Patents by Inventor FUSAO USUI

FUSAO USUI 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: 20100144697
    Abstract: The present invention provides a pharmaceutical composition containing a calcium channel blocker of the following formula or a pharmacologically acceptable salt thereof and a pharmacologically acceptable alkaline material which is added to an extent such that an aqueous solution or dispersion solution of said pharmaceutical composition containing a calcium channel blocker has a pH of at least 8: [wherein R1 represents an optionally substituted C1-C4 alkyl group, an amino group or a cyano group; R2 represents an optionally substituted C1-C4 alkyl group, a substituted C3-C4 alkenyl group, or a substituted 4- to 6-membered cyclic amino group; R3 represents a substituted phenyl group; R4 represents an optionally substituted C1-C4 alkoxycarbonyl group, a 1,3,2-phosphorinan-2-yl group, or a 5,5-dimethyl-1,3,2-phosphorinan-2-yl group, R5 represents a C1-C4 alkyl group].
    Type: Application
    Filed: February 3, 2010
    Publication date: June 10, 2010
    Applicants: SANKYO COMPANY, LIMITED, UBE INDUSTRIES, LTD.
    Inventors: Naoki Wakiyama, Fusao Usui, Kenji Nishimura
  • Publication number: 20100144696
    Abstract: The present invention provides a pharmaceutical composition containing a calcium channel blocker of the following formula or a pharmacologically acceptable salt thereof and a pharmacologically acceptable alkaline material which is added to an extent such that an aqueous solution or dispersion solution of said pharmaceutical composition containing a calcium channel blocker has a pH of at least 8: [wherein R1 represents an optionally substituted C1-C4 alkyl group, an amino group or a cyano group; R2 represents an optionally substituted C1-C4 alkyl group, a substituted C3-C4 alkenyl group, or a substituted 4- to 6-membered cyclic amino group; R3 represents a substituted phenyl group; R4 represents an optionally substituted C1-C4 alkoxycarbonyl group, a 1,3,2-phosphorinan-2-yl group, or a 5,5-dimethyl-1,3,2-phosphorinan-2-yl group, R5 represents a C1-C4 alkyl group].
    Type: Application
    Filed: February 3, 2010
    Publication date: June 10, 2010
    Applicants: SANKYO COMPANY, LIMITED, UBE INDUSTRIES, LTD.
    Inventors: Naoki Wakiyama, Fusao Usui, Kenji Nishimura
  • Publication number: 20070142442
    Abstract: The present invention provides a pharmaceutical composition containing a calcium channel blocker of the following formula or a pharmacologically acceptable salt thereof and a pharmacologically acceptable alkaline material which is added to an extent such that an aqueous solution or dispersion solution of said pharmaceutical composition containing a calcium channel blocker has a pH of at least 8: [wherein R1 represents an optionally substituted C1-C4 alkyl group, an amino group or a cyano group; R2 represents an optionally substituted C1-C4 alkyl group, a substituted C3-C4 alkenyl group, or a substituted 4- to 6-membered cyclic amino group; R3 represents a substituted phenyl group; R4 represents an optionally substituted C1-C4 alkoxycarbonyl group, a 1,3,2-phosphorinan-2-yl group, or a 5,5-dimethyl-1,3,2-phosphorinan-2-yl group, R5 represents a C1-C4 alkyl group].
    Type: Application
    Filed: February 8, 2007
    Publication date: June 21, 2007
    Applicants: SANKYO COMPANY, LIMITED, UBE INDUSTRIES, LTD.
    Inventors: Naoki Wakiyama, Fusao Usui, Kenji Nishimura
  • Publication number: 20030073670
    Abstract: The present invention provides a pharmaceutical composition containing a calcium channel blocker of the following formula or a pharmacologically acceptable salt thereof and a pharmacologically acceptable alkaline material which is added to an extent such that an aqueous solution or dispersion solution of said pharmaceutical composition containing a calcium channel blocker has a pH of at least 8: 1
    Type: Application
    Filed: October 10, 2002
    Publication date: April 17, 2003
    Applicant: SANKYO COMPANY, LIMITED
    Inventors: Naoki Wakiyama, Fusao Usui, Kenji Nishimura
  • Publication number: 20020015732
    Abstract: A formulation of a 5&agr;-reductase inhibitor for oral administration, which comprises a composition obtained by grinding a mixture of an azasteroid, a water-soluble polymer and a disintegrant.
    Type: Application
    Filed: August 4, 1998
    Publication date: February 7, 2002
    Inventors: FUSAO USUI, YUKO OHUCHI, AKIRA KUSAI