Patents by Inventor Walter Lunsmann

Walter Lunsmann 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: 20170273932
    Abstract: This disclosure features compositions (e.g., re-constitutable solids, such as lyophilized cakes; or liquid compositions, such as solutions or suspensions, e.g., reconstituted lyophilized cakes) that are suitable for subcutaneous administration. The compositions include a crystalline form (e.g., Form A) of 6-O-(4-dimethylaminoethoxy)cinnamoyl fumagillol, free base and one or more pharmaceutically acceptable excipients and/or one or more pharmaceutically acceptable carriers (e.g., one or more bulking agents; one or more dispersing agents; one or more buffers; one or more suspending agents; water, e.g., water for injection (“WFI”)).
    Type: Application
    Filed: August 24, 2015
    Publication date: September 28, 2017
    Inventors: James E. Vath, Michelle Howard-Sparks, Nancy Harper, David Dresback, Thomas Crawford, Gary Elliott, Walter Lunsmann, Grant Wilson, Jose Casillas
  • Patent number: 9717681
    Abstract: Improved formulations containing substituted imidazole derivatives of the general formula 1, formula (I) wherein Y is —CH2— or —CO—, R1 is H, halo or hydroxy, R2 is H or halo, and R3 is H or lower alkyl (e.g. C1 to C4 alkyl, preferably C1 or C2 alkyl), or a pharmaceutically acceptable salt, such as an acid addition salt, e.g. the hydrochloride, of a compound of the general formula (I), are in solid fast-dispersing dosage form suitable for pre-gastric absorption.
    Type: Grant
    Filed: November 3, 2003
    Date of Patent: August 1, 2017
    Assignee: R.P. Scherer Technologies, LLC
    Inventors: Susan Banbury, Päivi Juujärvi, Leon Grother, Walter Lunsmann, Owen Murray, Juha-Matti Savola
  • Publication number: 20070088057
    Abstract: Disclosed herein are compositions comprising a compound represented by structural formula (I): 2 g of which is reconstitutable in 10 mL of a water in less than 10 minutes, and methods for preparing these compositions. Also disclosed are compositions comprising a compound represented by structural formula (I) and a pharmaceutically acceptable excipient, wherein the molar ratio of said compound to said excipient is from 1:20 to 1:1, and methods for preparing these compositions.
    Type: Application
    Filed: August 10, 2006
    Publication date: April 19, 2007
    Inventors: Walter Lunsmann, Ninad Deshpanday
  • Publication number: 20060134194
    Abstract: Improved formulations containing substituted imidazole derivatives of the general formula 1, formula (I) wherein Y is —CH2— or —CO—, R1 is H, halo or hydroxy, R2 is H or halo, and R3 is H or lower alkyl (e.g. C1 to C4 alkyl, preferably C1 or C2 alkyl), or a pharmaceutically acceptable salt, such as an acid addition salt, e.g. the hydrochloride, of a compound of the general formula (I), are in solid fast-dispersing dosage form suitable for pre-gastric absorption.
    Type: Application
    Filed: November 3, 2003
    Publication date: June 22, 2006
    Inventors: Susan Banbury, Paivi Juujarvi, Leon Grother, Walter Lunsmann, Owen Murray, Juha-Matti Savola