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Patent Classification
Drug Delivery System, Oral Rinse/Cleansing/Care
-
Use of ozone for the treatment of bad breath
-
Composition and process for indicating the presence of soluble
fluoride ion in oral care compositions and method of making the same
-
Method of controlling release of antimicrobial agents in chewing gum
-
Fast dissolving orally consumable films
-
Gelatin soft capsule having the properties of
removal of oral smell and cleaning of oral cavity
-
Composition and method for promoting oral health
-
Composition
and method for inhibiting oral bacteria
-
Oral care composition
-
Stable
hydrogenated lupulone antibacterial oral compositions
-
Oral
care composition
-
Oral
cleansing: methods and compositions
-
Stable
zinc/citrate/CPC oral rinse formulations
Drug Delivery
System, Osmotic/Hydrostatic Delivery System
-
Hydrostatic
delivery system for controlled delivery of agent
-
Expandable osmotic composition and coating
suspension
-
Osmotic device containing venlafaxine and an anti-psychotic agent
-
Osmotic drug delivery system
-
Oral osmotic controlled drug delivery system for
a sparingly soluble drug
-
Soluble form osmotic dose delivery system
-
Soluble
form osmotic dose delivery system
-
Combined
diffusion/osmotic pumping drug delivery system
-
Osmotic
medicament releasing system
-
Soluble
form osmotic dose delivery system
-
Osmotic
delivery composition, solution, and method
-
Beneficial
agent delivery system with membrane plug and method for controlling
delivery of beneficial agents
-
Osmotic
drug delivery system
Drug Delivery System, Other
-
Formulations
and methods for providing prolonged local anesthesia
-
Hydrophilic
binary systems for the administration of lipophilic compounds
Drug Delivery System,
Packaging
-
Moisture resistant
container systems for rapidly bioavailable dosage forms
-
Moisture resistant
container systems for rapidly bioavailable dosage forms
-
Medicinal product package for eradication therapy
-
Blister package for
pharmaceutical treatment card
-
Preparation consisting of a film, sheet or wafer-shaped form of
administration with a two-layered structure and an integrated
identification marking
-
Packaged ophthalmic perfusate and cleaning fluid
bag
-
Antioxidant enriched adhesive compositions and
storage containers therefor
-
Test system for characterizing the compatibility
of bioactive substances and polyvinylpyrrolidone
-
Packaged markable ingestible compressible object
-
Strip
pack
-
Dividable
tablet and press-through pack
-
Method
and apparatus for the interim storage of medicated oral dosage forms
-
Package
and packaging method for aqueous liquid materials
-
Container
with freeze-dried vaccine components
-
Preparation
consisting of a surface-adhering, film-like or wafer-like
administration form
-
Blister
pack arrangement
-
Childproof
package for active substance patches
-
Container
for ascorbic acid composition
Drug Delivery System,
Parenteral/Intrathecal/Peritoneal
-
Stabilized
synthetic immunogen delivery system
-
Naltrexone long
acting formulations and methods of use
-
Intravenous
delivery of polynucleotides to cells in mammalian limb
-
Multi-part
substitution infusion fluids and matching anticoagulants
-
Cross-linking
of low and high molecular weight polysaccharides preparation of
injectable monophase hydrogels and polysaccharides and hydrogels thus
obtained
-
Methods for the
formulation and manufacture of artesunic acid for injection
-
Injection vehicle
for polymer-based formulations
-
Dimethicone-containing
sustained release injection formulation
-
Long acting
injectable insulin composition and methods of making and using thereof
-
Pharmaceutical
formulation comprising ziconotide
-
Injectable methadone, methadone and naltrexone, or buprenorphine and
naltrexone microparticle compositions and their use in reducing
consumption of abused substances
-
Injectable
compositions for the controlled delivery of pharmacologically active
compound
-
Parenteral formulations
of a peptide for the treatment of systemic lupus erythematosus
-
Compositions for parenteral administration and sustained-release of
therapeutic agents
-
Sodium bicarbonate/sodium chloride micronized slurry
-
Antifungal parenteral products
-
Multi-part substitution
infusion fluids and matching anticoagulants
-
Injectable system for
controlled drug delivery
-
Sustained release pharmaceutical compositions for the parenteral
administration of hydrophilic compounds
-
Non-aqueous injectable formulations for extended release
of somatotropin
-
High drug loaded injectable microparticle compositions and
methods of treating opioid drug dependence
-
Injectable compositions for the controlled delivery of
pharmacologically active compound
-
Biochemically balanced peritoneal dialysis solutions
-
Stability for injection solutions
-
Antifungal parenteral products
-
Testosterone derivative
-
Prolonged release microspheres for injectable administration
-
Pharmaceutical composition comprising factor VIII and neutral liposomes
-
Method for preparing a calcium phosphate pasty
material for injection
-
Aqueous pharmaceutical composition containing
moxifloxacin or salts thereof
-
Stabilized difloxacin injectable solution
-
Enteral formulation
-
Formulation for the parenteral application of a
sodium channel blocker
-
Use of L-carnitine and its alkanoyl derivatives
as osmotic agents in solutions for medical use
-
Method for keeping the quality of aqueous
parenteral solution of thrombomodulin in storage and distribution
-
Freeze-dried pantoprazole preparation and
pantoprazole injection
-
Catheter flush solution and method for its use
-
Substitution infusion fluid and citrate anticoagulation
-
Emulsion stability
-
Injectable hyaluronic acid derivative with
pharmaceuticals/cells
-
Starch microparticles
-
Pharmaceutically acceptable starch
-
Method of preparing a solution, in particular a
dialysis or infusion solution
-
Stable particle in liquid formulationsStable particle in liquid formulations
-
Preparation of injectable suspensions having
improved injectability
-
Non-aqueous injectable formulation preparation
with pH adjusted for extended release of somatotropin
-
Stability for injection solutions
-
Concentrated injection and infusion solution for
intravenous administration
-
Method for inducing therapeutically-effective
proteins
-
Stability for injection solutions
-
Parenteral Cisplatin emulsion
-
Lyophilizate of lipid complex of water insoluble
camptothecins
-
Protected one-vial formulation for nucleic acid
molecules, methods of making the same by in-line mixing, and related
products and methods
-
Injectable pharmaceutical composition comprising
coated particles of camptothecin
-
Stabilized aqueous suspensions for parenteral use
-
Room temperature storable immunoglobulin
preparation for intravenous injection
-
Prefilled,
low particle, sterile disposable syringe for injecting preparations
and procedure for manufacture
-
Injectable
depot gel composition and method of preparing the composition
-
Method
and device for producing a parenteral medicament
-
Clear, injectable formulation of an anesthetic
compound
-
Cylinder
ampoule
-
Finger
brace for hypodermic syringe
-
Prefilled
ampoules and manufacture thereof
-
Injectable hyaluronate-sulfated polysaccharide
conjugates
-
Compositions
and methods for production and use of an injectable naturally secreted
extracellular matrix
-
Process for producing immunoglobulins for
intravenous administration and other immunoglobulin products
-
Infusion
pump with an electronically loadable drug library and a user interface
for loading the library
-
Needleless
injector drug capsule and filling method
-
Drug
delivery compositions suitable for intravenous injection
-
Pharmaceutical
composition in form of solid lipidic microparticles suitable to
parenteral administration
-
Needleless
syringe
-
Stable
calcitriol solution for packaging into vials
-
Aqueous
solution of t-PA
-
Auto-injection
device
-
Injectable
bio-active glass in a dextran suspension
-
Composition
and method for stable injectable liquids
-
Stabilized
insulin compositions
-
Injection
viral treatment
-
Parenteral
water-miscible non intensely colored injectable composition of
non-steroidal anti-inflammatory drugs
-
Peritoneal
dialysis solution
-
Injectable
formulations of nanoparticulate naproxen
-
Stable
mitoxantrone solutions
-
Injectable
composition
-
Propofol
composition
-
Injectable
hydrogel compositions
-
Container
filled with infusion liquids and infusion preparation
-
Intravenous
form of thalidomide for treating immunological diseases
-
Methods
for universally distributing therapeutic agents to the brain
-
Stable
intravenously-administrable immune globulin preparation
-
Needle-less
parenteral introduction device
-
Methods
and compositions useful for administration of chemotherapeutic agents
-
Pharmaceutical
injection solution containing taxol
-
Administration
of an injectable antibiotic in the ear of an animal
-
Injectable
chondrocyte-carrier suspension for treatment of vesicoureteral reflux
and incontinence
-
Long
acting injectable parasiticidal composition and the process for its
preparation
-
Parenteral
metolazone formulations
-
Parenteral
pimaricin as treatment of systemic infections
-
Stable
liquid paracetamol compositions, and method for preparing same
-
Stable
prostaglandin E1-containing injectable composition
-
Pharmaceutical
composition containing cyclosporin A
- Stable
aqueous solution having high concentrations of calcium and phosphate
ions and solid complex
- Stabilized
pharmaceutical compositions containing dobutamine
-
Crystalline
protein controlled release compositions
-
Compositions
and method for treating migraine
-
Stable
vaccine compositions for parenteral administration, a method for their
use, and a process for their preparation
-
Nonaqueous
compositions for parenteral administration
Drug Delivery System,
Pediatric
-
Pediatric formulation of gatifloxacin
-
Pediatric
method of use of bambuterol
Drug Delivery System,
Pellet/Bolus
-
Continuous
melt spheronization apparatus and process for the production of
pharmaceutical pellets
-
Drug carrier pellet production process
-
Controlled absorption diltiazem pharmaceutical formulation
-
Pellets and process for production thereof
-
Controlled release oral dosage form
-
Rapidly decomposing chitosan-based pellets
-
Polyethylene glycol matrix pellets for greasy,
oily or sticky drug substances
-
Systems
and methods for local delivery of an agent
-
Fast
decomposing pellets
-
Pharmaceutical
delivery device and method of preparation therefor
-
System
and methods for local delivery of an agent
-
Inhalation
composition containing lactose pellets
-
Orally
administrable nifedipine pellet and process for the preparation
thereof
-
Pharmaceutical
pellet formulation
-
Omeprazole
formulation
-
System
and methods for local delivery of an agent
-
Controlled
absorption diltiazem pharmaceutical formulation
-
Pellet
for administration to ruminants
Drug Delivery System,
Peptide/Protein/Nucleic Acid
-
Nanoparticles
for protein/peptide delivery and delivery means thereof
-
Stabilized
preparations of serine endopeptidases, their preparation and use
-
Fast-acting oral
peptide pharmaceutical products
-
Polymeric carrier for
delivery of small interfering RNA
-
Transmembrane
delivery peptide and bio-material comprising the same
-
Concentrated
protein lyophilates, methods, and uses
-
Method for
stabilization of proteins in solution
-
Pharmaceutical
compositions and methods for peptide treatment
-
Stabilized liquid
polypeptide-containing pharmaceutical compositions
-
Intravenous
delivery of polynucleotides to cells in mammalian limb
-
Methods for increasing
protein polyethylene glycol (PEG) conjugation
-
Immunoglobulin
fusion proteins
-
Method for
stabilization of proteins in solution
-
Stable
polypeptide formulations
-
Plasma cryoprecipitate
substantially free of plasminogen
-
Zinc-containing
sustained-release composition, its preparation, and method for producing the
same
-
Nanoparticles
for protein drug delivery
-
Reducing the
immunogenicity of fusion proteins
-
Stable protein storage and
stable nucleic acid storage in recoverable form
-
Binding compounds
specific for cysteine-rich soluble protein C23
-
Nanoparticles
for protein drug delivery
-
Stoichiometric conjugates of biocompatible polymers at the unpaired
cysteine residue of the wild-type G-CSF
-
Nanoparticles
for protein drug delivery
-
Intravascular
delivery of nucleic acid
-
Microparticles
with adsorbed polypeptide-containing molecules
-
Protein and peptide
delivery to mammalian cells in vitro
-
Nanoparticles
for protein/peptide delivery and delivery means
-
Dendritic
encapsulation of active agents
-
Stabilized
soluble glycoprotein trimers
-
Cosmetic or
pharmaceutical composition containing peptides
-
Intravascular
delivery of nucleic acid
-
Stabilized protein crystals, formulations
comprising them and methods of making them
-
Hydrophobic biomolecular structure
-
Stable lipid-comprising drug delivery
complexes and methods for their production
-
Peptides and medicinal compositions
containing the same
-
Sustained release formulation
-
Formulations for amylin agonist peptides
-
Nanoparticles for
protein drug delivery
-
Nucleic acid-containing complex
-
Stable non-aqueous single phase viscous vehicles and formulations
utilizing such vehicle
-
Method for determining release of a peptide from a sustained release
polylactide formulation
-
Methods of delivering
aerosolized polynucleotides to the respiratory tract
-
Peptides as solubilizing excipients for transforming growth factor beta
proteins
-
Nuclear targeting by
means of bacterial proteins
-
Long-term stabilized
formulations
-
Stabilization of
pharmaceutical protein formulations with small peptides
-
Compositions and methods for drug delivery using pH sensitive molecules
-
Method for directed packaging of molecular substances in protein shells
-
Micellar systems
-
Stabilized proteins
-
Controlled nucleic acid delivery systems
-
Process of making a
compound by forming a polymer from a template drug
-
Aquespheres, their preparation and uses
thereof
-
Povidone-containing carriers for polypeptide growth factors
-
Reducing the immunogenicity of fusion proteins
-
Stabilization of cardiac troponin I subunits and complexes
-
Polyol/oil suspensions for the sustained release of proteins
-
Interferon and albumin fusion protein
-
Stable spray-dried protein formulations
-
N-terminally chemically modified protein compositions and methods
-
Slow release protein polymers
-
Methods and compositions for enhancing the delivery of a nucleic acid to a
cell
-
Compositions and methods for drug delivery using
pH sensitive molecules
-
Polynucleotide complex delivery
-
Proteins stabilized with polysaccharide gums
-
Particle delivery techniques
-
Identification of peptides that facilitate uptake
and cytoplasmic and/or nuclear transport of proteins, DNA and virues
-
Formation of polyampholytes in the presence of a
polyion
-
Reduced-viscosity concentrated protein
formulations
-
Compositions and methods for topical delivery of
oligonucleotides
-
Stabilizer for
pharmacons
-
Protein formulation
-
Polyampholytes for delivering polyions to a cell
-
Compositions for inhalation
-
Solid preparations for oral administration of
drugs relating to genes
-
Granule containing enzyme, corn starch and sugar
layered on an inert particle
-
Methods for quantitative analysis of nucleic acid amplification reaction
-
Sequence and method for genetic engineering of
proteins with cell membrane translocating activity
-
Method for targeted delivery of nucleic acids
-
Process for producing composite preparation
containing nucleic acid
-
Compositions and methods for drug delivery using
amphiphile binding molecules
-
Process for the stabilization of proteins in
complex mixtures during their storage in aqueous solvents
-
Sublingual compositions comprising thymosin
fraction 5 and methods for administration thereof
-
Methods for encapsulating nucleic acids in lipid
bilayers
-
Stable protein and nucleic acid formulations
using non-aqueous, anhydrous, aprotic, hydrophobic, non-polar vehicles
with low reactivity
-
Slow release protein polymers
-
Poliovirus replicons encoding therapeutic agents
and uses thereof
-
Oral delivery of peptides using enzyme-cleavable
membrane translocators
-
Compositions for inhalation
-
Self-assembling colloidal carriers for protein
delivery
-
Delivery of biologically active polypeptides
-
Stabilizing diluent for polypeptides and antigens
-
Inhaleable spray dried 4-helix bundle protein
powders having minimized aggregation
-
Site protected protein modification
-
Process for producing composite preparation
containing nucleic acid
-
Stabilized protein crystals formulations
containing them and methods of making them
-
Aerosol formulations of peptides and proteins
-
Stabilized liquid polypeptide-containing
pharmaceutical compositions
-
Pharmaceutical compositions for prolonged peptide
release and preparation method
-
Temperature sensitive gel for sustained delivery
of protein drugs
-
Pharmaceutical compositions comprised of stabilized peptide particles
-
Reverse micelles for delivery of nucleic acids
-
Granule containing protein and salt layered on an
inert particle
-
Protein occlusion for delivery of small molecules
-
Process for fractionating polyethylene glycol
(PEG) --protein adducts and an adduct of PEG and granulocyt-macrophage
colony stimulating factor
-
Intravascular
delivery of non-viral nucleic acid
-
Process
of making a compound by forming a polymer from a template drug
-
Sustained GnRH
peptide-release formulation
-
Method
of enhancing the delivery of nucleic acids using silica nanoparticles
-
Delivery
of nucleic acid materials
-
Compositions and methods for nucleic acid
delivery to the lung
-
Transforming growth factor .beta. crystals
-
Peptide/lipid
complex formation by co-lyophilization
-
Methods
and compositions for peptide synthesis
-
Proteinic
drug delivery system using aerosolized membrane-mimetic amphiphiles
-
Process
for stabilizing proteins
-
Method
to detect proteins
-
Proteinic
drug delivery system using membrane mimetics
-
Controlled
release delivery of peptide or protein
-
Synthetic
peptides and vaccines comprising same
-
Synthesis
of polymer bio-active conjugates
-
Stabilizing
solutions for proteins and peptides
-
Use
of locally applied DNA fragments
-
Delivery
of polypeptide-encoding plasmid DNA into the cytosol of macrophages by
attenuated listeria suicide bacteria
-
Process
of making a compound by forming a polymer from a template drug
-
Non-aqueous
polar aprotic peptide formulations
-
Preparation
of lipid-nucleic acid particles using a solvent extraction and direct
hydration method
-
Peptide
copolymer compositions
-
Oral
peptide pharmaceutical products
-
Process
to manufacture implants containing bioactive peptides
-
Liposomal
transfection method
-
Preparation
of stable formulations of lipid-nucleic acid complexes for efficient
in vivo delivery
-
Stabilized
conjugates of uncomplexed subunits of multimeric proteins
-
Aqueous
formulations of peptides
-
Preparation
of protein microparticles by supercritical fluid precipitation
-
PVA
or PEG conjugates of peptides for epitope-specific immunosuppression
-
Controlled
release polypeptide compositions and methods of treating inflammatory
bowel disease
-
Chemical
modification of repetitive polymers to enhance water solubility
- Stable
preparation for the treatment of blood coagulation disorders
-
Method
of protein therapy by orally administering crosslinked protein
crystals
-
Sustained-release
protein formulations
-
Peptide
formulation
-
Intravaginal
preparation containing physiologically active peptide
-
Crystalline
protein controlled release compositions
-
Powder
formulations containing melezitose as a diluent
-
Method
and compositions for solubilization and stabilization of polypeptides,
especially proteins
-
Peptide/protein
suspending formulations
Drug Delivery System,
Personal Care/OTC Products
-
Methods and
compositions for enhancing collagen and proteoglycan synthesis in the
skin
-
Personal care article
with distinct active zone
-
Lactic acid producing bacteria for use as probiotic organisms in the
human vagina
-
High efficacy gel with low glycol content
-
Use of ozone for the treatment of bad breath
-
Composition and method for inhibiting polar capsule discharge and
protecting a subject from nematocyst sting
-
Sweet with a rough texture intended for the treatment of halitosis
-
Method to produce a tampon that inhibits exoprotein production from gram
positive bacteria
-
Methods for preparing pharmaceutical formulations
-
Gelatin soft capsule having the properties of
removal of oral smell and cleaning of oral cavity
-
Emulsification systems and emulsions
-
Dentrifice comprising calcium carbonate granules
-
Method of disinfecting contact lens and
disinfecting liquid for the method
-
Ambroxol-containing lozenge
-
Inhibition of exoprotein production from gram
positive bacteria
-
Method of reducing eye irritation
-
Engineered polypeptides in personal care applications
-
Compositions and methods for treating eye discomfort
-
Antiviral compositions for tissue paper
-
Use of fats to replace silicone in cosmetic
and/or pharmaceutical preparations
-
Low temperature process for making stable
anhydrous solutions of antiperspirant active in selected 1,2-diol solvents
-
Method
for preparing ultraviolet radiation-absorbing compositions
-
Antiperspirant
actives from a glass form and products made therewith
-
Methods
for quantitating the efficacy of oral care products
-
Thickened aqueous surfactant solutions
- Thermochromic flowable topical personal care
product
- Use
of silica as agent for controlling the degradation of bicarbonate,
resulting mixture and its application
- Silicone
solvents for antiperspirant salts
- Non-spherical
and non-platelet forms of pyrithione salts and methods of making same
- Diaper
with osmotic pressure control
- Chemical
linker compositions
- Non-irritating
composition for treating acne and other skin conditions
- Fluidized
polymer suspensions of cationic polysaccharides in emollients and use
thereof in preparing personal care compositions
- Fluidized
polymer suspensions of cationic polysaccharides in polyols and use
thereof in personal care compositions
Drug Delivery System, Pouch
-
Digestible
pouch and method for administering medications to an animal
Drug Delivery System, Powder
-
Solubilizing
aids in powder form for solid pharmaceutical presentation forms
-
Powdery preparation for
nasal administration
-
Phospholipid-based powders for drug delivery
-
Storage stable powder compositions of interleukin-4 receptor
-
Pharmaceutical formulation comprising amoxycillin and clavulanate
-
Process for preparing powder formulations
-
Water soluble powders and tablets
-
Storage stable powder compositions of interleukin-4 receptor
-
Particle delivery techniques
-
Powder Composition for nasal administration
-
Anti-fungal powder having enhanced excipient
properties
-
Method of manufacturing powder particles
-
Powdery nasal compositions
-
Powder compositions comprising a skin irritation
reducing agent
-
Clump-free
liquid dispersible powder compositions and process for making the same
-
Powdered
pharmaceutical formulations having improved dispersibility
-
Medical
powder
-
Powdered
pharmaceutical formulations having improved dispersibility
-
Powder compositions
-
Powders
for inhalation
-
Method
for producing powder formulation comprising an insulin
-
Free-flowing
dry particles
-
Compositions
and methods for nucleic acid delivery to the lung
-
Water
soluble powder form compositions and their applications thereof
-
Controlled
release insufflation carrier for medicaments
Drug Delivery System, Preservative
-
Preserved pharmaceutical formulations
-
Preserved pharmaceutical formulations
-
Preserved pharmaceutical compositions comprising cyclodextrins
-
Use of lacrophyl preparation in eye drops containing therapeutically
active compounds
- Preserved
cyclodextrin-containing compositions
- Bis-amido
polybiguanides and the use thereof to disinfect contact lenses and
preserve pharmaceutical compositions
- Preserving
system and its use in a cosmetic or pharmaceutical composition
Drug Delivery System, Prodrug
-
Prodrug of an ICE
inhibitor
-
Activation of
peptide prodrugs by hK2
-
Use of specifically
engineered enzymes to enhance the efficacy of prodrugs
-
Abuse-resistant
amphetamine prodrugs
-
Abuse-resistant
amphetamine prodrugs
-
Heparin prodrugs
and drug delivery stents formed therefrom
-
Prodrugs of
pharmaceuticals with improved bioavailability
-
Tissue specific
prodrugs
-
Nonporous
microparticle-prodrug conjugates for treatment of infection
-
Use of specifically
engineered enzymes to enhance the efficacy of prodrugs
-
Heparin prodrugs and
drug delivery stents formed therefrom
-
Water soluble
paclitaxel prodrugs
-
Prodrugs of thrombin
inhibitors
-
P450/acetaminophen genetically directed enzyme prodrug therapy (GDEPT)
-
Fusion proteins for prodrug activation
-
Prodrug compositions and drug delivery methods using synthetic
receptors
-
Anaerobe targeted enzyme-mediated prodrug therapy
-
Pharmaceutical formulation comprising a low molecular weight thrombin
inhibitor and its prodrug
-
Vector for expression of GPI-enzyme hybrid
-
Mutual prodrug of amlodipine and atorvastatin
-
Method of targeting pharmaceuticals to motor
neurons
-
Selenium-containing pro-drugs for cancer therapy
-
Stabilized thyroxine compounds
-
Medical use of gene and vector encoding a
multisubstrate deoxyribonucleoside kinase
-
Anaerobe targeted enzyme-mediated prodrug therapy
-
Sensitizing
cells to compounds using lipid-mediated gene and compound delivery
-
Prodrugs
with enhanced penetration into cells
-
Gene construct encoding a heterologous prodrug-activating
enzyme and a cell targeting moiety
-
Self-assembled taxo-diterpenoid nanostructures
-
Water
soluble paclitaxel prodrugs
-
Prodrugs
activated by targeted catalytic proteins
-
Prodrugs
with enhanced penetration into cells
-
Prodrugs,
their preparation and use as pharmaceuticals
-
Polar
drug of prodrug compositions with extended shelf-life storage and a
method of making thereof
-
Liposomal
prodrugs comprising derivatives of camptothecin and methods of
treating cancer using these prodrugs
-
Prodrugs
of proton pump inhibitors
-
Prodrugs
comprising fluorinated amphiphiles
-
Surface
expression of enzyme in gene directed prodrug therapy
-
Prodrugs
with enhanced penetration into cells
-
Prodrugs
their preparation and use as pharmaceuticals
Drug Delivery System, Quick
Dissolving
-
Co-processed
carbohydrate system as a quick-dissolve matrix for solid dosage forms
-
Stable
foam composition
-
Rapidly
dissolving robust dosage form
-
Delivery
of controlled-release system(s)
Drug Delivery System, Radiation
Guided
-
Intracorporeal medicaments for high energy
phototherapeutic treatment of disease
- X-ray
guided drug delivery
Drug Delivery System, Radical, Free
- Method for
the preparation of free radical pharmaceuticals, diagnostics and
devices using selenium conjugates
Drug
Delivery System,
Resistance, Abuse
-
Process for the
production of an abuse-proofed solid dosage form
-
Opioid
agonist/antagonist combinations
Drug Delivery System, Sachet
- Sachet
formulations
Drug Delivery System, Saline Solution
-
Hypoosmotic saline solutions, method for
preparing same and medicines based on said solution
Drug Delivery System, Semi-Solid/Cream/Ointment
-
Use of octenidine
dihydrochloride in semisolid preparations
-
Ophthalmic ointments for treating infective eye
disease
-
Use of fats to replace silicone in cosmetic
and/or pharmaceutical preparations
- Aerosol
ointment compositions for topical use
- Pharmaceutical
gel preparation applicable to mucosal surfaces and body tissues
- Spill
resistant pharmaceutical compositions in semi-solid form
Drug Delivery System, Solid
Solution/Dispersion
-
Solid dispersions
comprising tacrolimus
-
Stabilised solid
drug dispersions in an organic carrier and a process for preparing the
same
-
Pharmaceutical compositions comprising
33-epi-chloro-33-desoxy-ascomycin solid dispersions
-
Rapidly disintegrable pharmaceutical composition
-
Pharmaceutical compositions for poorly soluble
drugs
-
Solid dose delivery vehicle and methods of making
same
-
Solid dispersion composition
-
Solid solution beadlet
-
Solid pharmaceutical dispersions
-
Aqueous process for manufacturing paroxetine
solid dispersions
-
Process
for the production of dry pharmaceutical forms and the thus obtained
pharmaceutical compositions
-
Pharmaceutical
compositions comprising rafamycin coprecipitates
-
Method
of producing a solid dispersion of a poorly water soluble drug
-
Solid solution of an antifungal agent with enhanced
bioavailability
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