FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to pharmaceutics, particularly to solid pharmaceutical compositions for the immune system suppression and multiple sclerosis treatment. The pharmaceutical composition exhibiting improved flowability contains a S1P receptor modulator representing 2-amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol or a pharmaceutically acceptable salt thereof, lactulose, polyethylene glycol-6000 and polyvinylpyrrolidone. What is also described is a drug preparation containing 2- amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol or a pharmaceutically acceptable salt thereof, in the form of a tablet or capsule, placed in pharmaceutically acceptable package, and a method for preparing the drug preparation for oral administration.
EFFECT: invention provides a uniform distribution of the active ingredient in the solid composition, high stability and improved flowability of the solid pharmaceutical composition; the improved flowability of the composition presented in the invention enables using the same on automated equipment.
15 cl, 1 tbl, 4 ex
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Authors
Dates
2013-10-27—Published
2012-07-11—Filed