The objective of this study is to assess the safety and tolerability of topical ocular PAN-90806 in patients with proliferative diabetic retinopathy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Valley Retina Institute
Harlingen, Texas, United States
Valley Retina Institute
McAllen, Texas, United States
Number of Patients with Adverse Events
Safety will be assessed based upon the incidence of all adverse events, ocular and systemic
Time frame: 2 months
The mean change in best-corrected visual acuity from baseline
Time frame: Week 8
Change in preretinal neovascularization
descriptive observations of the presence and extent as determined by ultra-wide field fluorescein angiography (FA) and color fundus photography (FP)
Time frame: Week 4 and Week 8
The mean number of rescue treatments during the study
Time frame: Week 8
Time to first rescue treatment
Time frame: up to Week 8
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