| 摘要 |
<p><P>PROBLEM TO BE SOLVED: To provide an effective treating method by which the defects in conventional functional therapy, medicament therapy and blood circulation-repairing technique, and recently proposed gene therapy, intramuscular transplantation of a myeloid cell, and the like, for obstructive arteriosclerosis can be solved. <P>SOLUTION: The subject therapeutic drug effective for ischemic disease contains a human granulocyte colony-stimulating factor (human G-CSF) as an active ingredient. The therapeutic agent can be the one for the ischemic disease such as ischemic cerebrovascular disease and ischemic heart disease. <P>COPYRIGHT: (C)2006,JPO&NCIPI</p> |
