摘要 |
<p>The present invention provides, among other things, methods and compositions for treating muscular dystrophy, in particular, Duchenne muscular dystrophy (DMD). In some embodiments, a method according to the present invention includes administering to an individual who is suffering from or susceptible to DMD an effective amount of an anti-Flt-1 antibody, or antigen binding fragment thereof, such that at least one symptom or feature of DMD is reduced in intensity, severity, or frequency, or has delayed onset.</p> |
申请人 |
REGENTS OF THE UNIVERSITY OF MINNESOTA;SHIRE HUMAN GENETIC THERAPIES, INC. |
发明人 |
JOSIAH, SERENE;LUBY, THOMAS M.;ASAKURA, ATSUSHI;KEEFE, DENNIS;CHARNAS, LAWRENCE |