Patents by Inventor Pamela J. Nakhle

Pamela J. Nakhle 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: 20110097713
    Abstract: Compositions and methods for determining an optimal dose of a medication for a subject are described that include determining the subject's genotype for the CYP2C9 and VKORC1 genes and determining the dose of the medication based on the genotype. Articles of manufacture also are provided that include polynucleotides for genotyping.
    Type: Application
    Filed: August 21, 2009
    Publication date: April 28, 2011
    Inventors: Thomas Briggs, James R. Johnson, Jeremy C. Pridgen, Michael P. Murphy, Suzanne L. Phillips, Pamela J. Nakhle
  • Publication number: 20100137426
    Abstract: Reference controls for use with pharmacogenomic testing, and methods for their identification, preparation, and use, are disclosed. The reference controls can confirm that pharmacogenomic testing correctly identifies individuals that do or do not have the mutation of interest, in both clinical trial and patient treatment settings. The reference controls can be selected to include one or more mutations to be identified, and prescreened to confirm that they bind to one or more of the primers used in the pharmacogenomic testing. The reference controls are human genomic DNA that includes certain identified polymorphisms (mutations) of interest, ideally derived from individuals, pre-selected and optionally properly consented, which have one or more of the polymorphism(s) of interest.
    Type: Application
    Filed: May 1, 2009
    Publication date: June 3, 2010
    Applicant: PARAGON
    Inventors: Michael P. Murphy, L. Scott Clark, Pamela J. Nakhle, Kenneth G. Butz
  • Publication number: 20090197945
    Abstract: Reference controls for use with pharmacogenomic testing, and methods for their identification, preparation, and use, are disclosed. The reference controls can confirm that pharmacogenomic testing correctly identifies individuals that do or do not have the mutation of interest, in both clinical trial and patient treatment settings. The reference controls can be selected to include one or more mutations to be identified, and prescreened to confirm that they bind to one or more of the primers used in the pharmacogenomic testing. The reference controls are human genomic DNA that includes certain identified polymorphisms (mutations) of interest, ideally derived from individuals, pre-selected and optionally properly consented, which have one or more of the polymorphism(s) of interest.
    Type: Application
    Filed: January 29, 2007
    Publication date: August 6, 2009
    Inventors: Michael P. Murphy, Scott L. Clark, Pamela J. Nakhle, Kenneth G. Butz