Patents
Patents for A61K 9 - Medicinal preparations characterised by special physical form (299,044)
07/2003
07/03/2003WO2003053415A1 Pharmaceutical composition comprising skim milk powder
07/03/2003WO2003053414A2 Triggered release from proteinoid microspheres
07/03/2003WO2003053413A2 Sustained-release compositions
07/03/2003WO2003053412A1 Stable granulates containing s-adenosylmethionne and process for the preparation thereof
07/03/2003WO2003053411A1 Pulmonary delivery of aminoglycosides
07/03/2003WO2003053410A1 Particulate compositions
07/03/2003WO2003053409A1 Liposome composition for delivery of nucleic acid
07/03/2003WO2003053408A1 Liposomal tumor necrosis factor compositions
07/03/2003WO2003053407A1 Liposomal delivery of vitamin e based compounds
07/03/2003WO2003053406A1 Fluorinated particles for inhalation & pharmaceutical formulation
07/03/2003WO2003053405A1 Method and composition for dry eye treatment
07/03/2003WO2003053404A1 Pharmaceutical compositions comprising a cyclosporin, a hydrophilic surfactant and a lipophilic surfactant
07/03/2003WO2003053403A2 Pharmaceutical suspension for oral administration
07/03/2003WO2003053402A1 Zero-order sustained released dosage forms and method of making the same
07/03/2003WO2003053401A2 Formulation and dosage form for increasing oral bioavailability of hydrophilic macromolecules
07/03/2003WO2003053400A1 Formulation & dosage form for the controlled delivery of therapeutic agents
07/03/2003WO2003053399A2 Methods for wet granulating azithromycin
07/03/2003WO2003053369A1 Allantoin-containing preparations for administration as gels and aerosols
07/03/2003WO2003053365A2 Syn3 compositions and methods
07/03/2003WO2003053357A2 Method and related composition employing nanostructures
07/03/2003WO2003053350A2 Pharmaceutical compositions of orally active taxane derivatives having enhanced bioavailability
07/03/2003WO2003053336A2 Methods for the treatment of peripheral neural and vascular ailments
07/03/2003WO2003053325A2 Microencapsulation of drugs by solvent exchange
07/03/2003WO2003053292A1 Vaginal delivery of drugs
07/03/2003WO2003053221A2 Methods using proton pump inhibitors
07/03/2003WO2003053180A2 Undergarments containing active substances
07/03/2003WO2003053158A2 Malleable protein matrix and uses thereof
07/03/2003WO2003035136A3 System for administering a drug delivery device
07/03/2003WO2003026767A3 Lysin-deficient bacteriophages having reduced immunogenicity
07/03/2003WO2003026697A3 Organoleptically acceptable intraorally disintegrating compositions
07/03/2003WO2003026611A3 Preparation of submicron sized nanoparticles via dispersion and solvent or liquid phase removal
07/03/2003WO2003013476B1 Compositions and methods to prevent abuse of opioids
07/03/2003WO2003013440A3 Treatment and prevention of heat shock protein-associated diseases and conditions
07/03/2003WO2003011204A3 Drug delivery systems
07/03/2003WO2003005950A3 Pharmaceutical dispensing apparatus and method
07/03/2003WO2002085338B1 Ipratropium formulation for pulmonary inhalation
07/03/2003US20030125803 Stents/catheters for regrowth of endothelium
07/03/2003US20030125800 Drug-delivery endovascular stent and method for treating restenosis
07/03/2003US20030125714 Comprises inner compartments enclosed within semipermeable membrane coated with drugs; osmosis
07/03/2003US20030125659 Dosage of transdermal delivery systems
07/03/2003US20030125543 For addition to drugs as binder, disintegrant or excipient; bulk density; fluidized bed granulation
07/03/2003US20030125517 Lipopeptides; virosomal delivery systems for transporting drugs, nucleic acids and proteins
07/03/2003US20030125509 Indomethacin entrapped within polysaccaride (dextran) or proteins
07/03/2003US20030125391 Pharmaceutical solutions of modafinil compounds
07/03/2003US20030125388 5-Aminolevulinic acid formulation dissolved/dispersed in non-aqueous solvents
07/03/2003US20030125387 Antioestrogens, capable of eliciting complete ablation of the trophic effects of oestrogens; cancer therapy
07/03/2003US20030125385 Prepared by mixing gamma-hydroxybutyrate and a pH-adjusting agent in an aqueous medium
07/03/2003US20030125376 Intracorporeal medicaments for high energy phototherapeutic treatment of disease
07/03/2003US20030125351 Administering a heterocyclic amide compound to a glaucoma patient for inhibiting contraction of ciliary muscle; Rho kinase inhibitor
07/03/2003US20030125350 Combination of formoterol and a tiotropium salt
07/03/2003US20030125347 An oral dosage form containing an opiate and a capsaicinoid irritant, opiate is selected from codeine, hydrocodone, hydromorphone, levorphanol, meperidine, morphine, oxycodone and their salts for the traeatment of drug abuse
07/03/2003US20030125313 Prophylaxis/treatment of respiratory system disorders; administered by inhalation; potentiation; reversible airways obstruction, e.g., asthma, chronic obstructive pulmonary diseases (COPD) (e.g. bronchitis, emphysema); infections
07/03/2003US20030125310 Combine solutions of each vitamin, i.e, K, D's, E and A, in water or an inert oil and emulsify using a protective colloid; drying; fineness; discoloration inhibition; homogeneity; oxidation resistance
07/03/2003US20030125308 Antipruritic agents for external use
07/03/2003US20030125307 Transdermally administering a preparation containing only acetylsalicylic acid as an active ingredient; bronchial asthma, allergic rhinitis, atopic dermatitis; eczema, lichen Vidal; insect stings; pruritis; side effect reduction
07/03/2003US20030125302 Folic acid-polysaccharide complex, its preparation method and pharmaceutical composition containing the same as active component
07/03/2003US20030125294 Selective toxin expression in angiogenic endothelial cells
07/03/2003US20030125292 Synergistic stimulating immunoglobulin A (IgA) production by administering a nucleic acid encapsulated with a lipid and at least one antigen
07/03/2003US20030125263 Nucleic acid ligand complexes
07/03/2003US20030125252 Administering to a vertebrate an effective osteogenesis stimulating amount of an RAR (retinoic acid receptor) antagonist to treat both metabolic or non-metabolic diseases; RAR antisense oligonucleotide
07/03/2003US20030125244 Endoparasiticidal agents
07/03/2003US20030125238 Hemoglobin-based oxygen carriers are prepared by reacting hemoglobin with oxidatively ring-opened polysaccharides such as hydroxyethyl starch or dextran, and storing the resultant conjugate under conditions which allow it to transform to a
07/03/2003US20030125237 Controlled release preparation of insulin and its method
07/03/2003US20030125236 Phospholipids, bioactive agent and excipients and the pulmonary delivery thereof. Dry powder inhaled insulin formulations are disclosed. Improved formulations comprising DPPC, insulin and sodium citrate which are useful in the
07/03/2003US20030124613 Epitope testing using soluble HLA
07/03/2003US20030124368 Plurality of polyelectrolyte layers of alternating charge; hydrolytic degradation of a member of the polycationic layers, the polyanionic layers, and both.
07/03/2003US20030124291 Film structures and methods of making film structures
07/03/2003US20030124200 Sucralose, glucosamine and a beverage base, especially fruit juice; cartilage supplements include chondroitin, glucosamine, and hyaluronic acid
07/03/2003US20030124197 Following surgery or injury, delivering to an external portion of said body passageway or cavity a therapeutic agent; include microtubule stabilizing agents, fibrosis inducers, angiogenic factors, growth factors and cytokines
07/03/2003US20030124196 Pulsatile release compositions and methods for enhanced intestinal drug absorption
07/03/2003US20030124194 Amine functionalized superparamagnetic nanoparticles for the synthesis of bioconjugates and uses therefor
07/03/2003US20030124193 Atomizing nozzles include a liquid nozzle adapted to disperse a supply of liquid and a gas nozzle adapted to disperse a supply of gas; spray drying at a commercial plant scale.
07/03/2003US20030124191 Pharmaceutical or nutraceutical, surfactant, wetting agent and diluent; rapid release when contacted with mucosal surface
07/03/2003US20030124190 Methods and compositions for treating pain of the mucous membrane
07/03/2003US20030124189 Combination of chitosan and second polymer that are not covalently or ionically crosslinked, prepared by dissolving both polymers in an acidic aqueous solution, dehydrating and recovering
07/03/2003US20030124188 Oral pulsed dose drug delivery system
07/03/2003US20030124187 Having reduced weight compared to existing formulations; common intermediate granulate comprising a fixed ratio of amoxycillin and clavulanate, with differing ratios in the final formulation
07/03/2003US20030124186 Efavirenz tablet formulation having unique biopharmaceutical characteristics
07/03/2003US20030124185 Pharmaceutical formulation containing opioid agonist, opioid antagonist and bittering agent
07/03/2003US20030124184 Liquiflash particles and an excipient mass; friability of less than 1%; need for conventional super disintegrant and having a friability of less than 1%; no need for conventional superdisintegrant
07/03/2003US20030124183 Insert prepared by molding a flowable starting material embedded in a compressed dosage form that is coated with a thermal molded coating.
07/03/2003US20030124182 Oral capsule formulation with increased physical stability
07/03/2003US20030124181 Lipid carrier compositions with enhanced blood stability
07/03/2003US20030124180 Liposomes containing active substances
07/03/2003US20030124179 Transdermally administered tolterodine as anti-muscarinic agent for the treatment of overactive bladder
07/03/2003US20030124178 Soft, adherent, soluble oral patch
07/03/2003US20030124177 Compositions and methods for transdermal oxybutynin therapy
07/03/2003US20030124176 Use of a base in order to increase the flux of the active agent through a body surface while minimizing the likelihood of skin damage, irritation or sensitization.
07/03/2003US20030124175 Adhesive polymer layer; removable protective layer; promotes the formation of dermis and collagen production.
07/03/2003US20030124174 Method for treating non-neuropathic pain
07/03/2003US20030124169 Biocompatible, biodegradable matrix and a protein, produced by expression of recombinant DNA capable of inducing endochondral bone formation in association with said matrix
07/03/2003US20030124162 Pressing a sol phase of a solvent and gelling agent between liners; cooling to form a gel phase; and cutting the gel phase; free of a supporting substrate; large scale; drug, food and cosmetic delivery
07/03/2003US20030124160 Targeted drug delivery
07/03/2003US20030124151 Pamidronate solution
07/03/2003US20030124149 Bioactive absorbable microparticles as therapeutic vaccines
07/03/2003US20030124139 Reduced aggregation and proteolytic breakdown; dissolution buffer comprising at least one amorphous excipient, at least one amorphous buffer, and at least one MenC immunogen
07/03/2003US20030124119 Antibody is dissolved in a buffer solution containing as a buffer acetic acid, citric acid, phosphoric acid, and/or salts thereof and is a solution of pH 5 to 8.
07/03/2003US20030124112 Containing lysozyme, tris(hydroxymethyl)aminomethane, and optionally ascorbic acid, and/or citric acid and/or ethylenediaminetetraacetic acid
07/03/2003US20030124088 Preparation for preventing bile acid diarrhea
07/03/2003US20030124063 Premeasured single unit dose; may be free of anti-microbial preservatives, such as benzalkonium chloride.