Patents by Inventor Laura S. Lehman

Laura S. Lehman 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: 6770262
    Abstract: The present invention is directed to a method for the treatment of gastroparesis by the use of metoclopramide nasal formulation.
    Type: Grant
    Filed: March 29, 2001
    Date of Patent: August 3, 2004
    Assignee: Questcor Pharmaceuticals, Inc.
    Inventors: Laura S. Lehman, David Tierney, Anastassios D. Retzios, Michael Petrone, David Young, Carol B. Trapnell, Ruth Oliver
  • Publication number: 20030059374
    Abstract: The present invention is directed to a method for the treatment of gastroparesis by the use of metoclopramide nasal formulation.
    Type: Application
    Filed: August 15, 2002
    Publication date: March 27, 2003
    Inventors: Laura S. Lehman, David Tierney, Anastassios D. Retzios, Michael Petrone, David Young, Carol B. Trapnell, Ruth Oliver
  • Publication number: 20020065321
    Abstract: The present invention is directed to a method for the treatment of gastroparesis by the use of metoclopramide nasal formulation.
    Type: Application
    Filed: March 29, 2001
    Publication date: May 30, 2002
    Inventors: Laura S. Lehman, David Tierney, Anastassios D. Retzios, Michael Petrone, David Young, Carol B. Trapnell, Ruth Oliver
  • Patent number: 5503989
    Abstract: Methods of preparing a peptide having a C-terminal amide group from peptides having a C-terminal carboxyl group are provided.
    Type: Grant
    Filed: August 10, 1992
    Date of Patent: April 2, 1996
    Assignee: Amylin Pharmaceuticals, Inc.
    Inventors: Jeffrey A. Bibbs, Laura S. Lehman De Gaeta, Howard Jones
  • Patent number: 5449680
    Abstract: Novel 2,2-disubstituted glycerol-like compounds are disclosed for use as anti-allergic and anti-inflammatory compounds. The compounds are antagonists of platelet activating factor ("PAF"). Also disclosed are methods of synthesizing and using the compounds of the invention as well as pharmaceutical compositions thereof. The compounds have the formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are as defined in the specification.
    Type: Grant
    Filed: October 2, 1992
    Date of Patent: September 12, 1995
    Assignee: Schering Corporation
    Inventors: Daniel Solomon, James J. Kaminski, Steven K. White, Laura S. Lehman de Gaeta, Ashit K. Ganguly
  • Patent number: 5424394
    Abstract: Synthetic amylin and amylin analogs which have high biological activity and which are substantially free from deletion peptides and other contaminating peptides are provided. Also provided are methods for the solid phase peptide synthesis of amylin and amylin analogs.
    Type: Grant
    Filed: July 8, 1993
    Date of Patent: June 13, 1995
    Inventors: Laura S. Lehman de Gaeta, Elisabeth Albrecht
  • Patent number: 5185334
    Abstract: Novel 2,2-disubstituted glycerol-like compounds are disclosed for use as anti-allergic and anti-inflammatory compounds. The compounds are antagonists of platelet activating factor ("PAF"). Also disclosed are methods of synthesizing and using the compounds of the invention as well as pharmaceutical compositions thereof. The compounds have the formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are as defined in the specification.
    Type: Grant
    Filed: September 6, 1991
    Date of Patent: February 9, 1993
    Assignee: Schering Corporation
    Inventors: Daniel Solomon, James J. Kaminski, Steven K. White, Laura S. Lehman de Gaeta, Ashit K. Ganguly
  • Patent number: 5047399
    Abstract: Novel hydrophobic psuedo-peptides of formula I ##STR1## wherein R.sub.1 is lower alkyl or -CH.sub.2 CONR.sub.6 R.sub.7 ; R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are independently lower alkyl, cycloalkyl lower alkyl, aryl lower alkyl, heteroaryl lower alkyl, aryl lower alkoxy, substituted aryl lower alkyl, wherein the aryl portion is substituted with 1-3 substituents independently selected from lowr alkyl, hydroxyl, lower alkoxy and halogeno, substituted heteroaryl lower alkyl wherein the substituents on the heteroaryl portion are as defined for aryl lower alkyl, substituted cycloalkyl lower alkyl, wherein the substituents on the cycloalkyl portion are as defined for aryl lower alkyl, and substituted aryl lower alkoxy wherein the substituents are as defined for aryl lower alkyl;R.sub.6 and R.sub.7 are independently hydrogen or lower alkyl;X.sub.1, X.sub.2, X.sub.3, X.sub.4 and X.sub.5 are independently ##STR2## cis or trans --CR.sub.8 .dbd.CR.sub.9 --, --CHR.sub.8 CHR.sub.9 --, --CH.sub.2 NR.sub.
    Type: Grant
    Filed: July 13, 1988
    Date of Patent: September 10, 1991
    Assignee: Schering Corporation
    Inventors: Laura S. Lehman, Michael F. Czarniecki