Evaluating Abicipar for Safety and Treatment Effect in Patients With Neovascular Age-related Macular Degeneration (AMD)
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 50 - Any |
Updated: | 4/6/2019 |
Start Date: | May 23, 2018 |
End Date: | March 20, 2019 |
The objective of this study is to evaluate abicipar for safety and treatment effect in
patients with neovascular Age-related Macular Degeneration (AMD).
patients with neovascular Age-related Macular Degeneration (AMD).
Inclusion Criteria:
- Male or female patients, 50 years of age or older at the time of informed consent
- BCVA ≤ 78 and ≥ 24 letters (20/32 to 20/320 Snellen equivalents, respectively) at
screening and at baseline (Day 1, prior to treatment) visits in the study eye
- BCVA of 34 letters (Snellen equivalent 20/200) or better at baseline (Day 1, prior to
treatment) in the non-study eye
Exclusion Criteria:
- Active periocular, ocular, or intraocular infection at baseline (Day 1) (either eye)
- Previous or concurrent macular laser treatment ( study eye)
- Cataract or refractive surgery within 3 months prior to baseline ( study eye)
We found this trial at
39
sites
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