http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-112020022429-A2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-13
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4245
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filingDate 2018-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2d1a651c3a125d4fad60e0ac475e63c
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publicationDate 2021-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112020022429-A2
titleOfInvention addition of s1p1 receptor agonist salt and crystalline form thereof and pharmaceutical composition
abstract the present invention relates to a salt form and a crystalline form of a 1- {2-fluoro-4- [5- (4-isobutylphenyl) -1,2,4-oxadiazol-3-yl] acid drug benzyl} -3-azetidinecarboxylic (formula a) for the treatment of a disease or symptom mediated by the s1p1 receptor. also described in the present invention are a method of preparing the salt form or the crystalline form, a pharmaceutical composition of the salt form or the crystalline form and the use of the salt form or the crystalline form in the preparation of a medicament for treatment and / or prevention of a disease or symptom mediated by the s1p1 receptor. (The).
priorityDate 2018-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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