Patents by Inventor Richard J. Flanagan

Richard J. Flanagan 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: 7037252
    Abstract: Devices, systems, and methods are provided for transporting implants. In one embodiment, the implants are radioactive seeds contained within substantially transparent sleeves that can be sealed at both ends. Multiple sleeves can be placed in a transfer device that, in turn, can be placed in a canister for further protection. The entire assembly can be sterilized prior to shipment to the user. Upon receipt, one can verify the loading pattern and activity of each sleeve, open one of the seals, and transfer the contents into a brachytherapy needle.
    Type: Grant
    Filed: May 5, 2003
    Date of Patent: May 2, 2006
    Assignee: DRAXIS Specialty Pharmaceuticals, Inc.
    Inventors: Richard J. Flanagan, R. William Riddoch, Pierre Morel
  • Publication number: 20040225176
    Abstract: Devices, systems, and methods are provided for transporting implants. In one embodiment, the implants are radioactive seeds contained within substantially transparent sleeves that can be sealed at both ends. Multiple sleeves can be placed in a transfer device that, in turn, can be placed in a canister for further protection. The entire assembly can be sterilized prior to shipment to the user. Upon receipt, one can verify the loading pattern and activity of each sleeve, open one of the seals, and transfer the contents into a brachytherapy needle.
    Type: Application
    Filed: May 5, 2003
    Publication date: November 11, 2004
    Inventors: Richard J. Flanagan, R. William Riddoch, Pierre Morel
  • Patent number: 6623721
    Abstract: New types of hydroxamic acid-based bifunctional chelators are provided. These chelators are designed to chelate metal ions that can be detected either by their paramagnetic or radioactive properties. Conjugation with peptides or protein can be achieved by the presence of a linker moiety in the molecular structure of these chelators.
    Type: Grant
    Filed: December 18, 2000
    Date of Patent: September 23, 2003
    Assignee: Draximage, Inc.
    Inventors: Richard J. Flanagan, Jean-Marc Dufour
  • Publication number: 20020076377
    Abstract: New types of hydroxamic acid-based bifunctional chelators are provided. These chelators are designed to chelate metal ions that can be detected either by their paramagnetic or radioactive properties. Conjugation with peptides or protein can be achieved by the presence of a linker moiety in the molecular structure of these chelators.
    Type: Application
    Filed: December 18, 2000
    Publication date: June 20, 2002
    Inventors: Richard J. Flanagan, Jean-Marc Dufour
  • Patent number: 5632969
    Abstract: Novel N.sub.3 S.sub.2 chelating ligands can be chelated to a radiodetectable element, Tc or Re, and are useful for radiolabeling peptides. A group of peptides especially useful are somatostatin derivatives which are valuable of the selective detection or treatment of tumors with somatostatin receptors.
    Type: Grant
    Filed: October 13, 1994
    Date of Patent: May 27, 1997
    Assignee: Merck & Co., Inc.
    Inventors: Richard J. Flanagan, Jean-Marc Dufour, Keith T. Hogan
  • Patent number: 5601801
    Abstract: Angiotensin convening enzyme (ACE) inhibitors can be labelled with Iodine-123, Iodine-125, Iodine-127 or Iodine-131, useful to image the kidneys and lungs for diagnosis and treatment of diseases such as essential hypertension, renal artery stenosis, or diabetes which are associated with a change in the amount of ACE present in the human body.
    Type: Grant
    Filed: August 2, 1994
    Date of Patent: February 11, 1997
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Richard J. Flanagan, Duncan H. Hunter, Vincenzo Quiquero, Pamela Zabel
  • Patent number: 5565185
    Abstract: The present invention provides a no-carrier-added synthesis of radiolabeled meta-halobenzylguanidine by halodestannylation which comprises reacting a meta-trialkylstannylbenzylguanidine with a source of radionuclide of a halogen. The present invention also provides meta-trialkylstannylbenzylguanidine as intermediates in the afore-mentioned process.
    Type: Grant
    Filed: July 20, 1994
    Date of Patent: October 15, 1996
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Duncan H. Hunter, Alok Goel, Richard J. Flanagan
  • Patent number: 5556939
    Abstract: Technetium or rhenium radionuclide labelled chelate-hexapeptide complexes are useful for the selective detection or treatment of tumors with somatostatin receptors. In particular, compounds of formula: ##STR1## (wherein R, R.sup.1, R.sup.3 and A are as defined herein) incorporating an N3S2 chelate may be labelled with a radionuclide. The resulting complexes are useful as radioimaging agents or as radiopharmaceuticals for the treatment of certain tumors.
    Type: Grant
    Filed: October 13, 1994
    Date of Patent: September 17, 1996
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Richard J. Flanagan, Jean-Marc Dufour, Keith T. Hogan
  • Patent number: 5539138
    Abstract: The ligands HBED-SCN, HBPD-SCN, and HTDD-SCN are provided which have enhanced ease of reaction with peptides or proteins and which are suitable for chelating with radioisoptopes, especially Indium-.sup.III and Gallium-.sup.67.
    Type: Grant
    Filed: July 28, 1994
    Date of Patent: July 23, 1996
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Richard J. Flanagan, Keith T. Hogan, Jean-Marc Dufour, F. Peter Charleson
  • Patent number: 5306482
    Abstract: Benzalkonium chloride and benzethorium chloride are each useful in radiopharmaceutical preparations (optionally in the presence of a polymyxin or a polymyxin derivative) as bacteriostatic agents which are compatible with anti-oxidants.
    Type: Grant
    Filed: March 3, 1992
    Date of Patent: April 26, 1994
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Daniel Tartaglia, Richard J. Flanagan
  • Patent number: 5248764
    Abstract: Derivatives of synthetic fragments of mammalian atrial natriuretic factor (ANF) in which a chelate molecule is attached to the N-terminal of the peptide are described. The chelate component allows the facile labelling of these peptides with metallic isotopes such as Tc-99m, Ga-67, In-111 and others. These radioactive chelates are useful in determining the in vivo behavior and fate of derivatives of ANF.
    Type: Grant
    Filed: February 27, 1992
    Date of Patent: September 28, 1993
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Richard J. Flanagan, F. Peter Charleson
  • Patent number: 5227152
    Abstract: Benzalkonium chloride and benzethonium chloride are each useful in radiopharmaceutical preparations as bacteriostatic agents which are compatible with anti-oxidants.
    Type: Grant
    Filed: December 12, 1991
    Date of Patent: July 13, 1993
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Richard J. Flanagan, Daniel Tartaglia
  • Patent number: 5093105
    Abstract: Benzalkonium chloride and benzethonium chloride are each useful in radiopharmaceutical preparations as bacteriostatic agents which are compatible with anti-oxidants.
    Type: Grant
    Filed: April 9, 1991
    Date of Patent: March 3, 1992
    Assignee: Merck Frosst Canada, Inc.
    Inventors: Richard J. Flanagan, Daniel Tartaglia
  • Patent number: 4874601
    Abstract: A kit for the direct and rapid preparation of radiolabelled compounds is disclosed comprising a Resin-S-Hg-R component where R is an organic group together with MZ* where M is an alkali metal and Z* is a radiohalogen isotope.
    Type: Grant
    Filed: June 14, 1988
    Date of Patent: October 17, 1989
    Assignee: Merck & Co., Inc.
    Inventor: Richard J. Flanagan
  • Patent number: 4430321
    Abstract: Novel 6-bromo derivatives of cholesterol have the formula ##STR1## Such compounds are prepared from the known 6-iodocholesterol by treatment with cuprous bromide.These compounds, labelled with radioisotopes of Br-82 or Br-77, are localized in the adrenal, mammary and ovary tissue of female mammals and in the adrenal or prostate tissue of males when administered to such individuals. This provides a method for imaging adrenal, ovary or prostate tissue which is superior to use of the prior art 6-iodo-cholesterol.
    Type: Grant
    Filed: January 15, 1982
    Date of Patent: February 7, 1984
    Assignee: Merck Frosst Canada Inc.
    Inventors: Richard J. Flanagan, Leonard I. Wiebe