Patents
Patents for A61K 31 - Medicinal preparations containing organic active ingredients (785,912)
05/2008
05/29/2008US20080124300 stabilizing honey bee brood pheromone comprised of two or more of 16-20-carbon carboxylic acids, or their methyl or ethyl esters by incorporating an antioxidant
05/29/2008US20080124297 Hydrolytically cleaving a plurality of peptide bonds in an allergenic polypeptide, using enzymes to denature all allergens; treating asthma, allergic rhinitis and atopic eczema in both humans and animals
05/29/2008US20080124285 Merocyanine Derivatives for Cosmetic Use
05/29/2008US20080124280 Thyroid Hormone Analogs and Methods of Use
05/29/2008US20080124277 Human and Mouse Targeting Peptides Identified by Phage Display
05/29/2008US20080124270 Compounds Useful as Metal Chelators
05/29/2008DE112005001269T5 Polysaccharidextrakt aus Lycium barbarum als neuroprotektives Mittel gegen ß-Amyloidpeptidneurotoxizität Lycium barbarum from Polysaccharidextrakt as a neuroprotective agent against beta-amyloid peptide toxicity EUR
05/29/2008DE102006056458A1 Arzneimittelzubereitung von Tramadol und Acetaminophen The pharmaceutical preparation of tramadol and acetaminophen
05/29/2008DE102006054757A1 Neue aza-bicyclische Verbindungen und ihre Verwendung New aza-bicyclic compounds and their use
05/29/2008DE102006054205A1 Verwendung von Cytohesin-Inhibitoren zur chemischen Induktion von Langlebigkeit Use of Cytohesin inhibitors for chemical induction of longevity
05/29/2008DE10113974B4 Verwendung von racemischer und enantiomerenreiner Dihydroliponsäure oder deren Derivate zur Körpergewichtsreduzierung und/oder zur Verringerung des Appetits The use of racemic and enantiomerically pure dihydrolipoic acid or their derivatives for body weight reduction and / or for the reduction of appetite
05/29/2008CA2749074A1 Process for the preparation of sevelamer hydrochloride and formulation thereof
05/29/2008CA2706070A1 Therapeutic tetrahydroisoquinoline-based compositions for cancer therapy
05/29/2008CA2689293A1 Prostaglandin prodrugs
05/29/2008CA2679955A1 Novel chemotherapeutic agents against inflammation and cancer
05/29/2008CA2677335A1 Indozalyl sulphonamide derivatives useful as glucocorticoid modulators
05/29/2008CA2674359A1 Metabolically-stabilized inhibitors of fatty acid amide hydrolase
05/29/2008CA2673137A1 Prodrug salts of 2,4-pyrimidinediamine compounds and their uses
05/29/2008CA2671517A1 Method of radio-sensitizing tumors using a radio-sensitizing agent
05/29/2008CA2670846A1 Pharmaceutical compositions for the treatment of capillary arteriopathy
05/29/2008CA2670619A1 Dissolution and processing of cellulose
05/29/2008CA2670468A1 Melatonin derivatives and their use as antioxidants
05/29/2008CA2670439A1 Anticonvulsive pharmaceutical compositions
05/29/2008CA2670418A1 N-(methyl)-1h-pyrazol-3-amine, n-(methyl)-pyridin-2-amine and n-(methyl)-thiazol-2-amine derivatives for the treatment of diseases associated with amyloid or amyloid-like proteins, like e.g. alzheimers's
05/29/2008CA2670417A1 Tricarbonyl complexes with tridentate chelators for myocardium imaging
05/29/2008CA2670409A1 Compositions and methods of using same for treatment of a disease or disorder of the eye and/or the adnexa of the eye
05/29/2008CA2670405A1 Combination treatments for alzheimer's disease and related neurodegenerative diseases
05/29/2008CA2670404A1 Heteromonocyclic compound and use thereof
05/29/2008CA2670382A1 (r)-n-stereoisomers of 7,8-saturated-4,5-epoxy-morphinanium analogs
05/29/2008CA2670362A1 Compounds modulating c-fms and/or c-kit activity and uses therefor
05/29/2008CA2670340A1 Tetrahydrocyclopenta[b]indole compounds as androgen receptor modulators
05/29/2008CA2670328A1 Nucleoside aryl phosphoramidates and their use as anti-viral agents for the treatment of hepatitis c virus
05/29/2008CA2670290A1 Transdermal therapeutic system for administering the active substance buprenorphine
05/29/2008CA2670288A1 Methods of treating chronic inflammatory diseases using a gm-csf antagonist
05/29/2008CA2670276A1 Compounds useful for treating neurodegenerative disorders
05/29/2008CA2670207A1 Process for preparing a crystalline form of candesartan cilexetil
05/29/2008CA2670202A1 5-sulfanylmethyl-[1,2,4] triazol[1, 5-a] pyrimidin-7-ol derivatives as cxcr2 antagonists
05/29/2008CA2670165A1 2- [ (2-substituted) -ind0lizin-3-yl] -2-oxo-acetamide derivatives as antifungal agents
05/29/2008CA2670160A1 Methods for improving bioavailability of a renin inhibitor
05/29/2008CA2670157A1 Delivery system for risperidone
05/29/2008CA2670153A1 Stable powder formulation containing a novel anticholinergic agent
05/29/2008CA2670143A1 Pyrimidines and their use as cxcr2 receptor antagonists
05/29/2008CA2670136A1 7,8-saturated-4,5-epoxy-morphinanium analogs
05/29/2008CA2670099A1 Synthesis and biological activities of new tricyclic-bis-enones (tbes)
05/29/2008CA2670083A1 Heterobicyclic metalloprotease inhibitors
05/29/2008CA2670044A1 Heterobicyclic matrix metalloprotease inhibitors
05/29/2008CA2670042A1 Heterobicyclic matrix metalloprotease inhibitors
05/29/2008CA2670031A1 Heterobicyclic metalloprotease inhibitors
05/29/2008CA2670026A1 Heterotricyclic metalloprotease inhibitors
05/29/2008CA2669991A1 Imidazotriazines and imidazopyrimidines as kinase inhibitors
05/29/2008CA2669982A1 Combination therapy for proliferative disorders
05/29/2008CA2669935A1 Methods for preserving renal function using xanthine oxidoreductase inhibitors
05/29/2008CA2669888A1 Novel aza-bicyclic compounds and their use as stimulators of soluble guanylate cyclase
05/29/2008CA2669887A1 Metallo-oxidoreductase inhibitors using metal binding moieties in combination with targeting moieties
05/29/2008CA2669856A1 Hepatitis c virus inhibitors
05/29/2008CA2669846A1 Materials and methods for introducing genetic material into living cells
05/29/2008CA2669839A1 2-hydroxy-1,3-diaminopropane derivatives
05/29/2008CA2669833A1 Vaginal delivery system for mirtazapine
05/29/2008CA2669705A1 Stable parenteral formulation containing a rsv inhibitor of a benzodiazepine structure
05/29/2008CA2669579A1 5-sulfanylmethyl-pyrazolo [1,5-a] pyrimidin-7-ol derivatives as cxcr2 antagonists
05/29/2008CA2669447A1 Allosteric modulators of the a1 adenosine receptor
05/29/2008CA2669300A1 Use of arginase inhibitors in the treatment of asthma and allergic rhinitis
05/29/2008CA2669229A1 Method of treatment for inflammatory bowel disease
05/29/2008CA2669209A1 Use of lipid containing particles comprising quillaja saponins for the treatment of cancer
05/29/2008CA2669199A1 Salts and crystal forms of 2-methyl-2-[4-(3-methyl-2-oxo-8-quinolin-3-yl-2,3-dihydro-imidazo[4,5-c]quinolin-1-yl)-phenyl]-propionitrile
05/29/2008CA2669124A1 Benzocycloheptyl analogs having sphingosine 1-phosphate receptor activity
05/29/2008CA2669104A1 Hydrindane analogs having sphingosine 1-phosphate receptor agonist activity
05/29/2008CA2669102A1 Tetralin analogs having sphingosine 1-phosphate agonist activity
05/29/2008CA2669094A1 Method of preparing solid dosage forms of multi-phasic pharmaceutical compositions
05/29/2008CA2669084A1 Pak modulators
05/29/2008CA2669083A1 5, 6, or 7-substituted-3-(hetero)arylisoquinolinamine derivatives as antitumor agents
05/29/2008CA2668828A1 Crystalline forms of aliskiren hemifumarate
05/29/2008CA2668757A1 Composition for inhibiting nadph oxidase activity
05/29/2008CA2668661A1 Substituted pyrazole and triazole compounds as ksp inhibitors
05/29/2008CA2668652A1 Inhibitors of voltage-gated ion channels for use in treating pain and pruritis
05/29/2008CA2668471A1 Antioxidant dietary supplement compositions and methods for maintaining healthy skin
05/29/2008CA2668441A1 Formulations and uses of 2-hydroxy-5-phenylazobenzoic acid derivatives
05/29/2008CA2668369A1 5-hydroxymethyl-oxazolidin-2-one antibacterials
05/29/2008CA2668205A1 2-alkyl-indazole compounds for the treatment of certain cns-related disorders
05/29/2008CA2667494A1 Dual action, inhaled formulations providing both an immediate and sustained release profile
05/29/2008CA2666814A1 Combination therapy for treatment of viral infections
05/29/2008CA2666689A1 Medical device coatings and coated stents
05/29/2008CA2666405A1 Improved process for the preparation of (r)-(+)-4-(ethyiamino)-3,4-dihydro-2-(3- methoxypropyl)-2h-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide
05/29/2008CA2666371A1 Use of an indazolemethoxyalkanoic acid to prepare a pharmaceutical composition
05/29/2008CA2666224A1 Boronic acids and esters as inhibitors of fatty acid amide hydrolase
05/29/2008CA2666159A1 Novel crystal of (s)-(+)-2-(2-chlorophenyl)-2-hydroxy-ethyl carbamate
05/29/2008CA2665726A1 Pharmaceutical compositions
05/29/2008CA2665223A1 An enzyme regulating ether lipid signaling pathways
05/29/2008CA2665214A1 Novel imidazothiazoles and imidazoxazoles
05/29/2008CA2664126A1 The use of pregnane and androstane steroids for the manufacture of a pharmaceutical composition for the treatment of cns disorders
05/29/2008CA2662510A1 Transdermal therapeutic system with high rate of utilization of active substance and dosing accuracy
05/29/2008CA2658834A1 Bisphosphonate inhalant formulations and methods for using the same
05/29/2008CA2655310A1 Use of a2a adenosine receptor agonists in the treatment of ischemia
05/29/2008CA2650227A1 Substituted pyrazolopyrimidines
05/29/2008CA2636242A1 Heterobicyclic thiophene compounds and methods of use
05/28/2008EP1925941A1 Method for prediction of the efficacy of vascularization inhibitor
05/28/2008EP1925677A2 Marker genes for determining renal toxicity
05/28/2008EP1925676A1 Method for assay on the effect of vascularization inhibitor
05/28/2008EP1925665A1 Use of non-viral active agents manufactured with a molecular-biological method for treating acne
05/28/2008EP1925624A1 Use of squalenic acid for the formulation of an active principle in nanoparticle state