Predicate |
Object |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-96444 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-2871 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5355 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y304-21006 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-444 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-727 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-6432 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-4846 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4412 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-437 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-04 |
filingDate |
2020-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate |
2022-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
JP-2022519327-A |
titleOfInvention |
Treatment method of intracranial hemorrhage and evaluation method of effect |
abstract |
The present disclosure relates to compositions and methods useful for assessing hemostatic effects in patients suffering from intracranial hemorrhage while receiving anticoagulant treatment with factor Xa (fXa) inhibitors. The method is an fXa derivative that has a reduced catalytic activity in the patient as compared to the wild-type fXa protein, has the ability to bind to the factor Xa inhibitor, and is unable to construct a prothrombinase complex. The anti-fXa activity reflects the hemostatic effect in the patient, including the administration of; obtaining a blood sample from the patient after administration; and measuring the anti-fXa activity in the sample. Once the above assessments have been made, appropriate medical interventions can be performed. |
priorityDate |
2019-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |