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filingDate 2010-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc81b4db96277f77aacae4d019aab990
publicationDate 2010-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010163457-A
titleOfInvention Unit dose FGF-2 effective for angiogenesis and methods of use
abstract Disclosed are pharmaceutical compositions and methods for inducing angiogenesis in a human heart. A unit dose composition comprising 0.2 μg / kg to 48 μg / kg of FGF-2 of SEQ ID NO: 2 or an angiogenic active fragment or an angiogenic active mutein thereof in a pharmaceutically acceptable carrier. object. Method for treating a human patient for coronary artery disease (recombinant FGF-2 or angiogenic active fragment thereof in one or more coronary arteries or one peripheral vein in a stable and angiogenic effective dose Or a step of administering an angiogenic activity mutein). The single unit dose composition provides an angiogenic effect in human CAD patients that lasts 6 months before re-treatment is required. A method of administration that optimizes patient safety (fluid, heparin and / or infusion rate all play a role). [Selection figure] None
priorityDate 1998-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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