Patents by Inventor Henderik Frijlink

Henderik Frijlink has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20080058371
    Abstract: An antibacterial formulation suitable for injection into animals containing approximately 2-10% w/v difloxacin HCl, L-arginine base, propylene glycol, ethanol and/or benzyl alcohol, and water. The formulation is a solution having a pH of form 9 to 10. The formulation produces little or no tissue damage or irritation at the injection site.
    Type: Application
    Filed: August 24, 2007
    Publication date: March 6, 2008
    Applicant: WYETH
    Inventor: Henderik Frijlink
  • Publication number: 20070098864
    Abstract: In one embodiment, the present invention relates to methods for the preparation of pharmaceutical compositions comprising a lipophilic compound and a glass of a sugar, a sugar alcohol, a mixture of sugars and/or a mixture of sugars alcohols. The invention is further related to such pharmaceutical compositions and the use of such compositions in the treatment of various diseases and disorders.
    Type: Application
    Filed: July 10, 2006
    Publication date: May 3, 2007
    Inventors: Gerrit Zijlstra, Bastiaan Dickhoff, Dirk Van Drooge, Wouter Hinrichs, Henderik Frijlink
  • Publication number: 20060237010
    Abstract: A breath actuated dry powder inhaler, comprising a substantially disc shaped air circulation chamber for de-agglomeration of entrained powdered medicament using the energy of the inspiratory air stream. The chamber has a substantially circular or polygonal sidewall extending about a central axis between top and bottom walls of the chamber so that the height of the chamber is smaller than its diameter. A plurality of air supply channels disposed about the circumference of the chamber, which channels extend from joint or separate air inlets and which channels enter the chamber substantially tangentially to its sidewall. At least one of the supply channels extends through a powder dose supply region of the inhaler. The chamber further comprises an air outlet axially extending from a discharge opening in the centre of the top or bottom wall of the chamber and connects to a discharge channel that extends to a mouthpiece.
    Type: Application
    Filed: June 16, 2004
    Publication date: October 26, 2006
    Applicant: Rijksuniversiteit Groningen
    Inventors: Anne De Boer, Paul Hagedoorn, Henderik Frijlink
  • Publication number: 20060013874
    Abstract: The present invention relates to an extended release formulation of 3-amino-8-(1-piperazinyl)-2H-1-benzopyran-2-one or a pharmaceutically acceptable salt thereof or a hydrate of said pharmaceutically acceptable salt thereof. The invention further relates to the preparation of these extended release formulations and their use in the prevention or treatment of disorders, especially pain and CNS disorders such as depression, anxiety and movement disorders.
    Type: Application
    Filed: July 12, 2005
    Publication date: January 19, 2006
    Inventors: Nico Bruins, Henderik Frijlink, Michiel de Vries
  • Publication number: 20050266088
    Abstract: The present invention relates to a pharmaceutical composition comprising at least one lipophilic compound and at least one glass of a sugar, a sugar alcohol, a mixture of sugars, a mixture of sugar alcohols, or a mixture of at least one sugar and at least one sugar alcohol, wherein the lipophilic compound is incorporated in the sugar glass. The present invention further relates to a method for manufacturing such a pharmaceutical composition.
    Type: Application
    Filed: June 10, 2005
    Publication date: December 1, 2005
    Applicant: Rijksuniversiteit Groningen
    Inventors: Wouter Hinrichs, Dirk van Drooge, Henderik Frijlink
  • Publication number: 20050143417
    Abstract: An antibacterial formulation suitable for injection into animals containing approximately 2-10% w/v difloxacin HCl, L-arginine base, propylene glycol, ethanol and/or benzyl alcohol, and water. The formulation is a solution having a pH of form 9 to 10. The formulation produces little or no tissue damage or irritation at the injection site.
    Type: Application
    Filed: March 3, 2005
    Publication date: June 30, 2005
    Applicant: WYETH
    Inventor: Henderik Frijlink