Patents
Patents for A61K 47 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives (171,128)
03/2006
03/22/2006CN1750810A A low dose corticosteroid composition
03/22/2006CN1750809A Fast dissolving orally consumable films containing pharmaceutically active agents
03/22/2006CN1750183A Double function magnetic fluid and its preparing method
03/22/2006CN1748671A Slow releasing injection containing anti-mitosis medicine
03/22/2006CN1246047C A suspension comprising fibrinogen, thrombin and alcohol and a method of coating a carrier with the same
03/22/2006CN1246040C Process to make a sustained release formulation
03/22/2006CN1246039C Moxilfloxacin formulation containing common salt
03/22/2006CN1246038C Systemic delivery of oral vaccines of botulinus toxin
03/22/2006CN1246035C Medicine composition of macrolides or cyclosporin and polyoxide saturated hydoxy fatty acid
03/22/2006CN1245994C Use of salivary lactobacillus
03/22/2006CN1245991C Shark meat extract
03/22/2006CN1245985C Compositions containing ascorbic acid phosphoric acid esters
03/22/2006CN1245977C Liposome anti-neoplastic drugs and uses thereof
03/22/2006CN1245976C Pharmaceutical formulations in hydroxypropylmenthyl cellulose capsules
03/22/2006CN1245962C Novel process
03/22/2006CN1245961C Ultraviolet shielding adhesive preparation
03/22/2006CN1245960C Non-oral preparation having three-layer structure
03/22/2006CN1245958C Controlled release hydroxy-ketone
03/22/2006CN1245955C Thermoprotected microparticle compositions and process for terminal steam sterilization thereof
03/22/2006CN1245875C Solutions of alkoxylated alkanol amide surfactants and antimicrobial compounds
03/21/2006USRE39030 Fluoxetine enteric pellets and methods for their preparation and use
03/21/2006US7015352 Capable of permeating a desired biological compartment and releasing a biologically active molecule in active form to effect a therapeutic functional change in the compartment to which it is introduced
03/21/2006US7015306 Peptide analogs of neurotensin resistant to enzymatic degradation and retain high binding affinity for neurotensin receptors; metal chelating group on one end; replacing Arg8 with Gly(PipAm) ((N-amidinopiperidinyl)glycine) for example; useful for diagnostic and therapeutic purposes
03/21/2006US7015245 Formulation to enhance antioxidant potency of Vitamin E
03/21/2006US7015232 Stablizer retards cyclization and discoloration of quinapril
03/21/2006US7015202 Adjust migration of monocytes, lymphocytes or interleukins; controllinginfections
03/21/2006US7015200 Carbohydrates conjugated to optionally protected 4-hydroxybutyric acid; enhance the uptake of the drug and allows effective drug delivery to treat GHB-treatable disorders such as sleep disorders or drug withdrawal
03/21/2006US7014871 Iodine preparation composition
03/21/2006US7014869 Rapid dehydration of proteins
03/21/2006US7014867 Tablet comprising cetirizine and pseudoephedrine
03/21/2006US7014866 High dose solid unit oral pharmaceutical dosage form of amorphous nelfinavir mesylate and process for making same
03/21/2006US7014862 Chewable compositions containing a gel-forming extract of psyllium
03/21/2006US7014857 Anti-sepsis conjugate vaccine
03/21/2006US7014856 for stimulating or enhancing production of an antibody which recognizes a ganglioside; comprises a ganglioside or oligosaccharide portion conjugated to an immunogenic protein with a carrier and/or vehicle; cancer treatment
03/21/2006US7014855 inducing an immune response against a peptide component of an amyloid deposit; active administration of an immunogen or passive administration of an antibody or an active fragment or derivative of the antibody; Alzheimer's disease
03/21/2006US7014846 polyallylamine hydrochloride crosslinked with epichlorohydrin; phosphate removal from gastrointestinal tract; hyperphosphatemia; side effect reduction
03/21/2006US7014845 copolymer of a polysaccharide and a vinyl or acrylic polymer crosslinked with a diamine, amino acid or polypeptide; sustained release; as the polysaccharide is degraded by intestinal bacteria, an active steroidal or nonsteroidal drug is released for effective absorption
03/21/2006US7014841 Delivery of antiemetics through an inhalation route
03/21/2006US7014840 heating a thin coating to form a vapor then allowing to cool to form a condensation aerosol; kits
03/21/2006US7014838 Use of biomolecular targets in the treatment and visualization of brain tumors
03/21/2006CA2520337A1 Medicinal cooling emulsions
03/21/2006CA2443314C Method of imaging cell death in vivo
03/21/2006CA2443214C Vaccine composition comprising human papilloma virus 16 l1 virus-like particle (hpv 16 l1 vlp), human papilloma virus 18 l1 virus-like particle (hpv 18 l1 vlp) and 3-de-o-acylatedmonphosphoryl lipid a (3d-mpl) and alum
03/21/2006CA2369715C Fast-dispersing dosage forms containing fish gelatin
03/21/2006CA2339177C Thermally-inhibited starch prepared with oligosaccharides
03/21/2006CA2258159C Intraorally rapidly disintegrable tablet
03/21/2006CA2189863C Mucoadhesive emulsions containing cyclodextrin
03/21/2006CA2135535C Medicinal formulations containing thioctic acid or dihydrolipoic acid in the form of inclusion compounds with cyclodextrins or cyclodextrin derivatives and in the form of granulates, chewable or effervescent tablets
03/16/2006WO2006029150A2 Endogenously-formed conjugate of albumin
03/16/2006WO2006029089A2 Tetrahydrocannabinoid- protein conjugates for the production of antibodies for the detection of tεtrahydrocannabinoid components in saliva
03/16/2006WO2006028632A1 Aspartame and citrate flavored phosphate salt laxative
03/16/2006WO2006028361A1 Implants and microspheres for the sustained release of drugs for ophthalmic use and preparation methods thereof
03/16/2006WO2006028270A1 Rebamipide preparation for rectal administration to be prepared before using
03/16/2006WO2006028129A1 Medicinal preparation
03/16/2006WO2006028110A1 Process for producing water-soluble hyaluronic acid modification
03/16/2006WO2006027711A2 Prodrugs and codrugs containing bio- cleavable disulfide linkers
03/16/2006WO2006027685A2 Glycosylceramide adjuvant for saccharide antigens
03/16/2006WO2006027278A1 Testosterone gels comprising propylene glycol as penetration enhancer
03/16/2006WO2006027124A1 Pharmaceutical composition
03/16/2006WO2006027116A2 P277 peptide formulations or variants thereof having optimised stability
03/16/2006WO2006026829A1 Stable paste composition of enteric coated acid labile active agent and use thereof
03/16/2006WO2005115441A3 Compositions and methods for enhanced mucosal delivery of parathyroid hormone
03/16/2006WO2005106488A3 Diagnostics and therapeutics for diseases associated with g protein-coupled beta-2 adrenoceptor (adrb2)
03/16/2006WO2005105070A3 Therapeutic antimicrobial compositions and methods
03/16/2006WO2005094891A3 Method for solubilising peptide mixtures
03/16/2006WO2005084361A3 Multi-component biological transport systems
03/16/2006WO2005082942A3 Hydroxyethyl starch
03/16/2006WO2005082781A3 Method for preparing adjustably bioresorbable sol-gel derived sio2
03/16/2006WO2005072679A3 Adjuvant formulation containing an oily emulsion with jojoba oil
03/16/2006WO2005070468A3 Transglutaminase mediated conjugation of peptides
03/16/2006WO2005046561A3 Multilayer dosage form comprising a matrix that influences release of a modulatory substance
03/16/2006WO2004033663A3 Carbohydrate-based synthetic vaccines for hiv
03/16/2006WO2004016733A3 Nucleic acid and corresponding protein entitled 251p5g2 useful in treatment and detection of cancer
03/16/2006US20060058736 Novel vaccine
03/16/2006US20060058552 Solid preferably with an aspect ratio of 1 to 4 and a solubility in water at room temperature of at least 425 mg/ml.
03/16/2006US20060058541 Purifying polyoxyethylated castor oils with activated charcoal and pharmaceutical formulations thereof
03/16/2006US20060058513 Oxime conjugates and methods for their formation and use
03/16/2006US20060058506 Synthetic anti-candida albicans oligosaccharide based vaccines
03/16/2006US20060058413 Using crosslinked, porous vinylimidazole-divinylbenzene copolymers formed by specific radical suspension polymerization of a monomer mixture in presence of air and/or oxygen, a salt, and inert substance; biocompatible; removing free and albumin-bound toxins, drugs, bilirubin, and/or bile acids
03/16/2006US20060058399 Emulsion preconcentrates containing cyclosporin or a macrolide
03/16/2006US20060058381 Pharmaceutical formulation comprising (r)-bicalitamide
03/16/2006US20060058378 reducing neovascularization by administering mixture of acid such as citric acid, ascorbic acid
03/16/2006US20060058333 Analgesic compositions containing buprenorphine
03/16/2006US20060058332 sublingual administration of N-cyclopropylmethyl-7 alpha -[1-(S)-hydroxy-1,2,2-trimethylpropyl]6,14-endoethano-6,7,8,14-tetrahydro-nororipavine, in combination with naloxone, naltrexone or nalmefene; synergistic mixtures for the treatment of pain in humans or animals
03/16/2006US20060058279 Topical compositions comprising ascomycins
03/16/2006US20060058277 Use of oculosurface selective glucocorticoid in the treatment of dry eye
03/16/2006US20060058252 Methods and materials for treating human papillomavirus infections
03/16/2006US20060058251 Use of immunostimulatory nucleic acids containing unmethylated CpG dinucleotide sequences to treat viral infections; use with viral antigen in vaccine or without a viral antigen
03/16/2006US20060058228 nine amino acid, disulfide-constrained peptide that selectively bound and was internalized into colon cancer cells; exhibit decreased or a substantially nonexistent immunogenicity in an in vivo system
03/16/2006US20060058220 Hapten-carrier conjugates for use in drug-abuse therapy and methods for preparation of same
03/16/2006US20060057636 Composite peptide compounds for diagnosis and treatment of diseases caused by prion proteins
03/16/2006US20060057225 Stable pharmaceutical composition useful for treating gastrointestinal disorders
03/16/2006US20060057220 Fine spherical particles with satisfactory molecular orientation, spherical microcapsules comprising the same and processes for producing these
03/16/2006US20060057219 Method for preparing a polymer micelle pharmaceutical preparation containing drug for injection
03/16/2006US20060057218 N-[1-butyl-4-piperidinylmethyl[3,4-dihydro-2 oxazino[3,2-a indole-10 carboxamide as drugs with Cahpo4 or Ca3/po4/2 fillers or binders for use in treatment of irritable bowel syndrome, urinry incontience or arrhythmias
03/16/2006US20060057210 for oral administration, reducing the range in daily dosages required to control pain in human patients; specified mean maximum plasma concentration
03/16/2006US20060057201 Multicomponent pharmaceutical dosage form
03/16/2006US20060057195 Stable solid preparations
03/16/2006US20060057188 Dietary supplement energy-providing to skeletal muscles
03/16/2006US20060057187 Emulsions containing unsaturated fatty acids and esters thereof