This study will evaluate the preliminary safety and efficacy of PDS 1.0 in patients with neovascular AMD.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Unnamed facility
Riga, Latvia
Change in retinal thickness measured by Optical Coherence Tomography
Time frame: Monthly
Change in Best Corrected Visual Acuity
Time frame: Monthly
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