphere of inert material; b) a first intermediate coating comprising beclomethasone dipropionate and at least one physiologically acceptable excipient; c) a second modified-release gastro-resistant coating. The present invention also refers to a process for obtaining said compositions.Type: ApplicationFiled: August 2, 2011Publication date: June 6, 2013Applicant: SOFAR SPAInventor: Carla Labruzzo
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Publication number: 20130142881Abstract: A lip balm composition of natural ingredients, comprising : 54-70 wt. % of one or more oils, 22-28 wt. % beeswax, 3-4 wt. % propolis, 3-5 wt. % pomace, 0.02-3.2 wt. % antioxidant, and optional ingredients, whereby all components add to 100 wt. %.Type: ApplicationFiled: December 2, 2011Publication date: June 6, 2013Applicant: THE MOTHERVINE NUTRACEUTICAL CO. LLCInventor: Fountain ODOM
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Publication number: 20130142882Abstract: The present invention provides methods and compositions for treating, preventing, modifying (reducing), or managing bone cancer pain by cyclohexenone compounds.Type: ApplicationFiled: November 14, 2012Publication date: June 6, 2013Applicant: GOLDEN BIOTECHNOLOGY CORPORATIONInventor: GOLDEN BIOTECHNOLOGY CORPORATION
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Publication number: 20130142883Abstract: A medical food for the dietary management of depression and/or anxiety includes water containing from 0.0002 to 0.0278 mol. % of isotopologue HOD, preferably, from 0.0178 to 0.0278 mol. % of isotopologue HOD. Further, a method for the dietary management of depression and/or anxiety uses the step of administering to a subject in need thereof the medical food. Further, a method of the treatment of depression includes the steps of administering to a subject an antidepressant drug and administering to the subject the medical food. Further, a method of the treatment of anxiety includes the steps of administering to a subject an antianxiety drug and administering to the subject the medical food.Type: ApplicationFiled: November 27, 2012Publication date: June 6, 2013Inventors: Igor Anatolyevich Pomytkin, Anton Sergeevich Chernopyatko
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Publication number: 20130142884Abstract: A cream has at least two components, one of the components includes stable water clusters, and the cream is applied on a body to produce local surface effects, local deep effects, and non-local effects in the body.Type: ApplicationFiled: January 28, 2013Publication date: June 6, 2013Applicant: D & Y LaboratoriesInventor: D & Y Laboratories
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Publication number: 20130142885Abstract: The present invention relates to compositions and methods by which surface modification techniques can be used to modify wide range polymeric or metal substrates using metal nanoparticles.Type: ApplicationFiled: January 15, 2013Publication date: June 6, 2013Applicant: University of Virginia Patent Foundation, d/b/a University of Virginia Licensing & Venture GroupInventor: University of Virginia Patent Foundation, d/b/a University of Virginia Licensing & Ventures Group
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Publication number: 20130142886Abstract: A biocidal composition comprising 2,2-dibromomalonamide and a metal selected from silver, copper, and mixtures thereof, and its use for the control of microorganisms in aqueous and water-containing systems.Type: ApplicationFiled: August 3, 2011Publication date: June 6, 2013Applicants: DOW GLOBAL TECHNOLOGIES LLC, ROHM AND HAAS CHEMICALS LLCInventors: Freddie L. Singleton, Tirthankar Ghosh, Kimberly S. Cagle