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filingDate 1998-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_873886cdbf5f7793aab0acda1acbe841
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publicationDate 1998-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9857648-A1
titleOfInvention Methods of increasing the bioavailability of stable crystal polymorphs of a compound
abstract The present invention relates to methods of increasing the bioavailability of the most stable crystalline form of a compound. The invention also relates to particles of the most stable crystalline form of a compound having an average particle size of less than 400 nm. The invention further relates to pharmaceutical compositions comprising these particles and the use of such pharmaceutical compositions for treating diseases, such as HIV.
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