摘要:
The present invention is directed to modulators of eosinophilic and neutrophilic function and the use of such modulators for treatment of eosinophil-associated and neutrophil-associated diseases.
摘要:
The present invention provides a multi-layer tablet comprising: an effervescent layer comprising hydrochlorothiazide or amlodipine or its salt as an active ingredient, a carbonate salt, and an organic acid; and a telmisartan-containing layer.
摘要:
Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung einer Valsartan enthaltenden Tablette sowie ein Wirkstoffgranulat, das ausschließlich aus Valsartan oder einem pharmazeutisch verträglichen Salz davon und gegebenenfalls einem anderen Wirkstoff besteht, und dessen Verwendung in der Herstellung der Tablette.
摘要:
The invention comprises pharmaceutical compositions for the treatment of neuropathic pain, e.g. that associated with neuralgia, dystrophy or phantom limb pain. The pharmaceutical composition comprises cardiac glycosides and/or diuretics and is preferably topically applied in e.g. a gel. The invention also comprises methods of manufacturing such compositions.
摘要:
The present invention relates to the use of a potassium channel activator in the manufacture of a medicament for suppressing the fasting plasma insulin leveland/or postabsorptive insulin level in a mammal in need thereof, wherein the fasting and/or postabsorptive plasma insulin level is reduced to about 5 mU/1 or less. The present invention also relates to the use ofa potassium channel activator in the manufacture of a medicament for suppressing the fasting plasma insulin level and/or postabsorptive insulin level in a mammal in need thereof for treating or preventing obesity, obesity related disorders and conditions and other disorders and conditions related to weight gain in a mammal in need thereof,said method comprising orally administering to said mammal in need thereofa daily dosage of about 5 mg to about 1200 mg, calculated on a Diazoxide active weight basis.
摘要:
A selective ETA receptor antagonist for use in a method for enhancing glycemic control and/or insulin sensitivity in a human subject having diabetic nephropathy and/or metabolic syndrome is disclosed. A selective ETA receptor antagonist for use in treating a complex of comorbidities in an elderly diabetic human subject, wherein the selective ETA receptor antagonist is for administration in combination or as adjunctive therapy with (a) at least one additional agent that is (i) other than a selective ETA receptor antagonist and (ii) effective in treatment of diabetes and/or at least one of said comorbidities other than hypertension, and optionally (b) at least one antihypertensive other than a selective ETA receptor antagonist is disclosed. Further, a therapeutic combination comprising a selective ETA receptor antagonist and at least one antidiabetic, anti-obesity or antidyslipidemic agent other than a selective ETA receptor antagonist is disclosed.
摘要:
This application describes compositions, methods of treatment, and methods of manufacturing a medicament for reducing injury or damage to cells, tissues or organs during ischemia, reperfusion, or following ischemia or trauma. The methods for reducing damage to a cell, tissue or organ comprise administering an effective amount of a composition including (i) a potassium channel opener or agonist and/or adenosine receptor agonist; and (ii) an antiarrhythmic agent. The methods may further include postconditioning the cell, tissue or organ.
摘要:
Compounds of formula I active on protein kinases are described, as well as methods of using such compounds to treat diseases and conditions associated with aberrant activity of protein kinases. Formula (I) wherein Ar is optionally substituted heteroaryl; R 2 is hydrogen, lower alkyl or halogen; U is selected from the group consisting of -S(O) 2 -, -C(X)-, -C(X)-N(R 10 )-, and -S(O) 2 -N(R 10 )-; R 3 is optionally substituted lower alkyl, optionally substituted C3.6 cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl or optionally substituted heteroaryl; and wherein R 1 , R 3 , R 4 , m, L 1 , X R 10 are as described herein.