15
Participants
Start Date
August 31, 2004
Primary Completion Date
August 31, 2007
Study Completion Date
December 31, 2007
bevasiranib
bevasiranib
The first three patients enrolled will receive 0.1 mg Cand5 in the study eye, the next three patients enrolled will receive 0.33 mg Cand5 in the study eye, the following three patients enrolled will receive 1.0 mg Cand5 in the study eye, the following three patients enrolled will receive 1.5 mg Cand5 in the study eye, and the remaining three patients enrolled will receive 3.0 mg Cand5 in the study eye. The third patient enrolled at each dose level will complete their two-week visit before the next dose level group may be treated.
OPKO site, Morristown
OPKO Health, Inc.
INDUSTRY