Abstract: The present invention relates to solid state forms of N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide (Compound 1), pharmaceutical compositions thereof and methods therewith.
Type:
Grant
Filed:
January 26, 2012
Date of Patent:
April 2, 2013
Assignee:
Vertex Pharmaceuticals
Inventors:
Patricia Hurter, William Rowe, Christopher Ryan Young, Adriana Costache, Patrick R. Connelly, Mariusz Krawiec, Yuchuan Gong, Yushi Feng, Martin Trudeau
Abstract: The present invention relates to a process for preparing azabicyclic compounds that are useful intermediates for synthesizing pharmaceutical compounds or salts thereof.
Type:
Grant
Filed:
September 17, 2010
Date of Patent:
March 26, 2013
Assignee:
Vertex Pharmaceuticals
Inventors:
Narendra Bhalchandra Ambhaikar, Brian Richard Bear, Lev T. D. Fanning, Robert Hughes, Benjamin Littler
Abstract: The present invention is directed to a splice variant of a human sodium channel alpha subunit and methods and compositions for making and using the same.
Type:
Application
Filed:
April 1, 2009
Publication date:
October 22, 2009
Applicant:
VERTEX PHARMACEUTICALS
Inventors:
Kenneth J. McCormack, Christopher D. Raj
Abstract: The present invention is directed to mutants of HCV NS3/4A protease. More particularly, the present invention identifies mutant of HCV NS3/4A protease that are resistant to drug treatment.
Abstract: The present invention is directed to methods for ameliorating reproductive disorders. More specifically, the present invention describes methods and compositions for using IL-17 in the treatment of various infertility-related defects.
Type:
Application
Filed:
May 27, 2005
Publication date:
December 25, 2008
Applicant:
VERTEX PHARMACEUTICALS
Inventors:
Jugnu Jain, Matthew W. Harding, Ravi Ramachandran, Martyn Botfield
Abstract: The present invention relates to inhibiting the activity of non-genotype 1 hepatitis C virus (HCV) NS3-NS4A protease activity. More particularly, the invention relates to inhibiting the activity of the protease from HCV genotype-2 or HCV genotype-3. The methods of the invention emply inhibitors that act by interfering with the life cycle of the HCV and are also useful as antiviral agents. The invention further relates to compositions comprising such compounds either for ex vivo use or for administration to a patient suffering from genotype-2 or genotype-3 HCV infection. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention.