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Attorney: PFIZER INC.


Number of applications: 369
Last date: October 29, 2009

1                    
Application No.Application TitleIssue Date
20090270350Pyridinone Pyrazole Urea and Pyrimidinone Pyrazole Urea Derivatives
This invention is directed generally to substituted pyridinone and pyrimidinone compounds that generally inhibit p38 kinase, TNF, and/or cyclooxygeπase activity. Such substituted pyridinone and pyrimidinone compounds include compounds generally corresponding in structu...
10/29/2009
20090221546INHIBITORS OF FACTOR XA AND OTHER SERINE PROTEASES INVOLVED IN THE COAGULATION CASCADE
Compounds useful as intermediates for synthesis of compounds of Formula (1):

    • wherein A, ...
09/03/2009
20090181957BENZIMIDAZOLONE DERIVATIVES AS CB2 RECEPTOR LIGANDS
This invention relates to compounds of the formula (I): or pharmaceutically acceptable salts thereof, wherein: A, B, R1, R2 and R3 are each as described herein, and compositions containing such compounds and the use of such compounds in ...
07/16/2009
20090171071PYY Agonists and Uses Thereof
The invention provides PYY3-36 variants and pegylated derivatives thereof and compositions and methods useful in the treatment of conditions modulated by an NPY Y2 receptor agonist....
07/02/2009
20090170897Method of Treating Neuropathic Pain
The invention relates to the use of a CRTH2 receptor antagonist in the manufacture of a medicament for the treatment of neuropathic pain and to a method of treating neuropathic pain using an antagonist of CRTH2 receptor....
07/02/2009
20090170886ANDROGEN MODULATORS
The present invention is directed to a new class of benzonitriles and to their use as androgen receptor modulators. Other aspects of the invention are directed to the use of these compounds to decrease excess sebum secretions and to stimulate hair growth....
07/02/2009
20090170852NOVEL PYRAZOLE-BASED HMG CoA REDUCTASE INHIBITORS
Novel compounds and pharmaceutical compositions useful as hypocholesterolemic and hypolipidemic agents are described. More specifically, potent inhibitors of the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase (“HMG CoA reductase”) are described. Methods of u...
07/02/2009
20090170778PYY Agonists and Uses Thereof
The invention provides PYY3-36 variants and pegylated derivatives thereof and compositions and methods useful in the treatment of conditions modulated by an NPY Y2 receptor agonist....
07/02/2009
20090169595Controlled Release Polymeric Compositions of Bone Growth Promoting Compounds
The present invention is directed to an improved system for controlled release of a bone growth promoting compound and to a flowable composition for its formation. The flowable composition is composed of a bone growth promoting compound, a thermoplastic polymer and an o...
07/02/2009
20090162286Phosphodiesterase 10 Inhibition as Treatment for Obesity-Related and Metabolic Syndrome-Related Conditions
The present invention provides methods to decrease body weight and/or body fat in animals, e.g., in the treatment of overweight or obese patients (e.g., humans or companion animals), or as a means to produce leaner meat in food stock animals (e.g., cattle, chickens, pig...
06/25/2009
20090156685(R)-CHIRAL HALOGENATED SUBSTITUTED FUSED HETEROCYCLIC AMINO COMPOUNDS USEFUL FOR INHIBITING CHOLESTEROL ESTER TRANSFER PROTEIN ACTIVITY
The invention relates to substituted aryl and heteroaryl (R)-Chiral Halogenated 1-Substitutedamino-(n+1)-Alkanol compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for trea...
06/18/2009
20090156677Gabapentin-containing Solid Compositions and Process for Preparing the Same
The present invention provides a stabilized solid composition containing a 4-amino 3-substituted-butanoic acid derivative which can be obtained by incorporating a humectant as a stabilizer....
06/18/2009
200901566181-(1- (2-Ethoxyethyl)-3-Ethyl-7-(4-Methylpyridin-2-Ylamino) - 1H-Pyrazolo [4,3-D] Pyrimidin-5-YL) Piperidine-4-Carboxylic acid and salts thereof
The present invention comprises 1-(1-(2-ethoxyethyl)-3-ethyl-7-(4-methylpyridin-2-ylamino)-1H-pyrazolo[4,3-d]pyrimidin-5-yl)piperidine-4-carboxylic acid and its salts. The invention further comprises pharmaceutical compositions, methods of treatment, and synthetic metho...
06/18/2009
20090149431Eplerenone Drug Substance Having High Phase Purity
A novel crystalline form (Form L) of the aldosterone receptor antagonist drug eplerenone is provided having relatively high physical stability at normal temperatures of storage and use. Pharmaceutical compositions are also provided comprising Form L eplerenone, optional...
06/11/2009
20090131397ESTROGEN MODULATORS
The present application is directed to a new class of isoxazoles and their use as estrogen modulators....
05/21/2009
20090076152Novel Compounds Active as Muscarinic Receptor Antagonists
The invention relates to compounds of formula

processes and intermediates for their preparation, their use as muscarinic antagonists and pharmaceutical compositions containing them....

03/19/2009
20090048453Salt forms of [R-(R*,R*)]-2-(4-fluorophenyl)-beta, delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid
Novel salt forms of [R—(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid characterized by their X-ray powder diffraction pattern and solid-state NMR spectra are described, as well as methods fo...
02/19/2009
20080306282Novel Forms of [R-(R*,R*)]-2-(4-Fluorophenyl)-Beta,Delta-Dihydroxy-5-(1-Methylethyl)-3-Phenyl-4-[(Phenylamino)Carbonyl]-1H-Pyrrole-1-HeptanoicAcid Calcium Salt (2:1)
Novel forms of [R—(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid hemi calcium salt designated Form XX, Form XXI, Form XXII, Form XXIII, Form XXIV, Form XXV, Form XXVI, Form XXVII, Form XXVII...
12/11/2008
20080292707Pharmaceutical Compositions of Adsorbates of Amorphous Drug
Pharmaceutical compositions comprise a low-solubility drug adsorbed onto a high surface area substrate to form an adsorbate. The compositions in some embodiments include a concentration-enhancing polymer....
11/27/2008
20080294071Assay Method
An assay for the assessment of drug side effects particularly the side effect of dizziness comprising the steps of: providing a first control animal located on abeam; inducing the control animal to traverse the beam; recording the number of footslips made by the animal ...
11/27/2008
200802937671-Isopropyl-2-Oxo-1,2-Dihydropyridine-3-Carboxamide Derivatives Having 5-Ht4 Receptor Agonistic Activity
This invention provides a compound of formula (I): wherein R1 represents an alkyl group having from 1 to 4 carbon atoms or a halogen atom, R2 represents an alkyl group having from 1 to 4 carbon atoms, R3 represents a hydrogen atom or a h...
11/27/2008
20080293801Solid Amorphous Dispersions of An Mtp Inhibitor For Treatment of Obesity
A composition comprises a solid amorphous dispersion comprising (S)—N-{2-[benzyl(methyl)amino]-2-oxo-1-phenylethyl}-methyl-5-[4′-(trifluoromethyl)[1,1′-biphenyl]-2-carboxamido]-1H-indole-2-carboxamide and a polymer....
11/27/2008
20080293746COMBINATIONS COMPRISING PREGABALIN
The invention relates to a combination of pregabalin and 1-(2-ethoxyethyl)-5-[ethyl(methyl)amino]-N-mesyl-7-[(4-methyl-2-pyridyl)amino]-1H-pyrazolo[4,3-d]pyrimidine-3-carboxamide, to pharmaceutical compositions containing the combination, and to the use of the combinati...
11/27/2008
20080293633Pharmaceutical Formulations, Methods, and Dosing Regimens for the Treatment and Prevention of Acute Coronary Syndromes
The invention provides methods and formulations for treating and preventing acute coronary syndromes. The methods of the instant invention provide safe and effective doses of an Apolipoprotein A-I Milano: phospholipid complex to reduce and stabilize atherosclerotic plaq...
11/27/2008
20080287521Crystalline Forms Of [R-(R*,R*)-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methyl- Ethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic Acid Calcium Salt (2:1)
Novel crystalline forms of [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid hemi calcium salt designated Form V, Form VI, Form VII, Form VIII, Form IX, Form X, Form XI, Form XII, Form XIII, F...
11/20/2008
20080287479INHIBITORS OF SERINE PALMITOYLTRANSFERASE
This invention provides compounds of the formula:

useful in the inhibition or modulation of serine palmitoyl transferase and their use in methods of treatment or amelioration of type 2 diabetes, type 1 diabet...

11/20/2008
20080280875FUSED PHENYL AMIDO HETEROCYCLIC COMPOUNDS
The present invention relates to a compound of formula (I):

or a pharmaceutically acceptable salt or solvate thereof, wherein:

    11/13/2008
    20080282364Phosphodiesterase 9 Inhibition as Treatment for Obesity-Related Conditions
    The present invention is directed to methods to decrease body weight and/or body fat in an animal, e.g., in the treatment of overweight or obese patients (e.g., humans or companion animals), or as a means to produce leaner meat in food stock animals (e.g., cattle, chick...
    11/13/2008
    20080280877Azetidines
    The invention relates to EP2 antagonist azetidines of formula (I)

    wherein Ar, R1, X, and Z are as defined herein, to their use in medicine, particularly in the treatment of endometriosis and/or ute...

    11/13/2008
    20080267970Sulfonamide Derivatives For The Treatment of Diseases
    The invention relates to compounds of formula (1)

    and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds ac...

    10/30/2008
    20080269314Process for Forming Amorphous Atorvastatin
    A process for forming amorphous atorvastatin comprising the steps of dissolving atorvastatin in a non-hydroxylic solvent and removing the solvent by freeze-drying, as well as processes of dissolving atorvastatin in a hydroxylic solvent with a solubilizing agent or an al...
    10/30/2008
    20080269211Indazole Derivatives
    This invention relates to compounds of the formula (I):

    or pharmaceutically acceptable salts thereof, wherein: R1, R2, R3, A and m are each as described herein and composition...

    10/30/2008
    20080269310Synergistic Combinations
    This invention relates to synergistic combinations of non-steroidal antiinflammatory drugs, particularly carprofen, with alpha-2...
    10/30/2008
    20080269293PYRAZOLE DERIVATIVES AS ANTI-PLATELET AND ANTI-THROMBOTIC AGENTS
    This invention relates to novel compounds of formula (I)

    or stereoisomers or pharmaceutically acceptable salts thereof wherein Y, R1 through R9, and X1 through X7 a...

    10/30/2008
    20080269111METHOD OF TREATING DYSLIPIDEMIC DISORDER
    The invention provides methods of treating or preventing a condition or disorder associated with dyslipidemia with compositions comprising apolipoprotein-sphingomyelin complexes. The methods of the invention permit reduction, by 4- to 20-fold, of the amount of apolipopr...
    10/30/2008
    20080269233Piperidinoyl-Pyrrolidine and Piperidinoyl-Piperidine Compounds
    The present invention relates to a class of compounds of general formula (I)

    and the salts, hydrates, solvates, polymorphs and prodrugs wherein n, R6, R7 and R10 are as define...

    10/30/2008
    20080262074Salt Forms of [R-(R*,R*)]-2-(4-Fluorophenyl)-Beta,Delta-Dihydroxy-5-(1-Methylethyl)-3-(Phenyl-4-[(Phenylamino)Carbonyl]-1H-Pyrrole-1-Heptanoic Acid
    Novel salt forms of [R—(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid or solvates or hydrates thereof, as well as crystalline salts characterized by their X-ray powder diffraction pattern ar...
    10/23/2008
    20080261995Pharmaceutical Combination of a Pde-5 Inhibitor and a 5-Alpha Reductase Inhibitor
    This invention relates to the combined use of a PDE5 inhibitor and a 5-alpha reductase antagonist in the treatment of lower urinary tract symptoms (LUTS), such as urgency, frequency, nocturia and urge incontinence....
    10/23/2008
    20080255113Quinolonecarboxylic Acid Compounds Having 5-Ht4 Receptor Agonistic Activity
    This invention provides a compound of the formula (I): wherein Het represents a heterocyclic group having one nitrogen atom, to which B binds directly, and from 4 to 7 carbon atoms, and said heterocyclic group being unsubstituted or substituted by 1 to 4 substituents in...
    10/16/2008
    20080234252Compounds Useful in Therapy
    Compounds of formula (I),

    or a pharmaceutically acceptable salt, solvate, ester or amide thereof, wherein

    • R1 represents [CH
    09/25/2008
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