Patents by Inventor Eric P. Krenning

Eric P. Krenning 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).

  • Patent number: 8293873
    Abstract: The invention relates to a combination of a solution of a gelatin derivative and at least one amino acid, if desired in the form of a pharmaceutically acceptable salt or carboxylic acid derivative, for inhibiting renal uptake of substances, that are potentially damaging for the kidneys, in a living being.
    Type: Grant
    Filed: May 31, 2007
    Date of Patent: October 23, 2012
    Assignee: BioSynthema Inc.
    Inventors: Marion De Jong, Eric P. Krenning, Edgar Rolleman
  • Publication number: 20090318330
    Abstract: The invention relates to a combination of a solution of a gelatin derivative and at least one amino acid, if desired in the form of a pharmaceutically acceptable salt or carboxylic acid derivative, for inhibiting renal uptake of substances, that are potentially damaging for the kidneys, in a living being.
    Type: Application
    Filed: May 31, 2007
    Publication date: December 24, 2009
    Inventors: Marion De Jong, Eric P. Krenning, Edgar Rolleman
  • Patent number: 5776894
    Abstract: Somatostatin peptides bearing at least one chelating group for a detectable element, said chelating group being linked to an amino group of said peptide, and said amino group having no significant binding affinity for somatostatin receptors, in free or salt form, are complexed with a detectable element and are useful as a pharmaceutical, e.g. a radiopharmaceutical for in vivo imaging of somatostatin receptor positive tumors or for therapy.
    Type: Grant
    Filed: June 6, 1995
    Date of Patent: July 7, 1998
    Assignee: Novartis AG
    Inventors: Rainer Albert, Eric P. Krenning, Steven W. J. Lamberts, Janos Pless
  • Patent number: 5753627
    Abstract: Somatostatin peptides bearing at least one chelating group for a detectable element, said chelating group being linked to an amino group of said peptide, and said amino group having no significant binding affinity for somatostatin receptors, in free or salt form, are complexed with a detectable element and are useful as a pharmaceutical, e.g. a radiopharmaceutical for in vivo imaging of somatostatin receptor positive tumors or for therapy.
    Type: Grant
    Filed: June 6, 1995
    Date of Patent: May 19, 1998
    Assignee: Novartis AG
    Inventors: Rainer Albert, Eric P. Krenning, Steven W. J. Lamberts, Janos Pless
  • Patent number: 5324522
    Abstract: Disclosed are sustained release dosage forms of liothyronine, in combination with normal or sustained release of thyroxine in a molar ratio of about 1 to 50:1, especially 5 to 20:1, useful in thyroid hormone replacement therapy. Surprisingly, it is found that by incorporating liothyronine and optionally thyroxine into a prolonged action dosage form in the described ratios, that the side effects associated with thyroid hormone replacement therapy are greatly reduced or eliminated. The preparation can be a dosage form containing salts of both thyroxine and liothyronine which release in a sustained manner. The preparations will typically contain 5 to 25 .mu.g of liothryronine. Also disclosed are processes of manufacturing the pharmaceutical preparations. The compositions are useful in treating disease states such as hypothyroidism, hyperthyroidism (in combination with thyrostatic drugs), so-called "TSH" suppressive therapy, and depression.
    Type: Grant
    Filed: December 28, 1992
    Date of Patent: June 28, 1994
    Assignee: Akzo N.V.
    Inventors: Eric P. Krenning, Georg Hennemann