Table 1. Adverse event summary, study eye (year 3 safety population) (n (%)).

	All subjects who received active therapy for 3 years n = 161
Subjects with any adverse event	142 (88)
Subjects with an ocular adverse event	114 (71)
Injection-procedure related	84 (52)
Study-therapy related	19 (12)
Subjects with any serious adverse event	27 (17)
Subjects discontinuing due to an adverse event	5 (3)