Open Label Study for the Evaluation of Tolerability of Five Dose Levels of Cand5

PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

August 31, 2004

Primary Completion Date

August 31, 2007

Study Completion Date

December 31, 2007

Conditions
Macular Degeneration
Interventions
DRUG

bevasiranib

DRUG

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.

Trial Locations (1)

Unknown

OPKO site, Morristown

All Listed Sponsors
lead

OPKO Health, Inc.

INDUSTRY

NCT00722384 - Open Label Study for the Evaluation of Tolerability of Five Dose Levels of Cand5 | Biotech Hunter | Biotech Hunter