The objective is to evaluate the safety of intravitreal Fovista® (anti-PDGF BB) administered in combination with anti-VEGF therapy.
The objective is to evaluate the safety of intravitreal Fovista® (anti-PDGF BB) administered in combination with anti-VEGF therapy in either a "Simultaneous" Regimen (Fovista® administered with anti-VEGF same day) or "Pre-Treatment" Regimen (monotherapy Fovista® Day 0 followed by Fovista® administered in combination with anti-VEGF Day 2).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
101
Unnamed facility
Phoenix, Arizona, United States
Unnamed facility
Beverly Hills, California, United States
Unnamed facility
Sacramento, California, United States
Number of Subject With Non Serious Adverse Events (Reported by >5% of Subjects)
Number of subjects on either arm with non-serious adverse events (reported by \>5% of subjects)
Time frame: 2 years
Number of Subjects With Serious Adverse Events
Number of subjects with serious adverse events in each arm
Time frame: 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Sacramento, California, United States
Unnamed facility
Santa Ana, California, United States
Unnamed facility
Augusta, Georgia, United States
Unnamed facility
Oak Forest, Illinois, United States
Unnamed facility
Boston, Massachusetts, United States
Unnamed facility
Jackson, Michigan, United States
Unnamed facility
Minneapolis, Minnesota, United States
...and 3 more locations