Patents
Patents for A61K 9 - Medicinal preparations characterised by special physical form (299,044)
04/2006
04/04/2006US7022311 Powdery inhalational preparations and process for producing the same
04/04/2006US7021309 Method of use of monomeric insulin as a means for improving the reproducibility of inhaled insulin
04/04/2006US7021031 Process for making pre-formed objects
04/04/2006CA2281962C Emulsion including a hydrophilic thickening compound and a thickening copolymer, compounds including the said emulsion, and uses
04/04/2006CA2265532C Process for producing solid dosage forms by extrusion
04/04/2006CA2259407C Drug delivery devices and process of manufacture
04/04/2006CA2257305C Marking rapidly disintegrating dosage forms
04/04/2006CA2257303C Biconvex rapidly disintegrating dosage forms
04/04/2006CA2181072C Estradiol penetration enhancers
03/2006
03/31/2006WO2005027875A1 Particles
03/31/2006CA2576410A1 Particles
03/30/2006WO2006034467A2 Biocompatible hydrogel compositions
03/30/2006WO2006034397A2 Coating composition
03/30/2006WO2006034383A1 Viscoelastic solution or gel formulation, and methods of treating a body site with the same
03/30/2006WO2006034255A2 Methods of device-assisted drug delivery
03/30/2006WO2006034253A1 Low-emission adhesive composition based on a solvent
03/30/2006WO2006034239A2 Antimicrobial mesoporous silica nanoparticles
03/30/2006WO2006034147A2 Compositions and methods for the preparation and administration of poorly water soluble drugs
03/30/2006WO2006034080A2 Formulation comprising itraconazole
03/30/2006WO2006033948A2 Sustained local anesthetic composition containing preferably a sugar ester such as saib
03/30/2006WO2006033911A2 Methods of administering water-soluble prodrugs of propofol
03/30/2006WO2006033713A2 Methods for ciprofloxacin inhalation
03/30/2006WO2006033698A2 Tissue matrix system
03/30/2006WO2006033686A1 Angiogenesis factor and biological material
03/30/2006WO2006033604A1 A metered medication dose
03/30/2006WO2006033433A1 Wound remedy
03/30/2006WO2006033296A1 Novel block copolymer, micelle preparation, and anticancer agent containing the same as active ingredient
03/30/2006WO2006032762A2 Pharmaceutical composition comprising a solid dispersion with a polymer matrix containing a continuous polydextrose phase and a continuous phase of a polymer other than polydextrose
03/30/2006WO2006032676A1 Pharmaceutical composition comprising roflumilast or the n-oxide of roflumilast
03/30/2006WO2006032675A1 Aqueous pharmaceutical preparation comprising roflumilast
03/30/2006WO2006032624A1 Pharmaceutical composition for transdermal administration
03/30/2006WO2006032464A2 Method of treatment of acute exudative skin lesions and composition useful therefor
03/30/2006WO2006032386A1 Lyophilisate containing n-diaminomethylene-2-methyl-4,5-di-(methylsulfonyl)-benzamide
03/30/2006WO2006032364A1 Lozenges based on mucolytic drugs for inflammatory diseases of the mouth and pharynx
03/30/2006WO2006032144A1 Pharmaceutical compositions and methods relating to inhibiting fibrous adhesions or inflammatory disease using fucans from various echinoderm sources
03/30/2006WO2006032143A1 Pharmaceutical compositions and methods relating to inhibiting fibrous adhesions or inflammatory disease using low sulphate fucans
03/30/2006WO2006032089A1 Sustained release pharmaceutical composition
03/30/2006WO2006017374A3 Nutritional supplement composition and method
03/30/2006WO2006007856A3 Acidic solid oral compositions without erosive potential in saliva and method for determining erosive potential in saliva
03/30/2006WO2006006691A3 Solid dispersion of a p38 map kinase inhibitor
03/30/2006WO2005123034A8 Microparticulate systems for the oral administration of biologically active substances
03/30/2006WO2005105049A8 Orally disintegrating tablets and methods of manufacture
03/30/2006WO2005102279A3 Controlled gap techniques for fiber optics devices
03/30/2006WO2005102275A3 Galantamine salts, method of producing it and nasal composition thereof
03/30/2006WO2005102274A3 Method of stabilizing disordered cefovecin sodium salt
03/30/2006WO2005082331A3 Extended release tablets of clarithromycin
03/30/2006WO2005079751A3 Oral pharmaceutical compositions of candesartan cilexetil
03/30/2006WO2005070398A3 Pharmaceutical compositions of candesartan cilexetil stabilized with co-solvents
03/30/2006WO2005060940A3 Method for the production of a solid, orally applicable pharmaceutical composition
03/30/2006WO2005055955A3 DOSING METHODS FOR ß-D-2’,3’-DIDEOXY-2’,3’-DIDEHYDRO-5-FLUOROCYTIDINE ANTIVIRAL THERAPY
03/30/2006WO2005049024A3 Solid pharmaceutical preparation form
03/30/2006WO2005048993A3 Minimization of drug oxidation in drug irradiated excipients formulations
03/30/2006WO2005044246A3 Controlled release analgesic suspensions
03/30/2006WO2005044243A3 Transdermal analgesic systems having reduced abuse potential
03/30/2006WO2005037911A3 Heterofunctional copolymers of glycerol and polyethylene glycol, their conjugates and compositions
03/30/2006WO2005032512A3 Capsules of multilayered neutral polymer films associated by hydrogen bonding
03/30/2006WO2005030164A3 Improved controlled release dosage form including a banded engine
03/30/2006WO2005020912A3 Delivery of immune response modifier compounds
03/30/2006WO2005013896A3 Programmed immune responses using a vaccination node
03/30/2006WO2004089298A3 5-htp composition
03/30/2006US20060069382 Delivery device
03/30/2006US20060069203 core blocks formed of 2-methacryloyloxyethyl-2'-trimethylammonium ethylphosphate inner salt (MPC) and terminal blocks formed of 2-(diisopropylamino)ethyl methacrylate; ability to undergo changes, when exposed to selected stimuli, often reversibly. gelled by changing the pH ; for drug delivery systems
03/30/2006US20060069177 Homogenous dispersion of thermoplastic or elastomeric polymer/oligomer with reactive end groups, monofunctional and/or bifunctional acrylate or methacrylate monomer, multifunctional acrylated/methacrylated monomer having more than two functional groups, photoinitiator, and organic and inorganic filler
03/30/2006US20060069162 Transparent eye drops containing latanoprost
03/30/2006US20060069114 Liquid pharmaceutical formulations of palonosetron
03/30/2006US20060069113 Analgesic compositions containing buprenorphine
03/30/2006US20060069033 Use of poly-amminopyrrolecarboxamides alone or in combination with a cyclodextrin in the prophylaxis and treatment of animal parasitosis
03/30/2006US20060069018 Treating lung diseases selected from acute pneumonia, pulmonary fibrosis, pulmonary hypertension, chronic obstructive pulmonary disease (COPD), and asthma by administering (E)-[5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7,8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof
03/30/2006US20060069013 Pharmaceutical preparations comprising acid-stabilised insulin
03/30/2006US20060069010 Detoxification depot for Alzheimer's disease
03/30/2006US20060068080 Combinatorial discovery of nanomaterials
03/30/2006US20060068043 Aqueous solution of flavonoids and anthocyanins
03/30/2006US20060068034 nose spray lipophilic medicament comprising tetrahydrocannabinol and cannabidiol, and cannabis plant extract as the drug substance; free from self emulsifying agent and/or a fluorinated propellant; administered by a pump action spray
03/30/2006US20060068021 Sustained-release microencapsulated delivery system
03/30/2006US20060068019 Coated polyunsaturated fatty acid-containing particles and coated liquid pharmaceutical-containing particles
03/30/2006US20060068018 Extended release formulation
03/30/2006US20060068017 Extended release formulation
03/30/2006US20060068016 Paticulate product comprising pantethine
03/30/2006US20060068015 Particulate or in solid dosage forms; a combination of fibrate and HMG CoA reductase inhibitor statins or a pharmaceutically active salts, in dissolved form in order to ensure suitable bioavailability of both active ingredients upon oral administration
03/30/2006US20060068014 Ionic hydrogels with controlled aqueous fluid absorption
03/30/2006US20060068013 Non-adhesive elastic gelatin matrices
03/30/2006US20060068012 Process for preparing poly (vinyl alcohol) drug delivery devices with humidity control
03/30/2006US20060068011 Simultaneous encapsulation technique for use in pharmaceutical compositions
03/30/2006US20060068010 Method for improving the bioavailability of orally delivered therapeutics
03/30/2006US20060068009 Modified release ibuprofen dosage form
03/30/2006US20060068008 Lyophilized pharmaceutical compositions
03/30/2006US20060068007 Class of surfactant-like materials
03/30/2006US20060068006 Edible holographic products, particularly pharmaceuticals and methods and apparatus for producing same
03/30/2006US20060068005 Chewable electrolyte tablet
03/30/2006US20060068004 Buccal delivery of sea cucumber tablets
03/30/2006US20060068003 System for increasing compliance with medication regime
03/30/2006US20060068002 Extended release formulation
03/30/2006US20060068001 Administering antidepressant venlafaxine hydrochloride in extended release form; lower incidence of nausea and vomiting
03/30/2006US20060068000 24 hour extended release unit dosage of antidepressant venlafaxine hydrochloride, and a degradable coating so that venlafaxine is released in a peak, followed by a protracted, substantially linear decrease
03/30/2006US20060067999 Spheroids comprise a core of venlafaxine and a binder or filler; daily dosage with side effect reduction of nausea and vomiting
03/30/2006US20060067998 Liposomal curcumin for treatment of cancer
03/30/2006US20060067997 Phospholipid complexes of lexitropsins, their preparation and use in therapeutic formulations
03/30/2006US20060067996 Preventing/treating signs of skin stress/aging by bioenergetically modifying acupuncture points of the face or neck
03/30/2006US20060067995 Topical and/or transdermal bioactive compound delivery system
03/30/2006US20060067994 System for providing therapy to a body