Patents
Patents for A61K 31 - Medicinal preparations containing organic active ingredients (785,912)
05/2008
05/29/2008US20080125418 Benzimidazole derivatives and their use as kdr kinase protein inhibitors
05/29/2008US20080125417 4-Tert-Butyl-N-(2-methyl-3-{2-[4-(morpholine-4-carbonyl)-phenylamino]-pyrimidin-4-yl}-phenyl)-benzamide;enzyme inhibitors of Burton's tyrosine kinase (Btk); autoimmune diseases; antiinflammatory/-arthritic agents; X-linked agammaglobulinaemia; antiallergens; osteoporosis; determining the presence Btk
05/29/2008US20080125416 Sigma Receptor Inhibitors
05/29/2008US20080125415 Novel methods for treatment of diseases related to activated lymphocytes
05/29/2008US20080125414 Method of Treatment
05/29/2008US20080125413 Antagonist for calcitonin gene related peptide (Cgrp); azepinone ligands; migranes; headaches; 1-[(2-methoxyethyl)-2-oxo-6-phenylazepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide
05/29/2008US20080125412 Containing a diazacycloalkane ring, especially a 1,4-diazepane ring, e.g., N-p-((4-(alpha-phenylmethoxycarbonylmethyl)-1,4-diazepan-1-yl)phenyl)-o-biphenylcarboxamide, for the treatment of hyperlipidemia, obesity and type II diabetes.
05/29/2008US20080125411 Dispiro 1,2,4-trioxolane antimalarials
05/29/2008US20080125410 7-chloro-N,N-9-trimethyl-2-(6-methylpyridin-3-yl)-9H-pyrimido[4,5-b]indole-4-carboxamide; ethyl 7-chloro-9-methyl-2-phenyl-9H-pyrimido[4,5-b]indole-4-carboxylate; 4-[(4-azetidin-1-yl)piperidin-1-ylcarbonyl]-7-chloro-9-methyl-2-phenyl-9H-pyrimido-[4,5-b]indole; Alzheimer's or Parkinson's disease
05/29/2008US20080125409 N-tert-butyl-5-(5-methanesulfonylamino-2-pyridyl)-1-(6-methoxy-3-pyridyl)-1H-1,2,4-triazole-3-carboxamide; prophylactic and/or therapeutic agent for ischemic diseases; platelet aggregation suppressant
05/29/2008US20080125408 (5-propyl-2-oxo-1,3-dioxol-4-yl)methyl (5R,6S)-6-[(1R)-1-hydroxyethyl]-7-oxo-3-[[(1R,3S)-tetrahydro-1-oxido-3-thienyl]thio]-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate for teating bacterial infections such as bronchitis, sinusitis, otitis media, brain abscess, pneumonia etc; oral bioavailability
05/29/2008US20080125407 Method for preparation of fluticasone propionate
05/29/2008US20080125406 Method for Treating Primary and Secondary Forms of Glaucoma
05/29/2008US20080125405 Composition for treating or preventing olfactory disorder
05/29/2008US20080125404 purine and pyrimidine derivatives such as Roscovitine or 2-[(1-ethyl-2-hydroxyethyl)amino]-6-benzylamine-9-isopropylpurine or olomoucine or purvalanol A for treating human systemic lupus erythematosus associated with antinuclear antibodies; methylprednisolone
05/29/2008US20080125403 Method of Treating Men with Metabolic and Anthropometric Disorders
05/29/2008US20080125402 Methods of hormonal treatment utilizing ascending-dose extended cycle regimens
05/29/2008US20080125401 Use of estradiol valerate or 17beta-estradiol in combination with dienogest for oral therapy to maintain and/or increase feminine libido
05/29/2008US20080125400 Use of phosphoenolpyruvate derivatives
05/29/2008US20080125399 N-[3-(trifluoromethyl)pyridin-2-yl]-4-methyl-6-methyl-3-oxo-4-aza-5 alpha -androst-5-en-17 beta -acetamide; useful for the treatment of conditions caused by androgen deficiency such as osteoporosis, osteopenia, glucocorticoid-induced osteoporosis, periodontal disease, cancer cachexia, Alzheimer's disease
05/29/2008US20080125398 oxidation of 2-{[2-(Diisopropylamino)ethyl]thio}ethyl N,N,N',N'-tetrakis(2-chloroethyl)phosphorodiamidate to 2-{[2-(diisopropylamino)ethyl]sulfonyl}ethyl N,N,N',N'-tetrakis(2-chloroethyl)phosphorodiamidate; salt formation, anticarcinogenic agent
05/29/2008US20080125397 2 (SULFONYL)ETHYL N,N,N',N' tetrakis(2 chloroethyl)phosphorodia
05/29/2008US20080125396 2-Butyl-4-{[4-(difluoromethoxy)phenyl]amino}-5-phenylisothiazole-3(2H)-thione 1,1-dioxide; cardiovascular diseases such as atherosclerosis; inflammatory and Alzheimer's diseases, lipid disorders (dyslipidemias); thionation of the isothiazol-3 (2H)-one with Lawesson's reagent
05/29/2008US20080125395 Compositions and methods for the treatment of skin
05/29/2008US20080125394 Continuous slow release of a oral drug containing phosphorus binder such as polyallylamine HCL, polyallylamine carbonate, lanthanum carbonate, Al/OH/3, magnesium acetate, MgCO3, CaCO3, calcium acetate, calcium citrate, calcium alginate, styrene-divinylbenzene copolymer, chitosan for hyperphosphatemia
05/29/2008US20080125393 Methods of selectively treating diseases with specific glycosaminoglycan polymers
05/29/2008US20080125392 Glycolipids
05/29/2008US20080125391 administering to a mammal harboring a tumor which expresses HALRs, a Sindbis virus vector to treat the tumor, and the vector has not been modified to target a tumor-specific cellular determinant, has a preferential affinity for HALRs, a Sindbis virus E2 HALR binding domain; ganciclovir; gene therapy
05/29/2008US20080125390 Methods for Modulating Immune and Inflammatory Responses
05/29/2008US20080125389 Men1 is a marker and therapeutic target for breast and prostate cancer
05/29/2008US20080125388 treating or preventing a condition of excessive cell death by administering a nucleic acid molecule encoding a protein having CPG15-2 biological activity; acts as survival factor by rescuing hippocampal and cortical neurons from cell death; inhibiting activity of CPG15-2 for cancer treatment
05/29/2008US20080125387 Administering vector system that directs regulated erythropoietin (Epo) gene therapy in a manner that physiologically corrects the hematocrit levels in a patient in need of anemia treatment
05/29/2008US20080125385 Decreasing activity improves beta-adrenergic response; point mutations; gene expression inhibition
05/29/2008US20080125384 Simultaneous silencing and restoration of gene function
05/29/2008US20080125383 For host undergoing surgery or coronary artery bypass
05/29/2008US20080125382 Extracellular superoxide dismutase (EC-SOD) gene delivery to prevent oxidative injury
05/29/2008US20080125381 Such as 7-(2-thienyl)-3-(2-deoxy- beta -D-ribofuranosyl)-3H-imidazo[4,5-b]pyridine; anticancer agents
05/29/2008US20080125380 Fatty acid-anticancer conjugates and uses thereof
05/29/2008US20080125379 Contains 3-O-beta-D-Glucopyranosyl-4-methyl-ergost-7-en-3-ol
05/29/2008US20080125378 Use of Amygdalin Analogues for the Treatment of Psoriasis
05/29/2008US20080125377 Delivery system for antiangiogenic and antiinflammatory pharmaceuticals and method of use
05/29/2008US20080125376 Viricide against hepatitis virus; pyrrole derivatives as, for example, 3-acetyl-4,5-dimethyl-2-pyrrole carboxylic acid
05/29/2008US20080125375 Peptide like compounds for treating coronavirus or aviviridae virus; severe acute respiratory distress syndrome
05/29/2008US20080125364 Increasing formation of tight junctions by modulating occludin activity of transformed cells (induced by RAF1)
05/29/2008US20080125360 Use of polypeptide YY (PYY) administered parenterally to treat pain, abdominal pain, constipation and/or diarrhea from irritable bowel syndrome, functional dyspepsia; use in combination with antidepressants or antiemetics
05/29/2008US20080125358 Methods for Chk2 inhibitor patient selection
05/29/2008US20080125355 Endogenous Peptide and Active Subfragments Thereof
05/29/2008US20080125354 With triple helix and/or poly-proline type II transition state analog phosphorus based inhibitor comprising a phosphonamide, phosphinic peptide or phosphonate ester; e.g. (R,S)-2-Isopropyl-3-((1-(N-(9-Fluorenylmethoxycarbonyl)amino)-methyl)-adamantyloxyphosphinyl)propanoic acid; antitumor agents
05/29/2008US20080125351 Forming water-in-oil emulsion from aqueous phase (water soluble polypeptide and sugar) and oil phase comprising glycolic acid-lactic acid copolymer and solvent, adding silicone oil, hardening, drying; optimizing the silicone oil to polymer ratio to improve bioavailability of peptide drug
05/29/2008US20080124803 cDNA Corresponding to the antigenome of nonsegmented negative stranded RNA viruses and process for the production of such viruses
05/29/2008US20080124802 Method for labeling specific cells within living cells or tissues
05/29/2008US20080124743 Diagnostics and therapeutics for diseases associated with neuromedin u1 receptor (u1)
05/29/2008US20080124416 Therapeutic composition from goji (lycium barbarum l.), methods of making and using
05/29/2008US20080124413 Novel composition containing extracts of butyrospermum parkii and the use of such a composition for preparing a medicament or a dietary supplement for the treatment or prevention of inflammation hypersensitivity or pain
05/29/2008US20080124412 Methods for reducing circulating glucose levels
05/29/2008US20080124411 nasal strip; and an orally administered composition comprising a tissue-firming agent, a tissue-soothing agent, a tissue lubricant, and an expectorant; for combating snoring
05/29/2008US20080124408 includes an alkylamide fraction comprising a 2-ene alkylamide fraction and a 2,4-diene alkylamide fraction; for the prevention and treatment of colds and flu
05/29/2008US20080124407 Inhibiting cyp3a4 induction
05/29/2008US20080124404 reducing at least one of total cholesterol, LDL-cholesterol, free fatty acids, or triglycerides; composition comprising berberine or a pharmaceutically acceptable salt thereof and a multi-drug resistant pump (MDR) inhibitor
05/29/2008US20080124402 N-(Pyridin-3-Yl)-2-Phenylbutanamides As Androgen Receptor Modulators
05/29/2008US20080124401 Method of treating endothelial injury
05/29/2008US20080124400 Microparticles With High Loadings Of A Bioactive Agent
05/29/2008US20080124399 Such as capsules/beads of cyclobenzaprine hydrochloride
05/29/2008US20080124398 Modified release dosage forms of skeletal muscle relaxants
05/29/2008US20080124396 polymer synthesized by a cross-coupling reaction of polymer scaffold units and xenoantigens
05/29/2008US20080124393 Time-release agent containing poorly soluble agent such as clozapine; release the agent following administration for a time period ranging from about 2 to about 24 hours or longer
05/29/2008US20080124389 Nanoparticulate and Controlled Release Compositions Comprising Cyclosporine
05/29/2008US20080124388 tannins obtained through total or semi-chemical syntheses; can sufficiently promote early growth of new blood vessels in the infarct zone to quickly restore the coronary blood circulation once an ischemic event occurs
05/29/2008US20080124387 Methods and formulations for enhancing the absorption and decreasing the absorption variability of orally administered drugs, vitamins and nutrients
05/29/2008US20080124386 Apoptosis-mimicking synthetic entities and use thereof in medical treatment
05/29/2008US20080124385 Methods for Transmembrane Treatment and Prevention of Otitis Media
05/29/2008US20080124384 Heteroaryl Substituted Piperazinyl-Pyridine Analogues
05/29/2008US20080124381 sufficient film strength and rapid disintegration profiles; high and low molecular weight water soluble polymer, an active agent, hydroxypropyl methylcellulose, hydroxypropyl cellulose
05/29/2008US20080124379 Compositions and methods for making therapies delivered by viral vectors reversible for safety and allele-specificity
05/29/2008US20080124377 Formulation for controlled release of drugs by combining hydrophilic and hydrophobic agents
05/29/2008US20080124376 Ocular devices and methods of making and using thereof
05/29/2008US20080124375 Device and Methods of Sequential, Regional Delivery of Multiple Cyctotoxic Agents and Directed Assembly of Wound Repair Tissues
05/29/2008US20080124374 Decellularized bone marrow extracellular matrix
05/29/2008US20080124372 Morphology profiles for control of agent release rates from polymer matrices
05/29/2008US20080124367 50% by mass to 95% by mass of an oil constituent, which contains 10% by mass to 100% by mass of a solid or semisolid oil constituent, and 5% by mass to 50% by mass of particles; enhancing percutaneous absorption of a water-soluble agent
05/29/2008US20080124366 Methods and Compositions for Treating Tumors
05/29/2008US20080124365 Using single-stranded DNA template to generate antisense RNA sequences for treatment and prevention of viral infection and cell proliferative disorders; viricides; antitumor agents
05/29/2008US20080124354 Her-2 protein fragments, recombinant peptides comprising same, nucleotide molecules encoding same, recombinant vaccine vectors and immunogenic compositions comprising same, and methods for inducing immune response and treating cancer, comprising same
05/29/2008US20080124352 Methods to bypass CD4+ cells in the induction of an immune response
05/29/2008US20080124349 Method or Use of a Solubilized Glucan Product to Increase Immunostimulation in Animals
05/29/2008US20080124346 Chimeric metal binding protein for use in prevention and treatment of cancer, diabetes, cardiovascular disease, obesity, metabolic disease, neurodegenerative disease, gastrointestinal disease, autoimmune disease, rheumatological disease and infectious disease.
05/29/2008US20080124339 Monoclonal antibody specific to mucosal addressin cell adhesion molecule (MAdCAM) for use in prevention and treatment of inflammatory, gastrointestinal, liver disorders
05/29/2008US20080124338 Using mixture comprising immunoglobulin and terminal region of nuclear factor kappa beta as therapeutic tool in treatment of sexually transmitted, ocular, cancer and atherosclerotic disorders
05/29/2008US20080124335 Novel Polypeptide and the Use Thereof
05/29/2008US20080124333 Administering glutamate release inhibitor and glutamate receptor antagonist; antiapoptosis
05/29/2008US20080124331 Compositions and methods for the diagnosis and treatment of tumor
05/29/2008US20080124329 Conditioned Cell Immunization
05/29/2008US20080124323 Using fructooligosaccharides as components of probiotics for use in prevention and treatment of infection
05/29/2008US20080124322 Activation and inhibition of the immune system
05/29/2008US20080124317 Diagnos and Treatment of Fibrosis Related Pathology
05/29/2008US20080124312 Using topical skin treatment to combat age-related skin pigmentation, skin elasticity, color and smoothness disorders
05/29/2008US20080124309 Cell Surface Glycoprotein
05/29/2008US20080124306 Vigor Enhancement Via Administration of Pyrimidine Derivatives
05/29/2008US20080124303 Exhibits tubercin activity; immune enhancers such as glycyrrhizin (GR), glycyrrhetic acid, and Chinese herbal extracts
05/29/2008US20080124301 Oligonucleotide for use in prevention and treatment of cell proliferative and nervous system disorders; antisense agents