Parathyroid Hormone (pth) Or Derivative Patents (Class 514/11.8)
  • Publication number: 20110008297
    Abstract: Synthetic oxysterols can be made and can be used for the treatment of bone disorders, obesity, cardiovascular disorders, and neurological disorders.
    Type: Application
    Filed: December 3, 2008
    Publication date: January 13, 2011
    Applicant: The Regents of the University of California
    Inventors: Farhad Parhami, Michael E. Jung, Khanhlinh Nguyen, Dongwon Yoo, Woo-Kyun Kim
  • Publication number: 20110003004
    Abstract: Methods are provided for promoting the adsorption of an active agent to microparticles by modifying the structural properties of the active agent in order to facilitate favorable association to the microparticle.
    Type: Application
    Filed: September 16, 2010
    Publication date: January 6, 2011
    Applicant: Mannkind Corporation
    Inventors: Mark Hokenson, Keith A. Oberg
  • Publication number: 20100317574
    Abstract: Disclosed herein are fumaryl diketopiperazine (FDKP) compositions and microparticles having a specific trans isomer content of about 45% to about 65%. The FDKP microparticles can comprise a drug such as an endocrine hormone, including, peptide, including, insulin, glucagon, parathyroid hormones and the like and can be used to make a powder formulation for pulmonary delivery of the drug.
    Type: Application
    Filed: June 11, 2010
    Publication date: December 16, 2010
    Inventors: Kelly S. Kraft, Karla Somerville
  • Publication number: 20100297066
    Abstract: Novel biodegradable compositions are disclosed. The biodegradable compositions include at least one hydroxyl-terminated component and at least one bioactive peptide in a linear chain. The compositions may be utilized as medical devices including drug delivery devices, tissue adhesives and/or sealants.
    Type: Application
    Filed: May 14, 2008
    Publication date: November 25, 2010
    Inventors: Joshua B. Stopek, Brian Cuevas
  • Publication number: 20100297249
    Abstract: The invention provides a formulation for the administration of at least one therapeutic mammalian protein to a mammal, and for enhancing the absorption, distribution and release of the at least one therapeutic mammalian protein in or on the mammal, the formulation consisting of at least one therapeutic mammalian protein in a micro-emulsion which micro-emulsion is constituted by a dispersion of vesicles or microsponges of a fatty acid based component in an aqueous or other pharmacologically acceptable earner in which nitrous oxide is dissolved, the fatty acid based component comprising at least one long chain fatty acid based substance selected from the group consisting of free fatty acids and derivatives of free fatty acids It further provides a method of the effective delivery of at least one therapeutic mammalian protein to a mammal and for enhancing the therapeutic efficacy of such at least one therapeutic mammalian protein, the method comprising the step of administering the at least one therapeutic mamma
    Type: Application
    Filed: July 5, 2007
    Publication date: November 25, 2010
    Applicant: NORTH-WEST UNIVERSITY
    Inventors: Jeanetta Du Plessis, Anne Frederica Grobler, Abraham Frederik Kotze
  • Publication number: 20100292146
    Abstract: The present invention relates to a sliceable composite bone repair material comprising a porous block-shaped ceramic scaffold and a stabilizing polymer disposed therein. Said ceramic scaffold is a synthetic ceramic material or a naturally-derived material. Additionally said scaffold comprises interconnected macropores.
    Type: Application
    Filed: June 30, 2008
    Publication date: November 18, 2010
    Applicants: Straumann Holding AG, CAM Implants B.V.
    Inventors: Reinhart Seibl, Aaldert Rens Molenberg, Astrid Sylvia Neidhardt, Nienke Beuling
  • Publication number: 20100291160
    Abstract: Non-invasive drug delivery systems useful for the absorption of therapeutically active agents through the epithelial membrane are described. The non-invasive drug delivery system delivers a therapeutic active agent with an ionizable, or ionized, metal, transition metal or metal-containing vehicle. The non-invasive drug delivery system may also have a pH adjustable vehicle which facilitates the absorption of the therapeutic agents by altering the pH of the non-invasive drug delivery system at the site of administration. Also disclosed is a method for the pH “sweeping” of the administered therapeutic active agent to provide a consistent and reproducible absorption of the active agent. Certain formulations utilize low doses of active agents without altering the active agents from their current or previous form.
    Type: Application
    Filed: May 12, 2010
    Publication date: November 18, 2010
    Inventors: David R. Carver, Troy G. Fohrman, Sean William Reynolds
  • Publication number: 20100278924
    Abstract: Methods are provided for coating crystalline microparticles with an active agent by altering the surface properties of the microparticles in order to facilitate favorable association on the microparticle by the active agent. Type of surface properties that are altered by the disclosed methods include by electrostatic properties, hydrophobic properties and hydrogen bonding properties.
    Type: Application
    Filed: July 6, 2010
    Publication date: November 4, 2010
    Applicant: MANNKIND CORPORATION
    Inventors: Keith A. Oberg, Joseph Sulner
  • Publication number: 20100267633
    Abstract: The invention relates to substituted N-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamid derivatives which modulate androgen receptors to treat conditions such as: osteoporosis, peridontal disease, bone fracture, frailty, and sarcopenia.
    Type: Application
    Filed: September 22, 2006
    Publication date: October 21, 2010
    Inventors: Barbara Hanney, Yuntae Kim, Helen J. Mitchell, Jeffrey D. Musselman, James J. Perkins
  • Publication number: 20100247661
    Abstract: Methods are provided for promoting the adsorption of an active agent to microparticles by modifying the structural properties of the active agent in order to facilitate favorable association to the microparticle.
    Type: Application
    Filed: June 14, 2010
    Publication date: September 30, 2010
    Applicant: MannKind Corporation
    Inventors: Mark Hokenson, Keith A. Oberg