| Patents for A61K 31 - Medicinal preparations containing organic active ingredients (785,912) |
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| 08/26/2003 | US6610730 Viricides; protease inbhibitor |
| 08/26/2003 | US6610728 Method for treatment of non-rheumatoid arthritis |
| 08/26/2003 | US6610727 Antitumor agents |
| 08/26/2003 | US6610726 Compositions and agents for modulating cellular proliferation and angiogenesis |
| 08/26/2003 | US6610725 Fluorinated imidazoline benzodioxane, preparation and therapeutic uses thereof |
| 08/26/2003 | US6610724 3-Aminopyrazole inhibitors of cyclin dependent kinases |
| 08/26/2003 | US6610723 Imidazole derivatives |
| 08/26/2003 | US6610722 Inhibitors of prenyl-protein transferase |
| 08/26/2003 | US6610720 Method for treating or preventing emesis |
| 08/26/2003 | US6610719 Use of prostaglandin (PGE2) receptor a (EP4) selective agonists for the treatment of acute and chronic renal failure |
| 08/26/2003 | US6610718 And dosage forms for treating rheumatoid arthritis |
| 08/26/2003 | US6610716 Cyanomethyl substituted thiazoliums and imidazoliums and treatments of disorders associated with protein aging |
| 08/26/2003 | US6610715 Cathecol hydrazone derivatives, process for preparing the same and pharmaceutical composition containing the same |
| 08/26/2003 | US6610714 Non-nucleoside reverse transcriptase inhibitors |
| 08/26/2003 | US6610713 Treating cell with cholinergic agonist |
| 08/26/2003 | US6610711 4-phenylpiperidines for the treatment of pruritic dermatoses |
| 08/26/2003 | US6610708 Cyclic amino compounds |
| 08/26/2003 | US6610707 Heterocyclic compounds as inhibitors of rotomase enzymes |
| 08/26/2003 | US6610706 Crystalline form of 6-hydroxy-3-(4-[2-(piperidin-1-yl)ethoxy]phenoxy)-2-(4-methoxyphenyl)benzo[b]thiophene hydrochloride |
| 08/26/2003 | US6610704 Antithrombotic amides |
| 08/26/2003 | US6610703 Administering long-chain N-alkyl derivative of deoxynojirimycin having from nine to about twenty carbon atoms in alkyl chain |
| 08/26/2003 | US6610700 Inhibit binding of integrins to their ligands, use in immune or inflammatory disorders; 3-(4-((2,6-Naphthyridinyl)amino)-phenyl)-2-((2-(1-ethylpropyl)-3-oxo-1 -cyclopentenyl) amino)-propionic acid, for example |
| 08/26/2003 | US6610699 Use of L-carnitine and its alkanoyl derivatives in the preparation of medicaments with anticancer activity |
| 08/26/2003 | US6610698 Treatment of tumor necrosis factor-alpha, interleukin-1 beta, interleukin-6, and interleukin-8 mediated diseases |
| 08/26/2003 | US6610697 Substituted 2-aryl-3-(heteroaryl)-imidazo[1,2-a]pyrimidines, and related pharmaceutical compositions and methods |
| 08/26/2003 | US6610696 Such as 2-(4-(2-(2-(4-(3,5-dimethyl-isoxazol-4-yl)-phenyl)-5-methyloxazol-4-yl) -ethyoxy)-phenoxy)-2-methylpropionic acid for treatment of diabetes (lowering serum triglycerides) |
| 08/26/2003 | US6610695 Prophylaxis or treatment of CSBP/RK/p38 kinase mediated disease |
| 08/26/2003 | US6610693 Fructosamine oxidase: antagonists and inhibitors |
| 08/26/2003 | US6610692 Anticoagulants |
| 08/26/2003 | US6610691 Carboxylic acid derivatives, their production and use |
| 08/26/2003 | US6610690 Administering optically pure (S,S) enantiomer of reboxetine |
| 08/26/2003 | US6610688 For therapy of blood vessel proliferative disorders; fibrotic disorders; mesangial cell proliferative disorders; metabolic disorders; allergies; asthma; thrombosis; nervous system diseases; and cancer |
| 08/26/2003 | US6610687 Benzofuranylsulfonates |
| 08/26/2003 | US6610686 Use of pirenoxine for the protection of corneal tissues in photokeractomy |
| 08/26/2003 | US6610685 Fused indole derivatives |
| 08/26/2003 | US6610684 Fused azepinone cyclin dependent kinase inhibitors |
| 08/26/2003 | US6610683 Treatment of infectious disease using interleukin-1β-converting enzyme (ICE)/CED-3 family inhibitors |
| 08/26/2003 | US6610682 Comprising insulin resistance improving agents in combination with drugs selected from angiotensin II receptor antagonists and angiotensin converting enzyme inhibitors with a diluent or carrier |
| 08/26/2003 | US6610681 Neurotherapeutic clavulanate composition and method |
| 08/26/2003 | US6610678 Corticotropin-releasing factor antagonists; treating endocrine, psychiatric or neurologic disorders |
| 08/26/2003 | US6610676 Nitrate esters of corticoid compounds and pharmaceutical applications thereof |
| 08/26/2003 | US6610674 Method of treating inflammatory conditions with progesterone analogs |
| 08/26/2003 | US6610673 Solid dose forms containing bismuth |
| 08/26/2003 | US6610670 Cyclodextrin-drospirenone inclusion complexes |
| 08/26/2003 | US6610667 Compositions for treatment of disorders of the oesophagus |
| 08/26/2003 | US6610666 Hyaluronan product and process for manufacturing thereof |
| 08/26/2003 | US6610665 2-(purin-9-yl)-tetrahydrofuran-3, 4-diol derivatives |
| 08/26/2003 | US6610661 Immunostimulatory polynucleotide/immunomodulatory molecule conjugates |
| 08/26/2003 | US6610660 O2-arylated or O2-glycosylated 1-substituted diazen-1-ium-1,2-diolates and O2-substituted 1-[(2-carboxylato) pyrrolidin-1-yl] diazen-1-ium-1,2-diolates |
| 08/26/2003 | US6610652 Administration of at least one agent at a level which enhances NO and which does not appreciably alter normal systemic vascular tone |
| 08/26/2003 | US6610651 Molecules that home to various selected organs or tissues |
| 08/26/2003 | US6610650 Modulation of cellular transcription factor activity |
| 08/26/2003 | US6610624 Method for enhancing catalytic activity with supercritical fluids |
| 08/26/2003 | US6610541 Recombinant, active caspases and uses thereof |
| 08/26/2003 | US6610539 Modulate the expression of the ribonucleotide reductase or the secA genes in microorganisms. This invention is also related to methods of using such oligonucleotides in inhibiting the growth of microorganisms. These antisense oligonucleotides are |
| 08/26/2003 | US6610534 Induction of blood vessel formation through administration of polynucleotides encoding sphingosine kinases |
| 08/26/2003 | US6610523 Human mitogen-activated (MAP) kinase kinase isoforms (MKKs). MKKs mediate unique signal transduction pathways that activate human MAP kinases p38 and JNK, which result in activation of other factors, including activating |
| 08/26/2003 | US6610484 Identifying material from a breast duct |
| 08/26/2003 | US6610480 Identification of genes which are differentially expressed in hypertrophic cardiac tissue as compared to normal cardiac tissue. Accordingly, the present invention provides nucleotide sequences of genes and promotion or inhibition of the function |
| 08/26/2003 | US6610477 Human DNA mismatch repair proteins |
| 08/26/2003 | US6610329 Compositions for the delivery of antigens |
| 08/26/2003 | US6610328 Amoxicillin-clarithromycin antibiotic composition |
| 08/26/2003 | US6610327 Oral administration which comprises moxifloxacin, its salt and/or hydrate and lactose, to a process for its preparation, and to the use of this preparation for controlling bacterial infections in humans and animals. |
| 08/26/2003 | US6610326 Divalproex sodium tablets |
| 08/26/2003 | US6610325 Pharmaceutical medicine comprises an iron salt, not less than two polyols, a binding agent, a lubricating agent, and a flavoring agent. The dose of elemental iron is not less than 5 mg, and preferably 10 mg to 15 mg per tablet. The polyols are |
| 08/26/2003 | US6610324 Analgesics; rheumatic diseases; muscular disorders; sleep disorders |
| 08/26/2003 | US6610323 An enteric coated pharmaceutical dosage form comprising an H+,K+- ATPase inhibitor is disclosed. The dosage form comprises at least two portions of the H+,K+- ATPase inhibitor to be released in at least two consecutive pulses. |
| 08/26/2003 | US6610322 Liposome suspension forms spontaneously upon adding a diacylglycerol-PEG lipid to an aqueous solution when the lipid has appropriate packing parameters and the adding occurs above the melting temperature of the lipid. Combinations of lipids |
| 08/26/2003 | US6610321 Emulsion formulations for hydrophilic active agents |
| 08/26/2003 | US6610320 Mixture of cocoa plant extract and antichloesterol agent |
| 08/26/2003 | US6610319 Immune response modifier compounds for treatment of TH2 mediated and related diseases |
| 08/26/2003 | US6610318 Sterile ophthalmological gel preparation applicable in drops and process for producing it |
| 08/26/2003 | US6610315 Mixture of alcohol and water; presurgery scrub |
| 08/26/2003 | US6610314 Comprising one or more proton donating agents and an alkyl phosphate anionic surfactant: high activity against numerous bacteria and other microorganisms |
| 08/26/2003 | US6610307 Immunity against pasteurella haemolytica leukotoxin |
| 08/26/2003 | US6610297 Compositions for treating allergies that include either BSW17 mimotope peptides or antibodies raised against BSW17 mimotope peptides. Also disclosed are methods for the treatment of allergies which involve administration of BSW17 mimeotope |
| 08/26/2003 | US6610284 Preparation for prevention and healing of inflammation affections |
| 08/26/2003 | US6610283 Poly(diallylamine)-based bile acid sequestrants |
| 08/26/2003 | US6610274 Anti-inflammatory composition comprising tetracycline |
| 08/26/2003 | US6610273 Container is provided with a non-metal interior surface so as to reduce chemical degradation |
| 08/26/2003 | US6610272 Medicinal aerosol formulation comprising pioglitazone hydrochloride and a protective colloid amino acid stabilizer |
| 08/26/2003 | US6610271 System and method for intranasal administration of lorazepam |
| 08/26/2003 | US6610206 Buffered compositions for dialysis |
| 08/26/2003 | CA2150892C A ruminant feed composition and a method for improving feed efficiency |
| 08/26/2003 | CA2092211C Imidazole compounds, their preparation and use |
| 08/25/2003 | CA2419773A1 Matrix metalloproteinase and tumor necrosis factor inhibitors |
| 08/25/2003 | CA2405347A1 Medicament comprising nk4 gene or recombinant nk4 protein |
| 08/24/2003 | WO2003059144A2 Method and process for producing youthful-appearing, small-pored, and smooth skin |
| 08/24/2003 | CA2472450A1 Method and process for producing youthful-appearing, small-pored, and smooth skin |
| 08/23/2003 | CA2473075A1 Process for the manufacture of hmg-coa reductase inhibitory mevalonic acid derivatives |
| 08/22/2003 | CA2418930A1 Use of agents that modulate pde11a activity |
| 08/21/2003 | WO2003069327A1 Ion-sensitive field effect transistor and a method for producing a transistor of this type |
| 08/21/2003 | WO2003069303A2 Antimalarial and antiproliferative pharmacophore models, novel tryptanthrin compounds having increased solubility, and methods of making and using thereof |
| 08/21/2003 | WO2003069302A2 Alpha-substituted arylalkyl phosphonate derivatives |
| 08/21/2003 | WO2003068955A2 Streptomyces avermitilis gene directing the ratio of b2:b1 avermectins |
| 08/21/2003 | WO2003068946A1 Phenalenone derivatives, method for the production thereof and use of the same |
| 08/21/2003 | WO2003068939A2 Cks1 INHIBITORS |
| 08/21/2003 | WO2003068936A2 Inhibition of lung metastases by aerosol delivery of p53 gene and anti-cancer compounds |
| 08/21/2003 | WO2003068931A2 Purification of the leading front migratory cells |
| 08/21/2003 | WO2003068929A2 Methods of inhibiting hiv-1 vpr activity and hiv-1 infectivity using atr or rad17 inhibitors |