The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 15, 2019

Filed:

Jun. 19, 2014
Applicant:

Aicuris Anti-infective Cures Gmbh, Wuppertal, DE;

Inventors:

Wilfried Schwab, Werder, DE;

Dirk Jung, Dresden, DE;

Christian Schickaneder, Lauf an der Pegnitz, DE;

Welljanne Martens, Dresden, DE;

Michael Limmert, Dresden, DE;

Clemens Bothe, Leverkusen, DE;

Mathias Berwe, Sprockhovel, DE;

Nicole Rindermann, Bad Laer, DE;

Assignee:
Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C07D 239/84 (2006.01); A61P 31/00 (2006.01); A61P 31/14 (2006.01); A61P 31/18 (2006.01); A61P 31/20 (2006.01); A61P 31/12 (2006.01); A61K 31/517 (2006.01); A61K 9/00 (2006.01); A61K 47/02 (2006.01); A61K 47/12 (2006.01); A61K 47/32 (2006.01); A61K 47/38 (2006.01);
U.S. Cl.
CPC ...
C07D 239/84 (2013.01); A61K 9/0053 (2013.01); A61K 31/517 (2013.01); A61K 47/02 (2013.01); A61K 47/12 (2013.01); A61K 47/32 (2013.01); A61K 47/38 (2013.01); A61P 31/00 (2018.01); A61P 31/12 (2018.01); A61P 31/14 (2018.01); A61P 31/18 (2018.01); A61P 31/20 (2018.01);
Abstract

The present invention provides for amorphous Letermovir and orally administrable solid pharmaceutical formulations thereof (immediate release formulation). Said amorphous Letermovir is suitable for immediate release formulations when isolated out of an organic solution by either roller-drying said organic solution in a volatile organic solvent, in particular acetone, at a temperature of 30° C. to 60° C., and subsequently drying the amorphous Letermovir obtained, or isolating said amorphous Letermovir by precipitation from water miscible solvents selected from acetone or acetonitrile into excess water as anti-solvent, and subsequently filtrating or centrifuging the amorphous Letermovir obtained. The immediate release formulations of amorphous Letermovir are intended for use in methods of prophylaxis or methods of treatment of diseases associated with the group of Herpesviridae, preferably associated with cytomegalovirus (CMV), even more preferably associated with human cytomegalovirus (HCMV).


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