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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 59559. Отображено 100.
05-01-2012 дата публикации

Composition Comprising Vascular Endothelial Growth Factor (VEGF) for the Treatment of Hair Loss

Номер: US20120003300A1
Принадлежит: Pangaea Laboratories Ltd

A composition to treat hair loss and enhance hair growth and condition. The composition comprises: i) one or more of VEGF, a VEGF biomimetic peptide, and/or a VEGFR2 receptor agonist; ii) ciclopirox olamine; and iii) a pharmaceutically acceptable carrier.

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12-01-2012 дата публикации

5-chloro-4-hydroxy-1-methyl-2-oxo-n-phenyl-1,2-dihydroquinoline-3-carboxamide, salts and uses thereof

Номер: US20120010239A1
Автор: Ulf Tomas Fristedt
Принадлежит: Teva Pharmaceutical Industries LTD

The subject invention provides 5-chloro-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide, its salts and uses.

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26-01-2012 дата публикации

Combination of an insulin and a glp-1-agonist

Номер: US20120021978A1
Принадлежит: Sanofi Aventis Deutschland GmbH

The invention relates to a drug comprising at least one insulin and at least one GLP-1 receptor agonist.

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02-02-2012 дата публикации

Pyrazole compounds as crth2 antagonists

Номер: US20120028938A1
Принадлежит: BOEHRINGER INGELHEIM INTERNATIONAL GMBH

The present invention relates to pyrazole compounds of formula (I) and pharmaceutically acceptable salts thereof having CRTH2-activity, wherein W, L 1 , L 2 , X, L 3 , Y, R 1 and R 2 are as defined in the specification and claims, to their use as medicaments and to pharmaceutical formulations, containing said compounds or containing a combination of said compounds with one or more active substances.

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02-02-2012 дата публикации

7-azoniabicyclo[2.2.1]heptane derivatives, methods of production, and pharmaceutical uses thereof

Номер: US20120029044A1
Принадлежит: Theron Pharmaceuticals Inc

Muscarinic acetylcholine receptor antagonists and methods of using them for the treatment of muscarinic acetylcholine receptor-mediated diseases, such as pulmonary diseases, are provided.

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16-02-2012 дата публикации

Combination of pilocarpin and methimazol for treating charcot-marietooth disease and related disorders

Номер: US20120040940A1
Принадлежит: Pharnext SA

The present invention relates to compositions and methods for the treatment of the Charcot-Marie-Tooth disease and related peripheral neuropathies. More particularly, the invention relates to combined therapies for treating said disease by affecting simultaneously muscarinic receptor signaling and thyroid hormone pathway in a subject.

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08-03-2012 дата публикации

Novel kinase modulators

Номер: US20120059001A1

The present invention provides PI3K protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of kinase mediated diseases or disorders with them.

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29-03-2012 дата публикации

Methods of enhancing drug delivery and effectiveness of therapeutic agents

Номер: US20120076862A1
Принадлежит: Individual

The present invention in one aspect provides methods of enhancing uptake of a therapeutic agent in a target tissue as well as methods of treating a disease (such as cancer) or enhancing effectiveness of treatment with a therapeutic agent in an individual by co-administering a composition comprising nanoparticles comprising albumin and a poorly water soluble drug such as a taxane with the therapeutic agent. The present invention in another aspect provides a method of treatment or a method of selecting patients for treatment of a disease (such as cancer) with the combination of a therapeutic agent and a composition comprising nanoparticles comprising albumin and a poorly water soluble drug such as a taxane based on one or more characteristics of the target tissue that correlates or indicates the capability of getting enhanced therapeutic agent uptake as a result of the co-administration of the taxane nanoparticle composition in the target tissue (referred to as “the drug uptake capability”). Also provided are pharmaceutical compositions, article of manufacture, and kits useful for methods described herein.

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29-03-2012 дата публикации

Chemical compounds

Номер: US20120077828A1
Принадлежит: GlaxoSmithKline LLC

The invention is directed to substituted indoline derivatives. Specifically, the invention is directed to compounds according to Formula I: wherein R 1 , R 2 , and R 3 are defined herein. The compounds of the invention are inhibitors of PERK and can be useful in the treatment of cancer, ocular diseases, and diseases associated with activated unfolded protein response pathways, such as Alzheimer's disease, stroke, Type 1 diabetes Parkinson disease, Huntington's disease, amyotrophic lateral sclerosis, myocardial infarction, cardiovascular disease, atherosclerosis, and arrhythmias, and more specifically cancers of the breast, colon, pancreatic, and lung. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting PERK activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

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12-04-2012 дата публикации

Use of inhibitors of bruton's tyrosine kinase (btk)

Номер: US20120087915A1
Принадлежит: Pharmacyclics LLC

Disclosed herein are methods for treating a cancer comprising: a. administering a Btk inhibitor to a subject sufficient to result in an increase or appearance in the blood of a subpopulation of lymphocytes defined by immunophenotyping; b. determining the expression profile of one or more biomarkers from one or more subpopulation of lymphocytes; and c. administering a second agent based on the determined expression profile.

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12-04-2012 дата публикации

Interlaced method for treating cancer or a precancerous condition

Номер: US20120088807A1
Принадлежит: TAU THERAPEUTICS LLC

The present invention provides a method for treating a disease or condition in a mammal which comprises the steps of; administering a therapeutically effective amount of a T type calcium channel inhibitor to effectively slow or stop progression of eukaryotic cells through the S, G 2 and M phases of the cell cycle to increase the proportion of the eukaryotic cells in the G 1 phase, stopping administration of the T type calcium channel inhibitor for a period of time, and administering a dosage selected from the group consisting of a dosage of at least one chemotherapeutic agent, a dosage of radiation, and combinations thereof, to kill the proportion of eukaryotic cells progressing past the G 1 phase of the cell cycle after the stopping of the administration of the T type calcium channel inhibitor.

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19-04-2012 дата публикации

Peptide fragments for inducing synthesis of extracellular matrix proteins

Номер: US20120093740A1
Принадлежит: Helix Biomedix Inc

Short biologically active tetrapeptides are disclosed that are comprised of the sequences GxxG and PxxP where G (glycine) and P (proline) are maintained and x is a variable amino acid. The peptides can be used singly or in combination to stimulate production of extracellular matrix proteins in skin. A rapid, low-cost method of producing heterogenous formulations of tetrapeptides is disclosed.

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14-06-2012 дата публикации

Compositions and methods for the prevention and treatment of hypertension

Номер: US20120148691A1
Автор: Ming Li, Peng Peng
Принадлежит: Generex Pharmaceuticals Inc

Disclosed herein are compounds, extracts, and active fractions of the plant Geum japonicum and methods for preventing or treating hypertension. The compounds provided herein can be formulated into pharmaceutical compositions and medicaments that are useful in the disclosed methods. Also provided are the use of the compounds and extracts in preparing pharmaceutical formulations and medicaments.

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28-06-2012 дата публикации

Compounds and their use as BACE Inhibitors

Номер: US20120165347A1
Принадлежит: AstraZeneca AB

The present invention relates to compounds of formula (I) and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and/or prevention of Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy such as but not limited to cerebral amyloid angiopathy or hereditary cerebral hemorrhage, disorders associated with cognitive impairment such as but not limited to MCI (“mild cognitive impairment”), Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration.

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05-07-2012 дата публикации

Nutritional formulations including human milk oligosaccharides and antioxidants and uses thereof

Номер: US20120172327A1
Принадлежит: ABBOTT LABORATORIES

Disclosed are nutritional compositions including human milk oligosaccharides in combination with long chain polyunsaturated fatty acids and/or carotenoids that can be administered to preterm infants, term infants, toddlers, and children for reducing inflammation and the incidence of inflammatory diseases.

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19-07-2012 дата публикации

use of inhibitors of bruton's tyrosine kinase (btk)

Номер: US20120183535A1
Принадлежит: Pharmacyclics LLC

Disclosed herein are methods for treating a cancer comprising: a. administering a Btk inhibitor to a subject sufficient to result in an increase or appearance in the blood of a subpopulation of lymphocytes defined by immunophenotyping; b. determining the expression profile of one or more biomarkers from one or more subpopulation of lymphocytes; and c. administering a second agent based on the determined expression profile.

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26-07-2012 дата публикации

Methods and compositions to reduce oxidative stress

Номер: US20120190731A1
Автор: Louis M. Messina
Принадлежит: University of Massachusetts UMass

The invention relates to therapeutic applications for compositions that reduce the level of oxidative stress on cells in vivo or in vitro. The invention describes methods for improving the therapeutic properties of stem cells. The invention also provides combination therapies that are useful to balance the oxidative microenvironment of cells in vivo or in vitro.

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23-08-2012 дата публикации

Methods for protecting dopaminergic neurons from stress and promoting proliferation and differentiation of oligodendrocyte progenitors by nrg-2

Номер: US20120214737A1
Автор: Mark Marchionni
Принадлежит: Acorda Therapeutics Inc

The invention features methods of treatment and diagnosis using NRG-2 polypeptides, nucleic acid molecules, and antibodies. The invention also provides novel NRG-2 polypeptides and nucleic acid molecules.

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13-09-2012 дата публикации

Methods of treating cancer using 3-(5-amino-2-methyl-4-oxo-4h-quinazolin-3-yl)-piperidine-2,6-dione

Номер: US20120230983A1
Принадлежит: Celgene Corp

Provided herein are methods of treating, preventing and/or managing cancers, which comprise administering to a patient 3-(5-amino-2-methyl-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dione, or an enantiomer or a mixture of enantiomers thereof, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof.

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04-10-2012 дата публикации

Pth-containing therapeutic/prophylactic agent for osteoporosis, characterized in that pth is administered once a week in a unit dose of 100 to 200 units

Номер: US20120252729A1
Принадлежит: Asahi Kasei Pharma Corp

A method of treating osteoporosis by PTH that has excellent safety and high efficacy is disclosed, along with a method for inhibiting/preventing bone fractures by PTH that has excellent safety, as well as providing a drug to do this. A drug containing PTH as the active ingredient is disclosed, characterized in that a unit dose of PTH of 100 to 200 units is administered weekly in the above method.

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04-10-2012 дата публикации

Bicyclic pyridines and analogs as sirtuin modulators

Номер: US20120252780A1

Provided herein are novel sirtuin-modulating compounds and methods of use thereof. The sirtuin-modulating compounds may be used for increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benefit from increased mitochondrial activity. Also provided are compositions comprising a sirtuin-modulating compound in combination with another therapeutic agent.

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18-10-2012 дата публикации

Compositions for the treatment of cns-related conditions

Номер: US20120264782A1
Принадлежит: Adamas Pharmaceuticals Inc

The invention provides compositions comprising extended release memantine in combination with immediate release donepezil to a subject. Memantine in an extended release form containing 22.5 to 30 mg memantine or a pharmaceutically acceptable salt thereof in combination with donepezil achieves particular pharmacokinetic criteria such as change in plasma concentration of memantine over time and ratio of maximum memantine plasma concentration to mean memantine plasma concentration.

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01-11-2012 дата публикации

Tolerogenic synthetic nanocarriers for generating cd8+ regulatory t cells

Номер: US20120276155A1
Принадлежит: Selecta Biosciences Inc

Disclosed are synthetic nanocarrier methods, and related compositions, comprising administering MHC Class I-restricted and/or MHC Class II-restricted epitopes of an antigen and immunosuppressants in order to generate tolerogenic immune responses against the antigen, such as the generation of antigen-specific CD8+ regulatory T cells.

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01-11-2012 дата публикации

Tolerogenic synthetic nanocarrier compositions with transplantable graft antigens and methods of use

Номер: US20120276156A1
Принадлежит: Selecta Biosciences Inc

Disclosed are synthetic nanocarrier compositions, and related methods, comprising APC presentable transplant antigens and immunosuppressants that provide tolerogenic immune responses (e.g., a reduction in CD8+ T cell proliferation and/or activity) specific to the APC presentable transplant antigens.

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01-11-2012 дата публикации

Tolerogenic synthetic nanocarriers to reduce cytotoxic t lymphocyte responses

Номер: US20120276158A1
Принадлежит: Selecta Biosciences Inc

Disclosed are synthetic nanocarrier compositions, and related methods, comprising MHC Class I-restricted and/or MHC Class II-restricted epitopes associated with undesired CD8+ T cell responses and immunosuppressants that provide tolerogenic immune responses against antigens that comprise the epitopes.

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01-11-2012 дата публикации

Tolerogenic synthetic nanocarriers

Номер: US20120276159A1
Принадлежит: Selecta Biosciences Inc

This invention relates, at least in part, to compositions comprising synthetic nanocarriers and immunosuppressants that result in immune suppressive effects. Such compositions can further comprise antigen and provide antigen-specific tolerogenic immune responses.

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15-11-2012 дата публикации

Methods for the Treatment of CNS-Related Conditions

Номер: US20120288560A1
Принадлежит: Adamas Pharmaceuticals Inc

The invention provides methods for treating CNS-related conditions with amantadine and donepezil, in which the amantadine is in an extended release form, wherein the extended release amantadine formulation provides a change in plasma concentration as a function of time (dC/dT) that is less than 40% of the dC/dT of the same quantity of an immediate release form of amantadine.

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03-01-2013 дата публикации

Compositions and Methods for Inhibiting Gene Expression of Hepatitis B Virus

Номер: US20130005793A1
Принадлежит: Arrowhead Research Corp

The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of a Hepatitis B Virus gene. The invention also relates to a pharmaceutical composition comprising the dsRNA or nucleic acid molecules or vectors encoding the same together with a pharmaceutically acceptable carrier; methods for treating diseases caused by Hepatitis B Virus infection using said pharmaceutical composition; and methods for inhibiting the expression of a Hepatitis B Virus gene in a cell.

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28-02-2013 дата публикации

Antigen binding proteins to proprotein convertase subtilisin kexin type 9 (pcsk9)

Номер: US20130052201A1
Принадлежит: AMGEN INC

Antigen binding proteins that interact with Proprotein Convertase Subtilisin Kexin Type 9 (PCSK9) are described. Methods of treating hypercholesterolemia and other disorders by administering a pharmaceutically effective amount of an antigen binding protein to PCSK9 are described. Methods of detecting the amount of PCSK9 in a sample using an antigen binding protein to PCSK9 are described.

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04-04-2013 дата публикации

Baclofen and acamprosate based therapy of neurological disorders

Номер: US20130085122A1
Принадлежит: Pharnext SA

The present invention relates to combinations and methods for the treatment of neurological disorders related to glutamate excitotoxicity and Amyloid β toxicity. More specifically, the present invention relates to novel combinatorial therapies of Multiple Sclerosis, Alzheimer's disease, Alzheimer's disease related disorder, Amyotrophic Lateral Sclerosis, Parkinson's disease, Huntington's disease, neuropathic pain, alcoholic neuropathy, alcoholism or alcohol withdrawal, or spinal cord injury, based on Baclofen and Acamprosate combination.

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02-05-2013 дата публикации

Antimalarial Drug Which Contains 5-Aminolevulinic Acid or Derivative Thereof as Active Ingredient

Номер: US20130108710A1

Provided is an antimalarial drug which is useful for prevention and treatment of infectious diseases caused by malaria parasites. A preventive and/or therapeutic agent for malaria, which contains, as an active ingredient, 5-aminolevulinic acid (ALA), a derivative thereof, or a pharmacologically acceptable salt thereof, is used.

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02-05-2013 дата публикации

C7-Fluoro Substituted Tetracycline Compounds

Номер: US20130109657A1
Принадлежит: Tetraphase Pharmaceuticals Inc

The present invention is directed to a compound represented by Structural Formula (A): or a pharmaceutically acceptable salt thereof. The variables for Structural Formula (A) are defined herein. Also described is a pharmaceutical composition comprising the compound of Structural Formula (A) and its therapeutic use.

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09-05-2013 дата публикации

Hepatitis C Virus Inhibitors

Номер: US20130115193A1
Принадлежит: Bristol Myers Squibb Co

The present disclosure relates to compounds, compositions and methods for the treatment of Hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.

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09-05-2013 дата публикации

Formulations, salts and polymorphs of transnorsertraline and uses thereof

Номер: US20130116332A1
Принадлежит: SUNOVION PHARMACEUTICALS INC

Provided herein are pharmaceutical compositions comprising transnorsertraline, salts and polymorphic forms of transnorsertraline, methods of making the compositions, and methods for their use for the treatment of CNS diseases, including depression.

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13-06-2013 дата публикации

Compositions comprising kakadu plum extract or acai berry extract

Номер: US20130149401A1
Принадлежит: Kay Mary Inc

A topical skin care composition comprising kakadu plum extract or acai berry extract, or a combination of both, is disclosed. The composition can include a high oxygen radical absorbance capacity (ORAC) value. The composition can improve the skin's visual appearance, physiological functions, clinical properties, and/or biophysical properties.

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20-06-2013 дата публикации

Pharmaceutical compositions

Номер: US20130158077A1
Автор: Bjoern C. Kahrs
Принадлежит: ARES TRADING SA

The invention relates to pharmaceutical compositions comprising PPAR agonists and Nrf2 activators and methods of using combinations of PPAR agonists and Nrf2 activators for treating diseases such as psoriasis, asthma, multiple sclerosis, inflammatory bowel disease, and arthritis.

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11-07-2013 дата публикации

Pharmaceutical compositions comprising hydromorphone and naloxone

Номер: US20130178492A1
Принадлежит: Euro Celtique SA

The present invention relates to prolonged release pharmaceutical dosage forms, the manufacture thereof as well as their use for administration to human beings.

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18-07-2013 дата публикации

Methods for treating multiple myeloma using 4-(amino)-2-(2,6-dioxo(3-piperidyl))-isoindoline-1,3-dione in combination with proteasome inhibitor

Номер: US20130183381A1
Автор: Jerome B. Zeldis
Принадлежит: Celgene Corp

Methods of treating, preventing and/or managing cancer as well as and diseases and disorders associated with, or characterized by, undesired angiogenesis are disclosed. Specific methods encompass the administration of an immunomodulatory compound alone or in combination with a second active ingredient. The invention further relates to methods of reducing or avoiding adverse side effects associated with chemotherapy, radiation therapy, hormonal therapy, biological therapy or immunotherapy which comprise the administration of an immunomodulatory compound. Pharmaceutical compositions, single unit dosage forms, and kits suitable for use in methods of the invention are also disclosed.

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01-08-2013 дата публикации

Sphingosine 1 phosphate receptor modulators and methods of chiral synthesis

Номер: US20130196966A1
Принадлежит: Receptos LLC

Compounds that selectively modulate the sphingosine 1 phosphate receptor are provided including compounds which modulate subtype 1 of the S1P receptor. Methods of chiral synthesis of such compounds are provided. Uses, methods of treatment or prevention and methods of preparing inventive compositions including inventive compounds are provided in connection with the treatment or prevention of diseases, malconditions, and disorders for which modulation of the sphingosine 1 phosphate receptor is medically indicated.

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08-08-2013 дата публикации

Agent for use in the case of fructose intolerance

Номер: US20130202695A1
Принадлежит: Vitacare GmbH and Co KG

There is provided in accordance with embodiments of the invention a method of treating or reducing the effects in a subject of a condition selected from fructose intolerance and impaired fructose metabolism, the method comprising administering to a subject in need of such treatment or reduction an efficacious amount of a glucose isomerase, other than in combination with 5-D-fructose dehydrogenase. Other embodiments are also disclosed.

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22-08-2013 дата публикации

Novel treatment of prostate carcinoma

Номер: US20130219528A1
Автор: Per Borgstrom
Принадлежит: Pellficure Pharmaceuticals Inc

Disclosed herein are naphthoquinone analogs, such as plumbagin, pharmaceutical compositions that include naphthoquinone analogs, such as plumbagin, and methods of treating diseases and/or conditions such as cancer with naphthoquinone analogs, such as plumbagin. Also included are combination therapies wherein a naphthoquinone analog, such as plumbagin, and a hormone therapy agent are provided to a subject suffering from a condition such as cancer.

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29-08-2013 дата публикации

Delayed-release formulation for reducing the frequency of urination and method of use thereof

Номер: US20130224291A1
Автор: David A. Dill
Принадлежит: Wellesley Pharmaceuticals LLC

Methods and compositions for reducing the frequency of urination are disclosed. One method comprises administering to a subject in need thereof an effective amount of a pharmaceutical composition comprising an analgesic agent formulated in a delayed-release formulation. Another method comprises administering to a subject in need thereof an effective amount of a pharmaceutical composition comprising multiple active ingredients. Yet another method comprises administering to a subject in need thereof an effective amount of a diuretic followed with another administration of an pharmaceutical composition comprising an analgesic agent.

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29-08-2013 дата публикации

Sublingual films

Номер: US20130225626A1
Принадлежит: ARx LLC, Cynapsus Therapeutics Inc

The invention features sublingual film formulations of dopamine agonists and methods of treating Parkinson's disease, tremors, restless leg syndrome, sexual dysfunction, and depressive disorders therewith.

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05-09-2013 дата публикации

Selective sphingosine 1 phosphate receptor modulators and methods of chiral synthesis

Номер: US20130231326A1
Принадлежит: Receptos LLC

Compounds that selectively modulate the sphingosine 1 phosphate receptor are provided including compounds which modulate subtype 1 of the S1P receptor. Methods of chiral synthesis of such compounds are provided. Uses, methods of treatment or prevention and methods of preparing inventive compositions including inventive compounds are provided in connection with the treatment or prevention of diseases, malconditions, and disorders for which modulation of the sphingosine 1 phosphate receptor is medically indicated.

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19-09-2013 дата публикации

Methods for treating hcv

Номер: US20130243726A1
Принадлежит: GILEAD PHARMASSET LLC

This invention folates to combinations of therapeutic molecules useful for treating hepatitis C virus infection. The present invention relates to methods, uses, dosing regimens, and compositions,

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03-10-2013 дата публикации

Benzoic Acid, Benzoic Acid Derivatives and Heteroaryl Carboxylic Acid Conjugates of Hydrocodone, Prodrugs, Methods of Making and Use Thereof

Номер: US20130259909A1
Принадлежит: KemPharm Inc

The presently described technology provides compositions comprising aryl carboxylic acids chemically conjugated to hydrocodone (morphinan-6-one, 4,5-alpha-epoxy-3-methoxy-17-methyl) to form novel prodrugs/compositions of hydrocodone, including benzoates and heteroaryl carboxylic acids, which have a decreased potential for abuse of hydrocodone. The present technology also provides methods of treating patients, pharmaceutical kits and methods of synthesizing conjugates of the present technology.

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17-10-2013 дата публикации

Use of inhibitors of bruton's tyrosine kinase (btk)

Номер: US20130273030A1
Принадлежит: Pharmacyclics LLC

Disclosed herein are methods for treating a cancer comprising: a. administering a Btk inhibitor to a subject sufficient to result in an increase or appearance in the blood of a subpopulation of lymphocytes defined by immunophenotyping; b. determining the expression profile of one or more biomarkers from one or more subpopulation of lymphocytes; and c. administering a second agent based on the determined expression profile.

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14-11-2013 дата публикации

Systems and Methods for Treating an Opioid-Induced Adverse Pharmacodynamic Response

Номер: US20130303561A1
Принадлежит: Purdue Pharma LP

Disclosed in certain embodiments is a method of treating or preventing an opioid-induced adverse pharmacodynamic response comprising administering to a patient in need thereof an effective amount of buprenorphine.

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14-11-2013 дата публикации

NRF2 Screening Assays and Related Methods and Compositions

Номер: US20130303613A1
Автор: Matvey E. Lukashev
Принадлежит: BIOGEN IDEC MA INC

Provided are certain methods of screening, identifying, and evaluating neuroprotective compounds useful for treatment of neurological diseases, such as, e.g., multiple sclerosis (MS). The compounds described upregulate the cellular cytoprotective pathway regulated by Nrf2. Also provided are certain methods of utilizing such compounds in therapy for neurological disease, particularly, for slowing or reducing demyelination, axonal loss, or neuronal and oligodendrocyte death.

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28-11-2013 дата публикации

Solid Forms of N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide

Номер: US20130317060A1
Принадлежит: Vertex Pharmaceuticals Inc

The present invention relates to solid state forms of N—[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide (Compound 1), pharmaceutical compositions thereof and methods therewith.

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12-12-2013 дата публикации

Pharmaceutical Compositions

Номер: US20130330281A1
Принадлежит: Cipla Ltd

A pharmaceutical composition for inhalation comprising R (+) budesonide and one or more bronchodilators, and, optionally, one or more pharmaceutically acceptable excipients is described.

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12-12-2013 дата публикации

Composition containing human umbilical cord blood-derived mesenchymal stem cell for inducing differentiation and proliferation of neural precursor cells or neural stem cells to neural cells

Номер: US20130330306A1
Принадлежит: Medipost Co Ltd

A use of a composition comprising umbilical cord blood-derived mesenchymal stem cells for inducing differentiation and proliferation of neural precursor cells or neural stem cells to neural cells is provided, the composition being effective for the treatment of nerve injury diseases.

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26-12-2013 дата публикации

Anti-fatigue composition

Номер: US20130344179A1
Автор: Michel Grise
Принадлежит: Individual

The present invention relates to a food supplement composition for reducing fatigue, and/or improving recovery and resistance to fatigue. The composition comprised of collagen hydrolysate, blueberry extract and liquorice extract.

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26-12-2013 дата публикации

Human antibodies to the glucagon receptor

Номер: US20130344538A1
Принадлежит: Regeneron Pharmaceuticals Inc

The present invention provides antibodies that bind to the human glucagon receptor, designated GCGR and methods of using same. According to certain embodiments of the invention, the antibodies are fully human antibodies that bind to human GCGR. The antibodies of the invention are useful for lowering blood glucose levels and blood ketone levels and are also useful for the treatment of diseases and disorders associated with one or more GCGR biological activities, including the treatment of diabetes, diabetic ketoacidosis and long-term complications associated with diabetes, or other metabolic disorders characterized in part by elevated blood glucose levels.

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26-12-2013 дата публикации

Combination therapeutic composition

Номер: US20130345165A1
Принадлежит: Hoffmann La Roche Inc

Embodiments disclosed in the present application relate to a composition that can include a hepatitis C viral nucleoside polymerase inhibitor, or pharmaceutically acceptable salt or prodrug thereof, a hepatitis C viral protease inhibitor, or pharmaceutically acceptable salt or prodrug thereof, and a hepatitis C viral non-nucleoside polymerase inhibitor, or pharmaceutically acceptable salt or prodrug thereof. Additional embodiments disclosed relate to methods for treating a disease condition such as a hepatitis C virus infection, liver fibrosis and/or impaired liver function with a hepatitis C viral nucleoside polymerase inhibitor, or pharmaceutically acceptable salt or prodrug thereof, a hepatitis C viral protease inhibitor, or pharmaceutically acceptable salt or prodrug thereof, and a hepatitis C viral non-nucleoside polymerase inhibitor, or pharmaceutically acceptable salt or prodrug thereof.

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02-01-2014 дата публикации

Compositions and Methods for the Treatment of Catatonia

Номер: US20140005173A1
Автор: James CONOUR
Принадлежит: Individual

Compositions and methods for treating psychotic and neurological disorders in a subject are disclosed. The compositions and methods utilize a pharmaceutical compound that reverses or negates the effects of an NMDA receptor antagonist. The compositions and methods are effective in reducing at least catatonic features in the subject.

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16-01-2014 дата публикации

Il-17 binding proteins

Номер: US20140017246A1
Принадлежит: AbbVie Inc

Proteins that bind IL-17 and/or IL-17F are described along with there use in composition and methods for treating, preventing, and diagnosing IL-17 related diseases and for detecting IL-17 in cells, tissues, samples, and compositions.

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30-01-2014 дата публикации

Methods and Compositions for Treating Thyroid-Related Medical Conditions with Reduced Folates

Номер: US20140030359A1
Автор: Linzy O. Scott, Iii
Принадлежит: Individual

The present invention provides methods and compositions for treating thyroid-related medical conditions. Many thyroid-related medical conditions exist that go undiagnosed and untreated. These conditions may be prevented and treated with reduced folates and vitamin B12. Administration of reduced folates and vitamin B12 will prevent or treat cerebrospinal folate deficiency, which is linked to thyroid-related medical conditions. Administration of reduced folates and vitamin B12 will also prevent or treat conditions associated with masked megaloblastic anemia and hypothyroidism, and other conditions brought upon through improper thyroid function. Additionally, it is commonplace to treat many thyroid conditions with anti-thyroid drugs or thyroid stimulating drugs. This practice alone is also responsible for causing, or not beneficially addressing, adverse conditions that can be prevented or treated through the methods and compositions discussed herein.

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30-01-2014 дата публикации

Biomarkers for predicting sensitivity to cancer treatments

Номер: US20140031259A1
Принадлежит: Genentech Inc

Methods for predicting sensitivity to cancer treatments by assessing biomarkers and combinations of biomarkers include evaluating the presence of mutations to Akt, wherein the presence of said mutations correlates with the sensitivity of Akt inhibitors.

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06-02-2014 дата публикации

Materials and Methods for Treating Conditions Associated with Pathogenic Biofilm

Номер: US20140037688A1
Принадлежит: Quorum Innovations LLC

The subject invention provides materials and methods that effectively support innate immunity and/or disperse pathogenic biofilms using readily available, nontoxic, natural substances, while supporting restoration of normal microbiotic homeostasis. In one embodiment, the subject invention provides anti-biofilm compositions comprising one or more probiotic organisms, anti-microbial honey, and other ingredients such as prebiotic compounds, other hive products, green tea derivatives, other plant derivatives, and vitamin D3.

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06-02-2014 дата публикации

Inhibitors of bruton's tyrosine kinase

Номер: US20140039186A1
Принадлежит: Pharmacyclics LLC

Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.

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20-02-2014 дата публикации

Compositions and Methods for Reducing Blood Alcohol Content

Номер: US20140050702A1
Принадлежит: Life Well Lived LLC

Disclosed are compositions and methods for reducing blood alcohol content following alcohol consumption. The inventive compositions and methods rapidly reduce blood alcohol content and alleviate symptoms of intoxication in a subject having an elevated blood alcohol content due to alcohol consumption.

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20-03-2014 дата публикации

Compositions for enhancing nail health

Номер: US20140079655A1
Автор: John G. Walt
Принадлежит: Allergan Inc

The present invention is directed to compositions and methods for enhancing the health of nails and cuticles in a mammal, including humans. The compositions may be administered topically to the nail bed, nail matrix and cuticle in an amount effective to enhance nail health. The composition is also effective in strengthening and growing nails.

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20-03-2014 дата публикации

Composition comprising lipid nanoparticles and a corticosteroid or vitamin d derivative

Номер: US20140079785A1
Принадлежит: Leo Pharma AS

A pharmaceutical composition comprises, as a therapeutically active ingredient, a corticosteroid and/or vitamin D derivative incorporated as a solid solution or dispersion in lipid nanoparticles, said lipid nanoparticles being solid at ambient temperature and comprising a first lipid with a melting point above body temperature, the first lipid being a wax selected from the group consisting of esters of C 12-24 alcohols and C 12-24 fatty acids, glyceryl mono-, di- or triesters of C 12-24 fatty acids, C 12-24 fatty alcohols, and cholesterol, optionally a second lipid which is an oil at ambient temperature and miscible with the first lipid, and a pharmaceutically acceptable surfactant.

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20-03-2014 дата публикации

Treatment of cerebral ischemia

Номер: US20140080873A1
Принадлежит: Pharnext SA

The present invention relates to new compositions and methods for protecting neuronal cells from ischemic or hypoxic events. More precisely, this invention provides new combinatorial therapies that efficiently protect neuronal cells from ischemia or hypoxia.

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27-03-2014 дата публикации

N-((1r,2s,5r)-5-(tert-butylamino)-2-((s)-3-(7-tert-butylpyrazolo[1,5-a][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide, a dual modulator of chemokine receptor activity, crystalline forms and processes

Номер: US20140088109A1
Принадлежит: Bristol Myers Squibb Co

The present invention provides a novel antagonist: N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-a][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin -1-yl)cyclohexyl)acetamide: or a pharmaceutically acceptable salt, solvate or prodrug, thereof, having unexpected dual CCR-2 and CCR-5 receptor activity. Crystalline forms, metabolites, pharmaceutical compositions containing the same and methods of using the same as agents for the treatment of inflammatory diseases, allergic, autoimmune, metabolic, cancer and/or cardiovascular diseases are also disclosed. The present disclosure also provides processes for preparing compounds of Formula (I) as provided herein, including N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-a][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide. Compounds that are useful intermediates of the process are also provided herein.

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03-04-2014 дата публикации

Combination therapies

Номер: US20140093568A1
Автор: Gordon BRAY, Iris Chan
Принадлежит: Genentech Inc

The present invention relates generally to the fields of molecular biology and growth factor regulation. More specifically, the invention relates to therapies for the treatment of pathological conditions, such as cancer.

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03-04-2014 дата публикации

Pyrazolopyrimidines and related heterocycles as ck2 inhibitors

Номер: US20140094448A1
Принадлежит: Senhwa Biosciences Inc

The invention provides compounds that inhibit protein kinase CK2 activity (CK2 activity), and compositions containing such compounds. These compounds and compositions are useful for treating proliferative disorders such as cancer, as well as other kinase-associated conditions including inflammation, pain, and certain immunological disorders, and have the following general formula:

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10-04-2014 дата публикации

Natural combination hormone replacement formulations and therapies

Номер: US20140100205A1
Принадлежит: TherapeuticsMD Inc

Estrogen and progesterone replacement therapies are provided herein. Among others, the following formulations are provided herein: solubilized estradiol without progesterone; micronized progesterone without estradiol; micronized progesterone with partially solubilized progesterone; solubilized estradiol with micronized progesterone; solubilized estradiol with micronized progesterone in combination with partially solubilized progesterone; and solubilized estradiol with solubilized progesterone.

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04-01-2018 дата публикации

Herbal Tea Compositions for Babies

Номер: US20180000107A1
Автор: Bensalem Samah
Принадлежит:

Herbal tea compositions that, when consumed as a beverage by babies, eases common baby digestive discomforts and helps babies to sleep and feel better. The compositions comprise fennel seed, cumin seed. Some blends additionally contain dried chamomile flower. 1. An herbal tea composition , comprising:a predetermined amount of fennel seeds; anda predetermined amount of cumin seeds.2. The composition of claim 1 , wherein said predetermined amount of fennel seeds is from about 55% (by weight) to about 65% (by weight) of said composition.3. The composition of claim 2 , wherein said predetermined amount of cumin seeds is from about 35% (by weight) to about 45% (by weight) of said composition.4. The composition of claim 1 , further comprising a predetermined amount of dried chamomile flower.5. The composition of claim 4 , wherein said predetermined amount of dried chamomile flower is from about 5% (by weight) to about 15% (by weight) of said composition.6. The composition of claim 4 , wherein:said predetermined amount of fennel seeds if from about 45% (by weight) to about 55% (by weight) of said composition;said predetermined amount of cumin seeds is from about 35% (by weight) to about 45% (by weight) of said composition; andsaid predetermined amount of dried chamomile flower is from about 5% (by weight) to about 15% (by weight) of said composition. This application is a continuation-in-part of prior U.S. patent application Ser. No. 15/055,570, filed Feb. 27, 2016, which application is hereby incorporated by reference.The subject matter described herein relates generally to herbal tea compositions, and in particular to herbal tea compositions which provide medicinal benefits when consumed.Babies often have digestive discomforts such as gas, constipation, acid reflux and colic which prevent them from sleeping for prolonged periods of time, and causes them to be irritable.The present invention provides herbal tea compositions that, when consumed as a beverage by babies, ...

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07-01-2021 дата публикации

Methods of treating central nervous system disorders via administration of nanoparticles of an mtor inhibitor and an albumin

Номер: US20210000752A1
Автор: Neil P. Desai, Shihe HOU
Принадлежит: Abraxis Bioscience Llc

The present application provides methods of treating a CNS disorder (such as glioblastoma and epilepsy) in an individual, comprising systemically (e.g., intravenously or subcutaneously) administering to the individual an effective amount of a composition comprising nanoparticles comprising an mTOR inhibitor (such as a limus drug, such as sirolimus or a derivative thereof) and an albumin, optionally further comprising administering a second agent (such as an anti-VEGF antibody, a proteasome inhibitor, or an alkylating agent).

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07-01-2021 дата публикации

SPHINGOSINE PATHWAY MODULATING COMPOUNDS FOR THE TREATMENT OF CANCERS

Номер: US20210000766A1
Принадлежит: ENZO BIOCHEM, INC.

The invention provides methods and compositions for treating cancers and myeloproliferative disorders using sphingosine kinase-1 inhibitors, such as SK1-I, and selective sphingosine-1-phosphate receptor agonists, such as ozanimod. 1. A method for treating prostate cancer in a mammalian subject , comprising the step of:administering to a mammalian subject in need of treatment for prostate cancer an effective amount of ozanimod or a pharmaceutically acceptable salt thereof.2. The method of claim 1 , wherein the administering step comprises administering the hydrochloride salt of ozanimod to the mammalian subject.3. The method of claim 1 , wherein the mammalian subject is a human.4. The method of claim 3 , wherein the administering step comprises administering the hydrochloride salt of ozanimod to the mammalian subject. This application is a continuation of U.S. patent application Ser. No. 16/830,357 filed Mar. 26, 2020, which is a continuation of U.S. patent application Ser. No. 16/287,201 filed Feb. 27, 2019 (now U.S. patent no. 10,646,459), which is a divisional of U.S. patent application Ser. No. 16/017,345 filed June 25, 2018 (now U.S. Pat. No. 10,278,960), which claims the benefit of U.S. provisional patent application Ser. No. 62/524,221 filed Jun. 23, 2017, each of which is hereby incorporated by reference in its entirety.The invention relates to the field of pharmaceutical treatment of cancers.Sphingosine-1-phosphate (S1P) was discovered to be a bioactive signaling molecule over 20 years ago. Studies have since identified two related kinases, sphingosine kinase 1 and 2 (a/k/a sphingosine kinase “type I” and “type II” respectively, and SphK1 and SphK2 respectively), which catalyze the phosphorylation of sphingosine to S1P. Extracellular S1P can bind to and activate each of five S1P-specific, G protein-coupled receptors (designated S1PR) to regulate cellular and physiological processes in an autocrine or paracrine manner. Selective inhibitors of each of ...

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07-01-2021 дата публикации

Methods for treating urea cycle disorders

Номер: US20210000781A1
Принадлежит: Horizon Therapeutics LLC

Provided are methods of administering glycerol phenylbutyrate to a patient in need thereof, wherein said patient is also being treated with a CYP3A4 substrate having a narrow therapeutic index, midazolam or a pharmaceutically acceptable salt thereof, or celecoxib.

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03-01-2019 дата публикации

EMULSION FORMULATIONS OF AN NK-1 RECEPTOR ANTAGONIST AND USES THEREOF

Номер: US20190000762A1
Принадлежит:

Disclosed herein are novel pharmaceutical formulations of a neurokinin-1 (NK-1) receptor antagonist suitable for parenteral administration including intravenous administration. Also included are formulations including both the NK-1 receptor antagonist and dexamethasone sodium phosphate. The pharmaceutical formulations are stable oil-in-water emulsions for non-oral treatment of emesis and are particularly useful for treatment of subjects undergoing highly emetogenic cancer chemotherapy. 128.-. (canceled)29. A method for treating a subject in need thereof , comprising administering to the subject an injectable pharmaceutical emulsion , wherein the emulsion comprises:a neurokinase-1 (NK-1) receptor antagonist;11 wt/wt % to 15 wt/wt % of an emulsifier;an oil;a co-surfactant which comprises an alcohol;a tonicity agent;a pH modifier; andwater;wherein the pH of the emulsion ranges from about 7.5 to 9.0, and the ratio of the emulsifier to the NK-1 receptor antagonist ranges from about 18:1 to 22:1 (wt/wt %).30. The method according to claim 29 , wherein the ratio of the oil to the NK-1 receptor antagonist ranges from about 5:1 to 15:1 (wt/wt %).31. The method according to claim 29 , wherein the ratio of the oil to the NK-1 receptor antagonist ranges from about 10:1 to 15:1 (wt/wt %).32. The method according to claim 29 , wherein the ratio of emulsifier to oil ranges from about 1:1 to 3:1 (wt/wt %).33. The method according to claim 29 , wherein the emulsifier is a phospholipid.34. The method according to claim 29 , wherein the emulsifier is an egg lecithin.35. The method according to claim 29 , wherein the emulsion further comprises dexamethasone sodium phosphate claim 29 , wherein the dexamethasone sodium phosphate is present in the aqueous phase.36. The method according to claim 29 , wherein the NK-1 receptor antagonist is selected from the group consisting of rolapitant claim 29 , netupitant claim 29 , ezlopitant claim 29 , vestipitant claim 29 , serlopitant claim 29 , ...

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03-01-2019 дата публикации

USE OF RASAGILINE FOR THE TREATMENT OF RESTLESS LEGS SYNDROME

Номер: US20190000780A1
Автор: Blaugrund Eran, Levy Ruth
Принадлежит: TEVA PHARMACEUTICAL INDUSTRIES, LTD.

Disclosed are methods for the treatment of Restless Legs Syndrome comprising administering an amount of R(+)-N-propargyl-1-aminoindan or a pharmaceutically acceptable salt thereof. 1. A pharmaceutical composition comprising in unit dosage form R(+)-N-propargyl-1-aminoindan or a pharmaceutically acceptable salt thereof and at least one of pergolide, pramipexole, oxycodone, clonazepam, carbamazepine, gabapentin, valproate, ropinirole or clonidin. This application is a continuation of U.S. Ser. No. 14/524,993, filed Oct. 27, 2014, which is a continuation of U.S. Ser. No. 11/731,493, filed Mar. 30, 2007, which claims benefit of U.S. Provisional Application No. 60/788,617 filed Apr. 3, 2006, the entire contents of each of which in their entireties are hereby incorporated by reference.Throughout this application various publications, published patent applications and published patents are referenced. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which this invention pertains.Restless Legs Syndrome (“RLS”, also known as Ekbom Syndrome) is a neurological condition that expresses itself as an overwhelming urge to move the legs, usually caused by uncomfortable or unpleasant sensations in the legs at rest. Movement of the legs temporarily alleviates the discomfort. (Jones et al., Restless Legs Syndrome—A Review, December 1997, 14(6):430-2)The sensations occur during periods of inactivity, and are thus most intense in the evening and at night. RLS often causes difficulty staying or falling asleep, which leads to feelings of daytime tiredness or fatigue. RLS may cause involuntary jerking of the limbs during sleep and sometimes during wakefulness. Because of the nature of these symptoms, RLS is one of the most prevalent causes of sleep disorders such as sleep disturbance and insomnia. (Fox, G. N., Restless Legs Syndrome, January 1986, 33(1):147-52)RLS can ...

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03-01-2019 дата публикации

Combination medication for neuro-degenerative diseases and side-effects associated with cognition effecting pharmaceuticals

Номер: US20190000782A1
Принадлежит: Individual

The disclosure generally relates to pharmaceutical compositions including a benzhydrylsulfinylacetamide antidepressant and an amount of sodium chloride effective to increase a mean arterial blood pressure of a subject and methods for ameliorating symptoms of dementia including forms of dementia diagnosed as Alzheimer's disease and side-effects associated with the administration of cognition effecting pharmaceuticals.

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03-01-2019 дата публикации

METHODS OF DIAGNOSING AND TREATING INFECTED IMPLANTS

Номер: US20190000786A1
Автор: Johnson Lanny Leo
Принадлежит:

The present invention relates to methods for treating microbial infections on the surfaces of an implant or other surfaces near an implant in a patient. In particular, the methods are useful for treating biofilm infections. The methods include the use of minimally invasive techniques, including the use of ultra sound for facilitating the detection of biofilm infections on the implant or other surface of a patient and destroying the infection by administering an anthocyanin or an anthocyanidin or metabolite thereof. In particular, the administration of protocatechuic acid (PCA) or 2,4,6 trihydroxybenzaldehyde (2,4,6 THBA) for the treatment of an infected implant or other surface of a patient is described herein. 1. A method of treating a biofilm bacterial infection on a surface of an implant or a surface of a patient suspected of having a biofilm bacterial infection , the method comprising:removing a biofilm-forming bacteria by a minimally invasive technique comprising needle aspiration or an application of ultrasound or both to determine a presence of a biofilm around or on the surface of the implant or surface of the patient, wherein the minimally invasive technique dislodges the biofilm colony andinhibiting or destroying the biofilm colony and all biofilm-forming bacteria on or around the surface of the implant in the patient or surface of the patient by administering a composition comprising protocatechuic acid or 2,4,6-trihydroxybenzaldehyde or a mixture or combination thereof or administering pure crystals or a powder of protocatechuic acid or 2,4,6-trihydroxybenzaldehyde or a mixture or combination thereof in an amount effective to inhibit or destroy the biofilm on or about the surface of the implant in the patient or the surface of the patient.2. The method of claim 1 , wherein the ultrasound is applied at a frequency and power sufficient to dislodge the biofilm-forming bacteria off the surface of the implant in a patient or the surface of the patient.3. The ...

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03-01-2019 дата публикации

Tumor therapeutic agent

Номер: US20190000797A1
Принадлежит: Eisai R&D Management Co Ltd

A novel tumor therapeutic agent for a combination therapy is disclosed. More specifically, a tumor therapeutic agent used for a combination therapy of lenvatinib, ifosfamide, and etoposide is disclosed.

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03-01-2019 дата публикации

COMPOSITION COMPRISING A DIINDOLYLMETHANE AND A RETINOID TO TREAT A SKIN CONDITION

Номер: US20190000800A1
Автор: ALPERT David
Принадлежит:

Provided is a composition for use in treating a skin condition, the composition comprising: 134-. (canceled)36. The dosage form of claim 35 , wherein the ratio (mg:μg) of the first and the second component is from about 10:3000 to about 500:200.37. The dosage form of claim 35 , wherein the ratio (mg:μg) of the first and the second component is from about 75:800 to about 300:200.38. The dosage form of claim 35 , wherein the ratio (mg:IU) of the first and the second component is from about 75:10000 to about 300:2500.39. The dosage form of claim 35 , wherein the ratio (mg:mg) of the first and the second component is from about 75:5.3 to about 300:1.3.40. The dosage form of claim 35 , wherein the dosage form comprises a first capsule comprising the first component and a second capsule comprising the second component.41. The dosage form of claim 35 , wherein the dosage form comprises a capsule comprising the first component and the second component claim 35 , wherein the first and the second component are provided in a single formulation.42. The dosage form of claim 41 , wherein the single formulation comprises a blended powder comprising the first and the second component.43. The dosage form of claim 35 , wherein the dosage form comprises a first tablet comprising the first component and a second tablet comprising the second component.44. The dosage form of claim 35 , wherein the dosage form comprises a tablet comprising the first component and the second component claim 35 , wherein the first and the second component are provided in a single formulation.45. The dosage form of claim 35 , wherein the first component is in a microencapsulated form.46. The dosage form of claim 35 , further comprising at least one excipient selected from the group consisting of: tricalcium phosphate claim 35 , cellulose fiber claim 35 , ascorbic acid claim 35 , silicon dioxide claim 35 , magnesium stearate claim 35 , and any combination thereof.47. The dosage form of claim 35 , wherein a ...

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04-01-2018 дата публикации

TREATMENT FOR NON-ALCOHOLIC FATTY LIVER DISEASES

Номер: US20180000775A1
Принадлежит:

The present invention relates to the use of mixtures of vitamin E and polyunsaturated fatty acids (PUFAs) as agents for the prevention, control and/or treatment of conditions associated with excessive fat accumulation in the liver which is not caused by alcohol abuse. This includes prevention, control and/or treatment of non-alcoholic steatosis in the liver—known as non-alcoholic fatty liver disease (NAFLD)—and/or non-alcoholic steatohepatitis (NASH) in a subject in need thereof. In particular, the present invention relates to the use of such compounds comprising vitamin E and PUFAs as active ingredients in the manufacture of medicaments for the prevention, control and/or treatment of conditions related to NAFLD. 1. Combination of vitamin E and polyunsaturated fatty acid (PUFA) in the use of prevention , control or treatment of non-alcoholic fat accumulation in the liver in a subject in need thereof , preferably for prevention , control or treatment of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis , wherein the ratio of vitamin E and polyunsaturated fatty acids is administered in the range of about 1:1 to about 1:5 , or in the range of about 4:1 to about 20:1 , wherein the vitamin E is calculated as α-tocopherol and the ratio is calculated as weight ratio.2. Combination according to claim 1 , wherein the vitamin E is selected from the group consisting of α-tocopherol claim 1 , β-tocopherol claim 1 , γ-tocopherol claim 1 , δ-tocopherol and mixtures thereof claim 1 , preferably α-tocopherol and/or γ-tocopherol.3. Combination according to claim 1 , wherein the polyunsaturated fatty acid is selected from the group consisting of ω-3 claim 1 , ω-6 claim 1 , ω-9 polyunsaturated fatty acids and oxylipins derived therefrom claim 1 , preferably ω-6 or ω-3 PUFAs claim 1 , more preferably selected from ω-3 α-linolenic acid claim 1 , ω-3 eicosapentaenoic acid claim 1 , ω-3 docosapentaenoic acid claim 1 , ω-3 docosahexaenoic claim 1 , ω-3 docosatetraenoic ...

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04-01-2018 дата публикации

Pharmaceutical composition for the treatment of mycosis

Номер: US20180000783A1

The present invention relates to a pharmaceutical composition comprising a combination of benzydamine and an antimycotic active ingredient, said combination having a synergistic effect in the treatment of mycosis.

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07-01-2021 дата публикации

Methods and Compositions for Treating Thyroid-Related Medical Conditions with Reduced Folates

Номер: US20210000836A1
Автор: III Linzy O., Scott
Принадлежит:

The present invention provides methods and compositions for treating thyroid-related medical conditions. Many thyroid-related medical conditions exist that go undiagnosed and untreated. These conditions may be prevented and treated with reduced folates and vitamin B12. Administration of reduced folates and vitamin B12 will prevent or treat cerebrospinal folate deficiency, which is linked to thyroid-related medical conditions. Administration of reduced folates and vitamin B12 will also prevent or treat conditions associated with masked megaloblastic anemia and hypothyroidism, and other conditions brought upon through improper thyroid function. Additionally, it is commonplace to treat many thyroid conditions with anti-thyroid drugs or thyroid stimulating drugs. This practice alone is also responsible for causing, or not beneficially addressing, adverse conditions that can be prevented or treated through the methods and compositions discussed herein. 1. A method of preventing and treating thyroid-related medical conditions comprising the administration of a folate.2. The method of claim 1 , additionally comprising the administration of vitamin B12.3. The method of wherein the thyroid-related medical condition is brought upon by hypothyroidism or hyperthyroidism.4. The method of where the thyroid-related medical condition is cerebrospinal folate deficiency.5. The method of where the thyroid-related medical condition is masked megaloblastic anemia or a masked macrocytic anemia claim 1 , or a macrocytic anemia.6. The method of where the thyroid-related medical condition is hepatic dysfunction.7. The method of where the thyroid-related medical condition is hypothyroxinemia or other temporary period of hypothyroidism.8. The method of where the thyroid-related medical condition is presented in an individual that is treated with radioactive iodine claim 1 , has surgery on or related to the thyroid gland or undergoes any other method or procedure to reduce the size or activity ...

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07-01-2021 дата публикации

Heterocyclic compounds and uses thereof

Номер: US20210000837A1
Принадлежит: Infinity Pharmaceuticals Inc

Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

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02-01-2020 дата публикации

ZEAXANTHIN FOR TUMOR TREATMENT

Номер: US20200000740A1
Принадлежит: The New York Eye and Ear Infirmary

A composition comprising a pharmaceutically effective amount of zeaxanthin or its derivative for use in treating a malignant tumor and a method of using a pharmaceutically effective amount of zeaxanthin or its derivative either alone or together with one or more pharmaceutical agents for treating a malignant tumor. The tumor may be, but is not limited to breast cancer, cervix cancer, colon cancer, cutaneous melanoma, cutaneous squamous carcinoma, hepatocellular carcinoma, lung cancer, osteosarcoma, prostate cancer, and uveal melanoma. The pharmaceutically effective amount of zeaxanthin is generally above about 0.5 mg/kg/d to about 20 mg/kg/d. 19-. (canceled)10. A method of treating a malignant tumor comprising administering a composition comprising zeaxanthin in combination with one or more anti-malignant tumor agents to a subject in need thereof.11. The method of claim 10 , wherein the composition further comprises one or more pharmaceutically acceptable additives claim 10 , excipient claim 10 , adjuvant or carriers.12. The method of claim 10 , wherein the anti-malignant tumor agent is selected from 5-Fluorouracil claim 10 , Adriamycin claim 10 , Cytoxan claim 10 , Cisplatin claim 10 , and Avastin®.13. The method of claim 10 , wherein the subject is a patient diagnosed with a malignant tumor.14. The method of claim 10 , wherein the zeaxanthin is administered in an amount sufficient to induce apoptosis of the malignant tumor.15. The method of claim 10 , wherein the zeaxanthin is administered in an amount sufficient to delay progression of the malignant tumor.16. The method of claim 10 , wherein apoptosis is induced in the malignant tumor cells when exposed to zeaxanthin and wherein apoptosis is not induced in non-malignant tumor cells.17. The method of claim 10 , wherein the malignant tumor is selected from breast cancer claim 10 , cervix cancer claim 10 , colon cancer claim 10 , cutaneous melanoma claim 10 , cutaneous squamous carcinoma claim 10 , hepatocellular ...

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02-01-2020 дата публикации

Cenicriviroc combination therapy for the treatment of fibrosis

Номер: US20200000772A1
Автор: Eric Lefebvre
Принадлежит: Tobira Therapeutics Inc

Cenicriviroc (CVC) is an orally active antagonist of ligand binding to C-C chemokine receptor type 5 (CCR5) and C-C chemokine receptor type 2 (CCR2). CVC blocks the binding of RANTES. MIP-1α, and MIP-1β to CCR5, and of MCP-1/CCL2 to CCR2. Methods of treating fibrosis and related conditions comprising co-administration of CVC with FXR agonists, high dose vitamin E (>400 iU/d), a peroxisome proliferator-activated receptor alpha (PPAR-α) agonist, PPAR-γ agonist, PPAR-δ agonist and/or chemokine antagonists are provided herein.

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04-01-2018 дата публикации

(S)-N-(3-(6-ISOPROPOXYPYRIDIN-3-YL)-1H-INDAZOL-5-YL)-1-(2-(4-(4-(1-METHYL-1H-1,2,4-TRIAZOL-3-YL)PHENYL)-3,6-DIHYDROPYRIDIN-1(2H)-YL)-2-OXOETHYL)-3-(METHYLTHIO)PYRROLIDINE-3-CARBOXAMIDE COMPOSITIONS FOR PHARMACEUTICAL PREPARATIONS

Номер: US20180000803A1
Принадлежит: Merck Sharp & Dohme Corp.

The invention includes a granular composition comprising the active ingredient (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3- carboxamide, wherein a total amount of active ingredient comprises by weight % about 60-90% (5)-N-(3-(6-isopro-poxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)-3,6-di-hydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide Form 1 HCl, about 10-30% (5)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide amorphous HCl, and about 0-5% (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide amorphous free base. 1. A pharmaceutical tablet comprising the active ingredient (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1 ,2 ,4-triazol-3-yl)phenyl)-3 ,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide , wherein a total amount of active ingredient comprises by weight % about 60-90% (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1 ,2 ,4-triazol-3-yl)phenyl)-3 ,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide Form 1 HCl , about 10-30% (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1 ,2 ,4-triazol-3-yl)phenyl)-3 ,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide amorphous HCl , and about 0-5% (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1 ,2 ,4-triazol-3-yl)phenyl)-3 ,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide amorphous free base.2. A pharmaceutical tablet of wherein the total ...

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03-01-2019 дата публикации

DRUG COMBINATION PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USING THEM

Номер: US20190000802A1
Принадлежит:

The invention provides preparations, formulations, kits and other products of manufacture (e.g., blister packs) comprising combinations of beneficial ingredients that are serviceable as therapies for improving states and disease symptoms such as involving inflammation, excessive sympathoneural drive, cachexia, anorexia, and anorexia-cachexia, as well as stress or anxiety related thereto, and methods of making and using them. The invention provides compositions and therapies comprising use of a beta adrenergic antagonist (also called “beta blockers”, e.g., propranolol) in combination with an anti-inflammatory agent, e.g., a nonsteroidal anti-inflammatory drug (NSAID), an angiotensin-converting enzyme (ACE) inhibitor, an angiotensin receptor blocker (ARB), an anabolic steroid, a natural oil or fatty acid or any combination thereof. 135-. (canceled)37: The method of claim 36 , wherein the condition or disease comprises a maladaptive nutritional state secondary to the SIRS; anorexia; insulin resistance; anxiety; sleep disturbances; weakness; fatigue; lethargy; depression; malaise; or any combination thereof.38: The method of claim 36 , wherein the maladaptive nutritional state comprises cachexia or anorexia.39: The method of claim 38 , wherein the cachexia comprises cachexia secondary to cancer.40: The method of claim 38 , wherein the cachexia is defined as at least two of the symptoms selected from the group consisting of: 1) a hyper-inflammatory state claim 38 , 2) altered hormone levels and cytokine levels; 3) increased heart rate variability; 4) weight loss claim 38 , and 5) increased heart rate claim 38 , wherein optionally the increased heart rate is having a sustained elevated heart rate of at least about 6 bpm.4160-. (canceled)61: The method of claim 36 , wherein the therapeutic combination or the pharmaceutical composition further comprises a nutritional supplement.62: The method of claim 36 , wherein the member of the first drug group and member of the second ...

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04-01-2018 дата публикации

STABLE PHARMACEUTICAL COMPOSITIONS COMPRISING ANTIBACTERIAL AGENT

Номер: US20180000811A1
Принадлежит: WOCKHARDT LIMITED

Stable pharmaceutical compositions comprising a compound of Formula (I) or a stereoisomer or a pharmaceutically acceptable derivative thereof are disclosed. Formula (I) 2. The pharmaceutical composition according to claim 1 , wherein a compound of Formula (I) is present as L-alanine claim 1 , 1-[(5S)-2-carboxy-9-fluoro-6 claim 1 ,7-dihydro-5-methyl-1-oxo-1H claim 1 ,5H-benzo[i claim 1 ,j]quinolizin-8-yl]-4-piperidinyl ester claim 1 , methanesulfonate.3. The pharmaceutical composition according to any one of or claim 1 , comprising less than about 2% w/w of total impurity following storage for six months at a temperature of 40° C. and a relative humidity of 75%.4. The pharmaceutical composition according to any one of or claim 1 , comprising less than about 2% w/w of S-(−)-9-fluoro-8-(4-hydroxy-piperidin-1-yl)-5-methyl-6 claim 1 ,7-dihydro-1-oxo-1H claim 1 ,5H-benzo[i claim 1 ,j] quinolizine-2-carboxylic acid following storage for six months at a temperature of 40° C. and a relative humidity of 75%.5. The pharmaceutical composition according to any one of or claim 1 , comprising less than about 0.5% w/w of (S)-(−)-8-(4-L-alaninyl oxypiperidin-1-yl)-5-methyl-6 claim 1 ,7-dihydro-1-oxo-1H claim 1 ,5H-benzo[i claim 1 ,j] quinolizine-2-carboxylic acid claim 1 , methane sulfonic acid salt following storage for six months at a temperature of 40° C. and a relative humidity of 75%.6. The pharmaceutical composition according to any one of or claim 1 , comprising less than about 0.5% w/w of (S)-(−)-9-fluoro-8-(4-D-alaninyl oxypiperidin-1-yl)-5-methyl-6 claim 1 ,7-dihydro-1-oxo-1H claim 1 ,5H-benzo[i claim 1 ,j] quinolizine-2-carboxylic acid claim 1 , methane sulfonic acid salt following storage for six months at a temperature of 40° C. and a relative humidity of 75%.7. The pharmaceutical composition according to any one of or claim 1 , comprising less than about 0.1% w/w of (S)-(−)-9-fluoro-8-(4-(N-tert-butyloxy carbonyl-L-alaninyl)-oxypiperidin-1-yl)-5-methyl-6 claim 1 ,7- ...

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03-01-2019 дата публикации

ORGANIC COMPOUNDS

Номер: US20190000807A1
Принадлежит: INTRA-CELLULAR THERAPIES, INC.

The present invention relates to certain PDE2 inhibitory compounds, in free or salt form, pharmaceutical compositions containing such compounds and methods for the treatment of PDE2 mediated disorders. 5. A pharmaceutical composition comprising a compound according to claim 1 , in combination or association with a pharmaceutically acceptable diluents or carrier.6. A method for the treatment of a PDE2 mediated disorder comprising administering to a subject in need thereof an effective amount of a compound according to .7. The method of claim 6 , wherein the disorder is selected from the group consisting of neurological disorders (such as migraine; epilepsy; Alzheimer's disease; Parkinson's disease; brain injury; stroke; cerebrovascular diseases (including cerebral arteriosclerosis claim 6 , cerebral amyloid angiopathy claim 6 , hereditary cerebral hemorrhage claim 6 , and brain hypoxia-ischemia); spinal muscular atrophy; lateral sclerosis; multiple sclerosis; cognitive disorders (including amnesia claim 6 , senile dementia claim 6 , HIV associated dementia claim 6 , Alzheimer's associated dementia claim 6 , Huntington's associated dementia claim 6 , Lewy body dementia claim 6 , vascular dementia claim 6 , drug related dementia claim 6 , delirium claim 6 , and mild cognitive impairment); cognitive dysfunction associated with Parkinson's disease and depression; mental deficiency (including Down syndrome and fragile X syndrome); sleep disorders (including hypersomnia claim 6 , circadian rhythm sleep disorder claim 6 , insomnia claim 6 , parasomnia claim 6 , and sleep deprivation); psychiatric disorders (such as anxiety (including acute stress disorder claim 6 , generalized anxiety disorder claim 6 , social anxiety disorder claim 6 , panic disorder claim 6 , post-traumatic stress disorder (PTSD) claim 6 , obsessive-compulsive disorder claim 6 , specific phobia claim 6 , social phobia claim 6 , chronicanxiety disorder and obsessive compulsive disorder claim 6 ,); ...

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03-01-2019 дата публикации

Antifungal Compounds

Номер: US20190000814A1
Принадлежит: Amplyx Pharmaceuticals, Inc.

The technical field of the invention is in pharmaceutical compounds and methods. In an aspect, the disclosure provides macrolide compounds suitable for use as antifungal agents, as well as methods for their use and compositions containing the same. 7. The method of wherein the compound as a structure of Table 1.8. The method of further comprising detecting a resultant antifungal activity.9. An anti-fungal formulation comprising an effective amount of a compound having the structure of formula (I) claim 1 , and a second claim 1 , different antifungal agent.10. The formulation of claim 9 , wherein the second antifungal agent is selected from compounds according to formula (I) claim 9 , polyenes claim 9 , imidazoles claim 9 , triazoles claim 9 , thiazoles claim 9 , allylamines claim 9 , and echinochandins.11. A compound of formula I (supra) claim 9 , of Table 1 claim 9 , and/or according to any of the structures described herein.12. A pharmaceutical composition comprising a formulation according to in effective unit dosage.13. A pharmaceutical composition comprising a compound according to in effective unit dosage. Tacrolimus (also referred to as FK-506) is a compound known to have immunosuppressive activity. As an immunosuppressive, it is used in a variety of situations such as organ transplantations and eczema treatment. The structure of tacrolimus includes a macrocyclic lactone, and various structurally related macrolide compounds are known.Relevant art: US 2006/0035918; U.S. Pat. No. 5,457,111.In an aspect is a method for treating a patient suffering from a fungal infection, the method comprising administering to the patient an effective amount of a composition comprising a compound of formula (I)In formula (I), “a” is a double bond optionally present (provided that Ror Ris not present); Ris selected from alkyl, alkenyl, or is taken together with Ror Rto form a cycle; Rand Rare independently selected from —H and —OH, or Rand Rtogether form ═X, where X is selected ...

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03-01-2019 дата публикации

COMPOSITION COMPRISING COMBINATION OF RAPAMYCIN AND AN ACTIVATOR OF AMP KINASE AND USE THEREOF FOR TREATING DISEASES

Номер: US20190000815A1
Автор: Melin Jeffrey M.
Принадлежит:

A formulation, especially one that is topically administered, comprising a combination of rapamcycin and metformin in a molar ratio of about 20:1, 10:1, 5:1, 4:1, 3:1, or 1:1. The topical formulation may be a gel, an ointment, a cream or a lotion. The topical formulation may be used to treat a condition or disease of the skin or eye, wherein the condition or disease is associated with mTORC1 activation. 1. A composition for treating a disease or condition of the skin or eye , wherein the disease or condition is associated with mTORC1 activation , the composition comprising a combination of rapamycin and metformin , wherein the rapamycin is present in an amount in a range of about 0.01% to about 4.0% by weight and metformin is present in an amount in a range of about 0.00007% to about 2.0% by weight.2. The composition of claim 1 , wherein the rapamycin is present in an amount in a range of about 0.% to about 3.5% and the metformin in present in an amount in a range of about 0.002% to about 1.0% by weight.3. The composition of claim 1 , wherein the rapamycin in present in an amount of up to about 3.5% by weight and the metformin is present in an amount of up to about 2.0% by weight.4. The composition of claim 1 , wherein the amount of rapamycin is less than about 2.0% by weight.5. The composition of claim 1 , herein the amount metformin is less than about 1.5% by weight.6. The composition of claim 1 , wherein the composition is formulated for topical administration in a form selected from a gel claim 1 , an ointment claim 1 , a cream claim 1 , a lotion claim 1 , or liquid solution.7. A method for treating a disease or condition of the skin or eye in a subject claim 1 , wherein the disease or condition is associated with mTORC1 activation claim 1 , the method comprising: administering an effective amount of a formulation comprising a combination of rapamycin and metformin claim 1 , wherein the molar ratio of rapamycin to metformin is in the range of about 20:1 to about ...

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05-01-2017 дата публикации

Treatment of Neoplasia

Номер: US20170000795A1
Автор: David Cade, Michael Tapner
Принадлежит: Sirtex Medical Pty Ltd

A method of treating cancer in a patient comprising administering to the patient an a systemic chemotherapeutic drug regime in combination with radioactively doped particle, characterised in that the two therapies when introduced into the patient have an improved anticancer effect.

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03-01-2019 дата публикации

ANTICHOLINERGIC NEUROPROTECTIVE COMPOSITION AND METHODS

Номер: US20190000826A1
Принадлежит: CHASE PHARMACEUTICALS CORPORATION

The present invention relates to a pharmaceutical composition comprising propiverine, trospium or glycopyrrolate; and a non-anticholinergic antiemetic agent. It is also related to a pharmaceutical composition comprising a high dose of solifenacin or a pharmaceutically acceptable salts thereof; and a non-anticholinergic antiemetic agent. Pharmaceutical compositions containing high dose of nsPAChA for use for increasing the AChEI blood concentrations and for combating neurodegeneration are also described. The invention also relates to a method for inducing neuroprotection and combating neurodegeneration in a patient suffering from Alzheimer type dementia as well as to a method for increasing the blood levels of an acetyl choline esterase inhibitor (AChEI) in a human subject treated with an AChEI dose. 1. A pharmaceutical composition comprising a nsPAChA selected from the group consisting of propiverine and pharmaceutically acceptable salts thereof, in an amount which is equivalent to from 15 mg to 120 mg of propiverine hydrochloride; trospium pharmaceutically acceptable salts, in an amount which is equivalent to from 20 mg to 480 mg of trospium chloride; and glycopyrrolium pharmaceutically acceptable salts, in an amount which is equivalent to from 2 mg to 16 mg of glycopyrronium bromide; and (b) a non-anticholinergic antiemetic agent (naAEA); in admixture with a pharmaceutical carrier. The invention relates to a pharmaceutical composition comprising (a) a high dose of a non-selective peripheral anticholinergic agent (nsPAChA) selected from the group consisting of propiverine and pharmaceutically acceptable salts thereof, trospium and pharmaceutically acceptable salts thereof, glycopyrrolium and pharmaceutically acceptable salts thereof, and solifenacine and pharmaceutically acceptable salts thereof; (b) a non-anticholinergic antiemetic agent (naAEA); in admixture with a pharmaceutical carrier; and (c) a high dose of an acetylcholine esterase inhibitor (AChEI). This ...

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03-01-2019 дата публикации

Compositions and methods for treating drug-tolerant glioblastoma

Номер: US20190000831A1
Принадлежит: General Hospital Corp

The present invention provides compositions and methods for the treatment of drug-tolerant glioblastoma, and in particular glioblastoma stem cells. Specifically, the methods comprise contacting a glioblastoma stem cell with a platelet-derived growth factor receptor alpha inhibitor and one or more of a histone lysine demethylase inhibitor and a Notch inhibitor.

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03-01-2019 дата публикации

ABUSE-RESISTANT MUCOADHESIVE DEVICES FOR DELIVERY OF BUPRENORPHINE

Номер: US20190000833A1
Автор: Finn Andrew, Vasisht Niraj

The present invention provides abuse deterrent mucoadhesive devices for delivery of buprenorphine. Each device comprises a mucoadhesive layer and a backing layer, and the pH in each layer is selected, such that absorption of buprenorphine is maximized. 1. An abuse deterrent mucoadhesive device for use in managing pain or opioid dependence , the device comprising:a mucoadhesive layer comprising an effective amount of buprenorphine buffered to a pH of between about 4.0 and about 6.0; anda backing layer buffered to a pH between about 4.0 and about 4.8.28-. (canceled) This application is a continuation of U.S. patent application Ser. No. 15/213,137, filed Jul. 18, 2016; which is a continuation of U.S. patent application Ser. No. 14/704,955, filed on May 5, 2015; which is a continuation of U.S. patent application Ser. No. 14/499,651, filed on Sep. 29, 2014; which is a continuation of U.S. patent application Ser. No. 14/176,036, filed on Feb. 7, 2014; which is a continuation of U.S. patent application Ser. No. 13/590,094, filed on Aug. 20, 2012, now U.S. Pat. No. 8,703,177, issued on Apr. 22, 2014; which claims priority to U.S. Provisional Application No. 61/525,094, filed on Aug. 18, 2011. This application is also related to U.S. patent application Ser. No. 08/734,519, filed on Oct. 18, 1996, now U.S. Pat. No. 5,800,832, issued on Sep. 1, 1998; U.S. patent application Ser. No. 11/639,408, filed on Dec. 13, 2006; U.S. patent application Ser. No. 11/817,915, filed on Sep. 6, 2007; and U.S. patent application Ser. No. 13/184,306, filed on Jul. 15, 2011, now U.S. Pat. No. 8,147,866, issued on Apr. 3, 2012. The entire contents of each of the foregoing applications are incorporated herein by reference.Buprenorphine is a partial μ-opiate receptor agonist, an ORL1/nociceptin receptor agonist with high affinity, and slow association and dissociation from the receptors, and a κ-opiate receptor antagonist. Transmucosal bioavailability of buprenorphine is greater than its oral ...

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03-01-2019 дата публикации

BUPROPION AS A MODULATOR OF DRUG ACTIVITY

Номер: US20190000835A1
Автор: Tabuteau Herriot
Принадлежит:

Dosage forms, drug delivery systems, and methods related to sustained release of dextromethorphan or improved therapeutic effects are disclosed. Typically, bupropion or a related compound is orally administered to a human being to be treated with, or being treated with, dextromethorphan. 1. A method , comprising orally administering a dosage form to a human being twice daily for at least eight consecutive days , wherein the dosage form comprises a bupropion and a dextromethorphan , wherein the human being is an extensive metabolizer of dextromethorphan in need of treatment with dextromethorphan , and wherein on the eighth day that the dosage form is administered twice daily , the method results in a Cof dextromethorphan , that is: 1) at least about 40 ng/mL , and 2) at least about 15 times the Cof dextromethorphan that would be achieved by administering the same amount of the dextromethorphan without the bupropion twice daily for eight consecutive days.2. The method of claim 1 , wherein the dosage form is a solid.3. The method of claim 2 , wherein the solid oral dosage form further comprises a binder.4. The method of claim 2 , wherein the solid oral dosage form further comprises a disintegrating agent.5. The method of claim 2 , wherein the solid oral dosage form further comprises a lubricant.6. The method of claim 1 , wherein the dosage form is effective for immediate release of the dextromethorphan.7. The method of claim 1 , wherein the dosage form is effective for sustained release of the bupropion.8. The method of claim 1 , wherein the Cof dextromethorphan on the eighth day that the dosage form is administered twice daily is about 45 ng/mL to about 70 ng/mL.9. The method of claim 1 , wherein the Cof dextromethorphan on the eighth day that the dosage form is administered twice daily is about 50 ng/mL to about 60 ng/mL.10. The method of claim 1 , wherein the AUCof dextromethorphan on the eighth day that the dosage form is administered twice daily is about 400 ng·hr ...

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03-01-2019 дата публикации

Synthetic lethality and the treatment of cancer

Номер: US20190000838A1
Принадлежит: PACYLEX PHARMACEUTICALS Inc

Described herein are compounds, compositions and methods for treatment of cancer. Also described are methods and uses for identifying subject with cancer that are suitable for treatment with the compounds, composition and methods are described herein. In one aspect of the present invention, there is provided a method of treating a subject having a cancer deficient in NMT2, comprising: administering to said subject an NMT inhibitor.

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04-01-2018 дата публикации

COMPLEXES OF CELECOXIB AND ITS SALTS AND DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Номер: US20180000845A1
Принадлежит:

Disclosed herein are stable complexes with controlled particle size, increased apparent solubility and increased dissolution rate comprising as active compound Celecoxib, its salts, or derivatives thereof, which is useful in the treatment of osteoarthritis, rheumatoid arthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, acute pain especially in cancer related acute pain, primary dysmenorrhea. More specifically, the complexes possess instantaneous redispersibility, increased apparent solubility and permeability that provide faster onset of action for acute pain relief and lower GI related side effects. Further disclosed are methods of formulating and manufacturing the complexes described herein, pharmaceutical compositions, and uses and methods of treatment. 1. A stable complex comprising as active compound chosen from Celecoxib , its salts or derivatives thereof; and at least one complexation agent chosen from polyethylene glycol glycerides composed of mono- , di- and triglycerides and mono- and diesters of polyethylene glycol , hydroxypropylcellulose , poloxamers (copolymers of ethylene oxide and propylene oxide blocks) , vinylpyrrolidone/vinyl acetate copolymer , poly(2-ethyl-2-oxazoline) , polyvinylpyrrolidone , poly(maleic acid/methyl vinyl ether) , polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer , polyoxyl 15 hydroxystearate , ethylene oxide/propylene oxide tetra functional block copolymer , and d-alpha tocopheryl polyethylene glycol 1000 succinate; said complexes characterized in that it possesses at least one of the following properties:a. are instantaneously redispersable in physiological relevant mediab. are stable in solid form and in colloid solution and/or dispersion;c. have an apparent solubility in water of at least 1 mg/mL;{'sup': '−6', 'd. have a PAMPA permeability of at least 0.5×10cm/s when dispersed in FaSSIF or FeSSIF biorelevant media, which does not decrease in time at least for 1 month; and'}{'sup': '−6 ...

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03-01-2019 дата публикации

Combinations for the treatment of cancer

Номер: US20190000840A1
Принадлежит: Ignyta Inc

Described herein are combinations comprising a therapeutically effective amount of a first agent and a therapeutically effective amount of a second agent, wherein the first agent is an inhibitor of ALK, ROS1, TrkA, TrkB, or TrkC activity, or a combination thereof, and methods of using such combinations in the treatment of patients having cancer.

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03-01-2019 дата публикации

METHOD OF TREATING A BRAIN TUMOR

Номер: US20190000841A1
Автор: Huang Lan
Принадлежит:

Disclosed herein are methods of treating a brain tumor by administering Plinabulin. Some embodiments relate to treatment of glioblastoma multiforme by administering Plinabulin. 1. (canceled)2. A method of treating a brain tumor comprising administering an effective amount of plinabulin to a subject in need thereof , with the proviso that the brain tumor is not hemangiopericytoma.3. The method of claim 1 , wherein the cancer is selected from metastatic brain tumor claim 1 , anaplastic astrocytoma claim 1 , Central neurocytoma claim 1 , Choroid plexus carcinoma claim 1 , Choroid plexus papilloma claim 1 , Choroid plexus tumor claim 1 , Dysembryoplastic neuroepithelial tumor claim 1 , Ependymal tumor claim 1 , Fibrillary astrocytoma claim 1 , Giant-cell glioblastoma claim 1 , Glioblastoma multiforme claim 1 , Gliomatosis cerebri claim 1 , Gliosarcoma claim 1 , Medulloblastoma claim 1 , Medulloepithelioma claim 1 , Meningeal carcinomatosis claim 1 , Neuroblastoma claim 1 , Neurocytoma claim 1 , Oligoastrocytoma claim 1 , Oligodendroglioma claim 1 , Optic nerve sheath meningioma claim 1 , Pediatric ependymoma claim 1 , Pilocytic astrocytoma claim 1 , Pinealoblastoma claim 1 , Pineocytoma claim 1 , Pleomorphic anaplastic neuroblastoma claim 1 , Pleomorphic xanthoastrocytoma claim 1 , Primary central nervous system lymphoma claim 1 , Sphenoid wing meningioma claim 1 , Subependymal giant cell astrocytoma claim 1 , Subependymoma claim 1 , central nervous system myeloma claim 1 , and Trilateral retinoblastoma.4. The method of claim 1 , wherein the brain tumor is metastatic brain tumor claim 1 , anaplastic astrocytoma claim 1 , glioblastoma multiforme claim 1 , oligodendroglioma claim 1 , ependymomas claim 1 , or a combination thereof.5. The method of claim 1 , wherein the brain tumor is a glioblastoma multiforme.6. The method of claim 1 , wherein the brain tumor is a metastatic brain tumor.7. The method of claim 1 , further comprising administering an additional therapeutic ...

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