A Study of Abicipar Pegol in Patients With Neovascular Age-related Macular Degeneration
Completed · Phase 2 · Has a placebo group
Conditions studied: Macular Degeneration
In brief
This is a safety and efficacy study of abicipar pegol in patients with neovascular age-related macular degeneration to establish comparability between Japanese and non-Japanese.
Key facts
- Study ID
- NCT02181517
- Run by
- Allergan
- People needed
- 25
- Starts
- 2014-07-01
- Expected to finish
- 2015-03-01
- Last updated by the study team
- 2016-05-17
Who can join
Age: 50 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of wet age-related macular degeneration in at least 1 eye
- Best corrected visual acuity of 20/32 to 20/320 in the study eye and 20/200 or better in the fellow eye
You may not qualify if…
- Hypersensitivity, allergy, or anaphylactic reaction to iodine
- Cataract or refractive surgery within the last 3 months
- History of vitrectomy
Where it is running
- Study site — Phoenix, Arizona, United States
Full record on ClinicalTrials.gov
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