BACKGROUND
Conventional treatments for cancer, such as chemotherapy and radiation therapy, can be used to selectively kill rapidly dividing cancer cells in the body. Conventional treatments, however, exhibit poor target specificity. The efficacy of chemotherapy, for example, is hindered, because
FIELD OF INVENTION
The invention provides stable pharmaceutical compositions comprising tumor necrosis factor receptor Fc fusion protein (TNFR:Fc). The invention also provides methods of manufacturing the composition, method of administration and kits containing the same.
BACKGROUND OF
FIELD OF THE INVENTION
The present disclosure relates to methods for the detection and quantization of urinary polyamines and compositions for use therein. The methods and compositions described herein are useful in diagnosis of prostate cancer in patient.
BACKGROUND OF THE INVENTION
Prostate cancer
FIELD OF THE INVENTION
The present invention relates to compositions comprising inhibitors of ATP citrate lyase and/or tricarboxylate transporter and methods of using such compositions to treat individuals who have been diagnosed with cancer.
BACKGROUND OF THE INVENTION
Each year, more than one
CROSS REFERENCE TO RELATED APPLICATIONS
This is a national stage application based on PCT/JP2012/076020, filed on Oct. 5, 2012, which claims priority to Japanese Patent Application Nos. 2011-225383, filed on Oct. 12, 2011, and 2012-081346, filed on Mar. 30, 2012. This application claims the priority
BACKGROUND OF THE INVENTION
The leading cause of pulmonary and cerebral embolism is thrombophlebitis. Thromboembolism is caused by abnormalities of the blood vessel, the blood or the circulation resulting the formation of blood clots called thrombi. Within a short period of time, many of these blood
TECHNICAL FIELD
This invention relates generally to the chemical synthesis of steroids, and more particularly relates to the synthesis of anti-estrogenic and other therapeutic steroids such as 3-hydroxy-7.alpha.-methyl-21-[2'-methoxy-4'-(diethylaminomethyl)-phenoxy]- -19-norpregna-1,3,5(10)triene
TECHNICAL FIELD
This invention relates generally to the chemical synthesis of steroids, and more particularly relates to the synthesis of anti-estrogenic and other therapeutic steroids such as 3-hydroxy-7.alpha.-methyl-21-[2'-methoxy-4'-(diethylaminomethyl)-phenoxy]- 19-norpregna-1,3,5(10)triene
BACKGROUND OF THE INVENTION
The present invention relates to novel ruthenium labeled transferrin compounds, methods for preparing and purifying them, and their uses in nuclear medicine as a diagnostic tool, as well as possible uses in the treatment of tumors and abscesses.
The prior art discloses
BACKGROUND OF THE INVENTION
The present invention relates to a method for differentiating the source of occult gastrointestinal bleeding.
The common screening test for occult gastrointestinal bleeding is to test for fecal occult blood (FOB). An FOB test involves placing a sample of stool onto a
BACKGROUND OF THE INVENTION
Field of the Invention
This invention relates to a use of micronutrient formulations to reduce the effects of radiation on humans.
Description of the Related Art
Ionizing radiation (X-rays and gamma rays) has proven to be a double-edged sword in clinical Medicine since
TECHNICAL FIELD
This invention relates to combinations comprising (or consisting essentially of) one or more compounds of the formula (I') or (I) as defined herein (so including one or more specific salts of the compound 1-cyclopropyl-3-[3-(5-morpholin-4-ylmethyl-1H-benzoimidazol-2-yl)-1H-pyra-
FIELD OF THE INVENTION
The present invention relates to crystalline forms of citrate salts of N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-- 3-yl}phenyl)-N'-(3-fluorophenyl)urea, processes for preparing the crystalline forms, pharmaceutical formulations thereof, and
FIELD OF THE INVENTION
The present invention relates to crystalline forms of citrate salts of N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-- 3-yl}phenyl)-N'-(3-fluorophenyl)urea, processes for preparing the crystalline forms, pharmaceutical formulations thereof, and
BACKGROUND OF THE INVENTION
This invention relates to salt forms of 3-(4-bromo-2,6-difluoro-benzyloxy)-5-[3-(4-pyrrolidin-1-yl-butyl)-ureido]- isothiazole-4-carboxylic acid amide having the formula: ##STR2##
Formula I in its free base form is described in co-pending U.S. Ser. No. 09/316,837, filed
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