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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0fc2a22a9271507062ad7e07974d3c58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_61f88efcda59d7062a4252ecf6886f58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K47-62
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-48
filingDate 1992-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3eebf55525633ddf08c4fec4ecf1a05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5119f1f6ee478dc27cc0c51d0109230
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec1e1137b0fb67d8a07d13deb85dbe1b
publicationDate 1993-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0565620-A1
titleOfInvention MITOTOXIN FOR TREATMENT OF VESSEL DAMAGE.
abstract Patients with vascular lesions caused by the use of a balloon catheter or the like are treated with drugs containing conjugates comprising a ligand such as fibroblast base growth factor (bFGF) (or another fibroblast growth factor polypeptide), and a cytotoxic agent. The cytotoxic agent may consist of a ribosome inactivation protein (RIP), such as saporin, and is attached to the ligand via a chemical bond or prepared as a DNA chimera of recombination. The drug containing the conjugate is administered intravenously to patients after they have been treated for atherosclerosis in a manner that frequently causes vascular damage, particularly to the intima, this drug effectively preventing restenosis . The ligand binds to and activates high affinity bFGF receptors, these receptors being surprisingly expressed on smooth muscle cells in the lumen of blood vessels, thereby allowing the cytotoxic agent to penetrate target cells and eventually destroy unwanted proliferating cells.
priorityDate 1991-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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