http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-114012-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e1005fb53db203969fab84a916931d38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4ef33401e844e4f184c336b2c8325e17
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-17
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-04
filingDate 2018-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62c3b8ee9d52286f00e62b2041c9cd90
publicationDate 2020-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-114012-A1
titleOfInvention METHOD OF PROVIDING CELIPROLOL THERAPY TO A PATIENT
abstract This refers to the field of the treatment of an orphan disease, in particular the treatment of vascular Ehlers-Danlos syndrome (vEDS). More specifically, this relates to titre-up dosage regimens (eg, escalating dosage regimens) effective for treating vEDS patients with celiprolol. Claim 1: A method for treating vascular Ehlers-Danlos syndrome, which comprises administering to a patient in need thereof a daily dose of 80 to 100 mg of celiprolol, or an equivalent amount of a pharmaceutically acceptable salt thereof, and increasing the daily dose up to 360 to 440 mg within six months.
priorityDate 2017-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419553031
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2663

Total number of triples: 16.