Open-Label Study of Intravitreal ICON-1 in Patients With Choroidal Neovascularization Secondary to Age-related Macular Degeneration (AMD)



Status:Active, not recruiting
Conditions:Cardiology, Ocular
Therapuetic Areas:Cardiology / Vascular Diseases, Ophthalmology
Healthy:No
Age Range:50 - Any
Updated:11/10/2018
Start Date:March 26, 2018
End Date:June 2019

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A Phase 2 Randomized, Open-Label, Multicenter Study Evaluating Administration of Repeated Intravitreal Doses of ICON-1 in Patients With Choroidal Neovascularization Secondary to Age-related Macular Degeneration

The purpose of this study is to evaluate the safety and effects of repeated intravitreal
injections of ICON-1 0.6 mg administered as maintenance therapy or in combination with
aflibercept in patients with wet macular degeneration.


Inclusion Criteria:

- Males or females of any race, ≥50 years of age

- Active primary CNV secondary to AMD in the study eye

Exclusion Criteria:

- Any prior treatment of CNV or advanced AMD in the study eye, except for dietary
supplements or vitamins

- Any intraocular or ocular surface surgery (including cataract surgery and laser
procedures) in the study eye within 3 months

- Vitrectomy in the study eye
We found this trial at
8
sites
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Philadelphia, PA
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Ashland, OR
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Austin, TX
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Beverly Hills, California 90211
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from
Beverly Hills, CA
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McAllen, TX
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San Antonio, TX
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Santa Ana, CA
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Syracuse, NY
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