Abstract: Modified release pharmaceutical compositions (controlled release, sustained release, and/or extended release) of the R-(+) enantiomer of pramipexole (RPPX) and methods of using such compositions for the treatment of neurodegenerative diseases, or those related to mitochondrial dysfunction or increased oxidative stress are disclosed.
Type:
Grant
Filed:
March 14, 2008
Date of Patent:
September 3, 2013
Assignee:
Knopp Neurosciences, Inc.
Inventors:
Michael E. Bozik, Thomas Petzinger, Jr., Valentin Gribkoff
Abstract: Methods for preparing chirally purified substituted 4,5,6,7-tetrahydro-benzothiazole diamines such as, for example, (6R)2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole and purifying a dominant enantiomer of substituted 4,5,6,7-tetrahydro-benzothiazole diamines from entantiomerically enriched mixtures of substituted 4,5,6,7-tetrahydro-benzothiazole diamines are provided herein.
Type:
Grant
Filed:
March 14, 2008
Date of Patent:
August 27, 2013
Assignee:
Knopp Neurosciences, Inc.
Inventors:
Prasad Raje, Rajendrakumar Reddy Gadikota, Jian-Xie Chen, Olga V. Lapina, John M. McCall
Abstract: Pharmaceutical compositions of (R)-pramipexole and methods and kits of using such compositions for the treatment of neurodegenerative diseases, or those related to mitochondrial dysfunction or increased oxidative stress are disclosed.
Type:
Grant
Filed:
December 14, 2007
Date of Patent:
August 27, 2013
Assignee:
Knopp Neurosciences, Inc.
Inventors:
Michael E. Bozik, Thomas Petzinger, Jr., Valentin Gribkoff
Abstract: Compositions of predetermined amounts of R(+) pramipexole and S(?) pramipexole and methods of using the same, including for the treatment and prevention of Parkinson's disease, are provided.
Type:
Grant
Filed:
August 5, 2011
Date of Patent:
May 21, 2013
Assignee:
Knopp Neurosciences, Inc.
Inventors:
Michael E. Bozik, Thomas Petzinger, Jr., Valentin Gribkoff
Abstract: Pharmaceutical compositions of R(+) pramipexole and methods of using such compositions for the treatment or prevention of diseases associated with or related to mitochondrial dysfunction or increased oxidative stress are disclosed.
Abstract: Methods for preparing chirally purified substituted 4,5,6,7-tetrahydro-benzothiazole diamines such as, for example, (6R)2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole and purifying a dominant enantiomer of substituted 4,5,6,7-tetrahydro-benzothiazole diamines from entantiomerically enriched mixtures of substituted 4,5,6,7-tetrahydro-benzothiazole diamines are provided herein.
Abstract: Pharmaceutical compositions of R(+) pramipexole and methods of using such compositions for the treatment or prevention of diseases associated with or related to mitochondrial dysfunction or increased oxidative stress are disclosed.
Type:
Application
Filed:
May 9, 2012
Publication date:
September 6, 2012
Applicant:
Knopp Neurosciences Inc.
Inventors:
Michael E. Bozik, Gregory T. Hebrank, Thomas Petzinger, JR.
Abstract: Pharmaceutical compositions of R(+) pramipexole and methods of using such compositions for the treatment or prevention of diseases associated with or related to mitochondrial dysfunction or increased oxidative stress are disclosed.
Type:
Application
Filed:
February 28, 2011
Publication date:
September 15, 2011
Applicant:
Knopp Neurosciences Inc
Inventors:
Michael E. Bozik, Gregory T. Hebrank, Thomas Petzinger, JR.
Abstract: Compositions of predetermined amounts of R(+) pramipexole and S(?) pramipexole and methods of using the same, including for the treatment and prevention of Parkinson's disease, are provided.
Type:
Grant
Filed:
May 16, 2007
Date of Patent:
September 13, 2011
Assignee:
Knopp Neurosciences, Inc.
Inventors:
Michael E. Bozik, Thomas Petzinger, Jr., Valentin Gribkoff
Abstract: Pharmaceutical compositions of (R)-pramipexole and one or more secondary therapeutic agents such as, for example dopamine agonists, dopaminergic agonists, COMT inhibitors, MOA inhibitors, excitatory amino acid antagonists, growth factors, neurotrophic factors, antioxidants, anti-inflammatory agents, immunomodulators, anti-glutamatergics, ion channel blockers, ?-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists, heat shock protein inducers/protein disaggregators and downregulators, monoamine oxidase type B (MOAB) inhibitors, multi-target agents, kinase inhibitors, Bcl inducers, histone deacetylase (HDAC) mediators, glial modulators, mitochondrial energy promoting agents, myostatin inhibitors, caspase inhibitors and combinations thereof or those related to mitochondrial dysfunction or increased oxidative stress are disclosed.