Patents
Patents for A61K 47 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives (171,128)
05/2002
05/22/2002EP1102581B1 A microemulsion forming composition for the sustained release of an active agent
05/22/2002EP1089722B1 Matrix-type transdermal patch for steroid hormones
05/22/2002EP1014940B1 Ophthalmic composition including a cationic glycoside and an anionic therapeutic agent
05/22/2002EP0902681B1 Inhibition of selectin binding
05/22/2002EP0810822B1 Use of aerogels in agriculture
05/22/2002EP0804501B1 Microcapsules containing a stabiliser mixture made from chromane derivatives, inert organic solvents and organic phosphites or phosphonites and/or amines.
05/22/2002EP0797431B1 Aerosol formulations of peptides and proteins
05/22/2002EP0792110B1 Silicone compositions
05/22/2002EP0745085B1 Texaphyrin metal complexes having improved functionalization
05/22/2002EP0726947B1 Insecticidal toxins derived from funnel web (atrax or hadronyche) spiders
05/22/2002EP0650353B1 Palatable pharmaceutical compositions
05/22/2002CN1350456A Pharmaceutical compositions comprising a pyrimidine derivative and cyclodextrin
05/22/2002CN1350454A Apomorphine and sildenafil composition
05/22/2002CN1350450A Fast-dispersing dosage forms containing fish gelatin
05/22/2002CN1350435A A composition containing carvacrol and thymol for use as abactericide
05/22/2002CN1350009A Arylamine-o-quinone polymer and its prepn and use
05/21/2002US6391886 Oral compositions having improved consumer aesthetics
05/21/2002US6391879 Therapeutic anti-fungal nail preparation
05/21/2002US6391870 Dopaminergic agent
05/21/2002US6391857 Methods and compositions for endothelial binding
05/21/2002US6391832 Medical emulsion for lubrication and delivery of drugs
05/21/2002US6391565 Methods of detecting growth differentiation factor-3
05/21/2002US6391343 Particle comprising fibrinogen bound on surface of albumin matrix, capable of co-aggregation with platelets, and of aggregation in solution containing soluble fibrinogen at concentration not capable of clot formation by itself
05/21/2002US6391340 Dry powder pharmaceutical formulation
05/21/2002US6391336 Inorganic-polymer complexes for the controlled release of compounds including medicinals
05/21/2002US6391335 Effervescent drug delivery system for oral administration
05/21/2002US6391303 Orally administering to animal pharmaceutical formulation comprising antigen and delivery agent comprising at least one derivatized amino acid or salt thereof in amount sufficient to induce tolerance to antigen
05/21/2002US6391294 In situ formation of polymeric material
05/21/2002CA2330480C Controlled release formulation of divalproex sodium
05/21/2002CA2119932C Pressurized hydrofluoroalkane pharmaceutical aerosol compositions
05/21/2002CA1341359C Manufacturing process for a single-cell lifeform killing or growth inhibiting composition containing fluorine (f-) and lithium (li+)
05/20/2002WO2002039947A2 Carrier vectors through an epithelium with tight junctions
05/17/2002CA2363147A1 Stable lactase compositions
05/16/2002WO2002038775A2 METHODS FOR PRODUCING AND PURIFYING RECOMBINANT α-L-IDURONIDASE
05/16/2002WO2002038646A2 Novel polyesters, method for producing the same and depot medicaments produced from these polyesters
05/16/2002WO2002038609A2 Apolipoprotein conjugates
05/16/2002WO2002038591A1 Fap-activated anti-tumor compounds
05/16/2002WO2002038590A1 Fap-alpha-activated anti-tumor compounds
05/16/2002WO2002038577A2 Extended release erythromycin derivatives
05/16/2002WO2002038208A2 Device and method for the cessation of smoking
05/16/2002WO2002038187A1 Fap-activated anti-tumour prodrug
05/16/2002WO2002038186A1 Compositions of n-(methylethylaminocarbonyl)-4-(3-methylphenylamino)-3-pyridylsulfonamide and cyclic oligosaccharides
05/16/2002WO2002038185A2 Injectable sustained release delivery system with loperamide
05/16/2002WO2002038184A1 Oral pharmaceutical composition containing a block copolymer
05/16/2002WO2002038171A2 METHODS FOR TREATING DISEASES CAUSED BY DEFICIENCIES OF α-L-IDURONIDASE
05/16/2002WO2002038170A2 Stabilized inteferon compositions
05/16/2002WO2002038168A2 Use of selectin-binding active ingredients for the treatment of inflammatory and tumoral diseases
05/16/2002WO2002038161A1 Improved ophthalmic and contact lens solutions containing simple saccharides as preservative enhancers
05/16/2002WO2002038154A1 Novel medicament compositions based on tiotropium salts and on salmeterol salts
05/16/2002WO2002038139A1 Pharmaceutical preparation of percutaneous absorption type
05/16/2002WO2002038133A2 Compositions containing hydrolytically unstable compounds
05/16/2002WO2002038132A2 Soft capsules comprising a starch mixture having a reduced branching degree
05/16/2002WO2002038129A2 Delayed-release pharmaceutical formulations containing proinsulin c-peptide
05/16/2002WO2002038127A2 Particle formation methods and their products
05/16/2002WO2002038123A1 A skin cream composition
05/16/2002WO2002038105A2 Novel polyamine analog-amino acid conjugates useful as anticancer agents
05/16/2002WO2002038077A2 L-histidine in ophthalmic solutions
05/16/2002WO2002020026A3 Treatment of drug resistant organisms with nitric oxide
05/16/2002WO2002018448A3 Percarboxylated polysaccharides, and a process for their preparation
05/16/2002WO2002017892A3 Water-dispersible encapsulated sterols
05/16/2002WO2002013762A3 Improved solid pharmaceutical dosage formulation of hydrophobic drugs
05/16/2002WO2002009671A3 Microemulsion and micelle systems for solubilizing drugs
05/16/2002WO2002007770A3 Polymeric conjugates of antitumor agents
05/16/2002WO2001098364A3 Peptides, compositions and methods for the treatment of burkholderia cepacia
05/16/2002WO2001097851A3 Compositions and methods to improve the oral absorption of antimicrobial agents
05/16/2002WO2001091703A3 Low emulsifier multiple emulsions
05/16/2002WO2001089514A3 Pharmaceutical composition comprising a free-radical scavenging sedative agent and a metal ion chelating agent
05/16/2002WO2001088105A3 Production of dendritic cells from bone-marrow stem cells
05/16/2002WO2001087289A3 Propofol for treatment of sepsis
05/16/2002WO2001081405A3 Methods and compositions for the prevention and treatment of anemia
05/16/2002WO2001076638A3 Compositions for drug delivery
05/16/2002WO2001076597A3 A method of administering an antitumour compound using a polymer-camptothecin conjugate
05/16/2002WO2001070663A3 Novel amphipathic aldehydes and their use as adjuvants and immunoeffectors
05/16/2002WO2001068144A3 Biodegradable immunomodulatory formulations and methods for use thereof
05/16/2002WO2001068143A3 Immunomodulatory formulations and methods for use thereof
05/16/2002WO2001032125A3 Apparatus and process for preparing crystalline particles
05/16/2002US20020058853 Method of administering a therapeutically active substance
05/16/2002US20020058787 Mhc binding peptide oligomers and methods of use
05/16/2002US20020058714 Base material for dry direct tableting comprising low-substituted hydroxypropyl cellulose
05/16/2002US20020058695 Administering a bioavailability increasing effective amount of tetrahydropiperine, or an analog or derivative together with or proximate the administration of the nutrient or drug or other organic compound
05/16/2002US20020058674 Used for therapy of conditions associated with mucosal surfaces such as cervical dysphasia and cervical intraepithelial neoplasia
05/16/2002US20020058653 Administering cyclic polyamine compound to elevate white blood cell (WBC) count
05/16/2002US20020058650 Penetration enhancing and irritation reducing systems
05/16/2002US20020058647 Preparing a slurry of pamidronic acid in water, combining aqueous sodium hydroxide with slurry to obtain disodium pamidronate; packaging solution in sealed containers to obtain unit dosage
05/16/2002US20020058634 Formulation of nitrogen mustard
05/16/2002US20020058626 Increasing blood platelet formation by administering a parathyroid hormone or a derivative
05/16/2002US20020058624 Powder containing physiologically active peptide
05/16/2002US20020058616 Coadministration of a an oral bioavailability-enhancing agent (e.g., a cyclosporin F or ketoconazole) with a drug that exhibits poor or inconsistent oral bioavailability (e.g., paclitaxel, docetaxel or etoposide)
05/16/2002US20020058615 Endothelial specific targeting
05/16/2002US20020058614 Especially administered by direct injection into the afflicted cartilagenous region or joint.
05/16/2002US20020058611 Therapeutic agent is conjugated to the carrier via a biodegradable disulfide bond.
05/16/2002US20020058608 Buffered drug formulations for transdermal electrotransport delivery
05/16/2002US20020058601 Low-foaming; good biodegradability; can be used in polymer, antifoaming, biocidal, coating, fertilizer, pharmaceutical, and drilling fluid compositions.
05/16/2002US20020058318 Gels for encapsulation of biological materials
05/16/2002US20020058284 Methods and compositions for treating macrophage-mediated diseases
05/16/2002US20020058097 Gelling agents and gels containing them
05/16/2002US20020058069 Use of microparticles having a protein and an antibody adsorbed thereon for preparing a pharmaceutical composition for intranasal administration
05/16/2002US20020058067 Solid drug delivery system
05/16/2002US20020058066 Outer layer portion containing cilostazol, a water-insoluble substance, such as ethyl cellulose, and a hydrophilic hydrogel forming substance, such as hydroxypropyl methyl cellulose.
05/16/2002US20020058065 Insoluble drug particle compositions with improved fasted-fed effects