Patents by Inventor Karl Agger

Karl Agger 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: 20220288063
    Abstract: The present invention relates to lysine deficient protein kinase 1 (WNK1) inhibitors for use in treating patients with blood cancers, in particular leukemia and multiple myeloma.
    Type: Application
    Filed: August 11, 2020
    Publication date: September 15, 2022
    Inventors: Kristian Helin, Karl Agger
  • Patent number: 8420335
    Abstract: The present invention provides a method of testing the ability of a test compound to bind to and optionally modulate the activity of a protein of the JMJD2 subfamily of Jumonji proteins. The method comprises incubating a test compound with a protein of the JMJD2 subfamily of Jumonji proteins, a co-factor of said protein and, optionally, a substrate for demethylation. The method of the invention can be used for screening large numbers of compounds to identify a group of compounds that are candidate compounds for clinical use for treatment of certain cancers especially prostate cancers. Other compounds that do not have activity in the screening assays can be eliminated from further consideration as candidate compounds. The method of the invention therefore has utility in the pharmaceutical industry.
    Type: Grant
    Filed: March 14, 2007
    Date of Patent: April 16, 2013
    Assignee: Kobenhavns Universitet
    Inventors: Paul Cloos, Karl Agger, Jesper Christensen, Klaus H. Hansen, Kristian Helin
  • Publication number: 20090162945
    Abstract: The present invention provides a method of testing the ability of a test compound to bind to and optionally modulate the activity of a protein of the JMJD2 subfamily of Jumonji proteins. The method comprises incubating a test compound with a protein of the JMJD2 subfamily of Jumonji proteins, a co-factor of said protein and, optionally, a substrate for demethylation. The method of the invention can be used for screening large numbers of compounds to identify a group of compounds that are candidate compounds for clinical use for treatment of certain cancers especially prostate cancers. Other compounds that do not have activity in the screening assays can be eliminated from further consideration as candidate compounds. The method of the invention therefore has utility in the pharmaceutical industry.
    Type: Application
    Filed: March 14, 2007
    Publication date: June 25, 2009
    Inventors: Paul Cloos, Karl Agger, Jesper Christensen, Klaus H. Hansen, Kristian Helin