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filingDate 2003-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_006143ee1c27aabcebbf01f8eacbe355
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9fd673b79554c7c10e86453a7c18f3bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0847e511f9808b3bbc892d4dabb17efd
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publicationDate 2004-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004057953-A1
titleOfInvention Modified peptides as therapeutic agents
abstract The present invention concerns fusion of Fc domains with biologically active peptides and a process for preparing pharmaceutical agents using biologically active peptides. In this invention, pharmacologically active compounds are prepared by a process comprising: n a) selecting at least one peptide that modulates the activity of a protein of interest; and n b) preparing a pharmacologic agent comprising an Fc domain covalently linked to at least one amino acid of the selected peptide. n Linkage to the vehicle increases the half-life of the peptide, which otherwise would be quickly degraded in vivo. The preferred vehicle is an Fc domain. The peptide is preferably selected by phage display, E. coli display, ribosome display, RNA-peptide screening, or chemical-peptide screening.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008131431-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2275816-A2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010239579-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8377448-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2322931-A2
priorityDate 1998-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 2702.