Sulfur In R Patents (Class 514/618)
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Patent number: 7763661Abstract: This invention relates to novel substituted pentafluorosulfanylbenzenes of the formula I: and/or salts thereof as claimed, for use as a synthetic intermediates for preparing medicaments, diagnostic aids, liquid crystals, pesticides, herbicides, fungicides, nematicides, parasiticides, insecticides, acaricides, arthropodicides and polymers.Type: GrantFiled: March 9, 2007Date of Patent: July 27, 2010Assignee: sanofi-aventis Deutschland GmbHInventors: Heinz-Werner Kleemann, Remo Weck
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Publication number: 20100172957Abstract: Administration of at least one compound selected from (S)-2-dodecylsulfanyl-N-(4-hydroxy-2,3,5-trimethylphenyl)-2-phenylacetanilide (eflucimibe) of formula (I): or (R)-2-dodecylsulfanyl-N-(4-hydroxy-2,3,5-trimethylphenyl)-2-phenylacetanilide ((R) enantiomer), or pharmaceutically acceptable salt or pharmaceutically acceptable solvate thereof, is useful for preventing or treating disorders due to a sebaceous gland dysfunction in humans or animals, for example, acne and/or or any state or pathological condition related to an overproduction of sebum, e.g., seborrhoeic dermatitis, greasy skin or a greasy scalp.Type: ApplicationFiled: January 15, 2010Publication date: July 8, 2010Applicant: GALDERMA RESEARCH & DEVELOPMENTInventor: Thibaud BIADATTI-PORTAL
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Patent number: 7749540Abstract: Particle-forming compositions of modafinil compounds, and aqueous compositions of particles, wherein the particles comprise a modafinil compound, are disclosed, along with methods of their preparation, and their use in the treatment of diseases.Type: GrantFiled: October 11, 2001Date of Patent: July 6, 2010Assignee: Cephalon, Inc.Inventors: Martin J. Jacobs, Bradley T. McIntyre, Piyush R. Patel, David A. Dickason
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Patent number: 7745491Abstract: Compounds of Formula (I) wherein R1 is a cycloalkylsulphonyl group, or pharmaceutically acceptable salts thereof, are useful in the prophylactic and therapeutic treatment of hyperglycemia and diabetes.Type: GrantFiled: August 9, 2005Date of Patent: June 29, 2010Assignee: Prosidion LimitedInventors: Matthew Colin Thor Fyfe, Vilasben Kanji Shah
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Publication number: 20100151035Abstract: The present invention relates to a stable pharmaceutical composition of a poorly water-soluble drug with a view to increasing its solubility and bioavailability. The present invention relates to a solid dispersion of a poorly water-soluble drug.Type: ApplicationFiled: March 10, 2008Publication date: June 17, 2010Applicant: Sandoz AGInventors: Bharatrajan Ramaswami, Manisha Rajesh Patil, Aditi Das
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Publication number: 20100137401Abstract: The present invention relates to inhibitors of 11-? hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-? hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.Type: ApplicationFiled: February 2, 2010Publication date: June 3, 2010Applicant: Incyte CorporationInventors: Wenqing Yao, Colin Zhang, Jincong Zhuo, Meizhong Xu, Konstantinos Agrios, Brian Metcalf
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Publication number: 20100129444Abstract: The present invention is related to compositions of modafinil, including compositions of modafinil and one or more diluents, disintegrants, binders and lubricants, and the processes for their preparation thereof.Type: ApplicationFiled: January 29, 2010Publication date: May 27, 2010Applicant: Cephalon, Inc.Inventors: Vincent Corvari, George Grandolfi, Alpa Parikh
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Publication number: 20100112045Abstract: The present invention is directed to solid oral dosage forms comprising surface-treated particles comprising modafinil particles and a hydrophilic treating agent, methods of making the same, and uses thereof.Type: ApplicationFiled: January 6, 2010Publication date: May 6, 2010Applicant: CEPHALON, INC.Inventors: Salah U. AHMED, Muhammed A. HOSSAIN, Pruthvi R. KATIKANENI, Zhijun JIANG
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Patent number: 7704975Abstract: Mixtures of a modafinil compound with a cyclodextrin, methods for their use, and compositions thereof are disclosed, along with complexes comprising a modafinil compound and a cyclodextrin which are taste-masked and suitable for oral consumption in an aqueous solution.Type: GrantFiled: November 28, 2006Date of Patent: April 27, 2010Assignee: Cephalon, Inc.Inventors: Martin J. Jacobs, Piyush R. Patel
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Publication number: 20100080829Abstract: The present invention relates to a new lyophilized pharmaceutical composition capable of adhering to oral mucosal tissue for an extended period of time for delivering active pharmaceutical ingredient through the oral mucosal tissue using transmucosal absorption.Type: ApplicationFiled: October 1, 2009Publication date: April 1, 2010Applicants: CEPHALON FRANCE, CEPHALON, INC.Inventors: Claire Dulieu, Steve Durfee, Richard J. Holl, Tam Nguyen
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Patent number: 7687665Abstract: The present invention relates to inhibitors of 11-? hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-? hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.Type: GrantFiled: June 23, 2005Date of Patent: March 30, 2010Assignee: Incyte CorporationInventors: Wenqing Yao, Colin Zhang, Jincong Zhuo, Meizhong Xu, Konstantinos Agrios, Brian Metcalf
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Patent number: 7671093Abstract: A mixed co-crystal comprising an API, a first co-crystal former, and a second co-crystal former which is isomorphically substitutable with said first co-crystal former is described. A pharmaceutical composition comprising a mixed co-crystal, methods of making mixed co-crystals, and methods of using mixed co-crystals are also described.Type: GrantFiled: May 27, 2005Date of Patent: March 2, 2010Assignee: Transform Pharmaceuticals, Inc.Inventors: Matthew Peterson, Magali Bourghol Hickey, Mark Oliveira, Örn Almarsson, Julius Remenar
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Publication number: 20100048718Abstract: The invention relates to a polymorphic form of (?)-modafinil that produces a powder X-ray diffraction spectrum comprising intensity peaks corresponding to interplanar spacings of about 5.23, 5.03, 4.22 and 4.10 ?, and a process for the preparation thereof.Type: ApplicationFiled: July 22, 2009Publication date: February 25, 2010Applicant: Cephalon FranceInventors: Olivier Neckebrock, Laurent Courvoisier, Stephanie Graf, Gilles Serrure, Gerard Francois Coquerel, Sebastien Rose, Christine Besselievre, Franck Patrick Mallet, Adriaan Jan Van Langevelde
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Publication number: 20100048717Abstract: Compounds of formula (I): are found to be selective inhibitors of cathepsin B, and hence useful in treating a variety of pathological conditions.Type: ApplicationFiled: September 24, 2007Publication date: February 25, 2010Applicant: MERCK FROSST CANADA LTD, Merk & Co., Inc.Inventors: Jacques Yves Gauthier, Vouy-Linh Truong
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Publication number: 20100048719Abstract: The invention relates to a polymorphic form of (?)-modafinil that produces a powder X-ray diffraction spectrum comprising intensity peaks corresponding to interplanar spacings of about 12.31, 8.54, 7.27 and 3.62 ?, and a process for the preparation thereof.Type: ApplicationFiled: July 22, 2009Publication date: February 25, 2010Applicant: Cephalon FranceInventors: Olivier Neckebrock, Laurent Courvoisier, Stephanie Graf, Gilles Serrure, Gerard Francois Coquerel, Sebastien Rose, Christine Besselievre, Franck Patrick Mallet, Adriaan Jan Van Langevelde
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Publication number: 20100048720Abstract: The invention relates to a polymorphic form of (?)-modafinil that produces a powder X-ray diffraction spectrum comprising intensity peaks corresponding to interplanar spacings of about 14.14, 10.66, 7.80 and 4.02 ?, and a process for the preparation thereof.Type: ApplicationFiled: July 22, 2009Publication date: February 25, 2010Applicant: Cephalon FranceInventors: Olivier Neckebrock, Laurent Courvoisier, Stéphanie Graf, Gilles Serrure, Gérard Fransois Coquerel, Sébastien Rose, Christine Besselievre, Franck Patrick Mallet, Adriaan Jan Van Langevelde
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Publication number: 20100041657Abstract: The present invention relates to compounds of formula I, in which at least one of R5, R6 and R7 is SR12, S(O)R12 or S(O)2R12 group where R12 is a C1-6haloalkyl group, that act, as chemical uncouplers. Compounds of the invention are useful in the treatment, including prevention, of obesity, diabetes and a number of diseases or conditions associated therewith.Type: ApplicationFiled: May 11, 2006Publication date: February 18, 2010Applicant: NOVO NORDICK A/SInventors: Preben Houlberg Olesen, Holger Claus Hansen, Lise Brown Christiansen, Flemming Elmelund Nielsen, Anders Klarskov Petersen
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Publication number: 20100022653Abstract: The invention relates to a polymorphic form of (?)-modafinil that produces a powder X-ray diffraction spectrum comprising intensity peaks corresponding to interplanar spacings of about 8.54, 4.56, and 3.78 ?, and a process for the preparation thereof.Type: ApplicationFiled: July 22, 2009Publication date: January 28, 2010Applicant: Cephalon FranceInventors: Olivier NECKEBROCK, Laurent COURVOISIER, Stéphanie GRAF, Gilles SERRURE, Gérard Francois COQUEREL, Sébastien ROSE, Christine BESSELIEVRE, Franck Patrick MALLET, Adriaan Jan VAN LANGEVELDE
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Patent number: 7649020Abstract: Polymorphic forms of modafinil racemate, methods of preparation thereof, pharmaceutical compositions and methods of therapeutic treatment involving modafinil polymorphic forms.Type: GrantFiled: December 14, 2007Date of Patent: January 19, 2010Assignee: Cephalon FranceInventors: Michel Broquaire, Véronique Broquaire, legal representative, Laurent Courvoisier, Armand Frydman, Gerard Coquerel, Franck Mallet
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Publication number: 20100009983Abstract: The instant disclosure describes methods for treating diseases and conditions of the central and peripheral nervous system by stimulating or increasing neurogenesis. The disclosure includes compositions and methods based on use of a 5HTR agent, in combination with one or more other neurogenic agents, or anti-astrogenic agent, to stimulate or activate the formation of new nerve cells.Type: ApplicationFiled: June 25, 2009Publication date: January 14, 2010Applicant: BrainCells, Inc.Inventors: Carrolee Barlow, Todd A. Carter, Andrew Morse, Kai Treuner, Kym I. Lorrain
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Publication number: 20100010092Abstract: A method for relieving, treating, improving or attenuating one or more symptoms of RLS and related movement disorders such as PLMS, and snoring ICSD 780.53-1 is disclosed. The method includes the administration to a host afflicted with RLS or related disorder a pharmaceutically effective amount of a modafinil compound or a related compound. The method of the present invention is to treat a host to reduce or diminish snoring, the unpleasant leg sensations associated with unwanted leg movements and to diminish or eliminate the unwanted, involuntary leg movements at rest, awake or asleep, typically occurring in the evenings and at night.Type: ApplicationFiled: December 19, 2007Publication date: January 14, 2010Inventors: Thomas N. Lavin, Catherine H. Koo
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Publication number: 20100010093Abstract: The present invention relates to compounds of the formula (I) or a tautomer or prodrug thereof, or a pharmaceutically acceptable salt of said compound, tautomer or prodrug, wherein: R1, R2, R3, R4 and R5 are each independently selected from H, halo, CN, CF3 and CONH2; compositions containing such compounds and the uses of such compounds as antiparasitic agents.Type: ApplicationFiled: September 15, 2009Publication date: January 14, 2010Applicant: PFIZER LIMITEDInventors: Stuart Nicholas Comlay, Joanne Clare Hannam, William Howson, Christelle Lauret, Yogesh Anil Sabnis
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Publication number: 20090325999Abstract: This invention relates to personalized pharmaceutical kits, packaging, compositions, and methods for treatment of a mammal, comprising at least one antihistamine for treating an allergic disease or condition in a mammal, in combination with at least one wakefulness promoting agent for preventing sedative effects during day time use, while promoting the antihistamine and sedating effect during evening use.Type: ApplicationFiled: June 27, 2008Publication date: December 31, 2009Inventor: Jie Du
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Publication number: 20090325949Abstract: The instant disclosure describes methods for treating diseases and conditions of the central and peripheral nervous system by stimulating or increasing neurogenesis. The disclosure includes compositions and methods based on use of a 5HTR agent, optionally in combination with one or more other neurogenic agents, to stimulate or activate the formation of new nerve cells.Type: ApplicationFiled: June 25, 2009Publication date: December 31, 2009Applicant: BrainCells, Inc.Inventors: Carrolee Barlow, Todd Carter, Andrew Morse, Kai Treuner, Kym I. Lorrain
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Publication number: 20090318559Abstract: Methods and compositions comprising modafinil are described for treating premature ejaculation in a male individual.Type: ApplicationFiled: August 13, 2007Publication date: December 24, 2009Inventor: Daniel E. Katzman
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Publication number: 20090318560Abstract: The instant invention relates to pharmaceutical compositions comprising cathepsin K inhibitors as the active ingredient with excipients which include binders, diluents, lubricants, and disintegrants. Also disclosed are processes for making said pharmaceutical compositions for oral and intravenous delivery.Type: ApplicationFiled: February 22, 2008Publication date: December 24, 2009Inventors: Wayne Parent, Mahtab Afaghi, David Breslin, Mireille Granger, Lei Wang, Jeff Zimmerman
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Publication number: 20090317464Abstract: The invention provides a method and a composition for producing an anti-androgenic effect in a mammal. The method comprises administering a modified release pharmaceutical composition of bicalutamide to a mammal, with a reduced dosing frequency, for improved patient convenience and compliance. The composition of the invention also provides for a higher bioavailability and improved pharmacokinetic profile as compared to a conventional bicalutamide composition.Type: ApplicationFiled: July 5, 2007Publication date: December 24, 2009Applicant: PANACEA BIOTEC LTD.Inventors: Amarjit Singh, Sarabjit Singh, Shivanand Puthli
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Publication number: 20090317481Abstract: The invention provides an oral pharmaceutical composition comprising modafinil particles, wherein at least about 5% of said modafinil particles have a diameter greater than 200 microns.Type: ApplicationFiled: September 2, 2009Publication date: December 24, 2009Applicant: CEPHALON, INC.Inventors: Moshe Bentolila, Aldo Shusterman, Moshe Arkin, Joseph Kaspi
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Publication number: 20090312367Abstract: The invention relates to a combination of modafinil and at least one histamine H3 receptor antagonist or inverse agonist, which can be used in particular for the treatment of narcolepsy-cataplexy and more generally for disorders of sleep, wakefulness and vigilance.Type: ApplicationFiled: July 20, 2007Publication date: December 17, 2009Applicant: BioprojetInventors: Jean-Charles Schwartz, Jeanne-Marie Lecomte
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Publication number: 20090304663Abstract: A method of combating prostate cancer in a mammalian individual, the method comprising administering an inhibitor of glycogen synthase kinase-3 (GSK-3), or a polynucleotide which encodes an inhibitor of GSK-3, to the individual. A further anti-cancer agent can also be administered. Use of an inhibitor of GSK-3, or a polynucleotide which encodes an inhibitor of GSK-3, in the preparation of a medicament for combating prostate cancer. The medicament may contain a further anti-cancer agent.Type: ApplicationFiled: August 17, 2005Publication date: December 10, 2009Applicant: IMPERIAL INNOVATIONS LIMITEDInventor: Robert Martin Kypta
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Publication number: 20090292025Abstract: The invention encompasses crystalline forms of armodafinil, processes for preparing the crystalline forms, and pharmaceutical formulation.Type: ApplicationFiled: June 8, 2009Publication date: November 26, 2009Applicant: Teva Pharmaceutical Industries Ltd.Inventors: Viviana Braude, Rinat Moshkovits-Kaptsan, Sigalit Levi
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Patent number: 7622611Abstract: Pentafluorosulfanylbenzoylguanidines of formula I wherein R1 to R4 have the meanings stated in the claims, are suitable, for example, as antiarrhythmic medicaments with a cardioprotective component for the prophylaxis of infarction and treatment of infarction and for the treatment of angina pectoris. They also inhibit preventively the pathophysiological processes associated with the development of ischemia-induced damage, especially in the triggering of ischemia-induced cardiac arrhythmias.Type: GrantFiled: January 11, 2008Date of Patent: November 24, 2009Assignee: Sanofi-Aventis Deutschland GmbHInventor: Heinz-Werner Kleemann
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Patent number: 7622612Abstract: The present invention relates to tricyclic colchicine derivatives represented by the formulas (I) or (II), pharmaceutically acceptable salts thereof, and a method for providing an immuno-suppressive or immuno-modulating effect, an anti-proliferative effect, an anti-inflammatory effect or a method for treating cancer comprising administering to a patient an effective amount of one or more colchicine derivatives:Type: GrantFiled: July 10, 2006Date of Patent: November 24, 2009Assignees: Chemtech Research Incorporation, KT & G CorporationInventors: Dong Jo Chang, Eun Young Yoon, Gun Bong Lee, Soon Ok Kim, Wan Joo Kim
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Patent number: 7618651Abstract: The present invention relates to pharmaceutical compositions in the form of a gel for controlled- or sustained-release of a pharmaceutically active agent and to methods for treating or preventing or preventing a condition in an animal by administering to an animal in need thereof the pharmaceutical compositions. One particular type of condition for which the pharmaceutical compositions are useful is a microbial infection, e.g., of the skin, ear, or eye, especially for veterinary applications.Type: GrantFiled: June 24, 2004Date of Patent: November 17, 2009Assignee: IDEXX LaboratoriesInventor: Yerramilli V. S. N. Murthy
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Publication number: 20090281192Abstract: The invention relates to a polymorphic form of (?)-modafinil that produces a powder X-ray diffraction spectrum comprising intensity peaks corresponding to interplanar spacings of about 12.38, 8.58, 7.34, 5.00 and 4.09 ?, and a process for the preparation thereof.Type: ApplicationFiled: July 22, 2009Publication date: November 12, 2009Applicant: Cephalon FranceInventors: Olivier NECKEBROCK, Laurent COURVOISIER, Stéphanie GRAF, Gilles SERRURE, Gérard Francois COQUEREL, Sébastien ROSE, Christine BESSELIEVRE, Franck Patrick MALLET, Adriaan Jan VAN LAGEVELDE
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Publication number: 20090282496Abstract: Disclosed are compositions and methods for treating bladder cancer.Type: ApplicationFiled: April 3, 2009Publication date: November 12, 2009Applicant: University of Rochester Medical CenterInventor: Chawnshang Chang
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Publication number: 20090281193Abstract: The invention relates to a polymorphic form of (?)-modafinil that produces a powder X-ray diffraction spectrum comprising intensity peaks corresponding to interplanar spacings of about 9.45, 7.15, 5.13, 4.15 and 3.67 ?, and a process for the preparation thereof.Type: ApplicationFiled: July 22, 2009Publication date: November 12, 2009Applicant: Cephalon FranceInventors: Olivier Neckebrock, Laurent Courvoisier, Stephanie Graf, Gilles Serrure, Gérard François Coquerel, Sébastien Rose, Christine Besselievre, Franck Patrick Mallet, Adriaan Jan Van Langevelde
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Publication number: 20090270512Abstract: Disclosed herein are novel antagonists of the androgen receptor and androgen receptor mutations associated with clinical failure of currently prescribed anti-androgens and use of said antagonists in the treatment of conditions associated with inappropriate activation of the androgen receptor.Type: ApplicationFiled: May 15, 2009Publication date: October 29, 2009Inventors: John Tze-tzun Koh, Paula Lynn McGinley, Hongmu Pan
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Publication number: 20090270511Abstract: The present invention provides compounds of formula (I) which are prodrugs of inhibitors of cathepsin S and as such are useful in the prevention and treatment of cathepsin S dependent diseases and conditions including, but not limited to, chronic obstructive pulmonary disease (COPD) and pain.Type: ApplicationFiled: September 7, 2007Publication date: October 29, 2009Inventor: Jacques Yves Gauthier
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Publication number: 20090270510Abstract: The present invention relates to compounds of formula (I), or salts or solvates thereof, their use in the manufacture of medicaments for treating neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder. The invention further comprises processes to make these compounds and pharmaceutical formulations thereof.Type: ApplicationFiled: December 21, 2005Publication date: October 29, 2009Applicant: GLAXO GROUP LIMITEDInventors: Daniel Marcus Bradley, Clive Leslie Branch, Wai Ngor Chan, Steven Coulton, Martin Leonard Gilpin, Andrew Jonathan Harris, Justine Yeun Quai Lai, Jacqueline Anne Macritchie, Howard Robert Marshall, David John Nash, Roderick Alan Porter, Simone Spada, Kevin Michael Thewlis, Simon Edward Ward
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Patent number: 7598232Abstract: Compounds useful as antiproliferative agents, including, for example, anticancer agents, are provided according to formula (I); wherein: X, X1, X2, Ra, R1, R2,R3, R4, R5, R6, R7, g, M, y, a, b, d, e, V, W, Z and Q are as defined herein.Type: GrantFiled: February 28, 2003Date of Patent: October 6, 2009Assignees: Temple University - Of the Commonwealth System of Higher Education, Onconova Therapeutics, Inc.Inventors: E. Premkumar Reddy, M. V. Ramana Reddy, Stanley C. Bell
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Patent number: 7595344Abstract: Disclosed are sulphones which modulate the action of gamma-secretase. The compounds are useful in the treatment or prevention of Alzheimer's disease.Type: GrantFiled: May 6, 2008Date of Patent: September 29, 2009Assignee: Merck Sharp & Dohme LimitedInventors: Jose Luis Castro Pineiro, Ian Churcher, Kevin Dinnell, Timothy Harrison, Sonia Kerrad, Alan John Nadin, Paul Joseph Oakley, Andrew Pate Owens, Duncan Edward Shaw, Martin Richard Teall, Susannah William, Brian John Williams
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Publication number: 20090239829Abstract: There are described compounds having the general formula (I) below and their pharmaceutically acceptable salts thereof, wherein E, X, m, q, R1, R2, n and ZBG have the meanings reported in the description useful, in therapy, as inhibitors of zinc metalloproteinases.Type: ApplicationFiled: July 25, 2007Publication date: September 24, 2009Applicant: BRACCO IMAGING SPAInventors: Armando Rossello, Elisabetta Orlandini, Aldo Balsamo, Laura Panelli, Elisa Nuti
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Publication number: 20090233962Abstract: The present invention is to provide a compound represented by the general formula (1) exhibiting a high insecticidal effect and an insecticide comprising the compound as an active ingredient. The compound represented by the general formula (1) and an insecticide comprising the compound as an active ingredient, wherein, in the formula, A1, A2, A3 and A4 each represent a carbon atom or the like; R1 and R2 each represent a hydrogen atom or the like; G1 and G2 represent an oxygen atom or the like; Xs each represent a hydrogen atom, a halogen atom or the like; n represents an integer of 0 to 4; Q1 represents a substituted phenyl group, a substituted heterocyclic group or the like; Q2 represents a substituted phenyl group, a substituted heterocyclic group or the like.Type: ApplicationFiled: June 20, 2006Publication date: September 17, 2009Applicant: Mitsui Chemicals, Inc.Inventors: Akiyoshi Kai, Takeo Wakita, Hiroyuki Katsuta, Kei Yoshida, Hidetaka Tsukada, Yusuke Takahashi, Nobuyuki Kawahara, Michikazu Nomura, Hidenori Daido
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Patent number: 7566805Abstract: Co-crystals and solvates of racemic, enantiomerically pure, and enantiomerically mixed modafinil are formed and several important physical properties are modulated. The solubility, dissolution, bioavailability, dose response, and stability of modafinil can be modulated to improve efficacy in pharmaceutical compositions.Type: GrantFiled: September 4, 2004Date of Patent: July 28, 2009Assignee: Cephalon, Inc.Inventors: Magali Bourghol Hickey, Matthew Peterson, Orn Almarsson, Mark Oliveira
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Publication number: 20090175939Abstract: Methods and compositions are provided which comprise effective amounts of analgesic to treat a subject, including reducing or eliminating an adverse effect associated with the analgesic.Type: ApplicationFiled: January 9, 2009Publication date: July 9, 2009Applicant: Charleston Laboratories, Inc.Inventors: Paul Bosse, John Ameling, Bernard Schachtel, Ray Takigiku
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Publication number: 20090176853Abstract: The invention provides adamantane derivatives of formula (I), a process for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy. In formula (I) D represents CH2 or CH2CH2, E represents C(O)NH or NHC(O) and R3 represents a group of formula (I).Type: ApplicationFiled: December 4, 2008Publication date: July 9, 2009Inventors: Lilian Alcaraz, Moya Caffrey, Mark Furber, Timothy Luker, Michael Mortimore, Austen Pimm, Philip Thorne, Paul Willis
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Publication number: 20090176868Abstract: The invention relates to compounds of the general formula (I) wherein X, Y and W have the significances given in claim 1 and optionally the enantiomers thereof. The active ingredients have advantageous pesticidal properties. They are especially suitable for controlling parasites in and on warm-blooded animals.Type: ApplicationFiled: January 8, 2009Publication date: July 9, 2009Applicant: Novartis AGInventors: Noelle Gauvry, Thomas Goebel, Pierre Ducray, Francois Pautrat, Ronald Kaminsky, Martin Jung
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Patent number: 7553646Abstract: The present invention provides novel methods for the synthesis of racemic and enantiomers of modafinil via microbial oxidation-amidation transformation. The methods include the successive oxidation-amidation of benzhydrylsulfanyl carboxylic acid to produce racemic and enantiomers of modafinil using at least one microorganism of yeast, bacteria, or fungus. Also disclosed are pharmaceutical compositions of racemic and enantiomers of modafinil along with their use in the treatment of diseases, including attention deficit hyperactivity disorder and drug addiction.Type: GrantFiled: July 27, 2006Date of Patent: June 30, 2009Assignee: University of Iowa Research FoundationInventors: Horacio F. Olivo, Antonio Victor Osorio-Lozada
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Publication number: 20090156683Abstract: The present invention relates to a chemically stable formulation of florfenicol, (and structurally related compounds) in compositions such as soluble blended powders, granules, fast-dissolving tablets or pellets suitable for rapid release of the drug in water, and to methods and kits for treating animals with aqueous compositions including florfenicol.Type: ApplicationFiled: November 5, 2008Publication date: June 18, 2009Inventors: Robert D. Simmons, Serena Tongiani, Keith Alan Freehauf