Coated Capsules Patents (Class 424/463)
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Publication number: 20120321709Abstract: Disclosed are a complex formulation for oral administration comprising probiotic formulation and 5-HT4 receptor agonist, and a method for the preparation thereof.Type: ApplicationFiled: February 25, 2011Publication date: December 20, 2012Applicant: HANMI SCIENCE CO LTDInventors: Jong Soo Woo, Jae Hyun Park, Yong Il Kim, Dong Ho Kim, Jun Young Choi
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Publication number: 20120321706Abstract: Disclosed is a multi-layered gastroretentive dosage form for the controlled release of a poorly soluble drug or diagnostic in the stomach and gastrointestinal tract of a patient, folded into a capsule which disintegrates rapidly and the said multi-layered dosage form unfolds rapidly upon contact with the gastric juice. The mechanisms of the gastric retention are not dependent on and do not influence the materials and methods used in controlling the release of the said poorly soluble drug.Type: ApplicationFiled: October 19, 2010Publication date: December 20, 2012Applicant: INTEC PHARMA LTD.Inventors: Suher Masri, Eytan Moor, David Kirmayer, Elena Kluev, Giora Carni, Nadav Navon
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Publication number: 20120315329Abstract: Embodiments of the present invention relate generally to siloxane surface-modified hydrogel microparticles and pastes, methods for their preparation, and uses thereof for delivery of personal care and healthcare active ingredients, as well as agricultural active ingredients.Type: ApplicationFiled: February 17, 2011Publication date: December 13, 2012Applicant: Dow Corning CorporationInventors: Dongchan Ahn, James Thompson
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Publication number: 20120315328Abstract: A capsule of compound danshen dripping pills are disclosed. The color of the capsule's shell is orange, yellow, green or blue and all of these colors are in the wavelength range of 446-620 nm.Type: ApplicationFiled: February 17, 2011Publication date: December 13, 2012Applicant: Tasly Pharmaceutical Group Co., Ltd.Inventors: He Sun, Shuiping Zhou, Lanlan Zhang, Zhijuan Huang, Zhaohui Song
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Patent number: 8304220Abstract: Bone cages are disclosed including devices for biocompatible implantation. The structures of bone are useful for providing living cells and tissues as well as biologically active molecules to subjects.Type: GrantFiled: October 15, 2007Date of Patent: November 6, 2012Assignee: The Invention Science Fund I, LLCInventors: Ed Harlow, Edward K. Y. Jung, Robert Langer, Eric C. Leuthardt, Lowell L. Wood, Jr.
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Publication number: 20120269891Abstract: Disclosed herein are controlled-release oral pharmaceutical dosage forms comprising MGBG, and their application for the improved treatment of diseases with reduced side effects and/or longer time at maximum concentration.Type: ApplicationFiled: January 19, 2012Publication date: October 25, 2012Applicant: PATHOLOGICA LLCInventors: John McKearn, Jeremy Blitzer
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Patent number: 8287902Abstract: An ingestible capsule is provided for delivering medication to a subject. A capsule coating dissolves in a gastrointestinal tract of the subject. An inner core of the capsule has an outer surface associated therewith. The outer surface is disposed within the coating and expands when the coating dissolves. A medication is disposed on the outer surface, and the outer surface is configured such that the medication contacts an intestinal wall of the subject when the outer surface expands. Other embodiments are also provided.Type: GrantFiled: July 23, 2009Date of Patent: October 16, 2012Assignee: Rainbow Medical Ltd.Inventor: Yossi Gross
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Publication number: 20120258167Abstract: The present application provides a method for treating or preventing Celiac disease. In one embodiment the method comprises administering to a patient in need thereof a composition comprising minicapsules, wherein the minicapsules comprise a steroid in a liquid, semi-solid or solid core, the minicapsules having release profiles to release the steroid in an active form at one or more sites along the gastrointestinal tract, the one or more sites comprising the proximal small intestine beginning at the duodenum and ending at the ileum. In a related embodiment the method comprises administering budesonide to a patient in need thereof in a pre-solubilised drug delivery format.Type: ApplicationFiled: April 6, 2012Publication date: October 11, 2012Inventor: Ivan Coulter
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Publication number: 20120244216Abstract: Pharmaceutical compositions in unit dose form comprising a hard or soft capsule containing a fill consisting of one or more inert ingredients, and one or more coatings on the capsule, wherein at least one coating comprises at least one active pharmaceutical ingredient.Type: ApplicationFiled: June 7, 2012Publication date: September 27, 2012Inventors: Manish S. SHAH, Ray J. Difalco
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Publication number: 20120237599Abstract: The disclosure provides oral cysteamine and cystamine formulations useful for treating cystinosis and neurodegenerative diseases and disorders. The formulations provide controlled release compositions that improve quality of life and reduced side-effects.Type: ApplicationFiled: February 17, 2012Publication date: September 20, 2012Applicant: THE REGENTS OF THE UNIVERSITY OF CALIFORNIAInventors: Ranjan Dohil, Jerry Schneider
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Publication number: 20120231074Abstract: The present invention is directed to a solid dosage form comprising (i) a core comprising a benzimidazole; (ii) a separating layer comprising a water soluble polymer and glyceryl monostearate; and (iii) an enteric coating.Type: ApplicationFiled: November 5, 2010Publication date: September 13, 2012Inventors: Angel Santanach-Delisau, Luis Soler Ranzani, Pierandrea Esposito
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Publication number: 20120231073Abstract: Premixes of dexlansoprazole with pharmaceutical excipients, processes for preparing premixes, pharmaceutical formulations containing the premixes, and their use in treatment of erosive esophagitis and heartburn associated with non-erosive gastroesophageal reflux disease.Type: ApplicationFiled: May 18, 2012Publication date: September 13, 2012Applicants: DR. REDDY'S LABORATORIES, INC., DR. REDDY'S LABORATORIES LIMITEDInventors: Nagaraju Manne, Udaykumar Neelam, Sudhakar Reddy Baddam, Naveen Kumar Kolla, Venkata Nookaraju Sreedharala, Chandra Sekhar Veera Venkata Naga Bulusu
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Publication number: 20120219620Abstract: A supercritical fluid (SCF) extract of a cardiac glycoside-containing plant mass is provided. The extract can be included in a pharmaceutical composition containing an extract-solubilizing amount of solubilizer. Oleandrin is included within the extract when a cardiac glycoside-containing plant, such as Nerium oleander, is extracted by SCF extraction. The extract can also contain one or more other SCF extractable pharmacologically active agents. The composition can be used to treat a wide range of disorders that are therapeutically responsive to a cardiac glycoside.Type: ApplicationFiled: March 12, 2012Publication date: August 30, 2012Applicant: Phoenix Biotechnology, Inc.Inventors: O.Cradell Addington, Feng Zhang, John J. Koleng
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Patent number: 8252570Abstract: Bone cages are disclosed including devices for biocompatible implantation. The structures of bone are useful for providing living cells and tissues as well as biologically active molecules to subjects.Type: GrantFiled: September 12, 2007Date of Patent: August 28, 2012Assignee: The Invention Science Fund I, LLCInventors: Ed Harlow, Edward K. Y. Jung, Robert Langer, Eric C. Leuthardt, Lowell L. Wood, Jr.
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Patent number: 8252327Abstract: A dosage form that provides a controlled release solid dosage form for the oral administration of a central nervous system stimulant, preferably methylphenidate hydrochloride.Type: GrantFiled: July 11, 2011Date of Patent: August 28, 2012Assignee: Andrx Pharmaceuticals, Inc.Inventors: Manesh Dixit, Chih-Ming Chen, Xiu-Xiu Cheng, Jianbo Xie
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Publication number: 20120213848Abstract: A method for treating HIV and other intra-cellular parasites and toxins using intrabodies delivered to leukocytes.Type: ApplicationFiled: November 16, 2011Publication date: August 23, 2012Inventor: Brian P. Hanley
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Publication number: 20120207827Abstract: Embodiments of the invention relate generally to the use of formulations comprising DMSO and MSM to treat arthritis (such as osteoarthritis), pain, inflammation, and/or degeneration. DMSO and MSM formulations are administered orally and/or topically in several embodiments and provide effective treatment of both chronic and acute symptoms of arthritis (e.g., osteoarthritis), pain, inflammation, and/or degeneration. Solid forms of DMSO are provided in several embodiments.Type: ApplicationFiled: October 29, 2010Publication date: August 16, 2012Applicant: Abela Pharmaceuticals, Inc.Inventors: Colette Cozean, Jesse Cozean, Rodney Benjamin, Anthony Keller
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Publication number: 20120207826Abstract: There is disclosed herein a composition for treating extracellular parasitic infections, the composition comprising one or more of the following combinations: at least one quinolone or fluoroquinolone together with at least one tetracycline, iodoquinol, an azole or imidazole; or at least two agents selected from the group consisting of iodoquinol, thiazolidones, tetracycline, nitroimidazoles, cotrimoxazole and diloxanide furoate.Type: ApplicationFiled: October 22, 2010Publication date: August 16, 2012Inventors: Thomas Julius Borody, Soledad Carsula
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Publication number: 20120195964Abstract: The present invention provides, among other things, compositions and methods suitable for the treatment of hyperphosphatemia based on phosphate-binding magnesium salts. In some embodiments, the present invention provides compositions and methods suitable for the treatment of hyperphosphatemia based on the combination of phosphate-binding magnesium and an enteric coating.Type: ApplicationFiled: April 12, 2012Publication date: August 2, 2012Applicant: CYPRESS PHARMACEUTICAL, INC.Inventors: Robert L. Lewis, Charles E. Day
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Publication number: 20120164075Abstract: The present invention provides compositions containing endoxifen, formulations and liposomes of endoxifen, methods of preparation of such agents and formulations, and use of such agents and formulations for the treatment of a subject having or at risk for psychiatric and neurodegenerative diseases, infectious diseases, fertility disorders, osteoporosis, osteoarthritis, and/or cardiovascular diseases. Specifically, the present invention relates to compositions comprising endoxifen for use in the treatment of such disorders or predisposition to such disorders, for use in manufacture of medicaments for treating such disorders, and methods comprising use of such compositions in such treatments.Type: ApplicationFiled: May 21, 2010Publication date: June 28, 2012Applicant: JINA PHARMACEUTICALS, INC.Inventors: Ateeq Ahmad, Shoukath M. Ali, Moghis U. Ahmad, Saifuddin Sheikh, Imran Ahmad
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Publication number: 20120164209Abstract: An abuse resistant oral pharmaceutical composition, comprising: a barrier layer, comprising a first polymer; a diffusion layer, comprising a second polymer, substantially covering the barrier layer, wherein the diffusion layer is bonded to the barrier layer and comprises a drug that is substantially homogeneously distributed within the second polymer and diffuses from the diffusion layer within the gastrointestinal (GI) tract; and optionally an expansion layer comprising an expandable polymer, wherein the expansion layer is substantially covered by the barrier layer. Methods of making the same and methods of using the same are also provided.Type: ApplicationFiled: February 29, 2012Publication date: June 28, 2012Applicant: INSPIRION DELIVERY TECHNOLOGIIES, LLCInventors: Manish S. Shah, Ray Difalco
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Patent number: 8206741Abstract: The present invention is directed to drug dosage forms that release an agent that raises the pH of a patient's gastrointestinal tract, followed by a non-steroidal anti-inflammatory drug. The dosage form is designed so that the NSAID is not released until the intragastric pH has been raised to a safe level. The invention also encompasses methods of treating patients by administering this coordinated release, gastroprotective, antiarthritic/analgesic combination unit dosage form to achieve pain and symptom relief with a reduced risk of developing gastrointestinal damage such as ulcers, erosions and hemorrhages.Type: GrantFiled: May 16, 2005Date of Patent: June 26, 2012Assignee: POZEN Inc.Inventor: John R. Plachetka
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Publication number: 20120156277Abstract: An abuse resistant oral pharmaceutical composition, comprising: a barrier layer, comprising a first polymer; a diffusion layer, comprising a second polymer, substantially covering the barrier layer, wherein the diffusion layer is bonded to the barrier layer and comprises a drug that is substantially homogeneously distributed within the second polymer and diffuses from the diffusion layer within the gastrointestinal (GI) tract; and optionally an expansion layer comprising an expandable polymer, wherein the expansion layer is substantially covered by the barrier layer. Methods of making the same and methods of using the same are also provided.Type: ApplicationFiled: February 29, 2012Publication date: June 21, 2012Applicant: INSPIRION DELIVERY TECHNOLOGIES, LLCInventors: Manish S. Shah, Ray J. Difalco
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Publication number: 20120156290Abstract: Methods are provided which include converting oripavine to other opiates, including converting oripavine to naltrexone, buprenorphine, 14-hydroxymorphinone and/or converting 14-hydroxymorphinone to oxymorphone. Purification and salt formation are optionally included.Type: ApplicationFiled: February 28, 2012Publication date: June 21, 2012Applicant: PENICK CORPORATIONInventor: Bao-Shan HUANG
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Patent number: 8198265Abstract: A mechanism of macrophage-induced T cell suppression is the selective elimination of tryptophan and/or increase in one or more tryptophan metabolites within the local macrophage microenvironment. Studies demonstrate that expression of IDO can serve as a marker of suppression of T cell activation, and may play a significant role in allogeneic pregnancy and therefore other types of transplantation, and that inhibitors of IDO can be used to activate T cells and therefore enhance T cell activation when the T cells are suppressed by pregnancy, malignancy or a virus such as HIV. Inhibiting tryptophan degradation (and thereby increasing tryptophan concentration while decreasing tryptophan metabolite concentration), or supplementing tryptophan concentration, can therefore be used in addition to, or in place of, inhibitors of IDO.Type: GrantFiled: November 21, 2006Date of Patent: June 12, 2012Assignee: Medical College of Georgia Research Institute Inc.Inventors: David Munn, Andrew Mellor
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Publication number: 20120128767Abstract: The present invention provides novel calcium phosphate nanoparticles suitable for efficient encapsulation of biologically active molecules. The invention further provides pharmaceutical compositions comprising these nanoparticles, as well as methods of making such nanoparticles and using them as carriers for therapeutic delivery of biologically active macromolecules.Type: ApplicationFiled: May 1, 2009Publication date: May 24, 2012Inventors: William W. LEE, Feng LU
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Publication number: 20120128770Abstract: The present invention relates to 1 or 2 C16-C18 acyl glycerol based compounds which are capable of activating G-protein coupled receptor 119 and thereby stimulate GLP-1 release. Compounds of the present invention are useful in the prophylaxis and/or treatment of metabolic disorders and complications thereof, such as, type 2 diabetes mellitus (T2DM), obesity, insulin resistance, and cardiovascular disease.Type: ApplicationFiled: June 24, 2010Publication date: May 24, 2012Applicant: Kobenhavns UniversitetInventors: Harald S. Hansen, Thi Ai Diep, Jens Juul Holst, Mette Marie Rosenkilde, Niels Wellner Andersen
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Publication number: 20120121701Abstract: The invention relates to a method of co-administering a peptide or protein drug with an enzyme-resistant PGA-complexone compound orally so to mitigate enzyme attack in the gastrointestinal tract of an animal subject.Type: ApplicationFiled: December 13, 2011Publication date: May 17, 2012Inventors: Hsing-Wen Sung, Kiran Sonaje, Hosheng Tu
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Publication number: 20120114751Abstract: The present invention relates to a granular pharmaceutical composition comprising an HCV protease inhibitor and at least one poloxamer.Type: ApplicationFiled: November 8, 2011Publication date: May 10, 2012Inventors: Andreas Leiminer, Kai Lindenstruth, Dave Alan Miller, Emmanuel Scheubel, Navnit Hargovindas Shah
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Patent number: 8173158Abstract: The present invention relates to a method of treating a gastrointestinal disorder by administering to a patient in need of treatment thereof a pharmaceutical composition, wherein said pharmaceutical composition can be administered to the patient independent of the intake of food.Type: GrantFiled: October 10, 2008Date of Patent: May 8, 2012Assignee: Takeda Pharmaceuticals U.S.A., Inc.Inventors: Ronald D. Lee, Majid Vakily, Darcy Mulford, Jing-Tao Wu, Stuart Atkinson
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Publication number: 20120100210Abstract: Provided are improvements in and relating to pharmaceutical compositions for oral administration of polymeric biological drug substances and to methods of treatment using such compositions. In particular, an oral and/or mucosal pharmaceutical composition is provided, said composition comprising an enteric-coated drug substance, and also comprising an enteric-coated oligouronate, wherein said drug substance is a polymeric biological drug substance.Type: ApplicationFiled: March 23, 2010Publication date: April 26, 2012Applicant: NTNU TECHNOLOGY TRANSFER ASInventors: Kurt Ingar Draget, Catherine Taylor
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Publication number: 20120093926Abstract: The invention relates to a gastric resistant pharmaceutical or nutraceutical composition, comprising a core, comprising a pharmaceutical or nutraceutical active ingredient and a gastric resistant coating layer onto the core, wherein the release of the pharmaceutical or nutraceutical active ingredient is not more than 15% under in-vitro conditions at pH 1.Type: ApplicationFiled: April 13, 2011Publication date: April 19, 2012Applicant: Evonik Roehm GmbHInventors: Shraddha Ashok Bodinge, Priyanka Bansilal Haksar, Seema Yashwant Gawde, Hemant Karbhari Pagar, Hans-Ulrich Petereit
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Publication number: 20120087977Abstract: The invention relates to an aqueous medium containing an amino(meth)acrylate polymer or copolymer which is not soluble in demineralised water, characterized in that the medium has a content of an aqueous phase of at least 60% by weight and a content of up to 40% by weight of solids comprising the amino(meth)acrylate polymer or copolymer, whereby the aqueous phase is charged by a sufficient amount of carbon dioxide that effects the amino(meth)acrylate polymer or copolymer to be present in solute form in the medium. The aqueous medium may be used beneficially as a coating or binding solution for the spray coating or binding of pharmaceutical compositions or nutraceutical compositions or cosmetical compositions.Type: ApplicationFiled: July 30, 2009Publication date: April 12, 2012Applicant: Evonik Roehm GmbHInventors: Rosario Lizio, Michael Damm, Hans-Ulrich Petereit
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Publication number: 20120082720Abstract: The present invention describes dietary compositions and methods of using such compositions to treat chronic viral infections, including hepatitis B and hepatitis C infections.Type: ApplicationFiled: January 11, 2011Publication date: April 5, 2012Inventor: Sam Poon Ang
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Publication number: 20120082721Abstract: The present invention refers to a dosage form comprising an enteric coating in a specific amount, and to the use of enteric coating compositions for preparing a dosage form. Furthermore, the present invention also relates to a process for the preparation of a solid oral dosage form.Type: ApplicationFiled: May 28, 2010Publication date: April 5, 2012Applicant: H E X A L AktiengesellschaftInventors: Christian Buessing, Marco Marchesan, Andreas Krekeler
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Patent number: 8147871Abstract: The present invention is directed to novel pharmaceutically acceptable polymeric compositions suitable for melt extrusion and injection molding of single or multi-component pharmaceutical dosage forms comprising a plurality of drug substance containing sub-units, being capsule compartments and/or solid sub-units comprising a solid matrix of a polymer which contains a drug substance, the sub-units being connected together in the assembled dosage form.Type: GrantFiled: March 11, 2005Date of Patent: April 3, 2012Assignee: Capsugel Belgium BVBAInventors: Adrian Brown, Wayne M. Matthews, Daniel M. Margetson, Stephen Mark McAllister, Ronald K. Raby
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Publication number: 20120064156Abstract: The present invention is directed to drug dosage forms that release an agent that raises the pH of a patient's gastrointestinal tract, followed by a non-steroidal anti-inflammatory drug. The dosage form is designed so that the NSAID is not released until the intragastric pH has been raised to a safe level. The invention also encompasses methods of treating patients by administering this coordinated release, gastroprotective, antiarthritic/analgesic combination unit dosage form to achieve pain and symptom relief with a reduced risk of developing gastrointestinal damage such as ulcers, erosions and hemorrhages.Type: ApplicationFiled: August 23, 2011Publication date: March 15, 2012Inventor: John R. Plachetka
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Patent number: 8124123Abstract: A solid dosage form for oral administration comprising azithromycin in an amount below that which causes gastrointestinal side effects, which dosage form is a controlled release dosage form.Type: GrantFiled: December 17, 2007Date of Patent: February 28, 2012Assignee: Dow Pharmaceutical Sciences, Inc.Inventors: Radhakrishnan Pillai, Pramod Sarpotdar, David W. Osborne, Gordon J. Dow
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Publication number: 20120045509Abstract: The present invention refers to pharmaceutical composition comprising a DPP-IV inhibitor.Type: ApplicationFiled: October 27, 2011Publication date: February 23, 2012Inventors: Bernd Michael Loeffler, Alexander MacDonald, Cynthia Rocha, Eric Worth
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Patent number: 8114647Abstract: Bone cages are disclosed including devices for biocompatible implantation. The structures of bone are useful for providing living cells and tissues as well as biologically active molecules to subjects.Type: GrantFiled: October 18, 2007Date of Patent: February 14, 2012Assignee: The Invention Science Fund I, LLCInventors: Ed Harlow, Roderick A. Hyde, Edward K. Y. Jung, Robert Langer, Eric C. Leuthardt, Lowell L. Wood, Jr.
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Publication number: 20120034299Abstract: The present invention provides compositions for use in the prophylaxis or treatment of a condition arising from gluten intolerance, the compositions including at least partially purified caricain (or a biologically active fragment, analogue or variant thereof) alone or in combination with other suitable enzymes including bromelain, and/or an intestinal extract, as herein described. The present invention also provides methods of using such compositions for the prophylaxis or treatment of a condition arising from gluten intolerance.Type: ApplicationFiled: January 6, 2010Publication date: February 9, 2012Applicant: Glutagen Pty Ltd.Inventors: Teodor Stelmasiak, Hugh James Beatty Cornell
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Publication number: 20120027864Abstract: The invention relates generally to methods of making formulations for delivering biological agents to a patient. In one aspect, proliposomal drug-delivery systems for medicaments are provided. In another aspect, coated proliposomal formulations for poorly water soluble drugs, and methods for making the same, are provided. Certain embodiments of the present invention provide enhanced stability and bioavailability for pharmaceutical formulations.Type: ApplicationFiled: October 7, 2011Publication date: February 2, 2012Applicant: WESTERN UNIVERSITY OF HEALTH SCIENCESInventor: Guru V. BETAGERI
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Patent number: 8097278Abstract: The present invention provides a dosage form that prevents misuse of the medicament contained within. The dosage form contains an inactivating substance in combination with the medicament, wherein the two substances are separated by a permeable or semi-permeable partition. The partition becomes impermeable upon activation by a medical professional, thereby effectively sequestering the inactivating substance from the medicament and allowing for the intended administration of the medicament to the patient. Unless activated, however, the inactivating substance and medicament remain commingled in the dosage form, and any attempt to dispense the medicament before activation will result in the release of inactivated medicament.Type: GrantFiled: September 20, 2006Date of Patent: January 17, 2012Assignee: Purdue Pharma L. P.Inventor: Richard S. Sackler
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Publication number: 20120009256Abstract: Naturally occurring lecithins and/or oleic acid stimulate the growth and lactic acid producing activity of Lactobacillus and Bifidobacterium species of probiotic bacteria, and replace polysorbate 80 for those products. They can be used in naturally occurring form, or where they are to be combined with probiotics in a carrier, or they can be treated to yield a stable powdered form of these naturally oily compounds. They can be sold as combined prebiotic/probiotic formulations in the same carrier, or sold as separate dietary supplements, e.g., in capsule or tablet form, to be used with the probiotic formulation as desired.Type: ApplicationFiled: May 30, 2011Publication date: January 12, 2012Applicant: MASTER SUPPLEMENTS, INC.Inventors: Randolph S. Porubcan, Sonja Lea Yonak
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Publication number: 20120003307Abstract: The present invention is concerned with controlled release compositions for oral administration comprising levetiracetam; and with processes of preparing such controlled release compositions.Type: ApplicationFiled: November 26, 2008Publication date: January 5, 2012Applicant: RANBAXY LABORATORIES LIMITEDInventors: Namdev M. Kashid, Sunny Chopra, Sumit Madan, Vinod Arora
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Publication number: 20110311622Abstract: A method for administering pharmaceutical agents to a subject is provided. The method includes the steps of: a) providing a course of treatment for a subject, which course includes periodically administering an amount of medicine to the subject, which 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), which NPA provides at least one non-visual sensory cue; and b) varying the dosage amount of the APA within the periodically administered amount of medicine, while the amount of the NPA contained within each periodically administered amount of medicine is provided at a level that maintains the sensory cue at a substantially constant level.Type: ApplicationFiled: December 22, 2009Publication date: December 22, 2011Inventors: Joshua D. Levine, Robert A. Levine
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Publication number: 20110311621Abstract: The pharmaceutical compositions described herein include a suspension which comprises an admixture in solid form of a therapeutically effective amount of a therapeutic agent (such as CCK-8, octreotide), at least one salt of a medium chain fatty acid, a matrix forming polymer and a hydrophobic(lipophilic) medium. A surfactant may be included in the suspension. The pharmaceutical compositions may be formulated in a capsule or tablet for oral delivery. Methods of treating or preventing diseases by administering such compositions to affected subjects are also disclosed.Type: ApplicationFiled: March 16, 2011Publication date: December 22, 2011Inventors: Paul Salama, Irina Karmeli, Shmuel Tuvia, Karen Marom, Oshrat Harush-Frenkel, Dana Gelbaum, Roni Mamluk, Fredric David Price, Steven Ronald Peikin
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Publication number: 20110305755Abstract: A method for administering an active pharmaceutical agent (APA) is provided that includes the steps of: a) providing a medicine having a dose of at least one APA and at least one active botanical agent (ABA) or dietary supplement; and b) dosing the APA within the medicine such that within each subsequent dose of the medicine, the amount of the APA decreases and the amount of the ABA increases, or remains the same, or decreases relative to an earlier amount. A trace of the APA may or may not remain in the pill toward the end of medicine application.Type: ApplicationFiled: January 28, 2010Publication date: December 15, 2011Inventors: Joshua D. Levine, Robert A. Levine
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Publication number: 20110300213Abstract: The subject invention relates to a variety of formulations of bipolar trans carotenoids including pharmaceutical compositions for oral delivery of a bipolar trans carotenoid comprising i) a bipolar trans carotenoid, ii) a cyclodextrin, and iii) a coating. The invention also relates to preparation of such formulations and their uses.Type: ApplicationFiled: June 2, 2011Publication date: December 8, 2011Inventors: John L. Gainer, Robert Murray
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Publication number: 20110274750Abstract: An enteric formulation of duloxetine, its core and preparing method thereof are disclosed. The core comprises duloxetine or its salt and pharmaceutically acceptable excipients. The excipients include water-soluble hot melt materials selected from PEG, poloxamer, polyoxyl (40) stearate or their mixture. Based on the total weight of the core, the amount of water-soluble hot melt materials is 10%˜40% and the amount of duloxetine or its salt is 15˜60%. The core material is prepared by hot melt process. The enteric formulation comprises the core, a separating layer and an enteric layer.Type: ApplicationFiled: November 4, 2009Publication date: November 10, 2011Applicant: SHANGHAI ZHONGXI PHARMACEUTICAL CORPORATIONInventors: Yunhui Ding, Siji Zheng