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folinic acid/vėžys
Nuoroda įrašoma į mainų sritį
8 rezultatus
Method for treating tumors by the administration of tegafur, uracil, folinic acid, and cyclophosphamide
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FIELD OF THE INVENTION
The present invention is directed to the administration to a warm blooded animal including humans of the combination of tegafur, uracil, and folinic acid and its administration with cyclophosphamide for the treatment of tumors.
BACKGROUND OF THE INVENTION
5--Fluorouracil
Method for treating cancer using camptothecin derivatives and 5-fluorouracil
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This invention relates to an improved treatment for cancer comprising administering a combination of at least one camptothecin derivative and at least one other colorectal anticancer drug. More specifically, the invention relates to treatments for colorectal cancer comprising administering a
Method for treating cancer using camptothecin derivatives and 5-fluorouracil
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This invention relates to an improved treatment for cancer comprising administering a combination of at least one camptothecin derivative and at least one other colorectal anticancer drug. More specifically, the invention relates to treatments for colorectal cancer comprising administering a
Oral dosage form for administration of the combination of tegafur, uracil, folinic acid, and oxaliplatin and method of using the same
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FIELD OF THE INVENTION
The present invention is directed to an oral dosage form for administration to a warm blooded animal of the combination of tegafur, uracil, and folinic acid to potentiate coadministered oxaliplatin for the treatment of tumors.
BACKGROUND OF THE INVENTION
5-Fluorouracil (5-FU)
Compositions and methods for delivery of anti-cancer agents
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TECHNICAL FIELD
The present invention relates to pharmaceutical compositions for the treatment of cancer. In particular, the present invention relates to compositions comprising 5-fluorouracil, cyclodextrin and folinic acid and their use in the treatment of cancer.
BACKGROUND OF THE
SHMT inhibitors
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BACKGROUND OF THE DISCLOSURE
Serine catabolism is initiated by serine hydroxymethyltransferase (SHMT) activity, catalyzed in the cytosol by SHMT1 and in the mitochondria by SHMT2. SHMTs catalyze a reversible reaction converting serine to glycine, with concurrent methylene-tetrahydrofolate (THF)
Antitumor effect potentiator and antitumor agent
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CROSS REFERENCE TO RELATED APPLICATION
This application is a 35 USC .sctn.371 National Phase Entry Application from PCT/JP2004/003189, filed Mar. 11, 2004, and designating the U.S.
TECHNICAL FIELD
The present invention relates to an antitumor effect potentiator and an antitumor agent.
BACKGROUND
Antitumor effect potentiator and antitumor agent
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TECHNICAL FIELD
The present invention relates to an antitumor effect potentiator and an antitumor agent.
BACKGROUND ART
The research and development of antitumor agents has been actively pursued. A variety of effective antitumor agents are clinically used in the treatment of malignant tumors.
For
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