Patents by Inventor Masashi Kurimoto

Masashi Kurimoto 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: 20030129184
    Abstract: A monoclonal antibody which is specific to a polypeptide having a molecular weight of 18,500±3,000 daltons on SDS-PAGE and a pI of 4.9±1.0 on chromatofocusing. The monoclonal antibody is obtainable from hybridomas and can be used for the purification and detection of the polypeptide. The polypeptide strongly induces the IFN-&ggr; production by immunocompetent cells with only a small amount, and dose not cause serious side effects even when administered to human in a relatively-high dose.
    Type: Application
    Filed: December 24, 2002
    Publication date: July 10, 2003
    Applicant: KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO
    Inventors: Toshio Kunikata, Mutsuko Taniguchi, Keizo Kohno, Masashi Kurimoto
  • Publication number: 20030095946
    Abstract: An osteoclastgenic inhibitory agent which comprises an interleukin-18 and/or its functional equivalent. The agent can be arbitrarily used as an ingredient for cell culture and agents for regulating bone resorption and for osteoclast-related diseases, directed to treat and/or prevent hypercalcemia, osteoclastoma, osteoporosis, etc.
    Type: Application
    Filed: February 25, 1998
    Publication date: May 22, 2003
    Inventors: MATTHEW TODD GILLSPIE, NICOLE JOY HORWOOD, NOBUYUKI UDAGAWA, MASASHI KURIMOTO
  • Publication number: 20030092130
    Abstract: Disclosed are created stable polypeptides which are capable of inducing the production of interferon-gamma by immunocompetent cells. The present polypeptides contain specific amino acid sequences usually derived from the wild-type polypeptides, being capable of the production of interferon-gamma, by replacing the cysteine(s) with different amino acid(s). The present polypeptides possess a stability and an activity of inducing the production of IFN-&ggr; by immunocompetent cells, both of which are significantly higher than those of the wild-type polypeptides. In addition to the activity, the present polypeptides can exhibit remarkable activities of inducing the formation of killer cells and enhancing thier cytotoxicities. The present polypeptides are easily obtainable by the process according to the present invention using recombinant DNA techniques.
    Type: Application
    Filed: October 1, 2002
    Publication date: May 15, 2003
    Applicant: KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO
    Inventors: Kozo Yamamoto, Iwao Okamoto, Masashi Kurimoto
  • Patent number: 6559298
    Abstract: Disclosed are a polypeptide (including that in soluble form) as receptor for a novel cytokine, i.e., interleukin-18, a DNA encoding the polypeptide, and the uses of the polypeptide including pharmaceutical and neutralizer to interleukin-18. Pharmaceuticals with the polypeptide is useful to treat and prevent autoimmune and allergic disease because it suppresses and regulates excessive immunoreaction.
    Type: Grant
    Filed: April 24, 2000
    Date of Patent: May 6, 2003
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Kakuji Torigoe, Takanori Okura, Masashi Kurimoto
  • Patent number: 6555526
    Abstract: An ophthalmic pharmaceutical composition comprising trehalose as an effective ingredient and a pharmaceutically-acceptable carrier. The pharmaceutical composition is a safe, long-term continuously-administrable, therapeutic and/or prophylactic agent for the ophthalmologic clinical symptoms and signs in Sjögren syndrome.
    Type: Grant
    Filed: August 30, 2001
    Date of Patent: April 29, 2003
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Toshihiko Matsuo, Masashi Kurimoto, Hiroshi Yamauchi
  • Patent number: 6537547
    Abstract: Disclosed are polypeptides which originate from mammal, having L-asparaginase activity. The polypeptides are easily prepared by applying recombinant DNA techniques to DNAs encoding the polypeptides and they exert satisfactory effects in the treatment and/or the prevention for diseases caused by tumor cells dependent on L-asparagine, and cause no substantial serious side effects even when administered to humans in relatively-high dose.
    Type: Grant
    Filed: June 5, 1997
    Date of Patent: March 25, 2003
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Takeshi Ario, Madoka Taniai, Kozo Yamamoto, Masashi Kurimoto
  • Publication number: 20030039629
    Abstract: The objects of the present invention are to reveal a specific combination of human interferon-&agr; subtypes that remarkably enhances the expression of protein synthesis inhibitory genes, and to provide an expression enhancer comprising as effective ingredients interferon-&agr; subtypes in such a combination and uses thereof. The above objects are solved by providing an expression enhancer for protein synthesis inhibitory genes which comprises as effective ingredients interferon-&agr;2 and interferon-&agr;8 subtypes of human interferon-&agr;, and uses thereof including pharmaceuticals.
    Type: Application
    Filed: September 26, 2001
    Publication date: February 27, 2003
    Applicant: KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO
    Inventors: Yoshiaki Yanai, Osamu Sano, Masashi Kurimoto
  • Patent number: 6524625
    Abstract: A physiologically active extract comprising an ethyl acetate-soluble ingredient of an indigo plant, which is obtainable by soaking a raw indigo plant in an organic solvent used for extraction. The ethyl acetate-soluble ingredient includes tryptanthrin, 3,5,4′-trihydroxy-6,7-methylenedioxy-flavone, kaempferol, 3,5,7,4′-tetrahydroxy-6-methoxy-flavone, gallic acid, caffeic acid, indirubin, pheophorbide a, and methylpheophorbide a.
    Type: Grant
    Filed: June 25, 1999
    Date of Patent: February 25, 2003
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyuto
    Inventors: Hajime Aga, Shigeyuki Arai, Shigeharu Fukuda, Toshio Kunikata, Masashi Kurimoto
  • Patent number: 6509449
    Abstract: A monoclonal antibody which is specific to a polypeptide having a molecular weight of 18,500±3,000 daltons on SDS-PAGE and a pI of 4.9±1.0 on chromatofocusing. The monoclonal antibody is obtainable from hybridomas and can be used for the purification and detection of the polypeptide. The polypeptide strongly induces the IFN-&ggr; production by immunocompetent cells with only a small amount, and dose not cause serious side effects even when administered to human in a relatively-high dose.
    Type: Grant
    Filed: November 15, 2000
    Date of Patent: January 21, 2003
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Toshio Kunikata, Mutsuko Taniguchi, Keizo Kohno, Masashi Kurimoto
  • Publication number: 20030003132
    Abstract: The object of the present invention is to provide a mucosal immunoregulatory agent which has neither excessive stress nor care for side effects even when administrated repeatedly, and solves the objected by providing the mucosal immunoregulatory agent comprising trehalose.
    Type: Application
    Filed: July 8, 2002
    Publication date: January 2, 2003
    Inventors: Norie Arai, Toshiharu Hanaya, Shigeyuki Arai, Masashi Kurimoto
  • Patent number: 6476197
    Abstract: Disclosed are created stable polypeptides which are capable of inducing the production of interferon-gamma by immunocompetent cells. The present polypeptides contain specific amino acid sequences usually derived from the wild-type polypeptides, being capable of the production of interferon-gamma, by replacing the cysteine(s) with different amino acid(s). The present polypeptides possess a stability and an activity of inducing the production of IFN-&ggr; by immunocompetent cells, both of which are significantly higher than those of the wild-type polypeptides. In addition to the activity, the present polypeptides can exhibit remarkable activities of inducing the formation of killer cells and enhancing thier cytotoxicities. The present polypeptides are easily obtainable by the process according to the present invention using recombinant DNA techniques.
    Type: Grant
    Filed: December 1, 1997
    Date of Patent: November 5, 2002
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Kozo Yamamoto, Iwao Okamoto, Masashi Kurimoto
  • Publication number: 20020150555
    Abstract: An osteoclastgenic inhibitory agent which comprises an interleukin-18 and/or its functional equivalent. The agent can be arbitrarily used as an ingredient for cell culture and agents for regulating bone resorption and for osteoclast-related diseases, directed to treat and/or prevent hypercalcemia, osteoclastoma, osteoporosis, etc.
    Type: Application
    Filed: March 19, 2002
    Publication date: October 17, 2002
    Applicant: KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO
    Inventors: Matthew Todd Gillispie, Nicole Joy Horwood, Nobuyuki Udagawa, Masashi Kurimoto
  • Publication number: 20020128450
    Abstract: Disclosed are artificially produced peptide capable of neutralizing the biological activities of IL-18, which comprises a part or the whole of the variable regions in anti interleukin 18 antibody, including single chain variable region fragments and humanized antibodies, a process of producing the peptide, and uses thereof. The peptide is useful as pharmaceutical to treat and prevent diseases such as autoimmune diseases and inflammatory diseases, where the biological activities of interleukin-18 are involved.
    Type: Application
    Filed: August 8, 2001
    Publication date: September 12, 2002
    Applicant: KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO
    Inventors: Yoshihiro Nishida, Takanori Okura, Tadao Tanimoto, Masashi Kurimoto
  • Patent number: 6441138
    Abstract: A protein of human cell origin, which induces the IFN-&ggr; production by immunocompetent cells and has the amino acid sequence of SEQ ID NO:1 near at the N-terminus. It can be produced from human cells such as lymphoblasts, lymphocytes, monoblasts, monocytes, myeloblasts, myelocytes, granulocytes and macrophages, and used for preventing and/or treating IFN-&ggr; susceptive diseases.
    Type: Grant
    Filed: January 3, 2001
    Date of Patent: August 27, 2002
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Kenji Akita, Yoshiyuki Nukada, Mitsukiyo Fujii, Tadao Tanimoto, Masashi Kurimoto
  • Patent number: 6440446
    Abstract: An orally or parenterally administrable agent for anti-osteoporosis, comprising trehalose as an effective ingredient and optionally another ingredients, that exerts a satisfactory therapeutic/prophylactic effect on osteoporosis with lesser side effects.
    Type: Grant
    Filed: April 16, 1999
    Date of Patent: August 27, 2002
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Chiyo Yoshizane, Yasushi Nishizaki, Shigeyuki Arai, Masashi Kurimoto
  • Patent number: 6436396
    Abstract: Disclosed are polypeptides which originate from mammal, having L-asparaginase activity. The polypeptides are easily prepared by applying recombinant DNA techniques to DNAs encoding the polypeptides and they exert satisfactory effects in the treatment and/or the prevention for diseases caused by tumor cells dependent on L-asparagine, and cause no substantial serious side effects even when administered to humans in relatively-high dose.
    Type: Grant
    Filed: August 8, 2000
    Date of Patent: August 20, 2002
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Takeshi Ario, Madoka Taniai, Kozo Yamamoto, Masashi Kurimoto
  • Patent number: 6403079
    Abstract: A protein of human cell origin, which induces the IFN-&ggr; production by immunocompetent cells and has the amino acid sequence of SEQ ID NO:1 near at the N-terminus. It can be produced from human cells such as lymphoblasts, lymphocytes, monoblasts, monocytes, myeloblasts, myelocytes, granulocytes and macrophages, and used for preventing and/or treating IFN-&ggr; susceptive diseases.
    Type: Grant
    Filed: March 29, 2001
    Date of Patent: June 11, 2002
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Kenji Akita, Yoshiyuki Nukada, Mitsukiyo Fujii, Tadao Tanimoto, Masashi Kurimoto
  • Publication number: 20020068094
    Abstract: A physiologically active extract comprising an ethyl acetate-soluble ingredient of an indigo plant, which is obtainable by soaking a raw indigo plant in an organic solvent used for extraction. The ethyl acetate-soluble ingredient includes tryptanthrin, 3,5,4′-trihydroxy-6,7-methylenedioxy-flavone, kaempferol, 3,5,7,4′-tetrahydroxy-6-methoxy-flavone, gallic acid, caffeic acid, indirubin, pheophorbide a, and methylpheophorbide a.
    Type: Application
    Filed: June 25, 1999
    Publication date: June 6, 2002
    Inventors: HAJIME AGA, SHIGEYUKI ARAI, TOSHIO KUNIKATA, MASASHI KURIMOTO
  • Publication number: 20020055486
    Abstract: An ophthalmic pharmaceutical composition comprising trehalose as an effective ingredient and a pharmaceutically-acceptable carrier. The pharmaceutical composition is a safe, long-term continuously-administrable, therapeutic and/or prophylactic agent for the ophthalmologic clinical symptoms and signs in Sjögren syndrome.
    Type: Application
    Filed: August 30, 2001
    Publication date: May 9, 2002
    Applicant: KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO
    Inventors: Toshihiko Matsuo, Masashi Kurimoto, Hiroshi Yamauchi
  • Patent number: 6368845
    Abstract: Disclosed are polypeptides which originate from mammal, having L-asparaginase activity. The polypeptides are easily prepared by applying recombinant DNA techniques to DNAs encoding the polypeptides and they exert satisfactory effects in the treatment and/or the prevention for diseases caused by tumor cells dependent on L-asparagine, and cause no substantial serious side effects even when administered to humans in relatively-high dose.
    Type: Grant
    Filed: August 9, 2000
    Date of Patent: April 9, 2002
    Assignee: Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo
    Inventors: Takeshi Ario, Madoka Taniai, Kozo Yamamoto, Masashi Kurimoto