Patents
Patents for A61K 31 - Medicinal preparations containing organic active ingredients (785,912)
06/2004
06/24/2004WO2004052293A2 Recombinant vaccine against flavivirus infection
06/24/2004WO2004052292A2 Histone deacetylase inhibitor enhancement of trail-induced apoptosis
06/24/2004WO2004052289A2 Multilayered tablet containing pravastatin and aspirin
06/24/2004WO2004052287A2 Topical composition for heightened sensitivity
06/24/2004WO2004052285A2 Fat regulation
06/24/2004WO2004052284A2 Treatment of diabetes
06/24/2004WO2004052283A2 Superoxide dismutase mimics for the treatment of ocular disorders and diseases
06/24/2004WO2004052280A2 Anti-angiogenic compounds and their use in cancer treatment
06/24/2004WO2004052269A1 A method for preparing a medical solution for the manufacture of a medicament for peritoneal dialysis
06/24/2004WO2004052268A1 A method for preparing a medical solution for the manufacture of a medicament for peritoneal dialysis
06/24/2004WO2004052236A2 Methods and compositions for treatment of otitis media
06/24/2004WO2004052227A2 Superoxide dismutase mimics for the treatment of ocular disorders and diseases
06/24/2004WO2004052076A2 Mixed esters of dicarboxylic acids for use as pigment dispersants
06/24/2004WO2004039320A3 STEREOISOMERS OF p-HYDROXY-MILNACIPRAN, AND METHODS OF USE THEREOF
06/24/2004WO2004035020A3 Controlled release preparation
06/24/2004WO2004032864A3 X-nitro compounds, pharmaceutical compositions thereof and uses therof
06/24/2004WO2004030625A3 Synergistic methods and compositions for treating cancer
06/24/2004WO2004028570A3 A method for treating severe tinnitus
06/24/2004WO2004028469A3 Docohexaenoic acid for improved glycemic control
06/24/2004WO2004026258A3 Modulating vesicular monoamine transporter trafficking and function: a novel approach for the treatment of parkinson’s disease
06/24/2004WO2004026224A3 Process for preparing prostaglandin derivatives and starting materials for the same
06/24/2004WO2004024896A3 Phenyl-indole compounds
06/24/2004WO2004022716A3 Recombinatant mutants of rhabdovirus and methods of use thereof
06/24/2004WO2004022002A3 Combined immediate release and extended release analgesic composition
06/24/2004WO2004020403A3 A composition and method to augment and sustain neurotransmitter production
06/24/2004WO2004019873A9 Methods of promoting osteogenesis
06/24/2004WO2004019869A3 Indoles having anti-diabetic activity
06/24/2004WO2004019863A3 Combination therapy for treatment of fibrotic disorders
06/24/2004WO2004018044A8 N-(3-methoxy-5-methylpyrazin-2-yl)-2-(4-'1,3,4-oxadiazol-2-yl!phenyl)pyridine-3 sulphonamide as an anticancer agent
06/24/2004WO2004017922A3 Keto cannabinoids with therapeutic indications
06/24/2004WO2004017903A3 Methods for treating fungal infections
06/24/2004WO2004014309A3 Improved process for hydroxyazapirones
06/24/2004WO2004014304A3 Electrospun amorphous pharmaceutical compositions
06/24/2004WO2004012684A3 M3muscarinic acetylcholine receptor antagonists
06/24/2004WO2004011478A3 Anti-viral 7-deaza d-nucleosides and uses thereof
06/24/2004WO2004011425A3 Indole, azaindole and related heterocyclic ureido and thioureido piperazine derivatives
06/24/2004WO2004010938A3 Use of chymase inhibitors for the prevention and/or treatment of arterio-venous graft failure
06/24/2004WO2004006834A3 Leflunomide analogs for treating rheumatoid arthritis
06/24/2004WO2003105864A9 Methods and compositions involving aldose reductase inhibitors
06/24/2004WO2003105724A3 Novel maxi-k channel blockers, methods of use and process for making the same
06/24/2004WO2003103699A8 Use of ramoplanin to treat diseases associated with the use of antibiotics
06/24/2004WO2003103583A3 A method for using tethered bis(polyhydroxyphenyls) and o-alkyl derivatives thereof in treating inflammatory conditions of the central nervous system
06/24/2004WO2003101389B1 Relief of aids symptoms
06/24/2004WO2003099221A3 Methods for using jnk inhibitors for treating or preventing disease-related wasting
06/24/2004WO2003094839A8 Pyrimidinone compounds, compositions and methods
06/24/2004WO2003092580B1 Methods and compositions for treatment of central and peripheral nervous system disorders and novel compounds useful therefor
06/24/2004WO2003090690A3 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds and the compounds as such
06/24/2004WO2003075856A3 Methods, compositions, and kits for enhancing oligonucleotide-mediated nucleic acid sequence alteration using compositions comprising a histone deacetylase inhibitor, lambda phage beta protein, or hydroxyurea
06/24/2004WO2003072056A3 Intranasal administration of mc4-r agonists
06/24/2004WO2003064617A9 Pestalotiopsis microsporia isolates and compounds derived therefrom
06/24/2004WO2003057200A3 Compositions comprising inhibitors of dpp-iv and nep enzymes for the treatment of diabetes
06/24/2004WO2003053966A8 1-alkyl-1-azoniabicyclo [2.2.2] octane carbamate derivatives and their use as muscarinic receptor antagonists
06/24/2004WO2003051841A3 Compounds and uses thereof for decreasing activity of hormone-sensitive lipase
06/24/2004WO2003049686A3 Stabilization of hypoxia inducible factor (hif) alpha
06/24/2004WO2003047589A8 Pharmaceutical compositions containing 3,4-propinoperhydropurines and uses thereof for blocking neuronal transmission
06/24/2004WO2003024386A8 Use of potent, selective and non toxic c-kit inhibitors for treating interstitial cystitis
06/24/2004WO2002092594A8 Substituted 4h-chromenes and analogs as activators of caspases and inducers of apoptosis and the use thereof
06/24/2004WO2002072021A3 Agents and methods for the prevention of initial onset and recurrence of existing cancers
06/24/2004WO2002040056A9 Carrageenan viscoelastics for ocular surgery
06/24/2004WO2002038141A3 Compositions and methods for treatment of mild cognitive impairment
06/24/2004US20040122318 Tissue penetrating catheters having integral imaging transducers and their methods of use
06/24/2004US20040122254 Selective cyclooxygenase-2(COX-2) inhibitors; free of gastrointestinal side effects; treating eye disorders such as glaucoma or selective cyclooxygenase-2(COX-2) inhibitors, rheumatoid arthritis, arthritis, pain, inflammation
06/24/2004US20040122235 such as N-(2-Phenoxyphenyl)-N'-(thiazol-2-yl)urea; for treating diseases in which increasing glucokinase activity is beneficial (diabetes)
06/24/2004US20040122165 Hydrogel-forming system with hydrophobic and hydrophilic components
06/24/2004US20040122125 Lactone compounds as novel photoinitiators
06/24/2004US20040122110 comprising topical administration of vitamin A for treating, healing, or regeneration of ciliated epithelial structures of mucosal membranes; used in the context of surgery, and post-surgical healing
06/24/2004US20040122109 Preparation for hair and/or scalp
06/24/2004US20040122108 Betamimetics with a prolonged duration of activity, processes for preparing them, and their use as pharmaceutical compositions
06/24/2004US20040122107 Method of alleviating barometric-induced symptoms in airline passengers
06/24/2004US20040122105 Transdermal compositions
06/24/2004US20040122104 has an enteric coating that delays the release of milnacipran within the stomach, thereby avoiding side effects such as nausea, vomiting, bleeding due to irritation of the gastric mucosa, sleep disturbance, headache etc
06/24/2004US20040122103 humectant and skin barrier function reinforcing agent that improve the water retaining ability and barrier functions of the horny layer, are miscible and mixing stability
06/24/2004US20040122102 compounds are potent ocular hypotensives, and are suitable for the management of glaucoma; they also are smooth muscle relaxants with broad application in systemic hypertensive and pulmonary diseases, gastrointestinal, reproduction disorders etc
06/24/2004US20040122101 Polymorphs of suberoylanilide hydroxamic acid
06/24/2004US20040122100 which contain EP1 agonist (which activate EP1 receptor that is subtype of prostaglandin E2 receptor) as an active ingredient
06/24/2004US20040122097 Stimulation of in vivo production of proteins
06/24/2004US20040122096 using guanidine derivatives, preferably acylguanidines as NHE inhibitors
06/24/2004US20040122094 Isomers of conjugated linoleic acids at either the 1 and 3 or 2 positions of the acylglyceride molecule and another fatty acyl residue at the other of 1 and 3 OR 2 positions of acylglyceride molecule; useful as dietary supplements
06/24/2004US20040122092 Hydroxyphenylundecane, a process for their production and their use
06/24/2004US20040122090 capable of modulating the excitatory response of the neurons, inhibiting an excitotoxic effect, and promoting a neurotrophic effect, thereby providing a therapeutic effect that treats neuropsychiatric disorders
06/24/2004US20040122089 Analogs of andandamide and arvanil have been found to act at receptors; are useful in pain management, used as anti-proliferative/anti-tumor agents, vasodilators, and in other applications
06/24/2004US20040122088 Zinc-monocysteine complex and method of using zinc-cysteine complexes
06/24/2004US20040122087 Comprising 21-40 wt-% urea, and trace amounts of salts of zinc, copper and manganese and the balance an excipient; treating, protecting and re-epitheliazing skin disorders; wound healing agents; semisolids; moisture; microbiocides
06/24/2004US20040122086 Method for the production of anhydrous, pharmaceutical formulations of xanthogenates
06/24/2004US20040122085 Compounds based on 1-oxoisochroman or - phthalan such as phyllodulcin and hydrangenol; food, beverage and feed additives; alcohol abuse
06/24/2004US20040122084 7-Methyl-3.6,10,15-tetraoxapentacyclo [12.2.1.02,4. 05,7. 09,13]heptadec-1(17)-ene-11,16-dione derivatives; antitumor, -proliferative, -carcinogenic agents; viricides;DNA polymerase inhibitors; bactericides; solubility; stability; injections
06/24/2004US20040122083 Antitubulin assembly and cell growth inhibitor denominated "dioxostatin"
06/24/2004US20040122082 A drug, a food, a beverage or a feed, each having an effective ingredient of a coumarin and/or a chroman compound having an enhancing action for nerve growth factors (NGF) production; nervous system disorders; Alzheimer's disease; plant extracts
06/24/2004US20040122081 Intravenous formulation for a taxoid antitumor agent as a two-vial kit with the taxoid, solvent and buffer in one vial and cosolvent and buffer in the other; mixing prior to administration; improved solubility, stability and oxidation resistance
06/24/2004US20040122080 Synergist combinations of retinoid receptor ligands and selected cytotoxic agents for treatment of cancer
06/24/2004US20040122079 (R)-thiophene-2,5-dicarboxylic acid 2-hydroxyamide 5-[(1-thiophen-2-yl-ethyl)-amide], e.g.: antiproliferative agents; anticarcinogenic agents; enzyme inhibitors of histonedeacetylases; colon, breast, lung, prostate, rectal, stomach, bladder cancers
06/24/2004US20040122078 A compound having slowly-deactivating A-type K+ channel opening activity such as N-(5,5-dioxido-10-oxo-4,10-dihydrothieno[3,2-c][1]benzothiepin-9-yl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide
06/24/2004US20040122077 Administering a statin drug in an amount to promote angiogenesis in the tissue, preferably in situations where the subject is not otherwise in need of the drug ; activating Akt (protein kinase B) in vascular endothelial cells in vitro and in vivo
06/24/2004US20040122076 The use of 1-(iso)indolylsulfonamido-),4-(alkylamido-)benzenes and derivatives as 5-Ht6receptor antagonists; Alzheimer's disease; neurodegenerative diseases; prophylaxis
06/24/2004US20040122071 Fluconazole, a compound selected from a group consisting of fatty acid, fatty alcohol, higher fatty acid ester and lower alcohol and a base; favorable absorption and delivery through the human skin; low skin stimulation; stability; spreading
06/24/2004US20040122068 Pramipexole and salts, e.g. dichloride, for use in the prevention and/or treatment of HIV-associated encephalopathy; motor disorders, cognitive impairment and behavioural disorders;.brain disorders; cognition activators
06/24/2004US20040122067 Treatment of chronic heart failure
06/24/2004US20040122066 Oxadiazole derivatives having anticancer effects
06/24/2004US20040122065 Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or buccally
06/24/2004US20040122064 Enzyme inhibitors of both wild type and mutant variants of HIV reverse transcriptase, particularly resistant varieties; e.g.,N-{4-[(acetylamino)sulfonyl]-2-methylphenyl}-2-[4-chloro-2-(3-cyano-5-methylbenzoyl)phenoxy]acetamide