Patents
Patents for A61K 9 - Medicinal preparations characterised by special physical form (299,044)
06/2002
06/13/2002WO2002045693A1 Pharmaceutical preparation comprising an active dispersed on a matrix
06/13/2002WO2002045692A1 Pharmaceutical preparation in the form of a suspension comprising an acid-labile active ingredient
06/13/2002WO2002045691A2 Laboratory scale milling process
06/13/2002WO2002045690A1 Synthesis of small particles
06/13/2002WO2002045689A1 Compositions for sustained delivery of hydrophobic drugs and process for the preparation thereof
06/13/2002WO2002045688A2 Composition for treatment of inflammatory disorders
06/13/2002WO2002045687A2 Topical alcoholic solution of a salicylic acid derivative and acemannan
06/13/2002WO2002045686A2 Pharmaceutical paste comprising an acid-labile active ingredient
06/13/2002WO2002045685A2 Cristallizable/non crystallizable polymer composites
06/13/2002WO2002045684A2 Rapidly dispersing pharmaceutical composition comprising effervescent agents
06/13/2002WO2002045683A2 Reversible gelling system for ocular drug delivery
06/13/2002WO2002045682A1 Particulate inhalation carrier
06/13/2002WO2002045681A2 Solid polyunsaturated fatty acid compositions
06/13/2002WO2002045618A2 Oral capsule for administering tablets to animals
06/13/2002WO2002045575A2 Multicomponent biodegradable bioadhesive controlled release system for oral care products
06/13/2002WO2002045573A2 Condom with male genital desensitizer lubricant
06/13/2002WO2002045571A2 Fast dissolving tablet
06/13/2002WO2002038530A8 Carboxylic acid type lipid
06/13/2002WO2002022204A3 Transdermal electrotransport device and method for manufacturing same
06/13/2002WO2002022156A3 Topical formulations for delivery of interleukin-11
06/13/2002WO2002020554A3 Hiv peptides from conserved regions in gag p17 and 924 and their application in e.g. vaccines
06/13/2002WO2002017857A3 Methods and compositions for inhibiting angiogenesis
06/13/2002WO2002016442A3 Microparticle composition and method
06/13/2002WO2002009710A3 Paroxetine tablets and capsules
06/13/2002WO2002007712A3 Self-emulsifying drug delivery systems for extremely water-insoluble, lipophilic drugs
06/13/2002WO2002003998A3 Macrolide formulations for inhalation and methods of treatment of endobronchial infections
06/13/2002WO2002003962A3 Drug delivery system for poorly water soluble drugs
06/13/2002WO2002000173A3 Methods for use of delivery composition for expanding, activating, committing or mobilizing one or more pluripotent, self-renewing and committed stem cells
06/13/2002WO2001098297A3 A thiazine oxazolidinone
06/13/2002WO2001095884A3 Liposomal benzoquinazoline thymidylate synthase inhibitor formulations
06/13/2002WO2001094547A3 Molecular delivery vehicle for delivery of selected compounds to targets
06/13/2002WO2001093829A3 Powder compositions
06/13/2002WO2001089554A3 Treatment of acute coronary syndrome with glp-1
06/13/2002WO2001085257A3 Opioid antagonist compositions and dosage forms
06/13/2002WO2001082899A3 Cationic diagnostic, imaging and therapeutic agents associated with activated vascular sites
06/13/2002WO2001074839A3 Methods of making the 4-n-butylcyclohexanoic and the undecanoic acid esters of (7 alpha, 11 beta)-dimethyl-17 beta-hydroxy-4-estren-3-one and their medical use
06/13/2002WO2001072277A3 Immunotherapeutic methods and compositions
06/13/2002WO2001035942A3 Analgesic compositions containing buprenorphine
06/13/2002WO2001028538A3 Laxative preparation containing l-arginine
06/13/2002WO2000057838A3 Coating system
06/13/2002US20020073428 Downloading and transfer of audio or video data from video broadcasts
06/13/2002US20020072784 Microchip reservoir devices using wireless transmission of power and data
06/13/2002US20020072735 Multi-step drug dosage forms
06/13/2002US20020072734 Chip systems for the controlled emission of substances having a chemosensory effect
06/13/2002US20020072733 Devices, systems and methods for patient infusion
06/13/2002US20020072540 For therapy, prophylaxis and diagnosis of respiratory distress syndrome or other pulmonary diseases that are associated with deficiency of lung surfactant
06/13/2002US20020072498 Method for administering ciliary neurotrophic factor to the brain
06/13/2002US20020072480 Water-soluble, chlorhexidine-containing compositions and use thereof
06/13/2002US20020072121 Composition for use in stable transfer on nucleotide sequences into cells
06/13/2002US20020071908 Storage-stable particle, in particular carrier for carrier-bound reactions, and methods of producing said particle
06/13/2002US20020071902 Applying a polymer in solvent mixture with finely divided bioactive species such as heparin, and curing, where the particle size of the bioactive species is selected to affect delivery kinetics
06/13/2002US20020071874 Compositions containing therapeutically active components having enhanced solubility
06/13/2002US20020071872 Laxative composition
06/13/2002US20020071871 Produce substantially monodisperse particles or multimodal particles having well defined and controllable particle size distributions for pulmonary administration; spray drying
06/13/2002US20020071870 Particulates of a water-insoluble pharmaceutical having a solubility of less than 15 mg/ml in an aqueous carrier liquid, then microfluidizing said composition in the presence of at least 0.01% by weight of particulates of a dextrin.
06/13/2002US20020071869 Microparticle composition and method
06/13/2002US20020071868 Compound that enhances the bioavailability of biological agents, compound that enhances intracellular signaling processes, and compound that enhances cell proliferation and cell survival.
06/13/2002US20020071866 Controlling the depth of laser ablation of a dosage form during laser formation of an exit orifice in an outer wall of the dosage form.
06/13/2002US20020071865 Quick disintegrating tablet in buccal cavity and manufacturing method thereof
06/13/2002US20020071864 Rapidly disintegrable tablet for oral administration
06/13/2002US20020071863 Sustained release oral dosage form that is free of in-situ aggregation effect of the antiviral drug and provides substantially improved bioavailability of said antiviral drug.
06/13/2002US20020071862 Method of forcing the reverse transport of cholesterol from a body part to the liver while avoiding harmful disruptions of hepatic cholesterol homeostasis, and pharmaceutical compositions, and kit related thereto
06/13/2002US20020071861 System for dermal or transdermal application containing an iota-carrageenan and process for its preparation
06/13/2002US20020071860 Intraoral adhesive preparation
06/13/2002US20020071857 Rapidly disintegrating oral formulation of a cyclooxygenase-2 inhibitor
06/13/2002US20020071852 Products for topical applications comprising oil bodies
06/13/2002US20020071846 Vaccines comprising oil bodies
06/13/2002US20020071843 Targeted therapeutic agents
06/13/2002US20020071837 Preferred hyaluronidase enzyme is devoid of molecular weight fractions below 40,000 MW, between 60-70,000 MW and above 100,OOO MW
06/13/2002US20020071835 Bacterial strain, processed plant extracts, compositions containing same, processes for their preparation and their therapeutic and industrial applications
06/13/2002US20020071815 Antipsoriatic nail polish
06/13/2002US20020071812 Contain 1,1,1,2,3,3,3-heptafluoropropane; especially with a betamimetic, an anticholinergic, a steroid, an antiallergic or a PAF-antagonist or a combination of such compounds.
06/13/2002US20020071810 Container is provided with a non-metal interior surface so as to reduce chemical degradation
06/13/2002US20020071809 Effervescence as a penetration enhancer for drugs known, or suspected, of having poor bioavailability.
06/13/2002DE19958554C2 Mikroreservoirsystem auf Basis von Polysiloxanen und ambiphilen Lösemitteln und ihre Herstellung Microreservoir system based on polysiloxanes and ambiphilic solvents and their preparation
06/13/2002DE10061057A1 Chip-Systeme zur kontrollierten Emission chemosensorisch wirkender Stoffe Chip systems for the controlled emission chemosensory of active substances
06/13/2002DE10059822A1 Saure kosmetische, pharmazeutische und dermatologische Mittel Acid cosmetic, pharmaceutical and dermatological compositions
06/13/2002DE10059821A1 Tensidfreie kosmetische, dermatologische und pharmazeutische Mittel Surfactant-free cosmetic, dermatological and pharmaceutical agents
06/13/2002DE10059213A1 Preparing solid composition of poorly soluble compounds, useful e.g. for carotenoid animal feed additives, by flocculating a dispersion with protective colloid
06/13/2002DE10059151A1 Magnetische Partikel zur Zielgerichteten Regionalen Therapie Magnetic particles for Targeted Therapy Regional
06/13/2002DE10049137A1 Production of oily suspensions of water soluble vitamins comprises milling of vitamins in oil or dry milling and suspension in oil
06/13/2002CA2436692A1 Oral extended release formulation of gepirone
06/13/2002CA2436574A1 Laboratory scale milling process
06/13/2002CA2436570A1 Rapidly dispersing pharmaceutical composition comprising effervescent agents
06/13/2002CA2432549A1 Clear propofol compositions
06/13/2002CA2431179A1 Synthesis of small particles
06/13/2002CA2430874A1 Absorbing agents and cover layer which is impermeable to active substances and which contains channel-formers or removable protective layer of a transdermal therapeutic system
06/13/2002CA2429727A1 Solid polyunsaturated fatty acid compositions
06/13/2002CA2426988A1 Multicomponent compositions containing chitosan and methods of preparing same
06/12/2002EP1213351A2 Nucleic acid enzymes acquiring an activity for cleaving a target RNA by recognising another molecule
06/12/2002EP1213032A1 Treatment of diseases by site-specific instillation of cells or site-specific transformation of cells and kits therefor
06/12/2002EP1213020A2 Pharmaceutical compositions having appetite suppressant activity
06/12/2002EP1213018A1 Preventive and therapeutic agents for eye diseases
06/12/2002EP1213016A2 Chip systems for controlled emission of chemosensorically active agents
06/12/2002EP1213015A1 Oral pharmaceutical composition with delayed release of proton pump inhibitors
06/12/2002EP1213014A2 Process and system for controlled-release drug delivery
06/12/2002EP1213013A2 Process for preparing solid compositions of water-soluble, hardly water-soluble or water-insoluble active agents
06/12/2002EP1213012A2 Improvements in and relating to powders for use in dry powder inhalers
06/12/2002EP1212601A1 Glucose biosensor
06/12/2002EP1212349A1 Recombinant subunit vaccine