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filingDate 2002-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aaa1a7ffd588d0f71760e0d006bc5668
publicationDate 2004-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004258755-A1
titleOfInvention Freeze-dried pharmaceutical preparation
abstract For clinical application of cis[((1R,2R)-1,2-cyclohexanediamine-N,N′)bis(R 1 )]platinum(II) (R 1 is an alkanoyloxy group having 6 to 20 carbon atoms), the present invention aims at providing a formulation which prevents layer separation and changes in viscosity, shows fine suspendability, and which is easy to handle during administration. The formulation of the present invention is a lyophilized formulation for injection obtained by dissolving a cis[((1R,2R)-1,2-cyclohexanediamine-N,N′)bis(R 1 )]platinum(II) in 2 -methyl- 2 -propanol and lyophilizing this solution, which has a central particle size distribution of around 3-25 μm and a D90% value of not more than 40 μm.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2017080113-A1
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type http://data.epo.org/linked-data/def/patent/Publication

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