Abstract: The present invention relates to a new route of synthesis to obtain pharmaceutically acceptable Vismodegib. In addition, besides the synthesis also suitable pharmaceutical compositions and the use of the compound for the treatment of basal-cell carcinomas are disclosed.
Type:
Grant
Filed:
March 26, 2018
Date of Patent:
July 9, 2019
Assignee:
AZAD PHARMACEUTICAL INGREDIENTS AG
Inventors:
Christian Manfred Frech, Pasquale Gabriele Grieco, Christine Aebersold, Patrick Müller, Jan-Erik Ingenhoff, Miriam Oberholzer, Viktorya Rstakyan, Roman Gerber Aeschbacher
Abstract: The present invention is directed to novel processes for the preparation of paricalcitol to novel intermediates used in these processes, and to processes for preparation of the novel intermediates.
Type:
Grant
Filed:
July 22, 2009
Date of Patent:
December 15, 2015
Assignees:
AZAD PHARMACEUTICALS INGREDIENTS AG, UNIVERSITAT ZURICH
Inventors:
Thomas Bader, Alfred Stutz, Hans-Ulrich Bichsel, Changchun Fu
Abstract: The present invention relates to a new polymorphic or crystalline form of Pemetrexed Disodium, processes for its preparation and its use, in particular for the preparation of medicaments.
Type:
Grant
Filed:
November 24, 2010
Date of Patent:
November 3, 2015
Assignees:
Azad Pharmaceutical Ingredients AG, University of Zurich
Inventors:
Uwe Jens Albrecht, Hannes Helmboldt, Vsevolod Valerievich Nikolaev
Abstract: Process of preparing sterile brinzolamide using ethylene-oxide gas sterilisation, sterile brinzolamide obtainable by said process and pharmaceutical compositions comprising said sterile brinzolamide.
Type:
Application
Filed:
March 15, 2013
Publication date:
March 5, 2015
Applicant:
AZAD Pharmaceutical Ingredients AG
Inventors:
Van Van Khov-Tran, Frank Porstmann, Jan Ondracek, Gregory Grams
Abstract: The present invention relates to a new polymorphic or crystalline form of Pemetrexed Disodium, processes for its preparation and its use, in particular for the preparation of medicaments.
Type:
Application
Filed:
November 24, 2010
Publication date:
December 27, 2012
Applicants:
UNIVERSITY OF ZURICH, AZAD PHARMACEUTICAL INGREDIENTS AG
Inventors:
Uwe Jens Albrecht, Hannes Helmboldt, Vsevold Valerievich Nikolaev
Abstract: The present invention provides a novel polymorphic form of olopatadine hydrochloride ([(Z)-3-(dimethylamino)propylidene]-6,11-dihydrodibenz[b,e]oxepin-2-acetic acid hydrochloride), a selective histamine H1-receptor antagonist that is used for the treatment of ocular symptoms of seasonal allergic conjunctivitis. The present invention also provides novel methods for producing olopatadine on a large scale, and in a manner that is cost effective, provides a low level of impurities and eliminates the need to use the costly and dangerous base, butyllithium, which is used in prior art reactions for making olopatadine. The present invention further provides novel processes for carrying out a large scale production of 3-dimethylaminopropyltriphenylphosphonium bromide and its corresponding hydrobromide salt, which are employed in the production of olopatadine, and pharmaceutically acceptable salts of olopatadine.
Type:
Grant
Filed:
March 28, 2006
Date of Patent:
March 30, 2010
Assignees:
Azad Pharmaceutical Ingredients, AG, Universität Zürich
Inventors:
Thomas Bader, Hans-Ulrich Bichsel, Bruno Gilomen, Imelda Meyer-Wilmes, Mark Sundermeier